66 results on '"Persano, Mara"'
Search Results
52. Drug-related toxicity in breast cancer patients: a new path towards tailored treatment?—A narrative review
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Lai, Eleonora, primary, Persano, Mara, additional, Dubois, Marco, additional, Spanu, Dario, additional, Donisi, Clelia, additional, Pozzari, Marta, additional, Deias, Giulia, additional, Saba, Giorgio, additional, Migliari, Marco, additional, Liscia, Nicole, additional, Dessì, Mariele, additional, Scartozzi, Mario, additional, and Atzori, Francesco, additional
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- 2021
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53. Retrospective survival analysis in patients with metastatic pancreatic ductal adenocarcinoma with insulin-treated type 2 diabetes mellitus
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Pretta, Andrea, primary, Ziranu, Pina, additional, Puzzoni, Marco, additional, Lai, Eleonora, additional, Orsi, Giulia, additional, Liscia, Nicole, additional, Molinaro, Eleonora, additional, Mariani, Stefano, additional, Riggi, Laura, additional, Rovesti, Giulia, additional, Dubois, Marco, additional, Migliari, Marco, additional, Persano, Mara, additional, Saba, Giorgio, additional, Impera, Valentino, additional, Musio, Francesca, additional, Batzella, Erich, additional, Demurtas, Laura, additional, Pusceddu, Valeria, additional, Astara, Giorgio, additional, Faloppi, Luca, additional, Casadei Gardini, Andrea, additional, Andrikou, Kalliopi, additional, Cascinu, Stefano, additional, and Scartozzi, Mario, additional
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- 2020
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54. Molecular-Biology-Driven Treatment for Metastatic Colorectal Cancer
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Lai, Eleonora, primary, Liscia, Nicole, additional, Donisi, Clelia, additional, Mariani, Stefano, additional, Tolu, Simona, additional, Pretta, Andrea, additional, Persano, Mara, additional, Pinna, Giovanna, additional, Balconi, Francesca, additional, Pireddu, Annagrazia, additional, Impera, Valentino, additional, Dubois, Marco, additional, Migliari, Marco, additional, Spanu, Dario, additional, Saba, Giorgio, additional, Camera, Silvia, additional, Musio, Francesca, additional, Ziranu, Pina, additional, Puzzoni, Marco, additional, Demurtas, Laura, additional, Pusceddu, Valeria, additional, Dettori, Manuela, additional, Massa, Elena, additional, Atzori, Francesco, additional, Dessì, Mariele, additional, Astara, Giorgio, additional, Madeddu, Clelia, additional, and Scartozzi, Mario, additional
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- 2020
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55. Why precision medicine should be applied across the continuum of care for metastatic colorectal cancer patients
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Puzzoni, Marco, primary, Ziranu, Pina, additional, Demurtas, Laura, additional, Lai, Eleonora, additional, Mariani, Stefano, additional, Liscia, Nicole, additional, Soro, Paolo, additional, Pretta, Andrea, additional, Impera, Valentino, additional, Camera, Silvia, additional, Musio, Francesca, additional, Persano, Mara, additional, Donisi, Clelia, additional, Tolu, Simona, additional, Balconi, Francesca, additional, and Scartozzi, Mario, additional
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- 2020
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56. New therapeutic targets in pancreatic cancer
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Lai, Eleonora, primary, Puzzoni, Marco, additional, Ziranu, Pina, additional, Pretta, Andrea, additional, Impera, Valentino, additional, Mariani, Stefano, additional, Liscia, Nicole, additional, Soro, Paolo, additional, Musio, Francesca, additional, Persano, Mara, additional, Donisi, Clelia, additional, Tolu, Simona, additional, Balconi, Francesca, additional, Pireddu, Annagrazia, additional, Demurtas, Laura, additional, Pusceddu, Valeria, additional, Camera, Silvia, additional, Sclafani, Francesco, additional, and Scartozzi, Mario, additional
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- 2019
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57. Retrospective survival analysis in patients with metastatic pancreatic ductal adenocarcinoma with insulin-treated type 2 diabetes mellitus
