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Updated Overall Survival and Long-Term Safety With Ripretinib Versus Sunitinib in Patients With GI Stromal Tumor: Final Overall Survival Analysis From INTRIGUE

  • Michael C Heinrich
  • , Jean-Yves Blay
  • , Hans Gelderblom
  • , Suzanne George
  • , Patrick Schöffski
  • , Margaret von Mehren
  • , John R Zalcberg
  • , Robin L Jones
  • , Yoon-Koo Kang
  • , Albiruni Abdul Razak
  • , Jonathan Trent
  • , Steven Attia
  • , Axel Le Cesne
  • , Kjetil Boye
  • , David Goldstein
  • , César Sánchez
  • , Brittany L Siontis
  • , Paulina Cox
  • , Erika Davis
  • , Matthew L Sherman
  • Rodrigo Ruiz-Soto, Sebastian Bauer
  • VA Portland Veterans Health Care System
  • Centre Léon Bérard
  • Leiden University Medical Center
  • Dana-Farber Cancer Institute
  • University Hospitals Leuven
  • Monash University School of Public Health and Preventive Medicine and Department of Medical Oncology
  • The Institute of Cancer Research and Royal Marsden NHS Foundation Trust
  • University of Ulsan
  • Princess Margaret Cancer Center
  • University of Miami Health System
  • Mayo Clinic
  • Gustave Roussy
  • Oslo University Hospital
  • Prince of Wales Hospital
  • Center de Cáncer
  • Deciphera Pharmaceuticals, LLC.
  • University Hospital Essen

Research output: Contribution to journal › Article › peer-review

2 Scopus citations

Abstract

In the INTRIGUE phase III trial (ClinicalTrials.gov identifier: NCT03673501), adult patients with advanced gastrointestinal stromal tumor previously treated with imatinib were randomly assigned 1:1 to ripretinib 150 mg once daily or sunitinib 50 mg once daily (4 weeks on/2 weeks off). In the primary analysis, overall survival (OS) was immature. In this study, we report the final planned analysis of OS (key secondary end point), progression-free survival (PFS) on third-line therapy (second PFS; prespecified exploratory end point), and long-term safety. Final OS analysis was prespecified to occur with approximately 200 and ≥145 events in the overall and KIT exon 11 intention-to-treat (ITT) populations, respectively. As of March 15, 2023, there were 211 and 151 OS events in the overall ITT and KIT exon 11 ITT populations, respectively. Median OS was similar between second-line ripretinib and sunitinib in both populations (overall, 35.5 v 31.5 months; KIT exon 11, 35.5 v 32.8 months). Median second PFS (on third-line therapy) for the overall ITT population was similar between the ripretinib and sunitinib arms (7.7 v 7.4 months). Safety was consistent with the primary analysis. OS from this analysis was similar between arms, and second PFS suggests that receiving ripretinib did not adversely affect the PFS of third-line therapy.

Original languageEnglish
Pages (from-to)2239-2244
Number of pages6
JournalJournal of Clinical Oncology
Volume43
Issue number20
Early online dateMay 23 2025
DOIs
StatePublished - Jul 10 2025

Keywords

  • Adult
  • Aged
  • Antineoplastic Agents/therapeutic use
  • Female
  • Gastrointestinal Neoplasms/drug therapy
  • Gastrointestinal Stromal Tumors/drug therapy
  • Humans
  • Male
  • Middle Aged
  • Naphthyridines
  • Progression-Free Survival
  • Proto-Oncogene Proteins c-kit/genetics
  • Sunitinib/adverse effects
  • Urea/analogs & derivatives

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