AIMS: In KEYNOTE-859, pembrolizumab plus chemotherapy significantly improved overall survival (OS) versus placebo plus chemotherapy for participants with untreated locally advanced or metastatic HER2-negative gastric or gastroesophageal junction adenocarcinoma, with manageable safety. This post hoc analysis assessed Quality-adjusted Time Without Symptoms of disease progression or Toxicity of treatment (Q-TWiST). PARTICIPANTS AND METHODS: Survival time was grouped into three health states: TOX (time with any grade ≥3 adverse event AE before disease progression), TWiST (time before PD or death without grade ≥3 AEs), and REL (time from PD to death). Q-TWiST was the sum of restricted mean survival time (RMST) in each state, weighted by utilities estimated using the EQ-5D-5L questionnaire. Relative gains in Q-TWiST ≥15% were considered "clearly clinically important." RESULTS: RMST was longer in TOX (2.30 months 95% CI, 1.28 to 3.44) and TWiST (1.90 months 95% CI, -0.02 to 3.79) and shorter in REL (-0.28 months 95% CI, -2.43 to 2.01) with pembrolizumab plus chemotherapy versus chemotherapy at month 56, for a relative Q-TWiST gain of 20.90% (US algorithm) or 18.38% (standardized algorithm). CONCLUSIONS: A clearly clinically important Q-TWiST gain was observed with pembrolizumab plus chemotherapy versus chemotherapy in all participants. CLINICAL TRIALS REGISTRATION: www.ClinicalTrials.gov identifier is NCT03675737.
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Lucjan Wyrwicz
Vasiliki Kalampoki
Adriana Valderrama
Immunotherapy
Merck & Co., Inc., Rahway, NJ, USA (United States)
National Institute of Oncology
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Wyrwicz et al. (Sat,) studied this question.
www.synapsesocial.com/papers/69ddd8eee195c95cdefd679f — DOI: https://doi.org/10.1080/1750743x.2026.2647579