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Pretta, Andrea, Ziranu, Pina, Puzzoni, Marco, Lai, Eleonora, Orsi, Giulia, Liscia, Nicole, Molinaro, Eleonora, Mariani, Stefano, Riggi, Laura, Rovesti, Giulia, Dubois, Marco, Migliari, Marco, Persano, Mara, Saba, Giorgio, Impera, Valentino, Musio, Francesca, Batzella, Erich, Demurtas, Laura, Pusceddu, Valeria, Astara, Giorgio, Faloppi, Luca, Casadei Gardini, Andrea, Andrikou, Kalliopi, Cascinu, Stefano, and Scartozzi, Mario
- Abstract
Introduction: The association between pancreatic ductal adenocarcinoma (PDAC) and type 2 diabetes mellitus (DM2) has long been evaluated and the role of antidiabetic medications such as metformin has also been investigated. The objective of this study was to examine the association between insulin use and overall survival (OS) in patients with advanced PDAC and DM2.Methods: We retrospectively collected data from 164 patients, including an exploratory cohort of 96 patients from Medical Oncology Unit, University Hospital and University of Cagliari, Italy, and a validation cohort of 68 patients from Medical Oncology of Modena University Hospital. Patients had metastatic disease and received a first-line gemcitabine-based chemotherapy and, subsequently, a second-line fluoropyrimidines-based chemotherapy. We performed univariate analysis to evaluate correlation between long-term diabetes and overall survival. Then we performed multivariate analysis, adjusting for sex, metastatic sites, Eastern Cooperative Oncology Group Performance Status, Ca19.9 levels, N/L ratio, and lactate dehydrogenase levels at diagnosis, to confirm the independence of the variable.Results: In the exploratory cohort, DM2 was significantly associated with higher median OS at univariate analysis (16 vs 10 months; p= 0.004). This result was confirmed by validation cohort (11 months vs 6 months; p= 0.01). In multivariate analysis, insulin-treated patients compared with non diabetic patients showed a significantly increased survival of 4.6 months (p= 0.03).Conclusions: Patients with insulin-treated metastatic PDAC showed better OS than non diabetic patients, as demonstrated by both cohorts. The correlation between OS and insulin-treated DM2 should be investigated further through a prospective clinical trial.
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- 2021
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58. Thyroid dysfunction and immune checkpoint inhibitors: Effect on survival in elderly patients.
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Donisi, Clelia, Pretta, Andrea, Lai, Eleonora, Liscia, Nicole, Cadoni, Andrea, Persano, Mara, Mariani, Stefano, Pinna, Giovanna, Spanu, Dario, Saba, Giorgio, Migliari, Marco, Dubois, Marco, Atzori, Francesco, Dessì, Mariele, Puzzoni, Marco, Pusceddu, Valeria, Ziranu, Pina, Madeddu, Clelia, Massa, Elena, and Scartozzi, Mario
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- 2023
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59. Prognostic impact of depth of response (DpR) and early tumour shrinkage (ETS) in patients (pts) with BRAF V600E mutated (mut) metastatic colorectal cancer (mCRC) receiving targeted therapy (TT) as second-line treatment.
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Vetere, Guglielmo, Germani, Marco Maria, Bensi, Maria, Antoniotti, Carlotta, Lonardi, Sara, Passardi, Alessandro, Ghelardi, Filippo, Calegari, Maria Alessandra, Borelli, Beatrice, Santucci, Sara, Intini, Rossana, Cristarella, Eleonora, Persano, Mara, Puccini, Alberto, Lavacchi, Daniele, Noto, Laura, Zichi, Clizia, Giampieri, Riccardo, Salati, Massimiliano, and Cremolini, Chiara
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- 2023
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60. Real-World Data on Ivosidenib in Patients with Previously Treated Isocitrate Dehydrogenase 1-Mutated Intrahepatic Cholangiocarcinomas: An Early Exploratory Analysis
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Margherita Rimini, Valentina Burgio, Lorenzo Antonuzzo, Lorenza Rimassa, Ester Oneda, Daniele Lavacchi, Nicola Personeni, Francesca Ratti, Federica Pedica, Angelo Della Corte, Mara Persano, Francesco De Cobelli, Luca Aldrighetti, Mario Scartozzi, Stefano Cascinu, Andrea Casadei-Gardini, Rimini, Margherita, Burgio, Valentina, Antonuzzo, Lorenzo, Rimassa, Lorenza, Oneda, Ester, Lavacchi, Daniele, Personeni, Nicola, Ratti, Francesca, Pedica, Federica, Della Corte, Angelo, Persano, Mara, De Cobelli, Francesco, Aldrighetti, Luca, Scartozzi, Mario, Cascinu, Stefano, and Casadei-Gardini, Andrea
