17 results on '"Blake-Cerda M"'
Search Results
2. P2.08-04 Stereotactic Ablative Radiation Therapy to Lung Metastases Associates with Better Outcomes in Oligometastatic Lung Cancer: Prospective Study
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Blake-Cerda, M., primary, Ruiz, F. Lozano, additional, Magos, F. Maldonado, additional, De La Mata-Moya, D., additional, Diaz-Garcia, D.A., additional, Ramírez-Tirado, L., additional, Góngora, M.F. Cuevas, additional, Barrón, F., additional, Gerson, R., additional, and Arrieta, O.G., additional
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- 2019
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3. P1.01-117 Pulmonary Function Monitoring in Patients with Oligometastatic NSCLC Who Receive Stereotactic Body Radiation Therapy
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Arroyo-Hernandez, M., primary, Blake-Cerda, M., additional, Gochicoa-Rangel, L., additional, Monraz-Pérez, S., additional, Góngora, M.F. Cuevas, additional, Bautista, D. Valle, additional, Castillo, P.A. Barragán, additional, Magos, F. Maldonado, additional, Rodríguez, O., additional, Flores, D., additional, and Arrieta, O.G., additional
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- 2019
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4. MA 20.12 Longitudinal Evaluation of Pulmonary Function in Patients with Advanced NSCLC Treated with Concurrent Chemo-Radiotherapy
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Arroyo Hernandez, M., primary, Bouscoulet, L. Torre, additional, Bacon, L., additional, Lozano-Ruiz, F., additional, Gochicoa-Rangel, L., additional, García-Sancho, C., additional, Vergara, E., additional, Martínez Briseño, D., additional, Guzmán-Barragán, A., additional, Fernández Plata, R., additional, Blake Cerda, M., additional, Maldonado, F., additional, and Arrieta, O., additional
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- 2017
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5. Treatment Outcomes and Prognostic Factors in Mexican Patients with Endometrial Carcinoma: the Latin American Experience
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Flores-Balcázar, C., primary, Alvarado-Zermeño, A., additional, Blake-Cerda, M., additional, Mota-García, A., additional, Poitevin-Chacón, A., additional, Rosales-Pérez, S., additional, and Trejo-Duran, G., additional
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- 2012
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6. Long-term Survival in Patients with Non-small Cell Lung Cancer and Synchronous Brain Metastasis Treated with Whole-brain Radiotherapy and Thoracic Chemo-radiation
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De La Mata, M., primary, Arrieta, O., additional, Blake-Cerda, M., additional, Villareal-Garza, C., additional, Martinez-Barrera, L., additional, Zamora, J., additional, and Gallardo, D., additional
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- 2011
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7. Triple-negative breast cancer in Hispanic patients: High prevalence, poor prognosis, and association with menopausal status, body mass index, and parity.
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Lara-Medina F, Pérez-Sánchez V, Saavedra-Pérez D, Blake-Cerda M, Arce C, Motola-Kuba D, Villarreal-Garza C, González-Angulo AM, Bargalló E, Aguilar JL, Mohar A, and Arrieta O
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- 2011
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8. National Consensus of Diagnosis and treatment of non-small cell lung cancer
