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Phase II Randomized Trial of Carboplatin, Pemetrexed, and Bevacizumab With and Without Atezolizumab in Stage IV Nonsquamous Non-Small-Cell Lung Cancer Patients Who Harbor a Sensitizing EGFR Mutation or Have Never Smoked.
Bodor, J Nicholas; Patel, Jyoti D; Wakelee, Heather A; Levy, Benjamin P; Borghaei, Hossein; Pellini, Bruna; Costello, Michael R; Dowell, Jonathan E; Finley, Gene; Huang, Chao H; Neal, Joel W; Nieva, Jorge J; Puri, Sonam; Socinski, Mark A; Thomas, Christian; Ross, Eric A; Litwin, Samuel; Clapper, Margie L; Treat, Joseph.
Afiliación
  • Bodor JN; Department of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA.
  • Patel JD; Hematology Oncology Division, Northwestern University, Chicago, IL.
  • Wakelee HA; Department of Medical Oncology, Stanford Cancer Institute, Stanford, CA.
  • Levy BP; Department of Medical Oncology, Johns Hopkins Sidney Kimmel Cancer Center, Washington, DC.
  • Borghaei H; Department of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA.
  • Pellini B; Department of Thoracic Oncology, Moffitt Cancer Center, Tampa, FL.
  • Costello MR; Department of Hematology/Oncology, University of Pennsylvania Abramson Cancer Center at Chester County Hospital, West Chester, PA.
  • Dowell JE; Department of Hematology/Oncology, UT Southwestern Harold C. Simmons Comprehensive Cancer Center, Dallas, TX.
  • Finley G; Department of Medical Oncology, Allegheny Health Network, Pittsburgh, PA.
  • Huang CH; Department of Medical Oncology, University of Kansas Medical Center, Kansas City, KS.
  • Neal JW; Department of Medical Oncology, Stanford Cancer Institute, Stanford, CA.
  • Nieva JJ; Department of Medical Oncology, University of Southern California Norris Comprehensive Cancer Center, Los Angeles, CA.
  • Puri S; Division of Oncology, University of Utah Huntsman Cancer Institute, Salt Lake City, UT.
  • Socinski MA; Department of Medical Oncology, AdventHealth Cancer Institute, Orlando, FL.
  • Thomas C; New England Cancer Specialists, Scarborough, ME.
  • Ross EA; Department of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA.
  • Litwin S; Department of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA.
  • Clapper ML; Department of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA.
  • Treat J; Department of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA. Electronic address: joseph.treat2@fccc.edu.
Clin Lung Cancer ; 24(7): e242-e246, 2023 11.
Article en En | MEDLINE | ID: mdl-37451930
ABSTRACT

INTRODUCTION:

Patients with non-small-cell lung cancer (NSCLC) who have never smoked or have tumors with mutations in EGFR generally derive minimal benefit from single-agent PD-1/PD-L1 checkpoint inhibitors. Prior data indicate that adding PD-L1 inhibition to anti-VEGF and cytotoxic chemotherapy may be a promising approach to overcoming immunotherapy resistance in these patients, however prospective validation is needed. This trial in progress (NCT03786692) is evaluating patients with stage IV NSCLC who have never smoked or who have tumors with sensitizing EGFR alterations to determine if a 4-drug combination of atezolizumab, carboplatin, pemetrexed, and bevacizumab can improve outcomes compared to carboplatin, pemetrexed and bevacizumab without atezolizumab.

METHODS:

This is a randomized, phase II, multicenter study evaluating carboplatin, pemetrexed, bevacizumab with and without atezolizumab in 117 patients with stage IV nonsquamous NSCLC. Randomization is 2 to 1 favoring the atezolizumab containing arm. Eligible patients include 1) those with tumors with sensitizing EGFR alterations in exons 19 or 21 or 2) patients who have never smoked and have wild-type tumors (ie, no EGFR, ALK or ROS1 alterations). Patients are defined as having never smoked if they have smoked less than 100 cigarettes in a lifetime. Patients with EGFR-mutated tumors must have disease progression or intolerance to prior tyrosine kinase inhibitor (TKI) therapy. The primary endpoint is progression-free survival (PFS). Secondary endpoints include overall survival (OS), response rate, duration of response, and time to response.

CONCLUSION:

This phase II trial is accruing patients at U.S. sites through the National Comprehensive Cancer Network (NCCN). The trial opened in August 2019 and accrual is expected to be completed in the Fall of 2024.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Revista: Clin Lung Cancer Asunto de la revista: NEOPLASIAS Año: 2023 Tipo del documento: Article País de afiliación: Panamá

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Pulmón de Células no Pequeñas / Neoplasias Pulmonares Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Revista: Clin Lung Cancer Asunto de la revista: NEOPLASIAS Año: 2023 Tipo del documento: Article País de afiliación: Panamá