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Cholangiocarcinoma ,Cancer Research ,Bile Ducts, Intrahepatic ,Bile Duct Neoplasms ,Oncology ,Pyridines ,Mutation ,Glycine ,Humans ,Pharmacology (medical) ,Isocitrate Dehydrogenase - Abstract
The results of the phase III ClarIDHy trial have led to US FDA approval of ivosidenib as a therapeutic option for patients with locally advanced or metastatic cholangiocarcinoma (CCA) harboring isocitrate dehydrogenase 1 (IDH1) mutations.In this study, we report the first real-world experience including eight patients with previously treated locally advanced or metastatic IDH1-mutated CCA treated with ivosidenib.Patients treated with ivosidenib as second and third line for advanced CCA were collected with the aim of evaluating the survival outcomes. A molecular study has been performed by next-generation sequencing assay.After a median follow up of 9.4 months, median progression-free survival (PFS) from the start of treatment with ivosidenib was 4.4 months (95% confidence interval [CI] 3.3-5.8), whereas median overall survival (OS) was not reached. The disease control rate was 62.5%, with two patients achieving a partial response (25%); 12.5% of patients experienced a treatment-related adverse event (AE), but no grade 3 or higher AEs were reported. The observed grade 2 AEs were prolonged QT interval and hypomagnesemia (25% of the sample). Molecular profiling was performed on six of eight patients, highlighting TP53, BAP1, CDKN2A and CDKN2B as the most common co-altered genes in these patients.Efficacy outcomes were consistent with those reported in the ClarIDHy trial. Real-world experiences on larger samples are needed in order to confirm our results.
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- 2022
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61. Validation of the easy-to-use lenvatinib prognostic index to predict prognosis in advanced hepatocellular carcinoma patients treated with lenvatinib
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Margherita Rimini, Wonseok Kang, Valentina Burgio, Mara Persano, Tamoko Aoki, Shigeo Shimose, Toshifumi Tada, Takashi Kumada, Takuya Sho, Eleonora Lai, Ciro Celsa, Claudia Campani, Matteo Tonnini, Emiliano Tamburini, Atsushi Hiraoka, Koichi Takaguchi, Naoshi Nishida, Hideki Iwamoto, Ei Itobayashi, Kunihiko Tsuji, Naoya Sakamoto, Toru Ishikawa, Hidenori Toyoda, Masatoshi Kudo, Takumi Kawaguchi, Takeshi Hatanaka, Kazugiro Nouso, Goki Suda, Giuseppe Cabibbo, Fabio Marra, Angelo Della Corte, Francesca Ratti, Federica Pedica, Francesco De Cobelli, Luca Aldrighetti, Mario Scartozzi, Stefano Cascinu, Andrea Casadei‐Gardini, Rimini, Margherita, Kang, Wonseok, Burgio, Valentina, Persano, Mara, Aoki, Tamoko, Shimose, Shigeo, Tada, Toshifumi, Kumada, Takashi, Sho, Takuya, Lai, Eleonora, Celsa, Ciro, Campani, Claudia, Tonnini, Matteo, Tamburini, Emiliano, Hiraoka, Atsushi, Takaguchi, Koichi, Nishida, Naoshi, Iwamoto, Hideki, Itobayashi, Ei, Tsuji, Kunihiko, Sakamoto, Naoya, Ishikawa, Toru, Toyoda, Hidenori, Kudo, Masatoshi, Kawaguchi, Takumi, Hatanaka, Takeshi, Nouso, Kazugiro, Suda, Goki, Cabibbo, Giuseppe, Marra, Fabio, Della Corte, Angelo, Ratti, Francesca, Pedica, Federica, De Cobelli, Francesco, Aldrighetti, Luca, Scartozzi, Mario, Cascinu, Stefano, and Casadei-Gardini, Andrea
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Infectious Diseases ,Hepatology ,prognostic factors ,hepatocellular carcinoma ,lenvatinib - Abstract
Aim The identification of new prognostic factors able to stratify hepatocellular carcinoma patients candidate to first-line therapy is urgent. In the present work we validated the prognostic value of the lenvatinib prognostic index. Methods Data of Eastern and Western patients treated with lenvatinib as first-line for Barcelona Clinic Liver Cancer stage B or C hepatocellular carcinoma were recollected. The lenvatinib prognostic index was composed by three classes of risk according with our previous study. The "low risk" group includes patients with prognostic nutritional index (PNI) >43.3 and with previous transarterial chemoembolization. The "medium risk" group includes patients with PNI >43.3, but without previous transarterial chemoembolization and patients with PNI