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Arrieta O, Guzmán-de Alba E, Lf, Alba-López, Acosta-Espinoza A, Alatorre-Alexander J, Jf, Alexander-Meza, Sr, Allende-Pérez, Alvarado-Aguilar S, Me, Araujo-Navarrete, Lm, Argote-Greene, Ca, Aquino-Mendoza, Am, Astorga-Ramos, Austudillo-de la Vega H, Avilés-Salas A, Lj, Barajas-Figueroa, Barroso-Quiroga N, Blake-Cerda M, Pa, Cabrera-Galeana, Calderillo-Ruíz G, Ad, Campos-Parra, Am, Cano-Valdez, Capdeville-García D, Castillo-Ortega G, Casillas-Suárez C, Castillo-González P, Jf, Corona-Cruz, Me, Correa-Acevedo, Ss, Cortez-Ramírez, Ja, La Cruz-Vargas, Jg, La Garza-Salazar, Md, La Mata-Moya, Me, Domínguez-Flores, Hr, Domínguez-Malagón, Lm, Domínguez-Parra, Domínguez-Peregrina A, Durán-Alcocer J, Mi, Enríquez-Aceves, Elizondo-Ríos A, Md, Escobedo-Sánchez, Pe, Villafranca, Flores-Cantisani A, Jp, Flores-Gutiérrez, Franco-Marina F, Ee, Franco-González, Ra, Franco-Topete, Fuentes-de la Peña H, Galicia-Amor S, Gallardo-Rincón D, Gamboa-Domínguez A, García-Andreu J, Cm, García-Cuéllar, Mc, García-Sancho-Figueroa, García-Torrentera R, Gerson-Cwilich R, Gómez-González A, Green-Schneeweiss L, Guillén-Núñez Mdel R, Gutiérrez-Velázquez H, Ibarra-Pérez C, Jiménez-Fuentes E, Juárez-Sánchez P, Juárez-Ramiro A, Kelly-García J, Kuri-Exsome R, Jm, Lázaro-León, León-Rodríguez E, Llanos-Osuna S, Loyola-García U, Js, López-González, Antuñano Fj, López Y., Ma, Loustaunau-Andrade, Eo, Macedo-Pérez, Machado-Villarroel L, Magallanes-Maciel M, Martínez-Barrera L, Martínez-Cedillo J, Martínez-Martínez G, Medina-Esparza A, Meneses-García A, Mohar-Betancourt A, Morales Blanhir J, Morales-Gómez J, Motola-Kuba D, Mp, Nájera-Cruz, Núñez-Valencia Cdel C, Ma, Ocampo-Ocampo, Md, Ochoa-Vázquez, Ca, Olivares-Torres, Palomar-Lever A, Patiño-Zarco M, Pérez-Padilla R, Yr, Peña-Alonso, Ar, Pérez-Romo, Aquilino Pérez M, Pm, Pinaya-Ruíz, Ma, Pointevin-Chacón, Jj, Poot-Braga, Posadas-Valay R, Ramirez-Márquez M, Reyes-Martínez I, Robledo-Pascual J, Rodríguez-Cid J, Ce, Rojas-Marín, Romero-Bielma E, Je, Rubio-Gutiérrez, Ja, Sáenz-Frías, Ma, Salazar-Lezama, Sánchez-Lara K, Sansores Martínez R, Santillán-Doherty P, Alejandro-Silva J, Jl, Téllez-Becerra, Toledo-Buenrostro V, Luis Torre-Bouscoulet, Torecillas-Torres L, Torres M, Tovar-Guzmán V, Jg, Turcott-Chaparro, Jj, Vázquez-Cortés, Me, Vázquez-Manríquez, Vilches-Cisneros N, Jf, Villegas-Elizondo, Mm, Zamboni, Zamora-Moreno J, and Jw, Zinser-Sierra
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Lung Neoplasms ,Carcinoma, Non-Small-Cell Lung ,Decision Trees ,Smoking ,Humans ,Mexico ,Algorithms ,Neoplasm Staging - Abstract
Mexican specialists in oncology, oncologic surgery, thoracic surgery, pneumology, pathology, molecular biology, anesthesiology, algology, psychology, nutrition, and rehabilitation (all of them experts in lung cancer treatment) in order to develop the National Consensus on Lung Cancer. The consensus has been developed as an answer to the need of updated Mexican guidelines for the optimal treatment of the disease, as well as to the requirements that such guidelines be established by multidisciplinary panel, depicting the current attention given to cancer lung cases in Mexico. Thus, this paper analyses the epidemiological review, screening, diagnosis, staging, pathology, translational medicine, and the suitable therapies for early, locally advanced, and metastatic disease in the first, second, and third lines of management, as well as rehabilitation and palliative measures.
