1,386 results on '"Tiseo, Marcello"'
Search Results
352. Syndrome of inappropriate anti-diuretic hormone secretion in cancer patients: results of the first multicenter Italian study
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Berardi, Rossana, primary, Mastroianni, Candida, additional, Lo Russo, Giuseppe, additional, Buosi, Roberta, additional, Santini, Daniele, additional, Montanino, Agnese, additional, Carnaghi, Carlo, additional, Tiseo, Marcello, additional, Chiari, Rita, additional, Camerini, Andrea, additional, Barni, Sandro, additional, De Marino, Valeria, additional, Ferrari, Daris, additional, Cristofano, Antonella, additional, Doni, Laura, additional, Freddari, Federica, additional, Fumagalli, Daniele, additional, Portalone, Luigi, additional, Sarmiento, Roberta, additional, Schinzari, Giovanni, additional, Sperandi, Francesca, additional, Tucci, Marcello, additional, Inno, Alessandro, additional, Ciuffreda, Libero, additional, Mariotti, Marita, additional, Mariani, Cinzia, additional, Caramanti, Miriam, additional, Torniai, Mariangela, additional, Gallucci, Rosaria, additional, Bennati, Chiara, additional, Bordi, Paola, additional, Buffoni, Lucio, additional, Galeassi, Achille, additional, Ghidini, Michele, additional, Grossi, Emidio, additional, Morabito, Alessandro, additional, Vincenzi, Bruno, additional, and Arvat, Emanuela, additional
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- 2019
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353. Trastuzumab Emtansine (T-DM1) in Patients with Previously Treated HER2-Overexpressing Metastatic Non–Small Cell Lung Cancer: Efficacy, Safety, and Biomarkers
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Peters, Solange, primary, Stahel, Rolf, additional, Bubendorf, Lukas, additional, Bonomi, Philip, additional, Villegas, Augusto, additional, Kowalski, Dariusz M., additional, Baik, Christina S., additional, Isla, Dolores, additional, Carpeno, Javier De Castro, additional, Garrido, Pilar, additional, Rittmeyer, Achim, additional, Tiseo, Marcello, additional, Meyenberg, Christoph, additional, de Haas, Sanne, additional, Lam, Lisa H., additional, Lu, Michael W., additional, and Stinchcombe, Thomas E., additional
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- 2019
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354. Metabolism of the EGFR tyrosin kinase inhibitor gefitinib by cytochrome P450 1A1 enzyme in EGFR-wild type non small cell lung cancer cell lines
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Alfieri Roberta R, Galetti Maricla, Tramonti Stefano, Andreoli Roberta, Mozzoni Paola, Cavazzoni Andrea, Bonelli Mara, Fumarola Claudia, La Monica Silvia, Galvani Elena, De Palma Giuseppe, Mutti Antonio, Mor Marco, Tiseo Marcello, Mari Ettore, Ardizzoni Andrea, and Petronini Pier
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Lung cancer ,EGFR ,gefitinib ,metabolism ,CYP1A1 ,Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,RC254-282 - Abstract
Abstract Background Gefitinib is a tyrosine kinase inhibitor (TKI) of the epidermal growth factor receptor (EGFR) especially effective in tumors with activating EGFR gene mutations while EGFR wild-type non small cell lung cancer (NSCLC) patients at present do not benefit from this treatment. The primary site of gefitinib metabolism is the liver, nevertheless tumor cell metabolism can significantly affect treatment effectiveness. Results In this study, we investigated the intracellular metabolism of gefitinib in a panel of EGFR wild-type gefitinib-sensitive and -resistant NSCLC cell lines, assessing the role of cytochrome P450 1A1 (CYP1A1) inhibition on gefitinib efficacy. Our results indicate that there is a significant difference in drug metabolism between gefitinib-sensitive and -resistant cell lines. Unexpectedly, only sensitive cells metabolized gefitinib, producing metabolites which were detected both inside and outside the cells. As a consequence of gefitinib metabolism, the intracellular level of gefitinib was markedly reduced after 12-24 h of treatment. Consistent with this observation, RT-PCR analysis and EROD assay showed that mRNA and activity of CYP1A1 were present at significant levels and were induced by gefitinib only in sensitive cells. Gefitinib metabolism was elevated in crowded cells, stimulated by exposure to cigarette smoke extract and prevented by hypoxic condition. It is worth noting that the metabolism of gefitinib in the sensitive cells is a consequence and not the cause of drug responsiveness, indeed treatment with a CYP1A1 inhibitor increased the efficacy of the drug because it prevented the fall in intracellular gefitinib level and significantly enhanced the inhibition of EGFR autophosphorylation, MAPK and PI3K/AKT/mTOR signalling pathways and cell proliferation. Conclusion Our findings suggest that gefitinib metabolism in lung cancer cells, elicited by CYP1A1 activity, might represent an early assessment of gefitinib responsiveness in NSCLC cells lacking activating mutations. On the other hand, in metabolizing cells, the inhibition of CYP1A1 might lead to increased local exposure to the active drug and thus increase gefitinib potency.
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- 2011
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355. Maintenance therapy in NSCLC: why? To whom? Which agent?
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Maione Paolo, Garassino Marina, Di Maio Massimo, Cortinovis Diego, Banna Giuseppe, Tiseo Marcello, Milella Michele, Novello Silvia, Martelli Olga, Vavalà Tiziana, and Bria Emilio
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Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,RC254-282 - Abstract
Abstract Maintenance therapy is emerging as a treatment strategy in the management of advanced non small cell lung cancer (NSCLC). Initial trials addressing the question of duration of combination chemotherapy failed to show any overall survival benefit for the prolonged administration over a fixed number of cycles with an increased risk for cumulative toxicity. Nowadays several agents with different ways of administration and a different pattern of toxicity have been formally investigated in the maintenance setting. Maintenance strategies include continuing with an agent already present in the induction regimen or switching to a different one. Taking into consideration that no comparative trials of maintenance with different chemotherapy drugs or targeted agents have been conducted, the choice and the duration of maintenance agents is largely empirical. Furthermore, it is still unknown and it remains an open question if this approach needs to be proposed to every patient in the case of partial/complete response or stable disease after the induction therapy. Here, we critically review available data on maintenance treatment, discussing the possibility to tailor the right treatment to the right patient, in an attempt to optimize costs and benefits of an ever-growing panel of different treatment options.
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- 2011
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356. PD-L1 SNPs as biomarkers to define benefit in patients with advanced NSCLC treated with immune checkpoint inhibitors
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Minari, Roberta, Bonatti, Francesco, Mazzaschi, Giulia, Dodi, Alessandra, Facchinetti, Francesco, Gelsomino, Francesco, Cinquegrani, Gloria, Squadrilli, Anna, Bordi, Paola, Buti, Sebastiano, Bersanelli, Melissa, Leonetti, Alessandro, Cosenza, Agnese, Ferri, Leonarda, Rapacchi, Elena, Quaini, Federico, Ardizzoni, Andrea, and Tiseo, Marcello
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Objective: To investigate the role of CTLA-4, PD-1(programmed death-1), and PD-L1(programmed death-ligand 1) single nucleotide polymorphisms (SNPs) in predicting clinical outcome of patients with advanced non-small cell lung cancer (NSCLC) treated with immune checkpoint inhibitors (ICIs).Methods: A total of 166 consecutive patients were included. We correlated SNPs with clinical benefit, progression-free survival, time to treatment failure, and overall survival and evaluated the incidence of SNPs in nonresponder and long clinical benefit groups.Results: Considering the entire cohort, no correlation was found between SNPs and clinical outcome; however, PD-L1rs4143815 SNP and the long clinical benefit group showed a statistically significant association (p= 0.02). The nonresponder cohort displayed distinctive PD-L1haplotype (p= 0.05).Conclusion: PD-L1SNPs seem to be marginally involved in predicting clinical outcome of NSCLC treated with ICI, but further investigations are required.
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- 2022
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357. Validation of a radiomic approach to decipher NSCLC immune microenvironment in surgically resected patients
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Trentini, Francesca, Mazzaschi, Giulia, Milanese, Gianluca, Pavone, Claudio, Madeddu, Denise, Gnetti, Letizia, Frati, Caterina, Lorusso, Bruno, Lagrasta, Costanza Anna Maria, Minari, Roberta, Ampollini, Luca, Ledda, Roberta Eufrasia, Silva, Mario, Sverzellati, Nicola, Quaini, Federico, Roti, Giovanni, and Tiseo, Marcello
- Abstract
Radiomics has emerged as a noninvasive tool endowed with the potential to intercept tumor characteristics thereby predicting clinical outcome. In a recent study on resected non-small cell lung cancer (NSCLC), we identified highly prognostic computed tomography (CT) -derived radiomic features (RFs), which in turn were able to discriminate hot from cold tumor immune microenvironment (TIME). We aimed at validating a radiomic model capable of dissecting specific TIME profiles bearing prognostic power in resected NSCLC. The validation cohort included 31 radically resected NSCLCs clinicopathologically matched with the training set (n = 69). TIME was classified in hot and cold according to a multiparametric immunohistochemical analysis involving PD-L1 score and incidence of immune effector phenotypes among tumor infiltrating lymphocytes (TILs). High- throughput radiomic features (n = 841) extracted from CT images were correlated to TIME parameters to ultimately define prognostic classes. We confirmed PD-1 to CD8 ratio as best predictor of clinical outcome among TIME characteristics. Significantly prolonged overall survival (OS) was observed in patients carrying hot (median OS not reached) vs cold (median OS 22 months; hazard ratio 0.28, 95% confidence interval 0.09 -0.82; p = 0.015) immune background, thus validating the prognostic impact of these two TIME categories in resected NSCLC. Importantly, in the validation setting, three out of eight previously identified RFs sharply distinguishing hot from cold TIME were endorsed. Among signature-related RFs, Wavelet-HHH_gldm_HighGrayLevelEmphasis highly performed as descriptor of hot immune contexture (area under the receiver operating characteristic curve 0.94, 95% confidence interval 0.81 -1.00; p = 0.01). Based on our findings, Radiomics may decipher specific TIME profiles providing a noninvasive prognostic approach in resected NSCLC and an exploitable predictive strategy in advanced cases.
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- 2022
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358. The role of miRNA-221 and miRNA-126 in patients with benign metastasizing leiomyoma of the lung: an overview with new interesting scenarios.
