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DOI 10.1016/j.lungcan.2023.107418

Медицинская библиотека · Lung cancer (Amsterdam, Netherlands) · 2023

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

Рандомизированное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

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.

CLINICALTRIAL: gov Identifier: NCT02763579.

Для цитирования: 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. Clinical and molecular characterization of long-term survivors with extensive-stage small cell lung cancer treated with first-line atezolizumab plus carboplatin and etoposide.. Lung cancer (Amsterdam, Netherlands). 2023. DOI: 10.1016/j.lungcan.2023.107418.

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