The KEYNOTE-811 trial of dual PD-1 and HER2 blockade in HER2-positive gastric cancer.
Yelena Y JanjigianAkihito KawazoePatricio YañezNing LiSara LonardiOleksii KolesnikOlga BarajasYuxian BaiLin ShenYong TangLucjan S WyrwiczJianming XuKohei ShitaraShukui QinEric Van CutsemJosep TaberneroLie LiSukrut ShahPooja BhagiaHyun Cheol ChungPublished in: Nature (2021)
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 adenocarcinomas 1-3 . 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 tumours 4 . Although adding the anti-programmed death 1 (PD-1) antibody pembrolizumab to chemotherapy does not significantly improve efficacy in advanced HER2-negative gastric cancer 5 , there are preclinical 6-19 and clinical 20,21 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 adenocarcinoma 22 ( 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.
Keyphrases
- phase iii
- epidermal growth factor receptor
- placebo controlled
- advanced non small cell lung cancer
- double blind
- phase ii
- locally advanced
- tyrosine kinase
- open label
- clinical trial
- combination therapy
- squamous cell carcinoma
- rectal cancer
- study protocol
- phase ii study
- endothelial cells
- randomized controlled trial
- small cell lung cancer
- induced pluripotent stem cells
- stem cells
- cell therapy
- mesenchymal stem cells
- pluripotent stem cells