| Literature DB >> 33358124 |
Camille Evrard1, Christophe Louvet2, Farid El Hajbi3, Frédéric DI Fiore4, Karine LE Malicot5, Thomas Aparicio6, Olivier Bouché7, Pierre Laurent-Puig8, Frédéric Bibeau9, Thierry Lecomte10, Astrid Lièvre11, Rosine Guimbaud12, Stefano Kim13, Aziz Zaanan14, Harry Sokol15, Benoist Chibaudel16, Jérome Desrame17, Sabrina Pierre5, Daniel Gonzalez5, Come Lepage18, David Tougeron19.
Abstract
Gastric or gastro-oesophageal junction (GEJ) adenocarcinomas present poor overall survival (OS). First-line chemotherapy regimen for patients with HER2-negative tumours is based on a doublet or triplet of fluoropyrimidine plus platinum salt ± taxane. Second-line chemotherapy (Docetaxel or Irinotecan) improves OS which nonetheless remains poor (around 5 months). The first results of immune checkpoint inhibitors (anti-PD-1) combined with chemotherapy in metastatic gastric and GEJ cancers were discordant in recent phase III trials. Data on dual-blockade (anti-PD-L1 or anti-PD-1 plus anti-CTLA-4) plus chemotherapy are lacking. DURIGAST is a randomised, multicenter, non-comparative, phase II study, evaluating safety and efficacy of FOLFIRI plus Durvalumab (anti-PD-L1) versus FOLFIRI plus Durvalumab and Tremelimumab (anti-CTLA-4) as second-line treatment of advanced gastric and GEJ adenocarcinoma. The primary objective is the rate of patients alive and without progression at 4 months. The main inclusion criteria are: patients with advanced gastric or GEJ adenocarcinoma, pre-treated with fluoropyrimidine + platinum salt ± taxane. Due to a lack of data on FOLFIRI, Durvalumab and Tremelimumab combination, a 2-step safety run-in phase has been performed before the randomised phase II. The safety run-in phase did not show any safety issue and the randomised phase II starts in September 2020.Entities:
Keywords: Adenocarcinoma; Chemotherapy; Gastric cancer; Immune checkpoint inhibitors
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Year: 2021 PMID: 33358124 DOI: 10.1016/j.dld.2020.11.036
Source DB: PubMed Journal: Dig Liver Dis ISSN: 1590-8658 Impact factor: 4.088