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Association details:
Evidence:
Evidence Level:
Sensitive: B - Late Trials
Title:

Deciphera Pharmaceuticals Announces Results from ctDNA Analysis from INTRIGUE Phase 3 Clinical Study Demonstrating Substantial Clinical Benefit of QINLOCK® in Second-Line GIST Patients with Mutations in KIT Exon 11 and 17/18 Only

Published date:
01/03/2023
Excerpt:
Deciphera Pharmaceuticals, Inc...announced findings of a planned exploratory analysis of data from the INTRIGUE Phase 3 clinical study of QINLOCK using circulating tumor DNA (ctDNA) from a subgroup of patients with gastrointestinal stromal tumor (GIST) previously treated with imatinib who harbor mutations in KIT exon 11 and 17/18 only..Patients with mutations in KIT exon 11 and exon 17/18 only had substantially improved progression-free survival (PFS), objective response rate (ORR), and overall survival (OS) with QINLOCK versus sunitinib.
Trial ID:
Evidence Level:
Sensitive: B - Late Trials
Title:

Clinical activity of ripretinib in patients with advanced gastrointestinal stromal tumor harboring heterogenous KIT/PDGFRA mutations in the phase 3 INVICTUS study

Published date:
09/09/2021
Excerpt:
Patients receiving ripretinib demonstrated progression-free survival (PFS) benefit vs placebo regardless of mutation status (hazard ratio 0.16) and in all assessed subgroups in Kaplan-Meier PFS analysis (exon 11, P <0.0001; exon 9, P=0.0023; exon 13, P <0.0001; exon 17, P <0.0001)....Ripretinib provided clinically meaningful activity across mutation subgroups in patients with advanced GIST...
DOI:
10.1158/1078-0432.CCR-21-1864
Trial ID:
Evidence Level:
Sensitive: C3 – Early Trials
Title:

The efficacy and safety of ripretinib in Chinese patients with advanced gastrointestinal stromal tumors: A multicenter, retrospective study.

Published date:
01/17/2023
Excerpt:
Patients with KIT exon 17/18 mutation had a longer PFS (hazard ratio, 0.097; 95% CI, 0.011 to 0.871; P = 0.037)….Ripretinib can provide clinical benefit in advanced GIST in real-world China with a favorable safety profile.
DOI:
10.1200/JCO.2023.41.3_suppl.800