TY - JOUR
T1 - Randomized phase III KEYNOTE-181 study of pembrolizumab versus chemotherapy in advanced esophageal cancer
AU - KEYNOTE-181 Investigators
AU - Kojima, Takashi
AU - Shah, Manish A.
AU - Muro, Kei
AU - Francois, Eric
AU - Adenis, Antoine
AU - Hsu, Chih Hung
AU - Doi, Toshihiko
AU - Moriwaki, Toshikazu
AU - Kim, Sung Bae
AU - Lee, Se Hoon
AU - Bennouna, Jaafar
AU - Kato, Ken
AU - Shen, Lin
AU - Enzinger, Peter
AU - Qin, Shu Kui
AU - Ferreira, Paula
AU - Chen, Jia
AU - Girotto, Gustavo
AU - de la Fouchardiere, Christelle
AU - Senellart, Helene
AU - Al-Rajabi, Raed
AU - Lordick, Florian
AU - Wang, Ruixue
AU - Suryawanshi, Shailaja
AU - Bhagia, Pooja
AU - Peter Kang, S.
AU - Metges, Jean Philippe
N1 - Publisher Copyright:
© 2020 by American Society of Clinical Oncology
PY - 2020/12/10
Y1 - 2020/12/10
N2 - PURPOSE Patients with advanced esophageal cancer have a poor prognosis and limited treatment options after first-line chemotherapy. PATIENTS AND METHODS In this open-label, phase III study, we randomly assigned (1:1) 628 patients with advanced/metastatic squamous cell carcinoma or adenocarcinoma of the esophagus, that progressed after one prior therapy, to pembrolizumab 200 mg every 3 weeks for up to 2 years or chemotherapy (investigator's choice of paclitaxel, docetaxel, or irinotecan). Primary end points were overall survival (OS) in patients with programmed death ligand-1 (PD-L1) combined positive score (CPS) $ 10, in patients with squamous cell carcinoma, and in all patients (one-sided a 0.9%, 0.8%, and 0.8%, respectively). RESULTS At final analysis, conducted 16 months after the last patient was randomly assigned, OS was prolonged with pembrolizumab versus chemotherapy for patients with CPS $ 10 (median, 9.3 v 6.7 months; hazard ratio [HR], 0.69 [95% CI, 0.52 to 0.93]; P 5.0074). Estimated 12-month OS rate was 43% (95% CI, 33.5% to 52.1%) with pembrolizumab versus 20% (95% CI, 13.5% to 28.3%) with chemotherapy. Median OS was 8.2 months versus 7.1 months (HR, 0.78 [95% CI, 0.63 to 0.96]; P 5.0095) in patients with squamous cell carcinoma and 7.1 months versus 7.1 months (HR, 0.89 [95% CI, 0.75 to 1.05]; P 5.0560) in all patients. Grade 3-5 treatment-related adverse events occurred in 18.2% of patients with pembrolizumab versus 40.9% in those who underwent chemotherapy. CONCLUSION Pembrolizumab prolonged OS versus chemotherapy as second-line therapy for advanced esophageal cancer in patients with PD-L1 CPS $ 10, with fewer treatment-related adverse events.
AB - PURPOSE Patients with advanced esophageal cancer have a poor prognosis and limited treatment options after first-line chemotherapy. PATIENTS AND METHODS In this open-label, phase III study, we randomly assigned (1:1) 628 patients with advanced/metastatic squamous cell carcinoma or adenocarcinoma of the esophagus, that progressed after one prior therapy, to pembrolizumab 200 mg every 3 weeks for up to 2 years or chemotherapy (investigator's choice of paclitaxel, docetaxel, or irinotecan). Primary end points were overall survival (OS) in patients with programmed death ligand-1 (PD-L1) combined positive score (CPS) $ 10, in patients with squamous cell carcinoma, and in all patients (one-sided a 0.9%, 0.8%, and 0.8%, respectively). RESULTS At final analysis, conducted 16 months after the last patient was randomly assigned, OS was prolonged with pembrolizumab versus chemotherapy for patients with CPS $ 10 (median, 9.3 v 6.7 months; hazard ratio [HR], 0.69 [95% CI, 0.52 to 0.93]; P 5.0074). Estimated 12-month OS rate was 43% (95% CI, 33.5% to 52.1%) with pembrolizumab versus 20% (95% CI, 13.5% to 28.3%) with chemotherapy. Median OS was 8.2 months versus 7.1 months (HR, 0.78 [95% CI, 0.63 to 0.96]; P 5.0095) in patients with squamous cell carcinoma and 7.1 months versus 7.1 months (HR, 0.89 [95% CI, 0.75 to 1.05]; P 5.0560) in all patients. Grade 3-5 treatment-related adverse events occurred in 18.2% of patients with pembrolizumab versus 40.9% in those who underwent chemotherapy. CONCLUSION Pembrolizumab prolonged OS versus chemotherapy as second-line therapy for advanced esophageal cancer in patients with PD-L1 CPS $ 10, with fewer treatment-related adverse events.
UR - https://www.scopus.com/pages/publications/85096380116
U2 - 10.1200/JCO.20.01888
DO - 10.1200/JCO.20.01888
M3 - Article
C2 - 33026938
AN - SCOPUS:85096380116
SN - 0732-183X
VL - 38
SP - 4138
EP - 4148
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 35
ER -