SKYSCRAPER-02: Tiragolumab in Combination With Atezolizumab Plus Chemotherapy in Untreated Extensive-Stage Small-Cell Lung Cancer

  • Charles M. Rudin
  • , Stephen V. Liu
  • , Ross A. Soo
  • , Shun Lu
  • , Min Hee Hong
  • , Jong Seok Lee
  • , Maciej Bryl
  • , Daphne W. Dumoulin
  • , Achim Rittmeyer
  • , Chao Hua Chiu
  • , Ozgur Ozyilkan
  • , Melissa Johnson
  • , Alejandro Navarro
  • , Silvia Novello
  • , Yuichi Ozawa
  • , Sammi Hiu Tam
  • , Namrata S. Patil
  • , Xiaohui Wen
  • , Meilin Huang
  • , Tien Hoang
  • Raymond Meng, Martin Reck

研究成果: 雜誌貢獻文章同行評審

68 引文 斯高帕斯(Scopus)

摘要

PURPOSE The phase III SKYSCRAPER-02 study determined whether the benefits of atezolizumab plus carboplatin and etoposide (CE) could be enhanced by the addition of tiragolumab in untreated extensive-stage small-cell lung cancer (ES-SCLC). We report final progression-free survival (PFS) and overall survival (OS) analyses. METHODS Patients received tiragolumab 600 mg/placebo, plus atezolizumab 1,200 mg and CE (four cycles), then maintenance tiragolumab/placebo plus atezolizumab. Primary end points were investigator-assessed PFS and OS in patients without history/presence of brain metastases (primary analysis set [PAS]). Additional end points included PFS and OS in all patients regardless of brain metastases status (full analysis set [FAS]), response, and safety. RESULTS Four hundred ninety patients were randomly assigned (FAS): 243 to tiragolumab armand 247 to control arm. At the cutoff date (February 6, 2022;median duration of follow-up, 14.3 months [PAS] and 13.9 months [FAS]), final analysis of PFS in the PAS (n = 397) did not reach statistical significance (stratified hazard ratio [HR], 1.11; P =. 3504; median, 5.4 months tiragolumab v 5.6 months control). At the cutoff date (September 6, 2022; median duration of follow-up, 21.2 months [FAS]), median OS in the PAS at final OS analysis was 13.1 months in both arms (stratified HR, 1.14; P =. 2859). Median PFS and OS in the FAS were consistent with the PAS. The proportion of patients with immune-mediated adverse events (AEs) in the tiragolumab and control arms was 54.4% and 49.2%, respectively (grade 3/4: 7.9% and 7.7%). AEs leading to treatment withdrawal occurred in 8.4% and 9.3% of tiragolumab- and control-treated patients, respectively. CONCLUSION Tiragolumab did not provide additional benefit over atezolizumab and CE in untreated ES-SCLC. The combination was well tolerated with no new safety signals.
原文英語
頁(從 - 到)324-335
頁數12
期刊Journal of Clinical Oncology
42
發行號3
DOIs
出版狀態已發佈 - 1月 20 2024

ASJC Scopus subject areas

  • 腫瘤科
  • 癌症研究

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