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Perioperative Durvalumab with Neoadjuvant Chemotherapy in Operable Bladder Cancer

  • T. Powles
  • , J. W. F. Catto
  • , M. D. Galsky
  • , H. Al-Ahmadie
  • , J. J. Meeks
  • , H. Nishiyama
  • , T. Q. Vu
  • , L. Antonuzzo
  • , P. Wiechno
  • , V. Atduev
  • , A. G. Kann
  • , T. H. Kim
  • , C. Suárez
  • , C. H. Chang
  • , F. Roghmann
  • , M. Özgüroğlu
  • , B. J. Eigl
  • , N. Oliveira
  • , T. Buchler
  • , M. Gadot
  • Y. Zakharia, J. Armstrong, A. Gupta, S. Hois, NIAGARA Investigators

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

BACKGROUND Neoadjuvant chemotherapy followed by radical cystectomy is the standard treatment for cisplatin-eligible patients with muscle-invasive bladder cancer. Adding perioperative immunotherapy may improve outcomes. METHODS In this phase 3, open-label, randomized trial, we assigned, in a 1:1 ratio, cisplatin-eligible patients with muscle-invasive bladder cancer to receive neoadjuvant durvalumab plus gemcitabine–cisplatin every 3 weeks for four cycles, followed by radical cystectomy and adjuvant durvalumab every 4 weeks for eight cycles (durvalumab group), or to receive neoadjuvant gemcitabine–cisplatin followed by radical cystectomy alone (comparison group). Event-free survival was one of two primary end points. Overall survival was the key secondary end point. RESULTS In total, 533 patients were assigned to the durvalumab group and 530 to the comparison group. The estimated event-free survival at 24 months was 67.8% (95% confidence interval [CI], 63.6 to 71.7) in the durvalumab group and 59.8% (95% CI, 55.4 to 64.0) in the comparison group (hazard ratio for progression, recurrence, not undergoing radical cystectomy, or death from any cause, 0.68; 95% CI, 0.56 to 0.82; P<0.001 by stratified log-rank test). The estimated overall survival at 24 months was 82.2% (95% CI, 78.7 to 85.2) in the durvalumab group and 75.2% (95% CI, 71.3 to 78.8) in the comparison group (hazard ratio for death, 0.75; 95% CI, 0.59 to 0.93; P=0.01 by stratified log-rank test). Treatment-related adverse events of grade 3 or 4 in severity occurred in 40.6% of the patients in the durvalumab group and in 40.9% of those in the comparison group; treatment-related adverse events leading to death occurred in 0.6% in each group. Radical cystectomy was performed in 88.0% of the patients in the durvalumab group and in 83.2% of those in the comparison group. CONCLUSIONS Perioperative durvalumab plus neoadjuvant chemotherapy led to significant improvements in event-free survival and overall survival as compared with neoadjuvant chemotherapy alone.
Original languageEnglish
Pages (from-to)1773-1786
JournalNew England journal of medicine
Volume391
Issue number19
DOIs
Publication statusPublished - 14 Nov 2024

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

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