Switch control inhibition of KIT and PDGFRA in patients with advanced gastrointestinal stromal tumor: A Phase I study of ripretinib Journal Article


Authors: Janku, F.; Abdul Razak, A. R.; Chi, P.; Heinrich, M. C.; Von Mehren, M.; Jones, R. L.; Ganjoo, K.; Trent, J.; Gelderblom, H.; Somaiah, N.; Hu, S.; Rosen, O.; Su, Y.; Ruiz-Soto, R.; Gordon, M.; George, S.
Article Title: Switch control inhibition of KIT and PDGFRA in patients with advanced gastrointestinal stromal tumor: A Phase I study of ripretinib
Abstract: PURPOSE In advanced gastrointestinal stromal tumor (GIST), there is an unmet need for therapies that target both primary and secondary mutations of pathogenic KIT/PDGFRA oncoproteins. Ripretinib is a novel switchcontrol kinase inhibitor designed to inhibit a wide range of KIT and PDGFRA mutations. PATIENTS AND METHODS This first-in-human, to our knowledge, phase I study of ripretinib (ClinicalTrials.gov identifier: NCT02571036) included a dose-escalation phase and subsequent expansion phase at the recommended phase II dose (RP2D). Eligible patients included those with advanced GIST, intolerant to or experienced progression on ≥ 1 line of systemic therapy, and other advanced malignancies. Safety, dose-limiting toxicities (DLTs), maximum-tolerated dose (MTD), and preliminary antitumor activity were evaluated. RESULTS At data cutoff (August 31, 2019), 258 patients (n = 184 GIST) were enrolled, with 68 patients in the dose-escalation phase. Three DLTs were reported: Grade 3 lipase increase (n = 2; 100 mg and 200 mg twice a day) and grade 4 increased creatine phosphokinase (n = 1; 150 mg once daily). MTD was not reached (maximum dose evaluated, 200 mg twice a day); 150 mg once daily was established as the RP2D. The most frequent (>30%) treatment-emergent adverse events in patients with GIST receiving ripretinib 150 mg once daily (n=142) were alopecia (n=88 [62.0%]), fatigue (n=78 [54.9%]),myalgia (n=69 [48.6%]), nausea (n=65 [45.8%]), palmar-plantar erythrodysesthesia (n =62 [43.7%]), constipation (n=56 [39.4%]), decreased appetite (n =48 [33.8%]), and diarrhea (n = 47 [33.1%]). Objective response rate (confirmed) of 11.3% (n = 16/142) ranging from 7.2% (n = 6/83; fourth line or greater) to 19.4% (n =6/31; second line) and median progression-free survival ranging from 5.5 months (fourth line or greater) to 10.7 months (second line), on the basis of investigator assessment, were observed. CONCLUSION Ripretinib is a well-tolerated, novel inhibitor of KIT and PDGFRA mutant kinases with promising activity in patients with refractory advanced GIST. © 2020 by American Society of Clinical Oncology.
Journal Title: Journal of Clinical Oncology
Volume: 38
Issue: 28
ISSN: 0732-183X
Publisher: American Society of Clinical Oncology  
Date Published: 2020-10-01
Start Page: 3294
End Page: 3303
Language: English
DOI: 10.1200/jco.20.00522
PUBMED: 32804590
PROVIDER: scopus
PMCID: PMC7526717
DOI/URL:
Notes: Article -- Export Date: 2 November 2020 -- Source: Scopus
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors
  1. Ping Chi
    172 Chi