9. National consensus of diagnosis and treatment of non-small cell lung cancer,Consenso nacional de diagnóstico y tratamiento del cáncer de pulmón de células no pequeñas
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Arrieta, O., Guzmán-De Alba, E., Alba-López, L. F., Acosta-Espinoza, A., Alatorre-Alexander, J., Alexander-Meza, J. F., Allende-Pérez, S. R., Alvarado-Aguilar, S., Araujo-Navarrete, M. E., Argote-Greene, L. M., Aquino-Mendoza, C. A., Astorga-Ramos, A. M., Astudillo-De La Vega, H., Avilés-Salas, A., Barajas-Figueroa, L. J., Barroso-Quiroga, N., Blake-Cerda, M., Cabrera-Galeana, P. A., Calderillo-Ruíz, G., Campos-Parra, A. D., Cano-Valdez, A. M., Capdeville-García, D., Castillo-Ortega, G., Casillas-Suárez, C., Castillo-González, P., Corona-Cruz, J. F., Correa-Acevedo, M. E., Cortez-Ramírez, S. S., Jhony A. De La Cruz-Vargas, La Garza-Salazar, J. G., La Mata-Moya, M. D., La Peña-Hinojosa, C., Domínguez-Flores, M. E., Domínguez-Malagón, H. R., Domínguez-Parra, L. M., Domínguez-Peregrina, A., Durán-Alcocer, J., Enríquez-Aceves, M. I., Elizondo-Ríos, A., Escobedo-Sánchez, M. D., Villafranca, P. E. -M, Flores-Cantisani, A., Flores-Gutiérrez, J. P., Franco-Marina, F., Franco-González, E. E., Franco-Topete, R. A., Fuentes-De La Peña, H., Galicia-Amor, S., Gallardo-Rincón, D., Gamboa-Domínguez, A., García-Andreu, J., García-Cuéllar, C. M., García-Sancho-Figueroa, M. C., García-Torrentera, R., Gerson-Cwilich, R., Gómez-González, A., Green-Schneeweiss, L., Del Rocío Guillén-Núñez, M., Gutiérrez-Velázquez, H., Ibarra-Pérez, C., Jiménez-Fuentes, E., Juárez-Sánchez, P., Juárez-Ramiro, A., Kelly-García, J., Kuri-Exsome, R., Lázaro-León, J. M., León-Rodríguez, E., Llanos-Osuna, S., Loyola-García, U., López-González, J. S., López Yde Antuñano, F. J., Loustaunau-Andrade, M. A., Macedo-Pérez, E. O., Machado-Villarroel, L., Magallanes-Maciel, M., Martínez-Barrera, L., Martínez-Cedillo, J., Martínez-Martínez, G., Medina-Esparza, A., Meneses-García, A., Mohar-Betancourt, A., Blanhir, J. M., Morales-Gómez, J., Motola-Kuba, D., Nájera-Cruz, M. P., Del Carmen Núñez-Valencia, C., Ocampo-Ocampo, M. A., Ochoa-Vázquez, M. D., Olivares-Torres, C. A., Palomar-Lever, A., Patiño-Zarco, M., Pérez-Padilla, R., Peña-Alonso, Y. R., Pérez-Romo, A. R., Pérez, M. A., Pinaya-Ruíz, P. M., Pointevin-Chacón, M. A., Poot-Braga, J. J., Posadas-Valay, R., Ramírez-Márquez, M., Reyes-Martínez, I., Robledo-Pascual, J., Rodríguez-Cid, J., Rojas-Marín, C. E., Romero-Bielma, E., Rubio-Gutiérrez, J. E., Sáenz-Frías, J. A., Salazar-Lezama, M. Á, Sánchez-Lara, K., Martínez, R. S., Santillán-Doherty, P., Alejandro-Silva, J., Téllez-Becerra, J. L., Toledo-Buenrostro, V., Torre-Bouscoulet, L., Torecillas-Torres, L., Torres, M., Tovar-Guzmán, V., Turcott-Chaparro, J. G., Vázquez-Cortés, J. J., Vázquez-Manríquez, M. E., Vilches-Cisneros, N., Villegas-Elizondo, J. F., Zamboni, M. M., Zamora-Moreno, J., and Zinser-Sierra, J. W.
10. Long-term survival in patients with non-small cell lung cancer and synchronous brain metastasis treated with whole-brain radiotherapy and thoracic chemoradiation
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Arrieta Oscar, Villarreal-Garza Cynthia, Zamora Jesús, Blake-Cerda Mónika, de la Mata María D, Zavala Diego G, Muñiz-Hernández Saé, and de la Garza Jaime
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NSCLC ,brain metastases ,chemoradiotherapy ,survival ,Medical physics. Medical radiology. Nuclear medicine ,R895-920 ,Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,RC254-282 - Abstract
Abstract Background Brain metastases occur in 30-50% of Non-small cell lung cancer (NSCLC) patients and confer a worse prognosis and quality of life. These patients are usually treated with Whole-brain radiotherapy (WBRT) followed by systemic therapy. Few studies have evaluated the role of chemoradiotherapy to the primary tumor after WBRT as definitive treatment in the management of these patients. Methods We reviewed the outcome of 30 patients with primary NSCLC and brain metastasis at diagnosis without evidence of other metastatic sites. Patients were treated with WBRT and after induction chemotherapy with paclitaxel and cisplatin for two cycles. In the absence of progression, concurrent chemoradiotherapy for the primary tumor with weekly paclitaxel and carboplatin was indicated, with a total effective dose of 60 Gy. If disease progression was ruled out, four chemotherapy cycles followed. Results Median Progression-free survival (PFS) and Overall survival (OS) were 8.43 ± 1.5 and 31.8 ± 15.8 months, respectively. PFS was 39.5% at 1 year and 24.7% at 2 years. The 1- and 2-year OS rates were 71.1 and 60.2%, respectively. Three-year OS was significantly superior for patients with N0-N1 stage disease vs. N2-N3 (60 vs. 24%, respectively; Response rate [RR], 0.03; p= 0.038). Conclusions Patients with NSCLC and brain metastasis might benefit from treatment with WBRT and concurrent thoracic chemoradiotherapy. The subgroup of N0-N1 patients appears to achieve the greatest benefit. The result of this study warrants a prospective trial to confirm the benefit of this treatment.
