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Pembrolizumab plus gemcitabine and cisplatin for advanced biliary tract cancer: longer-term follow-up from the randomised, double-blind, placebo-controlled, phase 3 KEYNOTE-966 trial.
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Ueno Makoto, Yoo Changhoon, Ren Zhenggang, Furuse Junji, Kelley Robin Kate, Chan Stephen Lam, Edeline Julien, Klümpen Heinz-Josef, Yau Thomas, Verslype Chris, Ozaka Masato, Bouattour Mohamed, Park Joon Oh, Vogel Arndt, Valle Juan W, Starkopf Liis, Malhotra Usha, Siegel Abby B, Qin Shukui, Finn Richard S, KEYNOTE-966 Investigatorst, KEYNOTE-966 Investigators
Аннотация
BACKGROUND: At the final analysis of KEYNOTE-966 (median follow-up 25·6 months), pembrolizumab plus gemcitabine and cisplatin (pembrolizumab group) versus placebo plus gemcitabine and cisplatin (placebo group) provided a statistically significant, clinically meaningful improvement in overall survival without any new safety signals in participants with advanced biliary tract cancer. We report results from a median study follow-up of 36·6 months (∼3 years).
METHODS: In the randomised, double-blind, placebo-controlled, phase 3 KEYNOTE-966 trial conducted at 175 medical centres worldwide, eligible participants aged ≥18 years with previously untreated advanced biliary tract cancer were randomly assigned (1:1) to pembrolizumab 200 mg or placebo intravenously every 3 weeks plus gemcitabine 1000 mg/m2 and cisplatin 25 mg/m2 intravenously on days 1 and 8 of every 3-week cycle. Randomisation was done using a central interactive voice-response system and stratified by geographical region, disease status, and site of origin in block sizes of four. The primary endpoint of overall survival was evaluated in the intention-to-treat population (all participants randomly assigned to a treatment). Safety was evaluated in the as-treated population, comprising all participants who received at least one dose of study treatment. As the primary endpoint was met at the final analysis, updated data are reported without p values. This study is registered at ClinicalTrials.gov, NCT04003636.
FINDINGS: Between Oct 4, 2019, and June 8, 2021, 1069 participants were randomly assigned to the pembrolizumab group (n = 533) or the placebo group (n = 536). Median follow-up at data cutoff (Nov 14, 2023) was 36·6 months (IQR 32·7-41·4). The hazard ratio for overall survival was 0·86 (95% CI, 0·75-0·98) with pembrolizumab versus placebo; estimated 36-month overall survival rates were 13% (95% CI, 11-17) in the pembrolizumab group and 11% (95% CI, 8-14) in the placebo group. Grade 3 or 4 treatment-related adverse events occurred in 370 (70%) of 529 participants in the pembrolizumab group and 367 (69%) of 534 participants in the placebo group. No new treatment-related deaths occurred since the final analysis.
INTERPRETATION: With extended follow-up, the survival benefit of pembrolizumab plus gemcitabine and cisplatin observed at the final analysis persists with approximately 3 years of follow-up, with no new safety signals among participants with previously untreated metastatic or unresectable biliary tract cancer.
FUNDING: Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA.
METHODS: In the randomised, double-blind, placebo-controlled, phase 3 KEYNOTE-966 trial conducted at 175 medical centres worldwide, eligible participants aged ≥18 years with previously untreated advanced biliary tract cancer were randomly assigned (1:1) to pembrolizumab 200 mg or placebo intravenously every 3 weeks plus gemcitabine 1000 mg/m2 and cisplatin 25 mg/m2 intravenously on days 1 and 8 of every 3-week cycle. Randomisation was done using a central interactive voice-response system and stratified by geographical region, disease status, and site of origin in block sizes of four. The primary endpoint of overall survival was evaluated in the intention-to-treat population (all participants randomly assigned to a treatment). Safety was evaluated in the as-treated population, comprising all participants who received at least one dose of study treatment. As the primary endpoint was met at the final analysis, updated data are reported without p values. This study is registered at ClinicalTrials.gov, NCT04003636.
FINDINGS: Between Oct 4, 2019, and June 8, 2021, 1069 participants were randomly assigned to the pembrolizumab group (n = 533) or the placebo group (n = 536). Median follow-up at data cutoff (Nov 14, 2023) was 36·6 months (IQR 32·7-41·4). The hazard ratio for overall survival was 0·86 (95% CI, 0·75-0·98) with pembrolizumab versus placebo; estimated 36-month overall survival rates were 13% (95% CI, 11-17) in the pembrolizumab group and 11% (95% CI, 8-14) in the placebo group. Grade 3 or 4 treatment-related adverse events occurred in 370 (70%) of 529 participants in the pembrolizumab group and 367 (69%) of 534 participants in the placebo group. No new treatment-related deaths occurred since the final analysis.
INTERPRETATION: With extended follow-up, the survival benefit of pembrolizumab plus gemcitabine and cisplatin observed at the final analysis persists with approximately 3 years of follow-up, with no new safety signals among participants with previously untreated metastatic or unresectable biliary tract cancer.
FUNDING: Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA.