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Clinical and molecular characterization of long-term survivors with extensive-stage small cell lung cancer treated with first-line atezolizumab plus carboplatin and etoposide.
Liu, Stephen V; Mok, Tony S K; Nabet, Barzin Y; Mansfield, Aaron S; De Boer, Richard; Losonczy, György; Sugawara, Shunichi; Dziadziuszko, Rafal; Krzakowski, Maciej; Smolin, Alexey; Hochmair, Maximilian J; Garassino, Marina C; Gay, Carl M; Heymach, John V; Byers, Lauren A; Lam, Sivuonthanh; Cardona, Andrés; Morris, Stefanie; Adler, Leah; Shames, David S; Reck, Martin.
Afiliação
  • Liu SV; Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA. Electronic address: stephen.v.liu@gunet.georgetown.edu.
  • Mok TSK; State Key Laboratory of Translational Oncology, The Chinese University of Hong Kong, Hong Kong, China.
  • Nabet BY; Genentech Inc., South San Francisco, CA, USA.
  • Mansfield AS; Division of Medical Oncology, Mayo Clinic, Rochester, MN, USA.
  • De Boer R; Peter MacCallum Cancer Centre, Melbourne, Australia.
  • Losonczy G; Department of Pulmonology, Semmelweis University, Budapest, Hungary.
  • Sugawara S; Sendai Kousei Hospital, Sendai, Japan.
  • Dziadziuszko R; Department of Oncology and Radiotherapy and Early Phase Clinical Trials Center, Medical University of Gdansk, Gdansk, Poland.
  • Krzakowski M; Maria Sklodowska Curie National Research Institute of Oncology, Warsaw, Poland.
  • Smolin A; Burdenko Main Military Clinical Hospital, Moscow, Russia.
  • Hochmair MJ; Karl Landsteiner Institute of Lung Research and Pulmonary Oncology, Vienna North Hospital Klinik Floridsdorf, Vienna, Austria.
  • Garassino MC; The University of Chicago Department of Hematology/Oncology, Chicago, IL, USA.
  • Gay CM; Department of Thoracic/Head & Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Heymach JV; Department of Thoracic/Head & Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Byers LA; Department of Thoracic/Head & Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Lam S; Genentech Inc., South San Francisco, CA, USA.
  • Cardona A; F. Hoffmann-La Roche Ltd., Basel, Switzerland.
  • Morris S; F. Hoffmann-La Roche Ltd., Basel, Switzerland.
  • Adler L; F. Hoffmann-La Roche Ltd., Basel, Switzerland.
  • Shames DS; Genentech Inc., South San Francisco, CA, USA.
  • Reck M; Lung Clinic Grosshansdorf, Airway Research Center North, German Center of Lung Research, Grosshansdorf, Germany.
Lung Cancer ; 186: 107418, 2023 12.
Article em En | MEDLINE | ID: mdl-37931445
ABSTRACT

OBJECTIVES:

In the Phase I/III IMpower133 study, first-line atezolizumab plus carboplatin and etoposide (CP/ET) treatment for extensive-stage small cell lung cancer (ES-SCLC) significantly improved overall survival (OS) and progression-free survival versus placebo plus CP/ET. We explored patient and disease characteristics associated with long-term survival in IMpower133, and associations of differential gene expression and SCLC-A (ASCL1-driven), SCLC-N (NEUROD1-driven), SCLC-P (POU2F3-driven), and SCLC-inflamed (SCLC-I) transcriptional subtypes with long-term survival. MATERIALS AND

METHODS:

Patients with previously untreated ES-SCLC were randomized 11 to four 21-day cycles of CP/ET with atezolizumab or placebo. Long-term survivors (LTS) were defined as patients who lived ≥ 18 months post randomization. A generalized linear model was used to evaluate the odds of living ≥ 18 months. Differential gene expression was analyzed using RNA-sequencing data in LTS and non-LTS. OS was assessed by T-effector and B-cell gene signature expression. Distribution of SCLC transcriptional subtypes was assessed in LTS and non-LTS.

RESULTS:

More LTS were in the atezolizumab arm (34%) than in the placebo arm (20%). The odds ratio for living ≥ 18 months in the atezolizumab arm versus the placebo arm was 2.1 (P < 0.03). Enhanced immune-related signaling was seen in LTS in both arms. Exploratory OS analyses showed atezolizumab treatment benefit versus placebo across T-effector and B-cell gene signature expression subgroups. A higher proportion of LTS than non-LTS in both arms had the SCLC-I subtype; this difference was particularly pronounced in the atezolizumab arm.

CONCLUSION:

These exploratory analyses suggest that long-term survival is more likely with atezolizumab than placebo in ES-SCLC, confirming the treatment benefit of the IMpower133 regimen. CLINICALTRIAL gov Identifier NCT02763579.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma de Pequenas Células do Pulmão / Neoplasias Pulmonares Limite: Humans Idioma: En Revista: Lung Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma de Pequenas Células do Pulmão / Neoplasias Pulmonares Limite: Humans Idioma: En Revista: Lung Cancer Assunto da revista: NEOPLASIAS Ano de publicação: 2023 Tipo de documento: Article