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- 2011
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11. Outcomes From Real-World Data on Intraoperative Electronic Radiotherapy for the Treatment of Early-Stage Breast Cancer: Long-Term Recurrence and Survival Outcomes From a Single Center.
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De la Mata D, Santiago-Concha BG, Bargalló-Rocha JE, Robles-Vidal CD, Gómez-Pue D, Castorena-Rojí G, Hinojosa-Gómez J, Flores-Vázquez F, Blake-Cerda M, Enriquez-Barrera M, and Maffuz-Aziz A
- Abstract
Purpose: This study is aimed at investigating the 10-year outcomes of intraoperative radiotherapy (IORT) in Mexican women with early breast cancer (EBC) treated at the Centro Medico ABC, Mexico City. Methods: A cohort study included women with early-stage invasive ductal carcinoma aged ≥ 45 years without prior oncologic treatment, tumor size ≤ 3.5 cm, cN0M0, positive hormone receptors, margins ≥ 2 mm, negative sentinel lymph nodes, and no extensive lymphovascular invasion. IORT was administered at 20 Gy for 20-30 min after a lumpectomy. Follow-up extended over 10 years and included clinical examinations every 6 months for the first 18 months, followed by annual mammograms and conventional examinations. Patients out of the criteria were excluded from this study because they were referred for additional surgery and/or whole-breast radiation therapy. Results: The study involved 238 patients with an average age of 61.1 years. The mean tumor size was 12 mm, and the percentages of lymphatic invasion, positive hormone receptors, and HER2/neu overexpression were 12.6%, 90.8%, and 2.1%, respectively. The median follow-up was 66.6 months (range: 1-126 months), and the overall survival and mastectomy-free rate reached 95.7% and 90%, respectively. Thirteen patients showed side effects; four recurrences were recorded, of which 50% were out-field relapses. The 5-year Kaplan-Meier probability of local relapses, mastectomy-free, and overall survival reached 97.5%, 100%, and 98%, respectively. Conclusions: This is the first 10-year report about the effect of IORT on Mexican women with EBC in the early stages. Strict adherence to the selection criteria in this study resulted in low rates of side effects, mortality, and local recurrences, demonstrating that IORT is an effective treatment alternative for patients with EBC. Studies with a longer follow-up period should be performed, as recurrences can occur in the long term., Competing Interests: The authors declare no conflicts of interest., (Copyright © 2024 Dolores De la Mata et al.)
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- 2024
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12. Prophylactic Cranial Irradiation Reduces Brain Metastases and Improves Overall Survival in High-Risk Metastatic Non-Small Cell Lung Cancer Patients: A Randomized phase 2 Study (PRoT-BM trial).
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Arrieta O, Maldonado F, Turcott JG, Zatarain-Barrón ZL, Barrón F, Blake-Cerda M, Cabrera-Miranda LA, Cardona AF, de la Garza JG, and Rosell R
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- Anaplastic Lymphoma Kinase genetics, Brain Neoplasms epidemiology, Brain Neoplasms mortality, Brain Neoplasms secondary, Carcinoembryonic Antigen blood, Carcinoma, Non-Small-Cell Lung genetics, Carcinoma, Non-Small-Cell Lung mortality, Carcinoma, Non-Small-Cell Lung secondary, Confidence Intervals, Female, Genes, erbB-1, Humans, Incidence, Lung Neoplasms genetics, Lung Neoplasms mortality, Male, Middle Aged, Progression-Free Survival, Proportional Hazards Models, Quality of Life, Radiation Dose Hypofractionation, Standard of Care, Brain Neoplasms prevention & control, Carcinoma, Non-Small-Cell Lung prevention & control, Cranial Irradiation, Lung Neoplasms pathology
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Purpose: To date, studies regarding the use of prophylactic cranial irradiation (PCI) versus standard of care (SoC) for patients with non-small cell lung cancer (NSCLC) have not shown a significant effect in terms of overall survival (OS). Additionally, the effect of PCI among high-risk patients has been scarcely studied. The objective of this randomized phase 2 study was to evaluate the role of PCI in a population of patients at high risk for development of brain metastases (BM)., Methods and Materials: Eligible patients had histologically confirmed NSCLC without baseline BM, harboring epidermal growth factor receptor mutations, anaplastic lymphoma kinase rearrangements, or elevated carcinoembryonic antigen levels at the time of