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Ventura, Luigi, Gnetti, Letizia, Rossi, Maurizio, Tiseo, Marcello, Giordano, Giovanna, Corradi, Massimo, Silva, Mario, Milanese, Gianluca, Minari, Roberta, Leonetti, Alessandro, Cattadori, Sara, Ampollini, Luca, Carbognani, Paolo, and Mozzoni, Paola
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Benign metastasizing leiomyoma (BML) is a rare disease characterized by extrauterine benign leiomyomatosis in patients with a previous or concomitant history of uterine leiomyoma. Currently, there are no specific criteria to predict the metastasizing ability of the uterine leiomyoma and the risk of malignant degeneration of pulmonary BML, and these are the aims of this study. We analyzed 10 uterine (three leiomyomas, four leiomyomas that gave rise to lung BML, three healthy tissues) and 11 pulmonary tissue samples (eight lung BML, three healthy tissues). Interestingly, one of the BML lesions exceptionally evolved into a leiomyosarcoma (case 2). Uterine leiomyoma microvascular density (MVD) was higher in the patients with uterine leiomyomas that gave rise to lung BML, reaching a peak in case 2. Strong positivity for the estrogen (ER) and progesterone (PR) receptors and a low proliferation index (Ki67 < 1%) were discovered both in patients with uterine leiomyoma and in patients with BML. Interestingly, in case 2, the last dedifferentiated leiomyosarcoma showed a weaker ER and PR positivity with a higher proliferation index (Ki67:30%). Regarding the uterine miRNA-126, a trend toward a hypo-expression between uterine leiomyoma and uterine leiomyoma that gave rise to lung BML was discovered, reaching the lowest level in case 2. Considering the pulmonary samples, we observed a higher miRNA-221 and a lower miRNA-126 expression in the leiomyosarcoma. We tried to better elucidate the biological behaviour of this rare disease. The analysis of the miRNA-221 and miRNA-126 could offer new diagnostic, prognostic and therapeutic perspectives. [ABSTRACT FROM AUTHOR]
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- 2021
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359. P3.02a-013 Brigatinib in Crizotinib-Refractory ALK+ NSCLC: Central Assessment and Updates from ALTA, a Pivotal Randomized Phase 2 Trial: Topic: ALK Clinical
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Camidge, D. Ross, Tiseo, Marcello, Ahn, Myung-Ju, Reckamp, Karen, Hansen, Karin, Kim, Sang-We, Huber, Rudolf, West, Howard, Groen, Harry, Hochmair, Maximilian, Leighl, Natasha, Gettinger, Scott, Langer, Corey, Paz-Ares, Luis, Smit, Egbert, Kim, Edward, Reichmann, William, Clackson, Tim, Kerstein, David, Haluska, Frank, and Kim, Dong-Wan
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- 2017
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360. Isolation of circulating lung tumour cells using a non-EpCAM-based capture method
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Bozzetti, Cecilia, Cavazzoni, Andrea, Carubbi, Cecilia, Mirandola, Prisco, Tiseo, Marcello, Petronini, Pier Giorgio, and Ardizzoni, Andrea
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- 2012
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361. Pneumothorax and pulmonary hemorrhage after CT-guided lung biopsy: incidence, clinical significance and correlation.
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Sabatino, Vittorio, Russo, Umberto, D'Amuri, Fabiano, Bevilacqua, Andrea, Pagnini, Francesco, Milanese, Gianluca, Gentili, Francesco, Nizzoli, Rita, Tiseo, Marcello, Pedrazzi, Giuseppe, and De Filippo, Massimo
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Objectives: To evaluate the incidence and clinical significance of pneumothorax (PTX) and pulmonary hemorrhage (PH) after CT-guided lung biopsy (CT-LB). To test correlations of PTX and chest tube insertion (CTI) with PH and other imaging and procedural parameters. Methods: Pre-procedural CT and CT-LB scans of 904 patients were examined. Incidence of PTX and PH and PH location (type-1 along needle track; type-2 perilesional) and severity according to its thickness (low grade < 6 mm; high grade > 6 mm) were recorded. PTX was considered clinically significant if treated with CTI, PH if treated with endoscopic/endovascular procedure. Binary logistic regression analyses were used to determine the effects of different imaging and procedural parameters on the likelihood to develop PTX, CTI and PH and to define their correlation. Results: PTX occurred in 306/904 cases (33.8%); CTI was required in 18/306 (5.9%). PH occurred in 296/904 cases (32.7%), and no case required treatment. Nodule-to-pleura distance (OR
PTX = 1.052; ORCTI = 1.046; ORPH 1.077), emphysema (ORPTX = 1.287; ORPH = 0.573), procedure time (ORPTX = 1.019; ORCTI = 1.039; ORPH = 1.019), target size (ORPTX = 0.982; ORPH = 0.968) and needle gauge (ORPTX = 0.487; ORCTI = 4.311; ORPH = 2.070) showed statistically significant correlation to PTX, CTI and PH. Type-1 PH showed a protective effect against PTX and CTI (ORPTX = 0.503; ORCTI = 0.416). Conclusion: PTX and PH have similar incidence after CT-guided lung biopsy. PH along needle track may represent a protective factor against development of PTX and against PTX requiring CTI. [ABSTRACT FROM AUTHOR]- Published
- 2021
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362. Final analysis of first-line chemo-immunotherapy in patients with advanced lung adenocarcinoma: an Italian real-world study.
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Tiseo, Marcello
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ADENOCARCINOMA ,IMMUNOTHERAPY ,TREATMENT effectiveness ,CANCER chemotherapy ,LUNG cancer ,TUMOR classification - Published
- 2023
363. Detection of ROS1 rearrangement in non-small cell lung cancer: current and future perspectives
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Rossi,Giulio, Jocollé,Genny, Conti,Antonia, Tiseo,Marcello, Zito Marino,Federica, Donati,Giovanni, Franco,Renato, Bono,Francesca, Barbisan,Francesca, and Facchinetti,Francesco
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Targets and Therapy [Lung Cancer] - Abstract
Giulio Rossi,1 Genny Jocollé,2 Antonia Conti,3 Marcello Tiseo,4 Federica Zito Marino,5,6 Giovanni Donati,7 Renato Franco,5,6 Francesca Bono,8 Francesca Barbisan,9 Francesco Facchinetti4,10 1Pathology Unit, 2Oncology Unit, Azienda USL Valle d’Aosta, Regional Hospital “Parini”, Aosta, 3Medical Illustrator, Riccione, 4Medical Oncology Unit, University Hospital of Parma, Parma, 5Pathology Unit, Istituto Nazionale Tumori Fondazione G. Pascale, 6Pathology Unit, Luigi Vanvitelli University of Campania, Naples, 7Unit of Thoracic and Senology Surgery, Azienda USL Valle d’Aosta, Regional Hospital “Parini”, Aosta, 8Unit of Pathologic Anatomy, San Gerardo Hospital, IRCCS, Monza, 9Pathology Unit, University Hospital, Azienda Ospedali Riuniti, Ancona, Italy; 10INSERM, U981, Gustave Roussy Cancer Campus, Villejuif, France Abstract: ROS1 rearrangement characterizes a small subset (1%–2%) of non-small cell lung cancer and is associated with slight/never smoking patients and adenocarcinoma histology. Identification of ROS1 rearrangement is mandatory to permit targeted therapy with specific inhibitors, demonstrating a significantly better survival when compared with conventional chemotherapy. Detection of ROS1 rearrangement is based on in situ (immunohistochemistry, fluorescence in situ hybridization) and extractive non-in situ assays. While fluorescence in situ hybridization still represents the gold standard in clinical trials, this technique may fail to recognize rearrangements of ROS1 with some gene fusion partner. On the other hand, immunohistochemistry is the most cost-effective screening technique, but it seems to be characterized by low specificity. Extractive molecular assays are expensive and laborious methods, but they specifically recognize almost all ROS1 fusions using a limited amount of mRNA even from formalin-fixed, paraffin-embedded tumor tissues. This review is a discussion on the present and futuristic diagnostic scenario of ROS1 identification in lung cancer. Keywords: lung, adenocarcinoma, ROS1, FISH, immunohistochemistry, NGS, rearrangement
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- 2017
364. Semiautomatic analysis on computed tomography in locally advanced or metastatic non-small cell lung cancer
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Colombi, Davide, Manna, Carmelinda, Montermini, Ilaria, Seletti, Valeria, Tiseo, Marcello, Fontana, Elisa, De Filippo, Massimo, Silva, Mario, Sverzellati, Nicola, DICIOTTI, STEFANO, Colombi, Davide, Manna, Carmelinda, Montermini, Ilaria, Seletti, Valeria, Diciotti, Stefano, Tiseo, Marcello, Fontana, Elisa, De Filippo, Massimo, Silva, Mario, and Sverzellati, Nicola
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Pulmonary and Respiratory Medicine ,Radiology, Nuclear Medicine and Imaging ,tumor volume ,multidetector computed tomography ,survival ,non-small cell lung cancer ,reproducibility of finding - Abstract
PURPOSE: The aim of the study was to compare both reproducibility and prognostic value of lesion size measurements obtained manually and semiautomatically on computed tomography in advanced non-small cell lung cancer (NSCLC). MATERIALS AND METHODS: Manual axial longest diameter, semiautomatic axial longest diameter, and volume of NSCLC lesions were independently analyzed by 4 readers at baseline and after at least 1 cycle of platinum-based chemotherapy. The prognostic value of the proportional change in lesion size between baseline and follow-up CT was evaluated using either RECIST or experimental thresholds derived from the quartiles of the changes as assessed manually or semiautomatically. RESULTS: Semiautomatic axial longest diameter (concordance correlation coefficient [CCC]: 0.980 to 0.987; variation coefficient [VC%]: 6% to 7.3%) and volume (CCC: 0.974 to 0.991; VC%: 5.6% to 9.5%) were more reproducible than manual axial longest diameter (CCC: 0.950 to 0.984; VC%: 6.4% to 11.7%). RECIST categories did not stratify patients with different survival durations. For 3/4 readers, a decrease of ≤ 70% in lesion volume was associated with shorter survival (median survival: 11 mo, P < 0.05; hazard ratio: 5 to 22.2, P < 0.05). CONCLUSIONS: In advanced NSCLC, semiautomatic measures were more reproducible than manual diameter, and volumetric measurement may better predict patient survival.
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- 2015
365. CEA and CYFRA 21-1 as prognostic biomarker and as a tool for treatment monitoring in advanced NSCLC treated with immune checkpoint inhibitors.
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Dall'Olio, Filippo G., Abbati, Francesca, Facchinetti, Francesco, Massucci, Maria, Melotti, Barbara, Squadrilli, Anna, Buti, Sebastiano, Formica, Francesca, Tiseo, Marcello, and Ardizzoni, Andrea
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Aims: To assess prognostic value of pre-therapy carcinoembryonic antigen (CEA) and cytokeratin-19 fragments (CYFRA 21-1) blood levels in non-small cell lung cancer (NSCLC) patients treated with immune-checkpoint inhibitors (ICIs) and their early change as predictor of benefit. Materials and methods: This is a retrospective cohort study including patients with stage IIIB–IV NSCLC who received anti PD-1/PD-L1 in first or advanced lines of therapy in two institutions. A control cohort of patients treated only with chemotherapy has been enrolled as well. Results: A total of 133 patients treated with nivolumab or atezolizumab were included in the test set, 74 treated with pembrolizumab first line in the validation set and 89 in the chemotherapy only cohort. CYFRA 21-1 >8 ng/mL was correlated with overall survival (OS) in the test set, validation set and in univariate and multivariate analysis (pooled cohort hazard ratio (HR) 1.90, 95% confidence interval (CI) 1.24–2.93, p 0.003). Early 20% reduction after the third cycle was correlated with OS for CEA (HR 0.12; 95% CI 0.04–0.33; p < 0.001), and for CYFRA 21-1 (HR 0.19; 95% CI 0.07–0.55; p 0.002) Conclusions: CYFRA 21-1 pre-therapy assessment provides clinicians with relevant prognostic information about patients treated with ICI. CEA and CYFRA 21-1 repeated measures could be useful as an early marker of benefit. [ABSTRACT FROM AUTHOR]
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- 2020
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366. Atezolizumab in a C o H ort of pretreated, advanced, non-small cell lung cancer patients with rare HistologiCal Subtyp E s (CHANCE trial).
