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Pembrolizumab for Persistent, Recurrent, or Metastatic Cervical Cancer

Authors :
Colombo, N
Dubot, C
Lorusso, D
Caceres, M
Hasegawa, K
Shapira-Frommer, R
Tewari, K
Salman, P
Hoyos Usta, E
Yañez, E
Gümüş, M
Olivera Hurtado de Mendoza, M
Samouëlian, V
Castonguay, V
Arkhipov, A
Toker, S
Li, K
Keefe, S
Monk, B
Colombo, Nicoletta
Dubot, Coraline
Lorusso, Domenica
Caceres, M Valeria
Hasegawa, Kosei
Shapira-Frommer, Ronnie
Tewari, Krishnansu S
Salman, Pamela
Hoyos Usta, Edwin
Yañez, Eduardo
Gümüş, Mahmut
Olivera Hurtado de Mendoza, Mivael
Samouëlian, Vanessa
Castonguay, Vincent
Arkhipov, Alexander
Toker, Sarper
Li, Kan
Keefe, Stephen M
Monk, Bradley J
Colombo, N
Dubot, C
Lorusso, D
Caceres, M
Hasegawa, K
Shapira-Frommer, R
Tewari, K
Salman, P
Hoyos Usta, E
Yañez, E
Gümüş, M
Olivera Hurtado de Mendoza, M
Samouëlian, V
Castonguay, V
Arkhipov, A
Toker, S
Li, K
Keefe, S
Monk, B
Colombo, Nicoletta
Dubot, Coraline
Lorusso, Domenica
Caceres, M Valeria
Hasegawa, Kosei
Shapira-Frommer, Ronnie
Tewari, Krishnansu S
Salman, Pamela
Hoyos Usta, Edwin
Yañez, Eduardo
Gümüş, Mahmut
Olivera Hurtado de Mendoza, Mivael
Samouëlian, Vanessa
Castonguay, Vincent
Arkhipov, Alexander
Toker, Sarper
Li, Kan
Keefe, Stephen M
Monk, Bradley J
Publication Year :
2021

Abstract

BACKGROUND Pembrolizumab has efficacy in programmed death ligand 1 (PD-L1)–positive metastatic or unresectable cervical cancer that has progressed during chemotherapy. We assessed the relative benefit of adding pembrolizumab to chemotherapy with or without bevacizumab. METHODS In a double-blind, phase 3 trial, we randomly assigned patients with persistent, recurrent, or metastatic cervical cancer in a 1:1 ratio to receive pembrolizumab (200 mg) or placebo every 3 weeks for up to 35 cycles plus platinum-based chemotherapy and, per investigator discretion, bevacizumab. The dual primary end points were progression-free survival and overall survival, each tested sequentially in patients with a PD-L1 combined positive score of 1 or more, in the intention-to-treat population, and in patients with a PD-L1 combined positive score of 10 or more. The combined positive score is defined as the number of PD-L1–staining cells divided by the total number of viable tumor cells, multiplied by 100. All results are from the protocol-specified first interim analysis. RESULTS In 548 patients with a PD-L1 combined positive score of 1 or more, median progression-free survival was 10.4 months in the pembrolizumab group and 8.2 months in the placebo group (hazard ratio for disease progression or death, 0.62; 95% confidence interval [CI], 0.50 to 0.77; P<0.001). In 617 patients in the intention-to-treat population, progression-free survival was 10.4 months and 8.2 months, respectively (hazard ratio, 0.65; 95% CI, 0.53 to 0.79; P<0.001). In 317 patients with a PD-L1 combined positive score of 10 or more, progression-free survival was 10.4 months and 8.1 months, respectively (hazard ratio, 0.58; 95% CI, 0.44 to 0.77; P<0.001). Overall survival at 24 months was 53.0% in the pembrolizumab group and 41.7% in the placebo group (hazard ratio for death, 0.64; 95% CI, 0.50 to 0.81; P<0.001), 50.4% and 40.4% (hazard ratio, 0.67; 95% CI, 0.54 to 0.84; P<0.001), and 54.4% and 44.6% (hazar

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1308940779
Document Type :
Electronic Resource