diagnosis. Participants received systemic therapy according to molecular status, those without progressive disease were then assigned to receive SoC or SoC + PCI (25 Gy in 10 fractions). The primary outcome was cumulative incidence of brain metastases (CBM). The secondary endpoints included progression-free survival and OS. Quality of life and neurocognitive function are discussed in a separate article (Clinicaltrials.gov: NCT01603849)., Results: From May 2012 to December 2017, 84 patients were enrolled in the study, with 41 patients allocated to receive PCI and 43 received SoC. Patients allocated to receive PCI had a CBM at 24 months of 7% versus 38% in those allocated to the SoC arm. PCI was associated with a hazard ratio of 0.12 (95% confidence interval, 0.035-0.42) for developing BM. A benefit in OS was also observed (64.5 vs 19.8 months; hazard ratio: 0.41 (95% confidence interval, 0.22-0.78; P =∙007)., Conclusions: Among a selected population at high risk for developing BM, PCI significantly decreased CBM in addition to increasing progression-free survival and OS. To our knowledge, this is the first study to evaluate PCI in epidermal growth factor receptor mutations, anaplastic lymphoma kinase rearrangements, or elevated carcinoembryonic antigen levels in patients with NSCLC, showing a significant improvement in CBM. This relevant information should be of particular importance in the context of patients without access to third-generation targeted agents. Further studies are warranted to ascertain this effect., (Copyright © 2021 Elsevier Inc. All rights reserved.)
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- 2021
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13. Consolidative stereotactic ablative radiotherapy (SABR) to intrapulmonary lesions is associated with prolonged progression-free survival and overall survival in oligometastatic NSCLC patients: A prospective phase 2 study.
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Blake-Cerda M, Lozano-Ruíz F, Maldonado-Magos F, de la Mata-Moya D, Díaz-García D, Lara-Mejía L, Zatarain-Barrón ZL, Cuevas-Góngora MF, Barron-Barron F, Corona-Cruz JF, Cabrera-Miranda L, Arroyo-Hernández M, Gerson R, and Arrieta O
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- Female, Humans, Male, Middle Aged, Positron Emission Tomography Computed Tomography, Progression-Free Survival, Prospective Studies, Treatment Outcome, Carcinoma, Non-Small-Cell Lung radiotherapy, Carcinoma, Non-Small-Cell Lung surgery, Lung Neoplasms radiotherapy, Lung Neoplasms surgery, Radiosurgery
- Abstract
Objectives: Stereotactic Ablative Radiotherapy (SABR) has shown high rates of local control and prolonged survival in early-stage non-small cell lung cancer (NSCLC), though its role in oligometastatic disease is undefined. This study aimed to evaluate SABR as a local consolidative therapy (LCT) in oligometastatic NSCLC patients., Methods: In this prospective, single-arm phase 2 trial, we sought to evaluate SABR in patients with stage IV NSCLC, with ≤ five lesions, including the primary tumor. Patients received initial systemic therapy according to international guidelines. Patients without progression after front-line therapy (two months of targeted therapy and ≥ four cycles of chemotherapy) were evaluated by an 18F-FDG-PET/CT to receive consolidative SABR (45-60 Gy in 3-5 fractions) to the primary and all intrapulmonary metastatic sites. The primary endpoint was progression-free survival (PFS); secondary endpoints were overall survival (OS) and toxicity., Results: A total of 47 patients were included. Mean age was 58.9 years, 59.6 % were female, 87.2 % had adenocarcinoma histology, and the contralateral lung was the main site of metastases in 42.6 %. All patients received systemic front-line therapy, chemotherapy in 61.7 %, and a tyrosine kinase inhibitor (TKI) in 38.3 %. Disease control rate (DCR) and complete metabolic response (CMR) to SABR were 93.6 % and 70.2 %. Median PFS was 34.3 months (95 %CI; 31.1-38.8) for the total cohort; patients with a CMR had a median PFS of 53.9 monthsvs.31.9 months in those without CMR (p = 0.011). Median OS was not reached.Grade 1, 2, and 3 pneumonitis were observed in 79.5 % (31/39), 12.8 % (5/39) and 7.7 % (3/39), respectively. No grade ≥4 toxicities were observed., Conclusion: The use of SABR as LCT in oligometastatic NSCLC patients was well tolerated and showed favorable results regarding PFS and OS compared with historical data. The benefit was significantly higher in patients who reached a CMR as assessed by 18F-FDG-PET/CT., (Copyright © 2020 Elsevier B.V. All rights reserved.)