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Gelsomino, Francesco, Lamberti, Giuseppe, Tiseo, Marcello, Rocco, Danilo, Pasello, Giulia, Cecere, Fabiana Letizia, Chella, Antonio, Grilli, Giada, Mandruzzato, Marcella, Tognetto, Michele, Garassino, Marina Chiara, Macerelli, Marianna, Novello, Silvia, Roila, Fausto, Colantonio, Ida, Grossi, Francesco, Fiorentino, Michelangelo, and Ardizzoni, Andrea
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Background: Although immunotherapy with immune-checkpoint inhibitors (ICIs) has profoundly changed the therapeutic scenario in the treatment of advanced non-small cell lung cancer (NSCLC), trials of ICIs only enrolled NSCLC patients with common histology. Atezolizumab was approved by the United States Food and Drug Administration (US FDA) in October 2016 and by the European Medicines Agency (EMA) in September 2017 for the treatment of patients with metastatic NSCLC whose disease progressed during or following platinum-containing chemotherapy, regardless of PD-L1 expression. Methods: We designed a single-arm, multicenter, two-stage phase II study and plan to enroll 43 patients. The primary objective of the study is to evaluate the antitumor activity of atezolizumab in advanced NSCLC patients with rare histology subtypes. Patients with prior atezolizumab or ICI treatment and with untreated, symptomatic, or progressing brain metastases will be excluded. The primary endpoint is disease control rate. Secondary objectives are toxicity and safety, overall response rate, progression-free survival, overall survival, and time to progression. Diagnosis of NSCLC with rare histology will be confirmed by central pathology revision, and will include: colloid carcinoma, fetal adenocarcinoma, non-endocrine large cell carcinoma, sarcomatoid carcinoma, salivary gland-type tumor, lymphoepithelioma-like carcinoma, and NUT-nuclear protein in testis carcinoma. Archival tumor tissue is required for correlative studies of PD-L1 expression on tumor cells and tumor infiltrating lymphocytes. Conclusions: Therapeutic options in NSCLC with rare histology subtypes, to be assessed in specifically designed trials, are an unmet need. This trial will help elucidate the role of atezolizumab as a viable option in this setting. [ABSTRACT FROM AUTHOR]
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- 2020
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367. Effect of the patient information brochure in communicating the risks associated with crizotinib treatment to patients with non-small cell lung cancer (NSCLC) in Europe.
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Kui Huang, Madison, Terri, Wehler, Beatrice, Tiseo, Marcello, Wilner, Keith D., and Jingping Mo
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NON-small-cell lung carcinoma ,INTERSTITIAL lung diseases ,HEPATOTOXICOLOGY - Abstract
Crizotinib (XALKORI®) is indicated for anaplastic lymphoma kinase-positive and ROS1-positive advanced non-small cell lung cancer. This study evaluated the distribution of the crizotinib patient information brochure (PIB) in Europe and patient knowledge of the key messages in the PIB. A cross-sectional survey was conducted in 10 European countries among patients who received crizotinib to ascertain whether each patient received and read the PIB, and his/her knowledge of its key messages on hepatotoxicity, interstitial lung disease/pneumonitis, QTc prolongation, bradycardia, and vision disorders. Of the 341 patients contacted, 40 responded (11.7%), and 39 patients were eligible. A total of 77% of respondents acknowledged receiving the PIB, of which, 93% reported reading it. Knowledge of the individual side effects ranged from 36% to 85%, and precautions for use ranged from 56% to 67%. Understanding the reasons for calling a physician ranged from 54% to 85%. Knowledge of each of the 6 key side effects was greater among readers of the PIB compared to non-readers or respondents who did not recall receiving the PIB. Approximately three-quarters of survey respondents recalled receiving the crizotinib PIB and respondents who read the PIB were more knowledgeable of the key side effects of crizotinib than those who did not read or receive. Caution should be taken in generalizing these results because of the potential for selection bias and small sample size. These survey results suggest that the crizotinib PIB may be an effective risk communication tool for crizotinib-treated patients in Europe. [ABSTRACT FROM AUTHOR]
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- 2020
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368. Upfront osimertinib in EGFR-mutated non-small cell lung cancer: is brain still a sanctuary?
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Leonetti, Alessandro, primary, Facchinetti, Francesco, additional, and Tiseo, Marcello, additional
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- 2018
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369. Brigatinib versus Crizotinib in ALK-Positive Non–Small-Cell Lung Cancer
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Camidge, D. Ross, primary, Kim, Hye Ryun, additional, Ahn, Myung-Ju, additional, Yang, James Chih-Hsin, additional, Han, Ji-Youn, additional, Lee, Jong-Seok, additional, Hochmair, Maximilian J., additional, Li, Jacky Yu-Chung, additional, Chang, Gee-Chen, additional, Lee, Ki Hyeong, additional, Gridelli, Cesare, additional, Delmonte, Angelo, additional, Garcia Campelo, Rosario, additional, Kim, Dong-Wan, additional, Bearz, Alessandra, additional, Griesinger, Frank, additional, Morabito, Alessandro, additional, Felip, Enriqueta, additional, Califano, Raffaele, additional, Ghosh, Sharmistha, additional, Spira, Alexander, additional, Gettinger, Scott N., additional, Tiseo, Marcello, additional, Gupta, Neeraj, additional, Haney, Jeff, additional, Kerstein, David, additional, and Popat, Sanjay, additional
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- 2018
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370. Meeting with triumph and disaster: Osimertinib in T790M-unknown CNS progression in EGFR-mutated non-small cell lung cancer
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Facchinetti, Francesco, primary, Bozzetti, Francesca, additional, Minari, Roberta, additional, Ceccon, Giovanni, additional, Zielli, Teresa, additional, Florindo, Irene, additional, Crisi, Girolamo, additional, and Tiseo, Marcello, additional
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- 2018
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371. The amount of activating EGFR mutations in circulating cell-free DNA is a marker to monitor osimertinib response
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Del Re, Marzia, primary, Bordi, Paola, additional, Rofi, Eleonora, additional, Restante, Giuliana, additional, Valleggi, Simona, additional, Minari, Roberta, additional, Crucitta, Stefania, additional, Arrigoni, Elena, additional, Chella, Antonio, additional, Morganti, Riccardo, additional, Tiseo, Marcello, additional, Petrini, Iacopo, additional, and Danesi, Romano, additional
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- 2018
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372. INfluenza Vaccine Indication During therapy with Immune checkpoint inhibitors: a transversal challenge. The INVIDIa study
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Bersanelli, Melissa, primary, Giannarelli, Diana, additional, Castrignanò, Paola, additional, Fornarini, Giuseppe, additional, Panni, Stefano, additional, Mazzoni, Francesca, additional, Tiseo, Marcello, additional, Rossetti, Sabrina, additional, Gambale, Elisabetta, additional, Rossi, Ernesto, additional, Papa, Anselmo, additional, Cortellini, Alessio, additional, Lolli, Cristian, additional, Ratta, Raffaele, additional, Michiara, Maria, additional, Milella, Michele, additional, De Luca, Emmanuele, additional, Sorarù, Mariella, additional, Mucciarini, Claudia, additional, Atzori, Francesco, additional, Banna, Giuseppe Luigi, additional, La Torre, Leonardo, additional, Vitale, Maria Giuseppa, additional, Massari, Francesco, additional, Rebuzzi, Sara Elena, additional, Facchini, Gaetano, additional, Schinzari, Giovanni, additional, Tomao, Silverio, additional, Bui, Simona, additional, Vaccaro, Vanja, additional, Procopio, Giuseppe, additional, De Giorgi, Ugo, additional, Santoni, Matteo, additional, Ficorella, Corrado, additional, Sabbatini, Roberto, additional, Maestri, Antonio, additional, Natoli, Clara, additional, De Tursi, Michele, additional, Di Maio, Massimo, additional, Rapacchi, Elena, additional, Pireddu, Annagrazia, additional, Sava, Teodoro, additional, Lipari, Helga, additional, Comito, Francesca, additional, Verzoni, Elena, additional, Leonardi, Francesco, additional, and Buti, Sebastiano, additional
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- 2018
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373. Enteral Administration of TKIs: Report of a Response to Ceritinib in an ALK-positive NSCLC Patient and Literature Review
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Facchinetti, Francesco, primary, Bordi, Paola, additional, Bini, Paola, additional, Bidin, Livia, additional, Camisa, Roberta, additional, and Tiseo, Marcello, additional
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- 2018
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374. Exploratory Analysis of Brigatinib Activity in Patients With Anaplastic Lymphoma Kinase-Positive Non–Small-Cell Lung Cancer and Brain Metastases in Two Clinical Trials
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Camidge, D. Ross, primary, Kim, Dong-Wan, additional, Tiseo, Marcello, additional, Langer, Corey J., additional, Ahn, Myung-Ju, additional, Shaw, Alice T., additional, Huber, Rudolf M., additional, Hochmair, Maximilian J., additional, Lee, Dae Ho, additional, Bazhenova, Lyudmila A., additional, Gold, Kathryn A., additional, Ou, Sai-Hong Ignatius, additional, West, Howard L., additional, Reichmann, William, additional, Haney, Jeff, additional, Clackson, Tim, additional, Kerstein, David, additional, and Gettinger, Scott N., additional
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- 2018
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375. Ventana ALK (D5F3) in the Detection of Patients Affected by Anaplastic Lymphoma Kinase-positive Non–Small-cell Lung Cancer: Clinical and Budget Effect
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Paolini, Davide, primary, Tiseo, Marcello, additional, Demma, Federica, additional, Furneri, Gianluca, additional, Dionisi, Matteo, additional, Akkermans, Marlene, additional, and Marchetti, Antonio, additional
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- 2018
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376. Widespread Nivolumab-induced Enteropathy in a Long Responder Non–Small-cell Lung Cancer Patient
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Facchinetti, Francesco, primary, Gnetti, Letizia, additional, Caruana, Pietro, additional, Fornaroli, Fabiola, additional, Luigi de'Angelis, Gian, additional, Sabato, Mariangela, additional, Ferri, Leonarda, additional, Cosenza, Agnese, additional, Bordi, Paola, additional, and Tiseo, Marcello, additional
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- 2018
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377. Sarcoid-like reaction mimicking disease progression in an ALK-positive lung cancer patient receiving lorlatinib
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Facchinetti, Francesco, primary, Gnetti, Letizia, additional, Balestra, Valeria, additional, Silva, Mario, additional, Silini, Enrico Maria, additional, Ventura, Luigi, additional, Majori, Maria, additional, Bordi, Paola, additional, and Tiseo, Marcello, additional
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- 2018
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378. NGR-hTNF in combination with best investigator choice in previously treated malignant pleural mesothelioma (NGR015): a randomised, double-blind, placebo-controlled phase 3 trial
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Gregorc, Vanesa, primary, Gaafar, Rabab M, additional, Favaretto, Adolfo, additional, Grossi, Francesco, additional, Jassem, Jacek, additional, Polychronis, Andreas, additional, Bidoli, Paolo, additional, Tiseo, Marcello, additional, Shah, Riyaz, additional, Taylor, Paul, additional, Novello, Silvia, additional, Muzio, Alberto, additional, Bearz, Alessandra, additional, Greillier, Laurent, additional, Fontana, Floriana, additional, Salini, Giulia, additional, Lambiase, Antonio, additional, and O'Brien, Mary, additional
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- 2018
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379. Family history of cancer as surrogate predictor for immunotherapy with anti-PD1/PD-L1 agents: preliminary report of the FAMI-L1 study
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Cortellini, Alessio, primary, Bersanelli, Melissa, additional, Buti, Sebastiano, additional, Gambale, Elisabetta, additional, Atzori, Francesco, additional, Zoratto, Federica, additional, Parisi, Alessandro, additional, Brocco, Davide, additional, Pireddu, Annagrazia, additional, Cannita, Katia, additional, Iacono, Daniela, additional, Migliorino, Maria R, additional, Gamucci, Teresa, additional, De Tursi, Michele, additional, Sidoni, Tina, additional, Tiseo, Marcello, additional, Michiara, Maria, additional, Papa, Anselmo, additional, Angius, Gesuino, additional, Tomao, Silverio, additional, Fargnoli, Maria C, additional, Natoli, Clara, additional, and Ficorella, Corrado, additional
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- 2018
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380. Concurrent Acquired BRAF V600E Mutation and MET Amplification as Resistance Mechanism of First-Line Osimertinib Treatment in a Patient with EGFR-Mutated NSCLC
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Minari, Roberta, primary, Bordi, Paola, additional, La Monica, Silvia, additional, Squadrilli, Anna, additional, Leonetti, Alessandro, additional, Bottarelli, Lorena, additional, Azzoni, Cinzia, additional, Lagrasta, Costanza Anna Maria, additional, Gnetti, Letizia, additional, Campanini, Nicoletta, additional, Petronini, Pier Giorgio, additional, Alfieri, Roberta, additional, and Tiseo, Marcello, additional
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- 2018
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381. Clinical and hematologic parameters address the outcomes of non-small-cell lung cancer patients treated with nivolumab
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Facchinetti, Francesco, primary, Veneziani, Michele, additional, Buti, Sebastiano, additional, Gelsomino, Francesco, additional, Squadrilli, Anna, additional, Bordi, Paola, additional, Bersanelli, Melissa, additional, Cosenza, Agnese, additional, Ferri, Leonarda, additional, Rapacchi, Elena, additional, Mazzaschi, Giulia, additional, Leonardi, Francesco, additional, Quaini, Federico, additional, Ardizzoni, Andrea, additional, Missale, Gabriele, additional, and Tiseo, Marcello, additional
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- 2018
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382. Brigatinib (BRG) in crizotinib (CRZ)-refractory ALK+ non–small cell lung cancer (NSCLC): Efficacy updates and exploratory analysis of CNS ORR and overall ORR by baseline (BL) brain lesion status.
