The KEYNOTE-811 trial of dual PD-1 and HER2 blockade in HER2-positive gastric cancer Journal Article


Authors: Janjigian, Y. Y.; Kawazoe, A.; Yañez, P.; Li, N.; Lonardi, S.; Kolesnik, O.; Barajas, O.; Bai, Y.; Shen, L.; Tang, Y.; Wyrwicz, L. S.; Xu, J.; Shitara, K.; Qin, S.; Van Cutsem, E.; Tabernero, J.; Li, L.; Shah, S.; Bhagia, P.; Chung, H. C.
Article Title: The KEYNOTE-811 trial of dual PD-1 and HER2 blockade in HER2-positive gastric cancer
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 III 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. © 2021, The Author(s), under exclusive licence to Springer Nature Limited.
Keywords: chemotherapy; tumor; antibody; cancer
Journal Title: Nature
Volume: 600
Issue: 7890
ISSN: 0028-0836
Publisher: Nature Publishing Group  
Date Published: 2021-12-23
Start Page: 727
End Page: 730
Language: English
DOI: 10.1038/s41586-021-04161-3
PUBMED: 34912120
PROVIDER: scopus
PMCID: PMC8959470
DOI/URL:
Notes: Article -- Export Date: 1 February 2022 -- Source: Scopus
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  1. Yelena Yuriy Janjigian
    394 Janjigian