Cancer Medicine (Oct 2020)

Duration of nivolumab for pretreated, advanced non–small‐cell lung cancer

  • Margaux Geier,
  • Renaud Descourt,
  • Romain Corre,
  • Guillaume Léveiller,
  • Régine Lamy,
  • Éric Goarant,
  • Jean‐Louis Bizec,
  • Cyril Bernier,
  • Gilles Quéré,
  • Karim Amrane,
  • Elisabeth Gaye,
  • François Lucia,
  • Emilie Burte,
  • Christos Chouaid,
  • Gilles Robinet

DOI
https://doi.org/10.1002/cam4.3120
Journal volume & issue
Vol. 9, no. 19
pp. 6923 – 6932

Abstract

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Abstract Background A standard of care for pretreated, advanced non–small‐cell lung cancers (NSCLCs), nivolumab has demonstrated long‐term benefit when administered for 2 years. We aimed to better discern an optimized administration duration by retrospectively analyzing real‐life long‐term efficacy in a prospective cohort. Methods All nivolumab‐treated adults with advanced NSCLCs (01/09/2015 to 30/09/2016) from nine French centers were eligible. On 31/12/2018, patients who are alive ≥ 2 years after starting nivolumab were defined as long‐term survivors (LTSs) and were divided into three nivolumab treatment groups: 2 years. Co‐primary endpoints were LTSs’ progression‐free survival (PFS) and overall survival (OS). Results The median follow‐up was 32 months (95% CI, 31.0 to 34.0). The 3‐year OS rate for the 259 cohort patients was 16.6%. Among them, 65 were LTSs: 47 treated 2 years. Their respective characteristics were: median age: 59, 52, and 58 years; smoking history: 92.9, 100, and 100%; adenocarcinomas: 66, 57.1, and 54.5%. LTSs’ median (m)PFS was 28.4 months; mOS was not reached. LTSs’ objective response rate was 61.6%. mOS was 32.7 months for those treated 2‐year group's 3‐year OS was longer. Twenty‐eight LTSs experienced no disease progression; 7 had durable complete responses. However, LTSs had more frequent and more severe adverse events. Conclusion In real‐life, prolonged nivolumab use provided long‐term benefit with 16.6% 3‐year OS and 25% LTSs. Survival tended to be prolonged with nivolumab continued beyond 2 years. Prospective randomized trials with adequate design are needed.

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