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Huber, Rudolf M., primary, Kim, Dong-Wan, additional, Ahn, Myung-Ju, additional, Langer, Corey J., additional, Tiseo, Marcello, additional, West, Howard, additional, Groen, Harry J.M., additional, Reckamp, Karen L., additional, Hochmair, Maximilian J., additional, Leighl, Natasha B., additional, Holmskov Hansen, Karin, additional, Gettinger, Scott N., additional, Paz-Ares, Luis G., additional, Kim, Edward S., additional, Smit, Egbert F., additional, Kim, Sang-We, additional, Reichmann, William, additional, Kerstein, David, additional, and Camidge, D. Ross, additional
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- 2018
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383. Prospective study on the role of cytidine deaminase activity in lung cancer patients treated with gemcitabine-platinum-based chemotherapy.
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Giovannetti, Elisa, primary, Tiseo, Marcello, additional, Honeywell, Richard J., additional, Boni, Luca, additional, Chartoire, Myriam, additional, Camerini, Andrea, additional, Mazzoni, Francesca, additional, Barbieri, Fausto, additional, Vittimberga, Isabella, additional, Peters, Godefridus J., additional, Rolfo, Christian Diego, additional, and Tibaldi, Carmelo, additional
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- 2018
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384. Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia (DIPNECH) Syndrome and Carcinoid Tumors With/Without NECH
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Mengoli, Maria Cecilia, primary, Rossi, Giulio, additional, Cavazza, Alberto, additional, Franco, Renato, additional, Marino, Federica Zito, additional, Migaldi, Mario, additional, Gnetti, Letizia, additional, Silini, Enrico Maria, additional, Ampollini, Luca, additional, Tiseo, Marcello, additional, Lococo, Filippo, additional, Fournel, Ludovic, additional, Spagnolo, Paolo, additional, Cottin, Vincent, additional, and Colby, Thomas V., additional
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- 2018
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385. BRAF in non-small cell lung cancer (NSCLC): Pickaxing another brick in the wall
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Leonetti, Alessandro, primary, Facchinetti, Francesco, additional, Rossi, Giulio, additional, Minari, Roberta, additional, Conti, Antonia, additional, Friboulet, Luc, additional, Tiseo, Marcello, additional, and Planchard, David, additional
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- 2018
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386. Is the door open to further investigation with antiangiogenesis in SCLC?
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Tiseo, Marcello, primary, Boni, Luca, additional, and Ardizzoni, Andrea, additional
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- 2018
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387. No room for statins in the quest for survival benefits in small cell lung cancer
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Facchinetti, Francesco, primary and Tiseo, Marcello, additional
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- 2018
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388. Is there still room for anti-angiogenic agents in small cell lung cancer?
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Brighenti, Matteo, primary and Tiseo, Marcello, additional
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- 2018
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389. Lung Toxicity in Non–Small-Cell Lung Cancer Patients Exposed to ALK Inhibitors: Report of a Peculiar Case and Systematic Review of the Literature
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Pellegrino, Benedetta, primary, Facchinetti, Francesco, additional, Bordi, Paola, additional, Silva, Mario, additional, Gnetti, Letizia, additional, and Tiseo, Marcello, additional
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- 2018
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390. Phase II Study of Everolimus in Patients With Thymoma and Thymic Carcinoma Previously Treated With Cisplatin-Based Chemotherapy
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Zucali, Paolo Andrea, primary, De Pas, Tommaso, additional, Palmieri, Giovannella, additional, Favaretto, Adolfo, additional, Chella, Antonio, additional, Tiseo, Marcello, additional, Caruso, Michele, additional, Simonelli, Matteo, additional, Perrino, Matteo, additional, De Vincenzo, Fabio, additional, Toffalorio, Francesca, additional, Damiano, Vincenzo, additional, Pasello, Giulia, additional, Garbella, Erika, additional, Ali, Marco, additional, Conforti, Fabio, additional, Ottaviano, Margaret, additional, Cioffi, Angela, additional, De Placido, Sabino, additional, Giordano, Laura, additional, Bertossi, Monica, additional, Destro, Annarita, additional, Di Tommaso, Luca, additional, and Santoro, Armando, additional
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- 2018
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391. Low PD-1 Expression in Cytotoxic CD8+ Tumor-Infiltrating Lymphocytes Confers an Immune-Privileged Tissue Microenvironment in NSCLC with a Prognostic and Predictive Value
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Mazzaschi, Giulia, primary, Madeddu, Denise, additional, Falco, Angela, additional, Bocchialini, Giovanni, additional, Goldoni, Matteo, additional, Sogni, Francesco, additional, Armani, Giovanna, additional, Lagrasta, Costanza Annamaria, additional, Lorusso, Bruno, additional, Mangiaracina, Chiara, additional, Vilella, Rocchina, additional, Frati, Caterina, additional, Alfieri, Roberta, additional, Ampollini, Luca, additional, Veneziani, Michele, additional, Silini, Enrico Maria, additional, Ardizzoni, Andrea, additional, Urbanek, Konrad, additional, Aversa, Franco, additional, Quaini, Federico, additional, and Tiseo, Marcello, additional
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- 2018
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392. Outcomes of First-Generation EGFR-TKIs Against Non-Small-Cell Lung Cancer Harboring Uncommon EGFR Mutations: A Post Hoc Analysis of the BE-POSITIVE Study
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Pilotto, Sara, primary, Rossi, Antonio, additional, Vavalà, Tiziana, additional, Follador, Alessandro, additional, Tiseo, Marcello, additional, Galetta, Domenico, additional, Morabito, Alessandro, additional, Di Maio, Massimo, additional, Martelli, Olga, additional, Caffo, Orazio, additional, Piovano, Pier Luigi, additional, Cortinovis, Diego, additional, Zilembo, Nicoletta, additional, Casartelli, Clelia, additional, Banna, Giuseppe Luigi, additional, Ardizzoia, Antonio, additional, Barzelloni, Maria Luisa, additional, Bearz, Alessandra, additional, Genestreti, Giovenzio, additional, Mucciarini, Claudia, additional, Filipazzi, Virginio, additional, Menis, Jessica, additional, Rizzo, Elisa, additional, Barbieri, Fausto, additional, Rijavec, Erika, additional, Cecere, Fabiana, additional, Spitaleri, Gianluca, additional, Bria, Emilio, additional, and Novello, Silvia, additional
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- 2018
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393. Listening understanding and acting (lung): focus on communicational issue in thoracic oncology
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Finocchiaro, Claudia Yvonne, primary, Rota, Alessandra, additional, Barbieri, Vito, additional, Bettini, Anna, additional, Bianco, Roberto, additional, Borra, Gloria, additional, Buffoni, Lucio, additional, Bulotta, Alessandra, additional, Carta, Annamaria, additional, Cortinovis, Diego, additional, Costanzo, Raffaele, additional, Cusmai, Antonio, additional, Danesi, Romano, additional, D’Argento, Ettore, additional, Del Conte, Alessandro, additional, Franchina, Tindara, additional, Gilli, Marina, additional, Gregorc, Vanesa, additional, Irtelli, Luciana, additional, Landi, Lorenza, additional, Malorgio, Francesco, additional, Mancuso, Gianfranco, additional, Martelli, Olga, additional, Mazzanti, Paola, additional, Melotti, Barbara, additional, Migliorino, Maria Rita, additional, Minotti, Vincenzo, additional, Montrone, Michele, additional, Morabito, Alessandro, additional, Roca, Elisa, additional, Romano, Giampiero, additional, Rossi, Antonio, additional, Savio, Giuseppa, additional, Tiseo, Marcello, additional, Boscardini, Ivano, additional, Piccolo, Lorenzo, additional, Pilotto, Sara, additional, and Malapelle, Umberto, additional
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- 2018
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394. Multiple primary malignancies involving lung cancer: a single-center experience
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Ventura, Luigi, Carbognani, Paolo, Gnetti, Letizia, Rossi, Maurizio, Tiseo, Marcello, Silini, Enrico Maria, Sverzellati, Nicola, Silva, Mario, Succi, Marcello, Braggio, Cesare, Cattadori, Sara, Bocchialini, Giovanni, Balestra, Valeria, Rusca, Michele, and Ampollini, Luca
- Abstract
Objective: Currently, unlike earlier years, patients affected by multiple primary malignancies (MPM) are significantly increased, thus representing a clinical-pathologic category worthy of attention. Their clinical features and prognosis still need to be studied thoroughly, and this is the aim of our study.Methods: Patients with MPM involving lung cancer admitted in our center between January 2006 and December 2016 were considered. Parametric and nonparametric testing was used for statistical comparisons. Univariate and multivariate analysis was used to evaluate the variables associated with a prognostic value.Results: MPM incidence was 19.8%. Among the 222 patients with MPM enrolled, 204 (91.8%) had two malignancies, while 18 (8.2%) had three malignancies, 38 (17.1%) were synchronous, 41 (18.5%) had lung cancer first (LCF) and 181 (81.5%) had other cancer first (OCF). A significant difference between the time of first cancer diagnosis to the second cancer diagnosis in the LCF vs OCF group was found (median 32 vs 51 months; p-value: 0.038). The most frequent anatomical sites of malignancies preceding or following lung cancer were prostate, colorectal, bladder, and larynx. Multivariate analysis revealed that sex, histologic pattern, and time and order of occurrence were independent factors for overall survival, with male sex, squamous cell lung carcinoma, synchronous and LCF MPM significantly associated with poorer overall survival.Conclusions: Prostate, colorectal, bladder, and larynx were the most frequent anatomical sites of malignancies preceding or following lung cancer. Male sex, squamous cell lung carcinoma, synchronous and LCF MPM might be associated with poorer prognosis.
