| Literature DB >> 34912120 |
Yelena Y Janjigian1, Akihito Kawazoe2, Patricio Yañez3, Ning Li4, Sara Lonardi5, Oleksii Kolesnik6, Olga Barajas7, Yuxian Bai8, Lin Shen9, Yong Tang10, Lucjan S Wyrwicz11, Jianming Xu12, Kohei Shitara2, Shukui Qin13, Eric Van Cutsem14, Josep Tabernero15, Lie Li16, Sukrut Shah16, Pooja Bhagia16, Hyun Cheol Chung17.
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.Entities:
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Year: 2021 PMID: 34912120 PMCID: PMC8959470 DOI: 10.1038/s41586-021-04161-3
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 69.504