4.5 Article

Clinical and molecular characterization of long-term survivors with extensive-stage small cell lung cancer treated with first-line atezolizumab plus carboplatin and etoposide

Journal

LUNG CANCER
Volume 186, Issue -, Pages -

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.lungcan.2023.107418

Keywords

(maximum 6): Small cell lung carcinoma; RNA Sequence analysis; Gene expression profiling; Immune checkpoint inhibitors; Carboplatin; Etoposide; Clinical trial IMpower133; Atezolizumab

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In the Phase I/III IMpower133 study, atezolizumab in combination with carboplatin and etoposide demonstrated improved overall survival and progression-free survival for patients with extensive-stage small cell lung cancer. The study also revealed associations between long-term survival and patient and disease characteristics, as well as differential gene expression and SCLC transcriptional subtypes.
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 1:1 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.

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