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- 2021
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395. Efficacy and safety of long-acting pasireotide or everolimus alone or in combination in patients with advanced carcinoids of the lung and thymus (LUNA) : an open-label, multicentre, randomised, phase 2 trial
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Ferolla, Piero, Brizzi, Maria Pia, Meyer, Tim, Mansoor, Wasat, Mazieres, Julien, Do Cao, Christine, Lena, Herve, Berruti, Alfredo, Damiano, Vincenzo, Buikhuisen, Wieneke, Gronbaek, Henning, Lombard-Bohas, Catherine, Grohe, Christian, Minotti, Vincenzo, Tiseo, Marcello, De Castro, Javier, Reed, Nicholas, Gislimberti, Gabriella, Singh, Neha, Stankovic, Miona, Öberg, Kjell, Baudin, Eric, Ferolla, Piero, Brizzi, Maria Pia, Meyer, Tim, Mansoor, Wasat, Mazieres, Julien, Do Cao, Christine, Lena, Herve, Berruti, Alfredo, Damiano, Vincenzo, Buikhuisen, Wieneke, Gronbaek, Henning, Lombard-Bohas, Catherine, Grohe, Christian, Minotti, Vincenzo, Tiseo, Marcello, De Castro, Javier, Reed, Nicholas, Gislimberti, Gabriella, Singh, Neha, Stankovic, Miona, Öberg, Kjell, and Baudin, Eric
- Abstract
Background There are no data from prospective studies focused exclusively on patients with advanced lung and thymic carcinoids. We aimed to assess the efficacy and safety of long-acting pasireotide and everolimus, administered alone or in combination, in patients with advanced carcinoids of the lung or thymus. Methods LUNA was a prospective, multicentre, randomised, open-label, phase 2 trial of adult patients (aged >18 years) with advanced (unresectable or metastatic), well differentiated carcinoid tumours of the lung or thymus, with radiological progression within 12 months before randomisation, and a WHO performance status of 0–2. At each centre, the investigator or their designee registered each patient using an interactive voice recognition system into one of the three treatment groups. The randomisation allocation sequence was generated by an external company; patients were randomly assigned (1:1:1) to receive treatment with long-acting pasireotide (60 mg intramuscularly every 28 days), everolimus (10 mg orally once daily), or both in combination, for the core 12-month treatment period. Patients were stratified by carcinoid type (typical vs atypical) and line of study treatment (first line vs others). The primary endpoint was the proportion of patients progression-free at month 9, defined as the proportion of patients with overall lesion assessment at month 9 showing a complete response, partial response, or stable disease according to local Response Evaluation Criteria in Solid Tumors, version 1.1, assessed in the intention-to-treat population. Safety was assessed in all patients who received at least one dose of study drug and had at least one post-baseline safety assessment. The trial is registered with ClinicalTrials.gov, number NCT01563354. The extension phase of the study is ongoing. Findings Between Aug 16, 2013, and Sept 30, 2014, 124 patients were enrolled from 36 centres in nine countries: 41 were allocated to the long-acting pasireotide group, 42
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- 2017
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396. A bug in the resistance to EGFR inhibitors: is there a role for Mycoplasma and cytidine deaminase in reducing the activity of osimertinib in lung cancer patients?
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Leonetti, Alessandro, Carbone, Daniela, Gregori, Alessandro, Tiseo, Marcello, Peters, Godefridus J., Deng, Dongmei, and Giovannetti, Elisa
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CYTIDINE deaminase ,EPIDERMAL growth factor receptors ,OSIMERTINIB ,LUNG cancer ,CANCER patients ,MYCOPLASMA diseases - Abstract
This article describes a retrospective study evaluating the relationship between I Mycoplasma hyorhinis i infection and epidermal growth factor receptor (EGFR) TKI resistance in 101 patients with I EGFR i -mutated lung adenocarcinoma. Dear Editor, With great interest we read the article " I Mycoplasma hyorhinis i infection promotes tyrosine kinase inhibitor (TKI) resistance in lung adenocarcinoma patients", by Dai et al. (Dai et al. [3]). [Extracted from the article]
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- 2021
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397. EPMA-World Congress 2015
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Abraham, Jella-Andrea, Golubnitschaja, Olga, Akhmetov, Ildar, Andrews, Russell J., Quintana, Leonidas, Baban, Babak, Liu, Jun Yao, Qin, Xu, Wang, Tailing, Mozaffari, Mahmood S., Bati, Viktoriia V., Meleshko, Tamara V., Levchuk, Olga B., Boyko, Nadiya V., Bauer, Joanna, Boerner, Ewa, Podbielska, Halina, Bomba, Alojz, Petrov, Viktor O., Drobnych, Volodymyr G., Bubnov, Rostyslav V., Bykova, Oksana M., Brunner-La Rocca, Hans-Peter, Fleischhacker, Lutz, Heemskerk, Frank, Helms, Thomas, Jaarsma, Tiny, Kinkorová, Judita, Ramaekers, Jan, Ruff, Peter, Schnur, Ivana, Vanoli, Emilio, Verdu, Jose, Grabovetskyi, Sergiy A., Mykhalchenko, Olena M., Tymoshok, Natalia O., Shcherbakov, Oleksandr B., Semeniv, Igor P., Spivak, Mykola Y., Ostapenko, Tetyana V., Kobyliak, Nazarii M., Zholobak, Nadiya M., Spivak, Mykola Ya., Cauchi, John Paul, Cherepakhin, Dmitrii, Bakay, Marina, Borovikov, Artem, Suchkov, Sergey, Cieślik, Barbara, Migasiewicz, Agnieszka, Podbielska, Maria-Luiza, Pelleter, Markus, Giemza, Agnieszka, Cirak, Sebahattin, Del Re, Marzia, Bordi, Paola, Citi, Valentina, Palombi, Marta, Pinto, Carmine, Tiseo, Marcello, Danesi, Romano, Einhorn, Lukas, Fazekas, Judit, Muhr, Martina, Schoos, Alexandra, Panakova, Lucia, Herrmann, Ina, Manzano-Szalai, Krisztina, Oida, Kumiko, Fiebiger, Edda, Singer, Josef, Jensen-Jarolim, Erika, Elnar, Arpiné A., Ouamara, Nadia, Boyko, Nadiya, Coumoul, Xavier, Antignac, Jean-Philippe, Le Bizec, Bruno, Eppe, Gauthier, Renaut, Jenny, Bonn, Torsten, Guignard, Cédric, Ferrante, Margherita, Chiusano, Maria Liusa, Cuzzocrea, Salvatore, O’Keeffe, Gerard, Cryan, John, Bisson, Michelle, Barakat, Amina, Hmamouchi, Ihsane, Zawia, Nasser, Kanthasamy, Anumantha, Kisby, Glen E., Alves, Rui, Pérez, Oscar Villacañas, Burgard, Kim, Spencer, Peter, Bomba, Norbert, Haranta, Martin, Zaitseva, Nina, May, Irina, Grojean, Stéphanie, Body-Malapel, Mathilde, Harari, Florencia, Harari, Raul, Yeghiazaryan, Kristina, Calabrese, Vittorio, Nemos, Christophe, Soulimani, Rachid, Evsevyeva, Maria E., Mishenko, Elena A., Kumukova, Zurida V., Chudnovsky, Evgeniy V., Smirnova, Tatyana A., Ivanova, Ludmila V., Eremin, Michail V., Rostovtseva, Maria V., Koshel, Vladimir I., Sergeeva, Oksana V., Konovalova, Nadesgda M., Girotra, Shantanu, Debald, Manuel, Kuhn, Walther, Goncharenko, Vadym M., Lushchyk, Ulyana, Grech, Godfrey, Konieczka, Katarzyna, Erwich, Jan Jaap, Costigliola, Vincenzo, Gembruch, Ulrich, Beniuk, Vasyl O., Kalenska, Olga V., Melnychuk, Olga, Gorbacheva, Irina A., Orekhova, Lyudmila Y., Tachalov, Vadim V., Grechanyk, Olena I., Abdullaiev, Rizvan Ya., Hagan, Suzanne, Martin, Eilidh, Pearce, Ian, Oliver, Katherine, Haytac, Cenk, Salimov, Fariz, Yoksul, Servin, Kunin, Anatoly A., Moiseeva, Natalia S., Herrera-Imbroda, Bernardo, del Río-González, Sergio, Lara, Maria Fernanda, Angulo, Antonia, Machuca Santa-Cruz, Francisco Javier, Ionescu, John, Isamulaeva, Alfiya Z., Magomedov, Shamil Sh., Isamulaeva, Aida I., Josifova, Tatjana, Kapalla, Marko, Kubáň, Juraj, Kent, Anthony, Fisher, Tom, Dias, Tilak, Topolčan, Ondřej, Kohl, Matthias, Kurchenko, Andrii I., Beniuk, Vasyl A., Strokan, Andriy M., Kzhyshkowska, Julia, Gudima, Alexandru, Stankevich, Ksenia S., Filimonov, Victor D., Klüter, Harald, Mamontova, Evgeniya M., Tverdokhlebov, Sergei I., Lushchyk, Ulyana B., Novytskyy, Viktor V., Babii, Igor P., Lushchyk, Nadiya G., Riabets, Lyudmyla S., Legka, Ivanna I., Marcus-Kalish, Mira, Mitelpunkt, Alexis, Galili, Tal, Shachar, Neta, Benjamini, Yoav, Dereń, Ewelina, Kunin, Dmitry A., Ippolitov, Yury A., Morozov, Alexei N., Chirkova, Natalia V., Aliev, Nakhid T., Abdelsayed, Rafik, Shi, Xing-Ming, Novák, Jaroslav, Štork, Milan, Zeman, Václav, Oosterhuis, Wytze P., Theodorsson, Elvar, Kudryavtseva, Tatyana V., Isaeva, Elena R., Loboda, Ekaterina S., Pazzagli, Mario, Malentacchi, Francesca, Mancini, Irene, Brandslund, Ivan, Vermeersch, Pieter, Schwab, Matthias, Marc, Janja, van Schaik, Ron H. N., Siest, Gerard, Di Resta, Chiara, Pleva, Matus, Juhar, Jozef, Polívka, Jiří, Janků, Filip, Pešta, Martin, Doležal, Jan, Králíčková, Milena, Lukešová, Alena, Müllerová, Nina, Ševčík, Petr, Rohan, Vladimír, Richter, Kneginja, Miloseva, Lence, Niklewski, Günter, Acker, Jens, Niklewski, Guenter, Safonicheva, Olga, Sautin, Maxim, Sinelnikova, Janna, Secer, Songül, von Bandemer, Stephan, Shapira, Niva, Shcherbakov, Aleksandr, Shumilovich, Bogdan R., Lipkind, Zhanna, Vorobieva, Yulia, Sudareva, Anastasiia V., Smokovski, Ivica, Milenkovic, Tatjana, Solís-Herrera, Arturo, Arias-Esparza, María del Carmen, Sridhar, Krishna Chander, Studneva, Maria, Song, Sihong, Creeden, James, Мandrik, Мark, Tofail, Syed A. M., Fiala, Ondřej, Karlíková, Marie, Svobodová, Šárka, Kučera, Radek, Fuchsová, Radka, Třeška, Vladislav, Šimánek, Václav, Pecen, Ladislav, Šoupal, Jan, Svačina, Štěpán, Tretyak, Evgeniya, Trovato, Francesca M., Martines, Giuseppe Fabio, Brischetto, Daniela, Catalano, Daniela, Musumeci, Giuseppe, Trovato, Guglielmo M., Tsangaris, George Th., Anagnostopoulos, Athanasios K., Verdú, José, Gutiérrez, German, Rovira, Jordi, Martinez, Marta, Green, Donna, Garson, Arthur, Tamburini, Elena, Cuomo, Stefano, Martinez-Leon, Juan, Abrisqueta, Teresa, Arredondo, Teresa, Vera, Cecilia, Fico, Giuseppe, Arribas, Fernando, Onderco, Martina, Vara, Isabel, Sambo, Francesco, Di Camillo, Barbara, Cobelli, Claudio, Facchinetti, Andrea, Bellazzi, Riccardo, Sacchi, Lucia, Dagliati, Arianna, Segnani, Daniele, Tibollo, Valentina, Ottaviano, Manuel, Gabriel, Rafael, Groop, Leif, Postma, Jacqueline, Martinez, Antonio, Hakaste, Liisa, Tuomi, Tiinamaija, Zarkogianni, Konstantia, Volchek, Igor, Pototskaya, Nina, Petrov, Andrey, Pototskaya, Nadezhda, Voog-Oras, Ülle, Jagur, Oksana, Leibur, Edvitar, Niibo, Priit, Jagomägi, Triin, Nguyen, Minh Son, Pruunsild, Chris, Piikov, Dagmar, Saag, Mare, Wang, Wei, Weinhäusel, Andreas, Pulverer, Walter, Wielscher, Matthias, Hofner, Manuela, Noehammer, Christa, Soldo, Regina, Hettegger, Peter, Gyurjan, Istvan, Kulovics, Ronald, Schönthaler, Silvia, Beikircher, Gabriel, Kriegner, Albert, Pabinger, Stephan, Vierlinger, Klemens, Yüzbaşıoğlu, Ayşe, and Özgüç, Meral
