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Abstract

Human epidermal growth factor receptor 2 (HER2, also known as ERBB2) amplification or overexpression occurs in approximately 20% of advanced gastric or gastro-oesophageal junction adenocarcinomas1-3. More than a decade ago, combination therapy with the anti-HER2 antibody trastuzumab and chemotherapy became the standard first-line treatment for patients with these types of tumours4. Although adding the anti-programmed death 1 (PD-1) antibody pembrolizumab to chemotherapy does not significantly improve efficacy in advanced HER2-negative gastric cancer5, there are preclinical6-19 and clinical20,21 rationales for adding pembrolizumab in HER2-positive disease. Here we describe results of the protocol-specified first interim analysis of the randomized, double-blind, placebo-controlled phase 111 KEYNOTE-811 study of pembrolizumab plus trastuzumab and chemotherapy for unresectable or metastatic, HER2-positive gastric or gastro-oesophageal junction adenocarcinoma22 (https://clinicaltrials.gov, NCT03615326). We show that adding pembrolizumab to trastuzumab and chemotherapy markedly reduces tumour size, induces complete responses in some participants, and significantly improves objective response rate.

Details

Title
The KEYNOTE-811 trial of dual PD-1 and HER2 blockade in HER2-positive gastric cancer
Author
Janjigian, Yelena Y 1 ; Kawazoe, Akihito 2 ; Yañez, Patricio 3 ; Li, Ning 4 ; Lonardi, Sara 5 ; Kolesnik, Oleksii; Barajas, Olga; Bai, Yuxian; Shen, Lin; Tang, Yong; Wyrwicz, Lucjan S; Xu, Jianming; Shitara, Kohei; Qin, Shukui; Van Cutsem, Eric; Tabernero, Josep; Li, Lie; Shah, Sukrut; Bhagia, Pooja; Chung, Hyun Cheol

 Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY, USA 
 National Cancer Hospital East, Kashiwa, Japan 
 Universidad de La Frontera, James Lind Cancer Research Center, Temuco, Chile 
 Henan Cancer Hospital, the Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, China 
 Istituto Oncologico Veneto IOV-IRCCS, Padova, Italy 
Pages
727-3,730A-730I
Section
Article
Publication year
2021
Publication date
Dec 23-Dec 30, 2021
Publisher
Nature Publishing Group
ISSN
00280836
e-ISSN
14764687
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2616227398
Copyright
Copyright Nature Publishing Group Dec 23-Dec 30, 2021