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- 2022
62. Introducing immunotherapy for advanced hepatocellular carcinoma patients: Too early or too fast?
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Francesca Musio, Nicole Liscia, Marco Migliari, Andrea Casadei Gardini, Mario Scartozzi, Giorgio Astara, Clelia Donisi, G. Pinna, Pina Ziranu, Clelia Madeddu, Mara Persano, Valeria Pusceddu, S. Tolu, Valentino Impera, Stefano Mariani, S. Camera, Dario Spanu, Marco Puzzoni, Andrea Pretta, Marco Dubois, Giorgio Saba, Francesca Balconi, Eleonora Lai, Annagrazia Pireddu, Lai, Eleonora, Astara, Giorgio, Ziranu, Pina, Pretta, Andrea, Migliari, Marco, Dubois, Marco, Donisi, Clelia, Mariani, Stefano, Liscia, Nicole, Impera, Valentino, Persano, Mara, Tolu, Simona, Balconi, Francesca, Pinna, Giovanna, Spanu, Dario, Pireddu, Annagrazia, Saba, Giorgio, Camera, Silvia, Musio, Francesca, Puzzoni, Marco, Pusceddu, Valeria, Madeddu, Clelia, Casadei Gardini, Andrea, and Scartozzi, Mario
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0301 basic medicine ,Adoptive cell transfer ,Advanced hepatocellular carcinoma ,Oncolytic virus ,Carcinoma, Hepatocellular ,medicine.medical_treatment ,Immune-related toxicity ,Cell therapy ,Immune checkpoint inhibitors ,03 medical and health sciences ,0302 clinical medicine ,Tumor Microenvironment ,Medicine ,Humans ,Immunologic Factors ,Vaccines ,business.industry ,Liver Neoplasms ,Cancer ,Antibodies, Monoclonal ,Hematology ,Immunotherapy ,medicine.disease ,digestive system diseases ,Clinical trial ,030104 developmental biology ,Oncology ,030220 oncology & carcinogenesis ,Hepatocellular carcinoma ,Cancer research ,Cytokines ,business ,Liver cancer - Abstract
Advanced hepatocellular carcinoma (HCC) is the most frequent liver cancer. Immunotherapy has been explored in this disease in order to improve survival outcomes. Nowadays, scientific research is focusing especially on immune checkpoint inhibitors, in particular anti-PD1, anti-PD-L1 and anti-CTLA4 monoclonal antibodies (mAbs), as single-agent or in combination with other immunotherapy agents, target therapies, anti-vascular endothelial growth factor (VEGF) and other agents targeting specific molecular pathways. Other immunotherapy strategies have been assessed or are under investigation in advanced HCC, namely cytokines, adoptive cell therapy, oncolytic virus, cancer vaccines. Each treatment presents specific efficacy and toxicity profiles, strictly related to their mechanism of action and to advanced HCC tumour microenvironment (TME). The aim of this review is to outline the state-of-the-art of immunotherapy in advanced HCC treatment, highlighting data on already investigated treatment strategies, safety and toxicity (including HBV/HCV-related HCC), and ongoing clinical trials focusing on new promising therapeutic weapons.
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- 2020
63. Impact of body mass index on the prognosis of unresectable HCC patients receiving first-line Lenvatinib or atezolizumab plus bevacizumab.