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Meeting Abstracts - Abstract
Table of contents A1 Predictive and prognostic biomarker panel for targeted application of radioembolisation improving individual outcomes in hepatocellular carcinoma Jella-Andrea Abraham, Olga Golubnitschaja A2 Integrated market access approach amplifying value of “Rx-CDx” Ildar Akhmetov A3 Disaster response: an opportunity to improve global healthcare Russell J. Andrews, Leonidas Quintana A4 USA PPPM: proscriptive, profligate, profiteering medicine-good for 1 % wealthy, not for 99 % unhealthy Russell J. Andrews A5 The role of IDO in a murine model of gingivitis: predictive and therapeutic potentials Babak Baban, Jun Yao Liu, Xu Qin, Tailing Wang, Mahmood S. Mozaffari A6 Specific diets for personalised treatment of diabetes type 2 Viktoriia V. Bati, Tamara V. Meleshko, Olga B. Levchuk, Nadiya V. Boyko A7 Towards personalized physiotherapeutic approach Joanna Bauer, Ewa Boerner, Halina Podbielska A8 Cells, animal, SHIME and in silico models for detection and verification of specific biomarkers of non-communicable chronic diseases Alojz Bomba, Viktor O. Petrov, Volodymyr G. Drobnych, Rostyslav V. Bubnov, Oksana M. Bykova, Nadiya V. Boyko A9 INTERACT-chronic care model: Self-treatment by patients with decision support e-Health solution Hans-Peter Brunner-La Rocca, Lutz Fleischhacker, Olga Golubnitschaja, Frank Heemskerk, Thomas Helms, Tiny Jaarsma, Judita Kinkorova, Jan Ramaekers, Peter Ruff, Ivana Schnur, Emilio Vanoli, Jose Verdu A10 PPPM in cardiovascular medicine in 2015 Hans-Peter Brunner-La Rocca A11 Magnetic resonance imaging of nanoparticles in mice, potential for theranostic and contrast media development – pilot results Rostyslav V. Bubnov, Sergiy A. Grabovetskyi, Olena M. Mykhalchenko, Natalia O. Tymoshok, Oleksandr B. Shcherbakov, Igor P. Semeniv, Mykola Y. Spivak A12 Ultrasound diagnosis for diabetic neuropathy - comparative study Rostyslav V. Bubnov, Tetyana V. Ostapenko A13 Ultrasound for stratification patients with diabetic foot ulcers for prevention and personalized treatment - pilot results Rostyslav V. Bubnov, Nazarii M. Kobyliak, Nadiya M. Zholobak, Mykola Ya. Spivak A14 Project ImaGenX – designing and executing a questionnaire on environment and lifestyle risk of breast cancer John Paul Cauchi A15 Genomics – a new structural brand of predictive, preventive and personalized medicine or the new driver as well? Dmitrii Cherepakhin, Marina Bakay, Artem Borovikov, Sergey Suchkov A16 Survey of questionnaires for evaluation of the quality of life in various medical fields Barbara Cieślik, Agnieszka Migasiewicz, Maria-Luiza Podbielska, Markus Pelleter, Agnieszka Giemza, Halina Podbielska A17 Personalized molecular treatment for muscular dystrophies Sebahattin Cirak A18 Secondary mutations in circulating tumour DNA for acquired drug resistance in patients with advanced ALK + NSCLC Marzia Del Re, Paola Bordi, Valentina Citi, Marta Palombi, Carmine Pinto, Marcello Tiseo, Romano Danesi A19 Recombinant species-specific FcεRI alpha proteins for diagnosis of IgE-mediated allergies in dogs, cats and horses Lukas Einhorn, Judit Fazekas, Martina Muhr, Alexandra Schoos, Lucia Panakova, Ina Herrmann, Krisztina Manzano-Szalai, Kumiko Oida, Edda Fiebiger, Josef Singer, Erika Jensen-Jarolim A20 Global methodology for developmental neurotoxicity testing in humans and animals early and chronically exposed to chemical contaminants Arpiné A. Elnar, Nadia Ouamara, Nadiya Boyko, Xavier Coumoul, Jean-Philippe Antignac, Bruno Le Bizec, Gauthier Eppe, Jenny Renaut, Torsten Bonn, Cédric Guignard, Margherita Ferrante, Maria Liusa Chiusano, Salvatore Cuzzocrea, Gerard O'Keeffe, John Cryan, Michelle Bisson, Amina Barakat, Ihsane Hmamouchi, Nasser Zawia, Anumantha Kanthasamy, Glen E. Kisby, Rui Alves, Oscar Villacañas Pérez, Kim Burgard, Peter Spencer, Norbert Bomba, Martin Haranta, Nina Zaitseva, Irina May, Stéphanie Grojean, Mathilde Body-Malapel, Florencia Harari, Raul Harari, Kristina Yeghiazaryan, Olga Golubnitschaja, Vittorio Calabrese, Christophe Nemos, Rachid Soulimani A21 Mental indicators at young people with attributes hypertension and pre-hypertension Maria E. Evsevyeva, Elena A. Mishenko, Zurida V. Kumukova, Evgeniy V. Chudnovsky, Tatyana A. Smirnova A22 On the approaches to the early diagnosis of stress-induced hypertension in young employees of State law enforcement agencies Maria E. Evsevyeva, Ludmila V. Ivanova, Michail V. Eremin, Maria V. Rostovtseva A23 Сentral aortic pressure and indexes of augmentation in young persons in view of risk factors Maria E. Evsevyeva, Michail V. Eremin, Vladimir I. Koshel, Oksana V. Sergeeva, Nadesgda M. Konovalova A24 Breast cancer prediction and prevention: Are reliable biomarkers in horizon? Shantanu Girotra, Olga Golubnitschaja A25 Flammer Syndrome and potential formation of pre-metastatic niches: A multi-centred study on phenotyping, patient stratification, prediction and potential prevention of aggressive breast cancer and metastatic disease Olga Golubnitschaja, Manuel Debald, Walther Kuhn, Kristina Yeghiazaryan, Rostyslav V. Bubnov, Vadym M. Goncharenko, Ulyana Lushchyk, Godfrey Grech, Katarzyna Konieczka A26 Innovative tools for prenatal diagnostics and monitoring: improving individual pregnancy outcomes and health-economy in EU Olga Golubnitschaja, Jan Jaap Erwich, Vincenzo Costigliola, Kristina Yeghiazaryan, Ulrich Gembruch A27 Immunohistochemical assessment of APUD cells in endometriosis Vadym M. Goncharenko, Vasyl O. Beniuk, Olga V. Kalenska, Rostyslav V. Bubnov A28 Updating personalized management algorithm of endometrial hyperplasia in pre-menopause women Vadym M. Goncharenko, Vasyl O. Beniuk, Rostyslav V. Bubnov, Olga Melnychuk A29 The personified treatment approach of polimorbid patients with periodontal inflammatory diseases Irina A. Gorbacheva, Lyudmila Y. Orekhova, Vadim V. Tachalov A30 Ukrainian experience in hybrid war – the challenge to update algorithms for personalized care and early prevention of different military injuries Olena I. Grechanyk, Rizvan Ya. Abdullaiev, Rostyslav V. Bubnov A31 Tear fluid biomarkers: a comparison of tear fluid sampling and storage protocols Suzanne Hagan, Eilidh Martin, Ian Pearce, Katherine Oliver A32 The correlation of dietary habits with gingival problems during menstruation Cenk Haytac, Fariz Salimov, Servin Yoksul, Anatoly A. Kunin, Natalia S. Moiseeva A33 Genomic medicine in a contemporary Spanish population of prostate cancer: our experience Bernardo Herrera-Imbroda, Sergio del Río-González, Maria Fernanda Lara, Antonia Angulo, Francisco Javier Machuca Santa-Cruz A34 Challenges, opportunities and collaborations for personalized medicine applicability in uro-oncological disease Bernardo Herrera-Imbroda, Sergio del Río-González, Maria Fernanda Lara A35 Metabolic hallmarks of cancer as targets for a personalized therapy John Ionescu A36 Influence of genetic polymorphism as a predictor of the development of periodontal disease in patients with gastric ulcer and 12 duodenal ulcer Alfiya Z. Isamulaeva, Anatoly A. Kunin, Shamil Sh. Magomedov, Aida I. Isamulaeva A37 Challenges in diabetic macular edema Tatjana Josifova A38 Overview of the EPMA strategies in laboratory medicine relevant for PPPM Marko Kapalla, Juraj Kubáň, Olga Golubnitschaja, Vincenzo Costigliola A39 EPMA initiative for effective organization of medical travel: European concepts and criteria Vincenzo Costigliola, Marko Kapalla, Juraj Kubáň, Olga Golubnitschaja A40 Design and innovation in e-textiles: implications for PPPM Anthony Kent, Tom Fisher, Tilak Dias A41 Biobank in Pilsen as a member of national node BBMRI_CZ Judita Kinkorová, Ondřej Topolčan A42 Big data in personalized medicine: hype and hope Matthias Kohl A43 The 3P approach as the platform of the European Dentistry Department (DPPPD) Anatoly A. Kunin, Natalia S. Moiseeva A44 The endometrium cytokine patterns for predictive diagnosis of proliferation severity and cancer prevention Andrii I. Kurchenko, Vasyl A. Beniuk, Vadym M. Goncharenko, Rostyslav V. Bubnov, Nadiya V. Boyko, Andriy M. Strokan A45 A monocyte-based in-vitro system for testing individual responses to the implanted material: future for personalized implant construction Julia Kzhyshkowska, Alexandru