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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
 Lam, Lyn Ley  ;  Pavlakis, Nick  ;  Shitara, Kohei  ;  Sjoquist, Katrin M.  ;  Martin, Andrew J.  ;  Yip, Sonia  ;  Kang, Yoon-Koo  ;  Bang, Yung-Jue  ;  Chen, Li-Tzong  ;  Moehler, Markus  ;  Bekaii-Saab, Tanios  ;  Alcindor, Thierry  ;  O'Callaghan, Christopher J.  ;  Tebbutt, Niall C.  ;  Hague, Wendy  ;  Chan, Howard  ;  Rha, Sun Young  ;  Lee, Keun-Wook  ;  Gebski, Val  ;  Jaworski, Anthony  ;  Zalcberg, John  ;  Price, Timothy  ;  Simes, John  ;  Goldstein, David 
Citation
 BMC CANCER, Vol.23(1), 2023-02 
Article Number
 180 
Journal Title
BMC CANCER
ISSN
 1471-2407 
Issue Date
2023-02
Keywords
Advanced gastro-oesophageal cancer ; Regorafenib ; Nivolumab ; Tyrosine kinase inhibitor ; Clinical trial
Abstract
BackgroundAdvanced 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/designINTEGRATE 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.DiscussionINTEGRATE 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.
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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