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INTEGRATE II: randomised phase III controlled trials of regorafenib containing regimens versus standard of care in refractory Advanced Gastro-Oesophageal Cancer (AGOC): a study by the Australasian Gastro-Intestinal Trials Group (AGITG)

Authors
 Lyn Ley Lam  ;  Nick Pavlakis  ;  Kohei Shitara  ;  Katrin M Sjoquist  ;  Andrew J Martin  ;  Sonia Yip  ;  Yoon-Koo Kang  ;  Yung-Jue Bang  ;  Li-Tzong Chen  ;  Markus Moehler  ;  Tanios Bekaii-Saab  ;  Thierry Alcindor  ;  Christopher J O'Callaghan  ;  Niall C Tebbutt  ;  Wendy Hague  ;  Howard Chan  ;  Sun Young Rha  ;  Keun-Wook Lee  ;  Val Gebski  ;  Anthony Jaworski  ;  John Zalcberg  ;  Timothy Price  ;  John Simes  ;  David Goldstein 
Citation
 BMC CANCER, Vol.23(1) : 1-12, 2023-02 
Journal Title
BMC CANCER
Issue Date
2023-02
MeSH
Adult ; Antineoplastic Combined Chemotherapy Protocols ; Double-Blind Method ; Esophageal Neoplasms* / drug therapy ; Humans ; Nivolumab / therapeutic use ; Pyridines / therapeutic use ; Randomized Controlled Trials as Topic ; Stomach Neoplasms* / drug therapy
Keywords
Advanced gastro-oesophageal cancer ; Clinical trial ; Nivolumab ; Regorafenib ; Tyrosine kinase inhibitor
Abstract
Background: Advanced gastro-oesophageal cancer (AGOC) carries a poor prognosis. No standard of care treatment options are available after first and second-line therapies. Regorafenib is an oral multi-targeted tyrosine kinase inhibitor targeting angiogenic, stromal, and oncogenic receptor tyrosine kinases. Regorafenib 160 mg daily prolonged progression free survival compared to placebo (INTEGRATE, phase 2). Regorafenib 80 mg daily in combination with nivolumab 3 mg/kg showed promising objective response rates (REGONIVO). Methods/design: INTEGRATE II (INTEGRATE IIa and IIb) platform comprises two international phase III randomised controlled trials (RCT) with 2:1 randomisation in favor of experimental intervention. INTEGRATE IIa (double-blind) compares regorafenib 160 mg daily on days 1 to 21 of each 28-day cycle to placebo. INTEGRATE IIb (open label) compares REGONIVO, regorafenib 90 mg days 1 to 21 in combination with intravenous nivolumab 240 mg days 1 and 15 each 28-day cycle with investigator’s choice of chemotherapy (control). Treatment continues until disease progression or intolerable adverse events as per protocol. Eligible participants include adults with AGOC who have failed two or more lines of treatment. Stratification is by location of tumour (INTEGRATE IIa only), geographic region, prior VEGF inhibitor and prior immunotherapy use (INTEGRATE IIb only). Primary endpoint is overall survival. Secondary endpoints are progression free survival, objective response rate, quality of life, and safety. Tertiary/correlative objectives include biomarker and pharmacokinetic evaluation. Discussion: INTEGRATE II provides a platform to evaluate the clinical utility of regorafenib alone, as well as regorafenib in combination with nivolumab in treatment of participants with refractory AGOC. Trial registration: INTEGRATE IIa prospectively registered 1 April 2016 Australia New Zealand Clinical Trial Registry: ACTRN12616000420448 (ClinicalTrials.gov NCT02773524). INTEGRATE IIb prospectively registered 10 May 2021 ClinicalTrials.gov: NCT04879368. © 2023, The Author(s).
Files in This Item:
T202400905.pdf Download
DOI
10.1186/s12885-023-10642-7
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Rha, Sun Young(라선영) ORCID logo https://orcid.org/0000-0002-2512-4531
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/198095
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