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- 2021
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14. Locoregional control and toxicity after pleurectomy/decortication and intensity-modulated pleural radiation therapy in patients with malignant pleural mesothelioma.
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Arrieta O, Lozano-Ruiz F, Blake-Cerda M, Catalán R, Lara-Mejía L, Salinas MÁ, Maldonado-Magos F, and Corona-Cruz JF
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- Aged, Aged, 80 and over, Female, Humans, Male, Mesothelioma, Malignant pathology, Middle Aged, Prospective Studies, Radiotherapy, Intensity-Modulated methods, Mesothelioma, Malignant radiotherapy, Pleural Neoplasms radiotherapy, Pleural Neoplasms surgery
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Background: Treatment of malignant pleural mesothelioma (MPM) represents a major challenge for oncologists. Multimodality treatment, which generally involves induction chemotherapy, surgery and radiotherapy have recently shown promising results. The aim of this study was to evaluate the locoregional control and toxicity of intensity modulated radiotherapy (IMRT) after pleurectomy and decortication (P/D) as part of trimodality therapy for patients with locally advanced MPM., Methods: We prospectively analyzed data from 20 patients with MPM treated at a single tertiary-care institution. Initially every patient received induction chemotherapy with platinum-based chemotherapy. After chemotherapy, patients without progression underwent P/D, and if feasible, hemi-thoracic IMRT was administered at a planned dose of 50.4-54 Gy in 28-30 fractions and treated with 9-11 noncoplanar fields., Results: A total of 15 of the 20 enrolled patients underwent P/D followed by IMRT to the hemi-thoracic cavity. The median total radiotherapy dose was 48.7 Gy (23.4-54 Gy). Radiation pneumonitis (RP) developed in nine patients (60%), and of these, two patients (13.3%) experienced G3 or G4 RP. The estimated locoregional-relapse-free survival at two years was 75.9%, and the main pattern of recurrence was distant (72.7%). For the entire cohort median follow-up was 22.7 months, median progression-free survival was 18.9 months and median overall survival 23.6 months., Conclusions: Platinum-based chemotherapy followed by lung-sparing surgery (P/D) and IMRT is a feasible and safe treatment modality that yields acceptable locoregional control in patients with locally advanced MPM; however, these results should be corroborated in larger studies., (© 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.)
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- 2020
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15. National Clinical Practice Guidelines for the management of non-small cell lung cancer in early, locally advanced and metastatic stages. Extended version.
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Barrón-Barrón F, Guzmán-De Alba E, Alatorre-Alexander J, Aldaco-Sarvider F, Bautista-Aragón Y, Blake-Cerda M, Blanco-Vázquez YC, Campos-Gómez S, Corona-Cruz JF, Iñiguez-García MA, Lozano-Ruiz FJ, Maldonado-Magos F, de la Mata-Moya D, Martínez-Barrera LM, Ramos-Prudencio R, Rodríguez-Cid J, Rivera-Rivera S, Trejo-Rosales RR, Aguilar-Ortíz MR, Astudillo-de la Vega H, Barajas-Figueroa LJ, Barroso-Quiroga N, Blanco-Salazar A, Castillo-Ortega G, Domínguez-Parra LM, Enriquez-Aceves MI, Fernández-Orozco A, Figueroa-Morales MA, Green-Schneewiss L, González-Garay JA, González Ramírez-Benfield R, Guadarrama-Orozco A, Guerrero-Ixtlahuac J, Hernández-Barajas D, Hernández-Montes de Oca R, Kelly-García J, Lázaro-León M, Silva-Bravo F, Tellez-Becerra JL, Macedo-Pérez EO, Maza-Ramos G, Mayorga-Butrón JL, Montaño-Velázquez BB, Murillo-Medina K, Narváez-Fernández S, Ochoa-Carrillo FJ, Olivares-Beltrán G, Olivares-Torres C, Ponce de León-Castillo M, Ponce-Viveros MA, Rubio-Gutiérrez JE, Sáenz-Frías JA, Silva-Vivas JA, Santillán-Doherty P, Soto-Ávila JJ, Toledo-Buenrostro V, Vargas-Abrego B, Velasco-Hidalgo L, Zapata-Tarres MM, Quintero-Beuló G, and Arrieta O
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- Algorithms, Carcinoma, Non-Small-Cell Lung pathology, Carcinoma, Non-Small-Cell Lung secondary, Early Medical Intervention, Humans, Lung Neoplasms pathology, Neoplasm Staging, Carcinoma, Non-Small-Cell Lung diagnosis, Carcinoma, Non-Small-Cell Lung therapy, Lung Neoplasms diagnosis, Lung Neoplasms therapy
- Abstract