Gudima, Ksenia S. Stankevich, Victor D. Filimonov4, Harald Klüter, Evgeniya M. Mamontova, Sergei I. Tverdokhlebov A46 Prediction and prevention of adverse health effects by meteorological factors: Biomarker patterns and creation of a device for self-monitoring and integrated care Ulyana B. Lushchyk, Viktor V. Novytskyy, Igor P. Babii, Nadiya G. Lushchyk, Lyudmyla S. Riabets, Ivanna I. Legka A47 Targeting "disease signatures" towards personalized healthcare Mira Marcus-Kalish, Alexis Mitelpunkt, Tal Galili, Neta Shachar, Yoav Benjamini A48 Influence of the skin imperfection on the personal quality of life and possible tools for objective diagnosis Agnieszka Migasiewicz, Markus Pelleter, Joanna Bauer, Ewelina Dereń, Halina Podbielska A49 The new direction in caries prevention based on the ultrastructure of dental hard tissues and filling materials Natalia S. Moiseeva, Anatoly A. Kunin, Dmitry A. Kunin A50 The use of LED radiation in prevention of dental diseases Natalia S. Moiseeva, Yury A. Ippolitov, Dmitry A. Kunin, Alexei N. Morozov, Natalia V. Chirkova, Nakhid T. Aliev A51 Status of endothelial progenitor cells in diabetic nephropathy: predictive and preventive potentials Mahmood S. Mozaffari, Jun Yao Liu, Babak Baban A52 The status of glucocorticoid-induced leucine zipper protein in salivary gland in Sjögren’s syndrome: predictive and personalized treatment potentials Mahmood S. Mozaffari, Jun Yao Liu, Rafik Abdelsayed, Xing-Ming Shi, Babak Baban A53 Maximal aerobic capacity - important quality marker of health Jaroslav Novák, Milan Štork, Václav Zeman A54 The EMPOWER project: laboratory medicine and Horizon 2020 Wytze P. Oosterhuis, Elvar Theodorsson A55 Personality profile manifestations in patient’s attitude to oral care and adherence to doctor’s prescriptions Lyudmila Y. Orekhova, Tatyana V. Kudryavtseva, Elena R. Isaeva, Vadim V. Tachalov, Ekaterina S. Loboda A56 Results of an European survey on personalized medicine addressed to directions of laboratory medicine Mario Pazzagli, Francesca Malentacchi, Irene Mancini, Ivan Brandslund, Pieter Vermeersch, Matthias Schwab, Janja Marc, Ron H.N. van Schaik, Gerard Siest, Elvar Theodorsson, Chiara Di Resta A57 MCI or early dementia predictive speech based diagnosis techniques Matus Pleva, Jozef Juhar A58 Personalized speech based mobile application for eHealth Matus Pleva, Jozef Juhar A59 Circulating tumor cell-free DNA as the biomarker in the management of cancer patients Jiří Polívka jr., Filip Janků, Martin Pešta, Jan Doležal, Milena Králíčková, Jiří Polívka A60 Complex stroke care – educational programme in Stroke Centre University Hospital Plzen Jiří Polívka, Alena Lukešová, Nina Müllerová, Petr Ševčík, Vladimír Rohan A61 Sleep apnea and sleep fragmentation contribute to brain aging Kneginja Richter, Lence Miloseva, Günter Niklewski A62 Personalised approach for sleep disturbances in shift workers Kneginja Richter, Jens Acker, Guenter Niklewski A63 Medical travel and innovative PPPM clusters: new concept of integration Olga Safonicheva, Vincenzo Costigliola A64 Medical travel and women health Olga Safonicheva A65 Continuity of generations in the training of specialists in the field of reconstructive microsurgery Maxim Sautin, Janna Sinelnikova, Sergey Suchkov A66 Telemonitoring of stroke patients – empirical evidence of individual risk management results from an observational study in Germany Songül Secer, Stephan von Bandemer A67 Women’s increasing breast cancer risk with n-6 fatty acid intake explained by estrogen-fatty acid interactive effect on DNA damage: implications for gender-specific nutrition within personalized medicine Niva Shapira A68 Cytobacterioscopy of the gingival crevicular fluid as a method for preventive diagnosis of periodontal diseases Aleksandr Shcherbakov, Anatoly A. Kunin, Natalia S. Moiseeva A69 Use of specially treated composites in dentistry to avoid violations of aesthetics Bogdan R. Shumilovich, Zhanna Lipkind, Yulia Vorobieva, Dmitry A. Kunin, Anastasiia V. Sudareva A70 National eHealth system – platform for preventive, predictive and personalized diabetes care Ivica Smokovski, Tatjana Milenkovic A72 The common energy levels of Prof. Szent-Györgyi, the intrinsic chemistry of melanin, and the muscle physiopathology. Implications in the context of Preventive, Predictive, and Personalized Medicine Arturo Solís-Herrera, María del Carmen Arias-Esparza, Sergey Suchkov A73 Plurality and individuality of hepatocellular carcinoma: PPPM perspectives Krishna Chander Sridhar, Olga Golubnitschaja A74 Strategic aspects of higher medical education reforms to secure newer educational platforms for getting biopharma professionals matures Maria Studneva, Sihong Song, James Creeden, Мark Мandrik, Sergey Suchkov A75 Overview of the strategies and activities of the European Federation of Clinical Chemistry and Laboratory Medicine, (EFLM) Elvar Theodorsson, EFLM A76 New spectroscopic techniques for point of care label free diagnostics Syed A. M. Tofail A77 Tumor markers for personalized medicine and oncology - the role of Laboratory Medicine Ondřej Topolčan, Judita Kinkorová, Ondřej Fiala, Marie Karlíková, Šárka Svobodová, Radek Kučera, Radka Fuchsová, Vladislav Třeška, Václav Šimánek, Ladislav Pecen, Jan Šoupal, Štěpán Svačina2 A78 Modern medical terminology (MMT) as a driver of the global educational reforms Evgeniya Tretyak, Maria Studneva, Sergey Suchkov A79 Juvenile hypertension; the relevance of novel predictive, preventive and personalized assessment of its determinants Francesca M. Trovato, G. Fabio Martines, Daniela Brischetto, Daniela Catalano, Giuseppe Musumeci, Guglielmo M. Trovato A80 Proteomarkers Biotech George Th. Tsangaris, Athanasios K. Anagnostopoulos A81 Proteomics and mass spectrometry based non-invasive prenatal testing of fetal health and pregnancy complications George Th. Tsangaris, Athanasios K. Anagnostopoulos A82 Integrated Ecosystem for an Integrated Care model for Heart Failure (HF) patients including related comorbidities (ZENITH) José Verdú, German Gutiérrez, Jordi Rovira, Marta Martinez, Lutz Fleischhacker, Donna Green, Arthur Garson, Elena Tamburini, Stefano Cuomo, Juan Martinez-Leon, Teresa Abrisqueta, Hans-Peter Brunner-La Rocca, Tiny Jaarsma, Teresa Arredondo, Cecilia Vera, Giuseppe Fico, Olga Golubnitschaja, Fernando Arribas, Martina Onderco, Isabel Vara, on behalf of ZENITH consortium A83 Predictive, preventive and personalized medicine in diabetes onset and complication (MOSAIC project) José Verdú, Francesco Sambo, Barbara Di Camillo, Claudio Cobelli, Andrea Facchinetti, Giuseppe Fico, Riccardo Bellazzi, Lucia Sacchi, Arianna Dagliati, Daniele Segnani, Valentina Tibollo, Manuel Ottaviano, Rafael Gabriel, Leif Groop, Jacqueline Postma, Antonio Martinez, Liisa Hakaste, Tiinamaija Tuomi, Konstantia Zarkogianni, on behalf of MOSAIC consortium A84 Possibilities for personalized therapy of diabetes using in vitro screening of insulin and oral hypoglycemic agents Igor Volchek, Nina Pototskaya, Andrey Petrov A85 The innovative technology for personalized therapy of human diseases based on in vitro drug screening Igor Volchek, Nadezhda Pototskaya, Andrey Petrov A86 Bone destruction and temporomandibular joint: predictive markers, pathogenetic aspects and quality of life Ülle Voog-Oras, Oksana Jagur, Edvitar Leibur, Priit Niibo, Triin Jagomägi, Minh Son Nguyen, Chris Pruunsild, Dagmar Piikov, Mare Saag A87 Sub-optimal health management – global vision for concepts in medical travel Wei Wang A88 Sub-optimal health management: synergic PPPM-TCAM approach Wei Wang A89 Innovative technologies for minimal invasive diagnostics Andreas Weinhäusel, Walter Pulverer, Matthias Wielscher, Manuela Hofner, Christa Noehammer, Regina Soldo, Peter Hettegger, Istvan Gyurjan, Ronald Kulovics, Silvia Schönthaler, Gabriel Beikircher, Albert Kriegner, Stephan Pabinger, Klemens Vierlinger A90 Rare disease diobanks for personalized medicine Ayşe Yüzbaşıoğlu, Meral Özgüç, Member of EuroBioBank - European Network of DNA, Cell and Tissue Banks for Rare Diseases
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- 2016
398. Global methodology for developmental neurotoxicity testing inhumans and animals early and chronically exposed to chemicalcontaminants