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Rimini M, Stefanini B, Tada T, Suda G, Shimose S, Kudo M, Finkelmeier F, Yoo C, Presa J, Amadeo E, Genovesi V, De Grandis MC, Iavarone M, Marra F, Foschi F, Tamburini E, Rossari F, Vitiello F, Bartalini L, Soldà C, Tovoli F, Vivaldi C, Lonardi S, Silletta M, Kumada T, Sakamoto N, Iwamoto H, Aoki T, Himmelsbach V, Montes M, Hiraoka A, Sho T, Niizeki T, Nishida N, Steup C, Hirooka M, Kariyama K, Tani J, Atsukawa M, Takaguchi K, Itobayashi E, Fukunishi S, Tsuji K, Ishikawa T, Tajiri K, Ochi H, Yasuda S, Toyoda H, Ogawa C, Nishimura T, Hatanaka T, Kakizaki S, Shimada N, Kawata K, Tada F, Ohama H, Nouso K, Morishita A, Tsutsui A, Nagano T, Itokawa N, Okubo T, Arai T, Imai M, Kosaka H, Naganuma A, Koizumi Y, Nakamura S, Kaibori M, Iijima H, Hiasa Y, Persano M, Camera S, Foti S, Aldrighetti L, Cascinu S, Casadei-Gardini A, and Piscaglia F
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- Humans, Bevacizumab therapeutic use, Body Mass Index, Overweight, Prognosis, Thinness, Antibodies, Monoclonal, Humanized therapeutic use, Carcinoma, Hepatocellular, Liver Neoplasms, Phenylurea Compounds therapeutic use, Quinolines therapeutic use
- Abstract
Introduction: Overweight is a negative prognostic factor in the general population in the long term. However, the role of body mass index (BMI) in the short-mid term in advanced tumours is unclear. The present analysis investigates the role of BMI weight classes in a large sample of patients affected by HCC and receiving atezolizumab plus bevacizumab or lenvatinib as first-line treatment., Methods and Material: The cohort included consecutive patients affected by BCLC-c and BCLC-B HCC patients from a multicenter international study group who received atezolizumab plus bevacizumab or lenvatinib as first-line therapy. Population was stratified according to the BMI in under-, over- and normal-weight according to the conventional thresholds. The primary objective of the study was to evaluate the prognostic and predictive impact of BMI in patients affected by advanced or intermediate HCC. Survival curves were estimated using the product-limit method of Kaplan-Meier. The role of stratification factors was analysed with log-rank tests., Results: 1292 consecutive patients with HCC were analysed. 466 (36%) patients were treated with lenvatinib and 826 (64%) patients were treated with atezolizumab plus bevacizumab. In the atezolizumab plus bevacizumab arm, 510 (62%) patients were normal-weight, 52 (6%) underweight and 264 (32%) overweight. At the univariate analysis for OS, underweight patients had significantly shorter OS compared to normal-weight patients, whereas no differences were found between normal-weight versus overweight. Multivariate analysis confirmed that underweight patients had significantly shorter OS compared to normal-weight patients (HR: 1.7; 95% CI: 1.0-2.8; p = .0323). In the lenvatinib arm, 26 patients (5.6%) were categorized as underweight, 256 (54.9%) as normal-weight, and 184 (39.5%) as overweight. At the univariate analysis for OS, no significant differences were found between normal-weight versus underweight and between normal-weight versus overweight, which was confirmed at multivariate analysis., Conclusion: Our analysis highlighted a prognostic role of BMI in a cohort of patients with advanced HCC who received atezolizumab plus bevacizumab, while no prognostic role for low BMI was apparent in patients who received lenvatinib., (© 2024 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
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- 2024
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64. α-FAtE: A new predictive score of response to atezolizumab plus bevacizumab for unresectable hepatocellular carcinoma.
