First-line pembrolizumab/placebo plus trastuzumab and chemotherapy in HER2-positive advanced gastric cancer: KEYNOTE-811

Author:

Chung Hyun Cheol1ORCID,Bang Yung-Jue2,S Fuchs Charles3,Qin Shu-Kui4,Satoh Taroh5,Shitara Kohei6,Tabernero Josep7,Van Cutsem Eric8,Alsina Maria7,Cao Zhu Alexander9,Lu Jia9,Bhagia Pooja9,Shih Chie-Schin9,Janjigian Yelena Y10

Affiliation:

1. Division of Medical Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, 03722, South Korea

2. Seoul National University College of Medicine, Seoul, 03080, South Korea

3. Yale Cancer Center, Smilow Cancer Hospital, New Haven, CT 06510, USA

4. Cancer Center of People's Liberation Army, Nanjing, 210002, China

5. Osaka University, Suita, Osaka, 565-0871, Japan

6. National Cancer Center Hospital East, Kashiwa, 277-8577, Japan

7. Vall d'Hebron University Hospital & Institute of Oncology, Barcelona, 08035, Spain

8. University Hospitals Gasthuisberg Leuven & KU Leuven, Leuven, 03001, Belgium

9. Department of Medical Oncology, Merck & Co., Inc., Kenilworth, NJ 07033, USA

10. Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA

Abstract

Treatment options for patients with HER2-positive advanced gastric cancer are limited, and the prognosis for these patients is poor. Pembrolizumab has demonstrated promising antitumor activity in patients with advanced gastric or gastroesophageal junction adenocarcinoma as monotherapy, in combination with chemotherapy and in combination with trastuzumab. Combining pembrolizumab with trastuzumab and chemotherapy may therefore provide a benefit for patients with advanced HER2-positive gastric cancer. Here we aimed to describe the design of and rationale for the randomized, double-blind, placebo-controlled Phase III KEYNOTE-811 study, which will evaluate the efficacy and safety of pembrolizumab or placebo in combination with trastuzumab and chemotherapy as first-line treatment for patients with advanced HER2-positive gastric or gastroesophageal junction adenocarcinoma. Clinical trial registration: NCT03615326 ( ClinicalTrials.gov )

Funder

Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., NJ, USA

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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