Objective: Lung cancer is one the leading causes of mortality worldwide. Symptomatic manifestations of the disease generally occur in the advanced-stage setting, and therefore an important number of patients have advanced or metastatic disease by the time they are diagnosed. This situation contributes to a poor prognosis in the treatment of lung cancer. Evidencebased clinical recommendations are of great value to support decision-making for daily practice, and thus improving health care quality and patient outcomes., Materials and Methods: This document was an initiative of the Mexican Society of Oncology (SMEO) in collaboration with Mexican Center of Clinical Excellence (Cenetec) according to Interna- tional Standards. Such standards included those described by the IOM, NICE, SIGN and GI-N. An interdisciplinary Guideline Development Group (GDG) was put together which included medical oncologists, surgical oncologistsc, radiation therapists, and methodologists with expertise in critical appraisal, sys- tematic reviews and clinical practice guidelines development., Results: 62 clinical questions were agreed among members of the GDG. With the evidence identified from systematic reviews, the GDG developed clinical recommendations using a Modified Delphi Panel technique. Patients' representatives validated them., Conclusions: These Clinical Practice Guideline aims to support the shared decision-making process for patients with different stages of non-small cell lung cancer. Our goal is to improve health-care quality on these patients., Competing Interests: Declaration of conflict of interests. The authors declare that they have no conflict of interests.
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- 2019
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16. A phase II trial of prolonged, continuous infusion of low-dose gemcitabine plus cisplatin in patients with advanced malignant pleural mesothelioma.
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Arrieta O, López-Macías D, Mendoza-García VO, Bacon-Fonseca L, Muñoz-Montaño W, Macedo-Pérez EO, Muñiz-Hernández S, Blake-Cerda M, and Corona-Cruz JF
- Subjects
- Adult, Aged, Aged, 80 and over, Antimetabolites, Antineoplastic administration & dosage, Antimetabolites, Antineoplastic adverse effects, Antineoplastic Agents administration & dosage, Antineoplastic Agents adverse effects, Cisplatin administration & dosage, Cisplatin adverse effects, Deoxycytidine administration & dosage, Deoxycytidine adverse effects, Deoxycytidine therapeutic use, Disease-Free Survival, Female, Humans, Lung Neoplasms mortality, Male, Mesothelioma mortality, Mesothelioma, Malignant, Middle Aged, Prognosis, Quality of Life, Survival Analysis, Gemcitabine, Antimetabolites, Antineoplastic therapeutic use, Antineoplastic Agents therapeutic use, Cisplatin therapeutic use, Deoxycytidine analogs & derivatives, Lung Neoplasms drug therapy, Mesothelioma drug therapy
- Abstract
Purpose: Low-dose, prolonged infusion of gemcitabine has effects similar to standard doses in several cancers. We evaluated the toxicity and efficacy of low-dose gemcitabine in prolonged infusion plus cisplatin in patients with advanced pleural mesothelioma., Methods: Patients with mesothelioma received gemcitabine (250 mg/m(2)) in a 6-h infusion plus cisplatin (35 mg/m(2)) on days 1 and 8 every three weeks. We used the modified response evaluation criteria in solid tumours. This study is registered in clinical trials (NCT01869023)., Results: We included 39 patients; 82.1 % were low risk according to the European Organisation for Research and Treatment of Cancer prognostic group. Partial response was observed in 53.8 % (21/39), stable disease in 33.3 % (13/39) and progression in 12.8 % (5/39). The median progression-free survival was 6.9 months (95 % CI 3.2-10.6 months), and the associated factors were the EORTC risk and histology. The median overall survival was 20.7 months (95 % CI 10.7-30.8 months). The functional, physical and emotional roles and dyspnoea, insomnia and pain symptom scales improved. The most commonly graded 3/4 side effects were neutropenia (24.4 %), lymphopenia (14.6 %), thrombocytopenia (14.7 %) and anaemia (12.2 %)., Conclusions: Low-dose, prolonged gemcitabine infusion plus cisplatin has acceptable toxicity and high efficacy with improved quality of life, representing an affordable regimen for the low-income population.
- Published
- 2014
- Full Text
- View/download PDF
17. [National consensus of diagnosis and treatment of non-small cell lung cancer].