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Rossari F, Tada T, Suda G, Shimose S, Kudo M, Yoo C, Cheon J, Finkelmeier F, Lim HY, Presa J, Masi G, Bergamo F, Amadeo E, Vitiello F, Kumada T, Sakamoto N, Iwamoto H, Aoki T, Chon HJ, Himmelsbach V, Iavarone M, Cabibbo G, Montes M, Foschi FG, Vivaldi C, Soldà C, Sho T, Niizeki T, Nishida N, Steup C, Hirooka M, Kariyama K, Tani J, Atsukawa M, Takaguchi K, Itobayashi E, Fukunishi S, Tsuji K, Ishikawa T, Tajiri K, Ochi H, Yasuda S, Toyoda H, Ogawa C, Nishimura T, Hatanaka T, Kakizaki S, Shimada N, Kawata K, Hiraoka A, Tada F, Ohama H, Nouso K, Morishita A, Tsutsui A, Nagano T, Itokawa N, Okubo T, Imai M, Kosaka H, Naganuma A, Koizumi Y, Nakamura S, Kaibori M, Iijima H, Hiasa Y, Persano M, Burgio V, Piscaglia F, Scartozzi M, Cascinu S, Casadei-Gardini A, and Rimini M
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- Humans, Bevacizumab therapeutic use, Prospective Studies, Carcinoma, Hepatocellular drug therapy, Liver Neoplasms drug therapy, Phenylurea Compounds, Quinolines, Antibodies, Monoclonal, Humanized
- Abstract
Atezolizumab plus bevacizumab (AB) and lenvatinib can be alternatively used as first-line systemic treatment of unresectable hepatocellular carcinoma (HCC). However, no direct comparison of the two regimens has been performed in randomized clinical trials, making the identification of baseline differential predictors of response of major relevance to tailor the best therapeutic option to each patient. Baseline clinical and laboratory characteristics of real-world AB-treated HCC patients were analyzed in uni- and multivariate analyses to find potential prognostic factors of overall survival (OS). Significant variables were incorporated in a composite score (α-FAtE) and it was tested for specificity and sensitivity in receiver operating characteristic (ROC) curve and in multivariate analysis for OS. The score was applied in uni- and multivariate analyses for OS of a comparable lenvatinib-treated HCC population. Finally, comparison between treatments was performed in patients with low and high α-FAtE scores and predictivity estimated by interaction analysis. Time-to-progression (TTP) was a secondary endpoint. OS of AB-treated HCC patients was statistically longer in those with α-fetoprotein <400 ng/mL (HR 0.62, p = .0407), alkaline phosphatase (ALP) <125 IU/L (HR 0.52, p = .0189) and eosinophil count ≥70/μL (HR 0.46, p = .0013). The α-FAtE score was generated by the sum of single points attributed to each variable among the above reported. In ROC curve analysis, superior sensitivity and specificity were achieved by the score compared to individual variables (AUC 0.794, p < .02). Patients with high score had longer OS (HR 0.44, p = .0009) and TTP (HR 0.34, p < .0001) compared to low score if treated with AB, but not with lenvatinib. Overall, AB was superior to lenvatinib in high score patients (HR 0.55, p = .0043) and inferior in low score ones (HR 1.75, p = .0227). At interaction test, low α-FAtE score resulted as negative predictive factor of response to AB (p = .0004). In conclusion, α-FAtE is a novel prognostic and predictive score of response to first-line AB for HCC patients that, if validated in prospective studies, could drive therapeutic choice between lenvatinib and AB., (© 2023 UICC.)
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- 2024
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65. Identification of Atezolizumab Plus Bevacizumab Prognostic Index via Recursive Partitioning Analysis in HCC: The ABE Index.
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Persano M, Rimini M, Tada T, Suda G, Shimose S, Kudo M, Cheon J, Finkelmeier F, Lim HY, Presa J, Masi G, Yoo C, Lonardi S, Pressiani T, Piscaglia F, Kumada T, Rimassa L, Scartozzi M, Cascinu S, and Casadei-Gardini A
- Subjects
- Humans, Prognosis, Bevacizumab therapeutic use, Serum Albumin, Bilirubin, Retrospective Studies, Carcinoma, Hepatocellular pathology, Liver Neoplasms pathology
- Abstract
Background/aim: The purpose of this study was to ascertain a novel prognostic index via recursive partitioning analysis (RPA) in hepatocellular carcinoma (HCC) patients being treated with the combination of atezolizumab plus bevacizumab (ABE) in first-line setting., Patients and Methods: A total of 784 patients with HCC were included in the analysis., Results: RPA identified three groups of patients: high-risk [Child-Pugh B (CP-B) patients; CP-A and Albumin-Bilirubin (ALBI)-2 patients; CP-A and ALBI-1 patients with macrovascular invasion (MVI), and alpha-fetoprotein (α-FP) ≥400 ng/ml]; intermediate-risk [CP-A and ALBI-1 patients with aspartate aminotransferase (AST) normal value (NV), and αFP ≥400 ng/ml, but without MVI; CP-A and ALBI-1 patients with AST increased value (IV), and neutrophil-lymphocyte ratio (NLR) ≥3, but without MVI]; low-risk (CP-A and ALBI-1 patients with AST NV, and αFP <400 ng/ml, but without MVI; CP-A and ALBI-1 patients with AST IV, and NLR <3, but without MVI; CP-A and ALBI-1 patients with MVI, and αFP <400 ng/ml). Overall survival was 7.0 months in high-risk patients (20.8%), 14.2 months in intermediate-risk patients (19.1%), and 22.5 months in low-risk patients (60.1%)., Conclusion: The ABE index allows for easy stratification of HCC patients treated with the combination of ABE in first-line setting., (Copyright © 2023 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.)
