1. Atezolizumab for First-Line Treatment of Metastatic Nonsquamous NSCLC
- Author
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Socinski, M. A., Jotte, R. M., Cappuzzo, F., Orlandi, F., Stroyakovskiy, D., Nogami, N., Rodriguez-Abreu, D., Moro-Sibilot, D., Thomas, C. A., Barlesi, F., Finley, G., Kelsch, C., Lee, A., Coleman, S., Deng, Y., Shen, Y., Kowanetz, M., Lopez-Chave, A., Sandler, A., Reck, M., Soto Parra, H, RS: GROW - R3 - Innovative Cancer Diagnostics & Therapy, Pulmonologie, and MUMC+: MA Med Staf Spec Longziekten (9)
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0301 basic medicine ,Oncology ,Male ,Vascular Endothelial Growth Factor A ,Lung Neoplasms ,MULTICENTER ,THERAPY ,B7-H1 Antigen ,Carboplatin ,chemistry.chemical_compound ,0302 clinical medicine ,Monoclonal ,Antineoplastic Combined Chemotherapy Protocols ,Medicine ,Anaplastic Lymphoma Kinase ,Neoplasm Metastasis ,Non-Small-Cell Lung ,DOCETAXEL ,education.field_of_study ,Aged ,Antibodies, Monoclonal ,Bevacizumab ,Carcinoma, Non-Small-Cell Lung ,Female ,Genes, erbB-1 ,Humans ,Middle Aged ,Mutation ,Paclitaxel ,Receptor Protein-Tyrosine Kinases ,Survival Analysis ,Immunotherapy ,Hazard ratio ,PHASE-III TRIAL ,General Medicine ,CHEMOTHERAPY ,OPEN-LABEL ,CANCER ,Docetaxel ,030220 oncology & carcinogenesis ,medicine.drug ,medicine.medical_specialty ,Population ,BEVACIZUMAB ,Antibodies ,03 medical and health sciences ,Atezolizumab ,Internal medicine ,Lung cancer ,education ,Survival analysis ,erbB-1 ,business.industry ,Carcinoma ,medicine.disease ,030104 developmental biology ,chemistry ,Genes ,ANTIBODY ,CELLS ,business - Abstract
Background The cancer-cell–killing property of atezolizumab may be enhanced by the blockade of vascular endothelial growth factor–mediated immunosuppression with bevacizumab. This open-label, phase 3 study evaluated atezolizumab plus bevacizumab plus chemotherapy in patients with metastatic nonsquamous non–small-cell lung cancer (NSCLC) who had not previously received chemotherapy. Methods We randomly assigned patients to receive atezolizumab plus carboplatin plus paclitaxel (ACP), bevacizumab plus carboplatin plus paclitaxel (BCP), or atezolizumab plus BCP (ABCP) every 3 weeks for four or six cycles, followed by maintenance therapy with atezolizumab, bevacizumab, or both. The two primary end points were investigator-assessed progression-free survival both among patients in the intention-to-treat population who had a wild-type genotype (WT population; patients with EGFR or ALK genetic alterations were excluded) and among patients in the WT population who had high expression of an effector T-cell (Teff) gene signature in the tumor (Teff-high WT population) and overall survival in the WT population. The ABCP group was compared with the BCP group before the ACP group was compared with the BCP group. Results In the WT population, 356 patients were assigned to the ABCP group, and 336 to the BCP group. The median progression-free survival was longer in the ABCP group than in the BCP group (8.3 months vs. 6.8 months; hazard ratio for disease progression or death, 0.62; 95% confidence interval [CI], 0.52 to 0.74; P
- Published
- 2018
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