- Author
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Arrieta O, Guzmán-de Alba E, Alba-López LF, Acosta-Espinoza A, Alatorre-Alexander J, Alexander-Meza JF, Allende-Pérez SR, Alvarado-Aguilar S, Araujo-Navarrete ME, Argote-Greene LM, Aquino-Mendoza CA, Astorga-Ramos AM, Austudillo-de la Vega H, Avilés-Salas A, Barajas-Figueroa LJ, Barroso-Quiroga N, Blake-Cerda M, Cabrera-Galeana PA, Calderillo-Ruíz G, Campos-Parra AD, Cano-Valdez AM, Capdeville-García D, Castillo-Ortega G, Casillas-Suárez C, Castillo-González P, Corona-Cruz JF, Correa-Acevedo ME, Cortez-Ramírez SS, de la Cruz-Vargas JA, de la Garza-Salazar JG, de la Mata-Moya MD, Domínguez-Flores ME, Domínguez-Malagón HR, Domínguez-Parra LM, Domínguez-Peregrina A, Durán-Alcocer J, Enríquez-Aceves MI, Elizondo-Ríos A, Escobedo-Sánchez MD, de Villafranca PE, Flores-Cantisani A, Flores-Gutiérrez JP, Franco-Marina F, Franco-González EE, Franco-Topete RA, Fuentes-de la Peña H, Galicia-Amor S, Gallardo-Rincón D, Gamboa-Domínguez A, García-Andreu J, García-Cuéllar CM, García-Sancho-Figueroa MC, García-Torrentera R, Gerson-Cwilich R, Gómez-González A, Green-Schneeweiss L, Guillén-Núñez Mdel R, Gutiérrez-Velázquez H, Ibarra-Pérez C, Jiménez-Fuentes E, Juárez-Sánchez P, Juárez-Ramiro A, Kelly-García J, Kuri-Exsome R, Lázaro-León JM, León-Rodríguez E, Llanos-Osuna S, Llanos-Osuna S, Loyola-García U, López-González JS, López y de Antuñano FJ, Loustaunau-Andrade MA, Macedo-Pérez EO, Machado-Villarroel L, Magallanes-Maciel M, Martínez-Barrera L, Martínez-Cedillo J, Martínez-Martínez G, Medina-Esparza A, Meneses-García A, Mohar-Betancourt A, Morales Blanhir J, Morales-Gómez J, Motola-Kuba D, Nájera-Cruz MP, Núñez-Valencia Cdel C, Ocampo-Ocampo MA, Ochoa-Vázquez MD, Olivares-Torres CA, Palomar-Lever A, Patiño-Zarco M, Pérez-Padilla R, Peña-Alonso YR, Pérez-Romo AR, Aquilino Pérez M, Pinaya-Ruíz PM, Pointevin-Chacón MA, Poot-Braga JJ, Posadas-Valay R, Ramirez-Márquez M, Reyes-Martínez I, Robledo-Pascual J, Rodríguez-Cid J, Rojas-Marín CE, Romero-Bielma E, Rubio-Gutiérrez JE, Sáenz-Frías JA, Salazar-Lezama MA, Sánchez-Lara K, Sansores Martínez R, Santillán-Doherty P, Alejandro-Silva J, Téllez-Becerra JL, Toledo-Buenrostro V, Torre-Bouscoulet L, Torecillas-Torres L, Torres M, Tovar-Guzmán V, Turcott-Chaparro JG, Vázquez-Cortés JJ, Vázquez-Manríquez ME, Vilches-Cisneros N, Villegas-Elizondo JF, Zamboni MM, Zamora-Moreno J, and Zinser-Sierra JW
- Subjects
- Algorithms, Carcinoma, Non-Small-Cell Lung complications, Carcinoma, Non-Small-Cell Lung etiology, Carcinoma, Non-Small-Cell Lung secondary, Decision Trees, Humans, Lung Neoplasms complications, Lung Neoplasms etiology, Mexico, Neoplasm Staging, Smoking adverse effects, Carcinoma, Non-Small-Cell Lung diagnosis, Carcinoma, Non-Small-Cell Lung therapy, Lung Neoplasms diagnosis, Lung Neoplasms therapy
- Abstract
Mexican specialists in oncology, oncologic surgery, thoracic surgery, pneumology, pathology, molecular biology, anesthesiology, algology, psychology, nutrition, and rehabilitation (all of them experts in lung cancer treatment) in order to develop the National Consensus on Lung Cancer. The consensus has been developed as an answer to the need of updated Mexican guidelines for the optimal treatment of the disease, as well as to the requirements that such guidelines be established by multidisciplinary panel, depicting the current attention given to cancer lung cases in Mexico. Thus, this paper analyses the epidemiological review, screening, diagnosis, staging, pathology, translational medicine, and the suitable therapies for early, locally advanced, and metastatic disease in the first, second, and third lines of management, as well as rehabilitation and palliative measures.
- Published
- 2013
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