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Abraham, Jella-Andrea, Golubnitschaja, Olga, Akhmetov, Ildar, Andrews, Russell J., Quintana, Leonidas, Baban, Babak, Liu, Jun Yao, Qin, Xu, Wang, Tailing, Mozaffari, Mahmood S., Bati, Viktoriia V., Meleshko, Tamara V., Levchuk, Olga B., Boyko, Nadiya V., Bauer, Joanna, Boerner, Ewa, Podbielska, Halina, Bomba, Alojz, Petrov, Viktor O., Drobnych, Volodymyr G., Bubnov, Rostyslav V., Bykova, Oksana M., Brunner-La Rocca, Hans-Peter, Fleischhacker, Lutz, Heemskerk, Frank, Helms, Thomas, Jaarsma, Tiny, Kinkorová, Judita, Ramaekers, Jan, Ruff, Peter, Schnur, Ivana, Vanoli, Emilio, Verdu, Jose, Grabovetskyi, Sergiy A., Mykhalchenko, Olena M., Tymoshok, Natalia O., Shcherbakov, Oleksandr B., Semeniv, Igor P., Spivak, Mykola Y., Ostapenko, Tetyana V., Kobyliak, Nazarii M., Zholobak, Nadiya M., Spivak, Mykola Ya., Cauchi, John Paul, Cherepakhin, Dmitrii, Bakay, Marina, Borovikov, Artem, Suchkov, Sergey, Cieślik, Barbara, Migasiewicz, Agnieszka, Podbielska, Maria-Luiza, Pelleter, Markus, Giemza, Agnieszka, Cirak, Sebahattin, Del Re, Marzia, Bordi, Paola, Citi, Valentina, Palombi, Marta, Pinto, Carmine, Tiseo, Marcello, Danesi, Romano, Einhorn, Lukas, Fazekas, Judit, Muhr, Martina, Schoos, Alexandra, Panakova, Lucia, Herrmann, Ina, Manzano-Szalai, Krisztina, Oida, Kumiko, Fiebiger, Edda, Singer, Josef, Jensen-Jarolim, Erika, Elnar, Arpiné A., Ouamara, Nadia, Boyko, Nadiya, Coumoul, Xavier, Antignac, Jean-Philippe, Le Bizec, Bruno, Eppe, Gauthier, Renaut, Jenny, Bonn, Torsten, Guignard, Cédric, Ferrante, Margherita, Chiusano, Maria Liusa, Cuzzocrea, Salvatore, O’Keeffe, Gerard, Cryan, John, Bisson, Michelle, Barakat, Amina, Hmamouchi, Ihsane, Zawia, Nasser, Kanthasamy, Anumantha, Kisby, Glen E., Alves, Rui, Pérez, Oscar Villacañas, Burgard, Kim, Spencer, Peter, Bomba, Norbert, Haranta, Martin, Zaitseva, Nina, May, Irina, Grojean, Stéphanie, Body-Malapel, Mathilde, Harari, Florencia, Harari, Raul, Yeghiazaryan, Kristina, Calabrese, Vittorio, Nemos, Christophe, Soulimani, Rachid, Evsevyeva, Maria E., Mishenko, Elena A., Kumukova, Zurida V., Chudnovsky, Evgeniy V., Smirnova, Tatyana A., Ivanova, Ludmila V., Eremin, Michail V., Rostovtseva, Maria V., Koshel, Vladimir I., Sergeeva, Oksana V., Konovalova, Nadesgda M., Girotra, Shantanu, Debald, Manuel, Kuhn, Walther, Goncharenko, Vadym M., Lushchyk, Ulyana, Grech, Godfrey, Konieczka, Katarzyna, Erwich, Jan Jaap, Costigliola, Vincenzo, Gembruch, Ulrich, Beniuk, Vasyl O., Kalenska, Olga V., Melnychuk, Olga, Gorbacheva, Irina A., Orekhova, Lyudmila Y., Tachalov, Vadim V., Grechanyk, Olena I., Abdullaiev, Rizvan Ya., Hagan, Suzanne, Martin, Eilidh, Pearce, Ian, Oliver, Katherine, Haytac, Cenk, Salimov, Fariz, Yoksul, Servin, Kunin, Anatoly A., Moiseeva, Natalia S., Herrera-Imbroda, Bernardo, del Río-González, Sergio, Lara, Maria Fernanda, Angulo, Antonia, Machuca Santa-Cruz, Francisco Javier, Ionescu, John, Isamulaeva, Alfiya Z., Magomedov, Shamil Sh., Isamulaeva, Aida I., Josifova, Tatjana, Kapalla, Marko, Kubáň, Juraj, Kent, Anthony, Fisher, Tom, Dias, Tilak, Topolčan, Ondřej, Kohl, Matthias, Kurchenko, Andrii I., Beniuk, Vasyl A., Strokan, Andriy M., Kzhyshkowska, Julia, Gudima, Alexandru, Stankevich, Ksenia S., Filimonov, Victor D., Klüter, Harald, Mamontova, Evgeniya M., Tverdokhlebov, Sergei I., Lushchyk, Ulyana B., Novytskyy, Viktor V., Babii, Igor P., Lushchyk, Nadiya G., Riabets, Lyudmyla S., Legka, Ivanna I., Marcus-Kalish, Mira, Mitelpunkt, Alexis, Galili, Tal, Shachar, Neta, Benjamini, Yoav, Dereń, Ewelina, Kunin, Dmitry A., Ippolitov, Yury A., Morozov, Alexei N., Chirkova, Natalia V., Aliev, Nakhid T., Abdelsayed, Rafik, Shi, Xing-Ming, Novák, Jaroslav, Štork, Milan, Zeman, Václav, Oosterhuis, Wytze P., Theodorsson, Elvar, Kudryavtseva, Tatyana V., Isaeva, Elena R., Loboda, Ekaterina S., Pazzagli, Mario, Malentacchi, Francesca, Mancini, Irene, Brandslund, Ivan, Vermeersch, Pieter, Schwab, Matthias, Marc, Janja, van Schaik, Ron H. N., Siest, Gerard, Di Resta, Chiara, Pleva, Matus, Juhar, Jozef, Polívka, Jiří, Janků, Filip, Pešta, Martin, Doležal, Jan, Králíčková, Milena, Lukešová, Alena, Müllerová, Nina, Ševčík, Petr, Rohan, Vladimír, Richter, Kneginja, Miloseva, Lence, Niklewski, Günter, Acker, Jens, Niklewski, Guenter, Safonicheva, Olga, Sautin, Maxim, Sinelnikova, Janna, Secer, Songül, von Bandemer, Stephan, Shapira, Niva, Shcherbakov, Aleksandr, Shumilovich, Bogdan R., Lipkind, Zhanna, Vorobieva, Yulia, Sudareva, Anastasiia V., Smokovski, Ivica, Milenkovic, Tatjana, Solís-Herrera, Arturo, Arias-Esparza, María del Carmen, Sridhar, Krishna Chander, Studneva, Maria, Song, Sihong, Creeden, James, Мandrik, Мark, Tofail, Syed A. M., Fiala, Ondřej, Karlíková, Marie, Svobodová, Šárka, Kučera, Radek, Fuchsová, Radka, Třeška, Vladislav, Šimánek, Václav, Pecen, Ladislav, Šoupal, Jan, Svačina, Štěpán, Tretyak, Evgeniya, Trovato, Francesca M., Martines, Giuseppe Fabio, Brischetto, Daniela, Catalano, Daniela, Musumeci, Giuseppe, Trovato, Guglielmo M., Tsangaris, George Th., Anagnostopoulos, Athanasios K., Verdú, José, Gutiérrez, German, Rovira, Jordi, Martinez, Marta, Green, Donna, Garson, Arthur, Tamburini, Elena, Cuomo, Stefano, Martinez-Leon, Juan, Abrisqueta, Teresa, Arredondo, Teresa, Vera, Cecilia, Fico, Giuseppe, Arribas, Fernando, Onderco, Martina, Vara, Isabel, Sambo, Francesco, Di Camillo, Barbara, Cobelli, Claudio, Facchinetti, Andrea, Bellazzi, Riccardo, Sacchi, Lucia, Dagliati, Arianna, Segnani, Daniele, Tibollo, Valentina, Ottaviano, Manuel, Gabriel, Rafael, Groop, Leif, Postma, Jacqueline, Martinez, Antonio, Hakaste, Liisa, Tuomi, Tiinamaija, Zarkogianni, Konstantia, Volchek, Igor, Pototskaya, Nina, Petrov, Andrey, Pototskaya, Nadezhda, Voog-Oras, Ülle, Jagur, Oksana, Leibur, Edvitar, Niibo, Priit, Jagomägi, Triin, Nguyen, Minh Son, Pruunsild, Chris, Piikov, Dagmar, Saag, Mare, Wang, Wei, Weinhäusel, Andreas, Pulverer, Walter, Wielscher, Matthias, Hofner, Manuela, Noehammer, Christa, Soldo, Regina, Hettegger, Peter, Gyurjan, Istvan, Kulovics, Ronald, Schönthaler, Silvia, Beikircher, Gabriel, Kriegner, Albert, Pabinger, Stephan, Vierlinger, Klemens, Yüzbaşıoğlu, Ayşe, and Özgüç, Meral
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- 2016
399. BE-POSITIVE: Beyond progression after tyrosine kinase inhibitor in EGFR- positive non small cell lung cancer patients. Results from a multicenter Italian observational study
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Vavalà, Tiziana, Follador, Alessandro, Tiseo, Marcello, Galetta, Domenico, Morabito, Alessandro, Di Maio, Massimo, Martelli, Olga, Caffo, Orazio, Piovano, Pier Luigi, Cortinovis, Diego, Zilembo, Nicoletta, Casartelli, Clelia, Banna, Giuseppe Luigi, Ardizzoia, Antonio, Barzelloni, Maria Luisa, Bearz, Alessandra, Genestreti, Giovenzio, Mucciarini, Claudia, Filipazzi, Virginio, Menis, Jessica, Rizzo, Elisa, Barbieri, Fausto, Rijavec, Erika, Cecere, Fabiana, Bria, Emilio, Spitaleri, Gianluca, Rossi, Antonio, and Novello, Silvia
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Male ,Pulmonary and Respiratory Medicine ,Cancer Research ,Lung Neoplasms ,Drug Resistance ,Acquired resistance ,EGFR mutation ,EGFR tyrosine kinase inhibitors ,First line ,Non small cell lung cancer ,Second line ,Oncology ,Risk Factors ,Carcinoma, Non-Small-Cell Lung ,80 and over ,Humans ,Neoplasm Metastasis ,Non-Small-Cell Lung ,Protein Kinase Inhibitors ,Aged ,Aged, 80 and over ,Disease Progression ,Drug Resistance, Neoplasm ,ErbB Receptors ,Female ,Italy ,Middle Aged ,Mutation ,Neoplasm Staging ,Retreatment ,Treatment Outcome ,Carcinoma ,Neoplasm - Abstract
Non-small-cell-lung-cancer (NSCLC) patients harbouring epidermal growth factor receptor (EGFR) mutations develop drug resistance after 9-12 months of EGFR tyrosine kinase inhibitors (TKIs) therapy pointing out the issue of the second-line treatment choice.From June 2009 until May 2013 patients affected by advanced NSCLC harbouring EGFR mutations receiving first-line TKI were collected mainly retrospectively in 24 Italian Centers. Primary objective was to describe the percentage of EGFR mutated patients receiving second-line therapy after progression to first-line EGFR-TKIs assessing the type, the activity in terms of objective response rate (ORR), efficacy in terms of progression free survival (PFS) and overall survival (OS), and safety of second-line treatment. Secondary objective was to describe the efficacy of first-line EGFR-TKIs.312 patients were included. Most of them were females (203, 65.1%), never smokers (200, 64.1%), with adenocarcinoma histology (290, 92.9%). The most common mutations were EGFR exon 19 deletion and L858R, detected in 186 and 97 cases (59.6% and 31.1%), respectively. At data cut-off, 274 patients (95.1%) received any second-line treatment (including best supportive care or local treatments only). A total of 163 patients received second-line systemic therapy with an ORR of 20.9% (95% CI:14.62-27.10), a median PFS and OS of 4.7 (95% CI:3.81-5.26) and 24.5 (95% CI:21.65-27.37) months, respectively. Grade 3-4 hematological and non-hematological toxicities were reported in 9% and 6.3% of 144 patients treated with chemotherapy while non-hematological toxicity was reported in 4 cases of the 17 patients receiving second-line target agents.BE-Positive is the first multicenter observational study reporting outcomes of therapies in a "real-life Caucasian EGFR-mutated population", highlighting the need of further researches about new treatment strategies in this setting.
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- 2016
400. Efficacy and safety of long-acting pasireotide or everolimus alone or in combination in patients with advanced carcinoids of the lung and thymus (LUNA): an open-label, multicentre, randomised, phase 2 trial
- Author
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Ferolla, Piero, primary, Brizzi, Maria Pia, additional, Meyer, Tim, additional, Mansoor, Wasat, additional, Mazieres, Julien, additional, Do Cao, Christine, additional, Léna, Hervé, additional, Berruti, Alfredo, additional, Damiano, Vincenzo, additional, Buikhuisen, Wieneke, additional, Grønbæk, Henning, additional, Lombard-Bohas, Catherine, additional, Grohé, Christian, additional, Minotti, Vincenzo, additional, Tiseo, Marcello, additional, De Castro, Javier, additional, Reed, Nicholas, additional, Gislimberti, Gabriella, additional, Singh, Neha, additional, Stankovic, Miona, additional, Öberg, Kjell, additional, and Baudin, Eric, additional
- Published
- 2017
- Full Text
- View/download PDF
Catalog
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