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- 2023
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66. Role of the Prognostic Nutritional Index in Predicting Survival in Advanced Hepatocellular Carcinoma Treated with Atezolizumab Plus Bevacizumab.
- Author
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Persano M, Rimini M, Tada T, Suda G, Shimose S, Kudo M, Cheon J, Finkelmeier F, Lim HY, Presa J, Masi G, Yoo C, Lonardi S, Stefanini B, Kumada T, Sakamoto N, Iwamoto H, Aoki T, Chon HJ, Himmelsbach V, Montes M, Vivaldi C, Soldà C, Hiraoka A, Sho T, Niizeki T, Nishida N, Steup C, Hirooka M, Kariyama K, Tani J, Atsukawa M, Takaguchi K, Itobayashi E, Fukunishi S, Tsuji K, Ishikawa T, Tajiri K, Ochi H, Yasuda S, Toyoda H, Ogawa C, Nishimura T, Hatanaka T, Kakizaki S, Shimada N, Kawata K, Tada F, Ohama H, Nouso K, Morishita A, Tsutsui A, Nagano T, Itokawa N, Okubo T, Arai T, Imai M, Kosaka H, Naganuma A, Koizumi Y, Nakamura S, Kaibori M, Iijima H, Hiasa Y, Burgio V, Della Corte A, Ratti F, De Cobelli F, Aldrighetti L, Scartozzi M, Cascinu S, and Casadei-Gardini A
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- Humans, Nutrition Assessment, Prognosis, Bevacizumab therapeutic use, Retrospective Studies, Albumins, Carcinoma, Hepatocellular drug therapy, Liver Neoplasms drug therapy
- Abstract
Introduction: The prognostic nutritional index (PNI) is a multiparametric score introduced by Onodera based on the blood levels of lymphocytes and albumin in patients with gastrointestinal neoplasms. Regarding hepatocellular carcinoma (HCC), its prognostic role has been shown in patients treated with sorafenib and lenvatinib. The aim of this real-world study was to investigate the association between clinical outcomes and PNI in patients being treated with atezolizumab plus bevacizumab., Methods: The overall cohort of this multicentric study included 871 consecutive HCC patients from 5 countries treated with atezolizumab plus bevacizumab in first-line therapy. The PNI was calculated as follows: 10 × serum albumin concentration (g/dL) + 0.005 × peripheral lymphocyte count (number/mm3)., Results: Data regarding lymphocyte counts and albumin levels were available for 773 patients; therefore, these patients were included in the final analysis. The cut-off point of the PNI was determined to be 41 by receiver operating characteristic analysis. 268 patients (34.7%) were categorized as the PNI-low group, while the remaining 505 (65.3%) patients as the PNI-high group. At the univariate analysis, high PNI was associated with longer overall survival (OS) (22.5 vs. 10.1 months, HR 0.34, p <0.01) and progression-free survival (PFS) (8.7 vs. 5.8 months, HR 0.63, p <0.01) compared to patients with low PNI. At the multivariate analysis, high versus low PNI resulted as an independent prognostic factor for OS (HR 0.49, p <0.01) and PFS (HR 0.82, p = 0.01). There was no difference in objective response rate between the two groups (high 26.1% vs. low 19.8%, p = 0.09), while disease control rate was significantly higher in the PNI-high group (76.8% vs. 66.4%, p = 0.01)., Conclusion: PNI is an independent prognostic factor for OS and PFS in HCC patients on first-line treatment with atezolizumab plus bevacizumab., (© 2023 S. Karger AG, Basel.)
- Published
- 2023
- Full Text
- View/download PDF
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