First-line regorafenib with nivolumab and chemotherapy in advanced oesophageal, gastric, or gastro-oesophageal junction cancer in the USA: a single-arm, single-centre, phase 2 trial.

BACKGROUND

The addition of nivolumab to chemotherapy improves survival in patients with advanced oesophagogastric (oesophageal, gastric, or gastro-oesophageal junction) adenocarcinoma; however, outcomes remain poor. We assessed the safety and activity of regorafenib in combination with nivolumab and chemotherapy in the first-line treatment of advanced oesophagogastric adenocarcinoma.

METHODS

This investigator-initiated, single-arm, phase 2 trial in adult patients (aged ≥18 years) with previously untreated, HER2-negative, metastatic oesophagogastric adenocarcinoma was done at the Memorial Sloan Kettering Cancer Center (New York, NY, USA). Eligible patients had measurable disease or non-measurable disease that was evaluable (defined by Response Evaluation Criteria in Solid Tumours [RECIST] version 1.1) and Eastern Cooperative Oncology Group performance status of 0 or 1. Patients received FOLFOX chemotherapy (fluorouracil [400 mg/m

FINDINGS

Between Feb 11, 2021, and May 4, 2022, 39 patients were enrolled, received at least one dose of study drug, and were included in safety analyses. 35 patients were evaluable for 6-month progression-free survival. Median age was 57 years (IQR 52-66), nine (26%) patients were women, 26 (74%) were men, 28 (80%) were White, and seven (20%) were Asian. At data cutoff (March 3, 2023), median follow-up was 18·1 months (IQR 12·7-20·4). The primary endpoint was reached, with 25 (71%; 95% CI 54-85) of 35 patients progression free at 6 months. Nine (26%) of 35 patients had disease progression and one (3%) patient died; the death was unrelated to treatment. The most common adverse event of any grade was fatigue (36 [92%] of 39). The most common grade 3 or 4 adverse events were decreased neutrophil count (18 [46%]), hypertension (six [15%]), dry skin, pruritus, or rash (five [13%]), and anaemia (four [10%]). Serious treatment-related adverse events occurred in ten (26%) patients, which were acute kidney injury (three [8%]), hepatotoxicity (two [5%]), sepsis (two [5%]), dry skin, pruritus, or rash (one [3%]), nausea (one [3%]), and gastric perforation (one [3%]). There were no treatment-related deaths.

INTERPRETATION

Regorafenib can be safely combined with nivolumab and chemotherapy and showed promising activity in HER2-negative metastatic oesophagogastric cancer. A randomised, phase 3 clinical trial is planned.

FUNDING

Bristol Myers Squibb, Bayer and National Institutes of Health/National Cancer Institute.

Informations de copyright

Copyright © 2023 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests SLC reports stock ownership in Pfizer, Moderna, and BioNTech. RHM reports consulting with PureTech Health, advisory board with IDEAYA Biosciences, and research funding from Nimbus Therapeutics. JFC reports an investigator role on a research study sponsored by Paige.AI. GYK reports consulting fees from AstraZeneca, Bristol-Myers Squibb, Merck, Pieris, and Zymeworks; and grants or contracts from AstraZeneca, Bristol-Myers Squibb, CARsgen, Zymeworks, Daiichi Sankyo, Oncolys, Pieris, and Adaptimmune. SBM reports honoraria from Natera, Bicara, Novartis, Basilea, Elevation Oncology, Purple Oncology, Pinetree Therapeutics, and Daiichi Sankyo; research support from Epic Sciences; grant funding from the Conquer Cancer Foundation; and research travel support from AstraZeneca outside of the submitted work. MAS reports consulting for Boston Scientific and Novo Nordisk. MEL reports ownership or equity interests with Apricity Health; intellectual property rights with John Wiley & Sons, and the Taylor & Francis Group; uncompensated provision of services for Oncoderm; and provision of services for Adgero Biopharmaceuticals, the American Academy of Dermatology, the American Society of Pediatric Hematology/Oncology, Apricity Health, AstraZeneca, Atlantic Canada Oncology Group, BGB Communications, Bicara Therapeutics, Deciphera, DelMar Pharmaceuticals, EMD Serono, GCO Global, Hoth Therapeutics, Incyte, Innovaderm Research, Johnson & Johnson, La Fonderie Ressources, La Roche-Posay, Loxo Oncology, Lutris Pharma, MJH Life Sciences, the Michigan Dermatological Society, NKMax America, NanOlogy, Novartis, Novartis Pharmaceuticals Corporation, Novocure, OnQuality Pharmaceuticals, Patient Resource, QED Therapeutics, RBC Consulting, RMEI Medical Education, Society for Immunotherapy of Cancer, Takeda Millennium, The Lynx Group, Tyra Biosciences, Varsona Pharmaceuticals, WebMD, Wolters Kluwer, and eSquared Communication Consulting. JS reports consulting for Paige.AI. MFB reports consulting for Eli Lilly and AstraZeneca (not related to this work). YYJ reports research funding from Bayer, Bristol Myers Squibb, Memorial Sloan Kettering Cancer Center Cycle for Survival, the United States Department of Defense, Eli Lilly, Fred's Team, Genentech/Roche, Merck, the National Cancer Institute, and RGENIX; advisory board or consulting with AbbVie, Amerisource Bergen, Ask-Gene Pharma, Arcus Biosciences, Astellas, Astra Zeneca, Basilea Pharmaceutica, Bayer, Bristol Myers Squibb, Clinical Care Options, Daiichi-Sankyo, Eli Lilly, Geneos Therapeutics, GlaxoSmithKline, Guardant Health, Imedex, Imugene, Lynx Health, Merck, Merck Serono, Mersana Therapeutics, Michael J Hennessy Associates, Paradigm Medical Communications, PeerView Institute, Pfizer, Research to Practice, RGENIX, Seagen, Silverback Therapeutics, and Zymeworks; and stock options in RGENIX. All other authors declare no competing interests.