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KEYNOTE-975 study design: a Phase III study of definitive chemoradiotherapy plus pembrolizumab in patients with esophageal carcinoma

Authors
 Manish A Shah  ;  Jaafar Bennouna  ;  Toshihiko Doi  ;  Lin Shen  ;  Ken Kato  ;  Antoine Adenis  ;  Harvey J Mamon  ;  Markus Moehler  ;  Xiaolong Fu  ;  Byoung Chul Cho  ;  Sonal Bordia  ;  Pooja Bhagia  ;  Chie-Schin Shih  ;  Anjali Desai  ;  Peter Enzinger 
Citation
 FUTURE ONCOLOGY, Vol.17(10) : 1143-1153, 2021-04 
Journal Title
FUTURE ONCOLOGY
ISSN
 1479-6694 
Issue Date
2021-04
MeSH
Antibodies, Monoclonal, Humanized / administration & dosage ; Antineoplastic Combined Chemotherapy Protocols / adverse effects ; Antineoplastic Combined Chemotherapy Protocols / therapeutic use* ; Chemoradiotherapy* ; Clinical Protocols* ; Combined Modality Therapy ; Esophageal Neoplasms / diagnosis ; Esophageal Neoplasms / therapy* ; Female ; Humans ; Male ; Research Design*
Keywords
chemotherapy ; esophageal adenocarcinoma ; esophageal cancer ; esophageal squamous cell carcinoma ; immunotherapy ; pembrolizumab ; radiotherapy
Abstract
Despite curative-intent treatment, most patients with locally advanced esophageal cancer will experience disease recurrence or locoregional progression, highlighting the need for new therapies. Current guidelines recommend definitive chemoradiotherapy in patients ineligible for surgical resection, but survival outcomes are poor. Pembrolizumab is well tolerated and provides promising antitumor activity in patients with previously treated, advanced, unresectable esophageal/esophagogastric junction cancer. Combining pembrolizumab with chemoradiotherapy may further improve outcomes in the first-line setting. Here, we describe the design and rationale for the double-blind, Phase III, placebo-controlled, randomized KEYNOTE-975 trial investigating pembrolizumab in combination with definitive chemoradiotherapy as first-line treatment in patients with locally advanced, unresectable esophageal/gastroesophageal junction cancer. Overall survival and event-free survival are the dual primary end points. Clinical trial registration: NCT04210115 (ClinicalTrials.gov).
Files in This Item:
T202126009.pdf Download
DOI
10.2217/fon-2020-0969
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Cho, Byoung Chul(조병철) ORCID logo https://orcid.org/0000-0002-5562-270X
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/190391
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