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Durvalumab, with or without tremelimumab, plus platinum-etoposide in first-line treatment of extensive-stage small-cell lung cancer: 3-year overall survival update from CASPIAN

  • L. Paz-Ares
  • , Y. Chen
  • , N. Reinmuth
  • , K. Hotta
  • , D. Trukhin
  • , G. Statsenko
  • , M. J. Hochmair
  • , M. Özgüroğlu
  • , J. H. Ji
  • , M. C. Garassino
  • , O. Voitko
  • , A. Poltoratskiy
  • , E. Musso
  • , L. Havel
  • , I. Bondarenko
  • , G. Losonczy
  • , N. Conev
  • , H. Mann
  • , T. B. Dalvi
  • , H. Jiang
  • J. W. Goldman
  • Hospital Universitario 12 de Octubre
  • Cancer & Hematology Centers of Western Michigan
  • Munich-Gauting
  • Okayama University
  • Odessa Regional Oncological Dispensary
  • Omsk Regional Cancer Center
  • Krankenhaus Nord
  • Istanbul University - Cerrahpaşa
  • Sungkyunkwan University
  • IRCCS Fondazione Istituto Nazionale per lo studio e la cura dei tumori - Milano
  • The University of Chicago
  • Kyiv City Clinical Oncological Centre
  • Russian Ministry of Health
  • AO Ospedali Riuniti PO Vincenzo Cervello
  • Charles University
  • Zaporizhia Medical Academy of Post-Gradate Education Ministry of Health of Ukraine
  • Semmelweis University
  • Clinic of Medical Oncology
  • AstraZeneca
  • University of California at Los Angeles

Research output: Contribution to journalArticlepeer-review

Abstract

Background: In the phase III CASPIAN study, first-line durvalumab in combination with etoposide plus either cisplatin or carboplatin (EP) significantly improved overall survival (OS) versus EP alone in extensive-stage small-cell lung cancer (ES-SCLC). Durvalumab plus tremelimumab plus EP numerically improved OS versus EP, but did not reach statistical significance. Here we report updated OS in censored patients after median follow-up of >3 years. Patients and methods: 805 patients with treatment-naïve ES-SCLC were randomized 1: 1: 1 to durvalumab plus EP, durvalumab plus tremelimumab plus EP, or EP. The two primary endpoints were OS for durvalumab plus EP versus EP and for durvalumab plus tremelimumab plus EP versus EP. Results: As of 22 March 2021 (median follow-up 39.4 months, 86% maturity), durvalumab plus EP continued to demonstrate improved OS versus EP: hazard ratio (HR) 0.71 [95% confidence interval (CI) 0.60-0.86; nominal P = 0.0003]; median OS was 12.9 versus 10.5 months, and 36-month OS rate was 17.6% versus 5.8%. Durvalumab plus tremelimumab plus EP continued to numerically improve OS versus EP: HR 0.81 (95% CI: 0.67-0.97; nominal P = 0.0200); median OS was 10.4 months, and 36-month OS rate was 15.3%. Twenty-seven and nineteen patients in the durvalumab plus EP and durvalumab plus tremelimumab plus EP arms, respectively, remained on durvalumab treatment at data cut-off. Conclusions: Three times more patients were estimated to be alive at 3 years when treated with durvalumab plus EP versus EP, with the majority still receiving durvalumab at data cut-off, further establishing durvalumab plus EP as first-line standard of care for ES-SCLC.

Original languageEnglish
Article number100408
JournalESMO Open
Volume7
Issue number2
DOIs
StatePublished - Apr 2022
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • CASPIAN
  • durvalumab
  • extensive-stage SCLC
  • overall survival
  • tremelimumab

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