KLI

Avapritinib Versus Regorafenib in Locally Advanced Unresectable or Metastatic GI Stromal Tumor: A Randomized, Open-Label Phase III Study

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Abstract
PURPOSEPrimary or secondary mutations in KIT or platelet-derived growth factor receptor alpha (PDGFRA) underlie tyrosine kinase inhibitor resistance in most GI stromal tumors (GISTs). Avapritinib selectively and potently inhibits KIT- and PDGFRA-mutant kinases. In the phase I NAVIGATOR study (NCT02508532), avapritinib showed clinical activity against PDGFRA D842V-mutant and later-line KIT-mutant GIST. VOYAGER (NCT03465722), a phase III study, evaluated efficacy and safety of avapritinib versus regorafenib as third-line or later treatment in patients with unresectable or metastatic GIST.PATIENTS AND METHODSVOYAGER randomly assigned patients 1:1 to avapritinib 300 mg once daily (4 weeks continuously) or regorafenib 160 mg once daily (3 weeks on and 1 week off). Primary end point was progression-free survival (PFS) by central radiology per RECIST version 1.1 modified for GIST. Secondary end points included objective response rate, overall survival, safety, disease control rate, and duration of response. Regorafenib to avapritinib crossover was permitted upon centrally confirmed disease progression.RESULTSFour hundred seventy-six patients were randomly assigned (avapritinib, n = 240; regorafenib, n = 236). Median PFS was not statistically different between avapritinib and regorafenib (hazard ratio, 1.25; 95% CI, 0.99 to 1.57; 4.2 v 5.6 months; P = .055). Overall survival data were immature at cutoff. Objective response rates were 17.1% and 7.2%, with durations of responses of 7.6 and 9.4 months for avapritinib and regorafenib; disease control rates were 41.7% (95% CI, 35.4 to 48.2) and 46.2% (95% CI, 39.7 to 52.8). Treatment-related adverse events (any grade, grade >= 3) were similar for avapritinib (92.5% and 55.2%) and regorafenib (96.2% and 57.7%).CONCLUSIONPrimary end point was not met. There was no significant difference in median PFS between avapritinib and regorafenib in patients with molecularly unselected, late-line GIST. Efficacy and safety data phase III VOYAGER study (avapritinib vs regorafenib, n=476)) as >= 3rd line for advanced GIST.
Author(s)
강윤구Jonathan TrentKate NewberryKevin HeLin ShenMargaret von MehrenMaria A. PantaleoMaria RocheMehdi BrahmiMichael C. HeinrichOlivier MirPaggy HewPatrick SchoffskiPeter HohenbergerPiotr RutkowskiRobin L JonesSebastian BauerShreyaskumar PatelSuzanne GeorgeVictor VillalobosWilliam
Issued Date
2021
Type
Article
DOI
10.1200/JCO.21.00217
URI
https://oak.ulsan.ac.kr/handle/2021.oak/8406
https://ulsan-primo.hosted.exlibrisgroup.com/primo-explore/fulldisplay?docid=TN_cdi_crossref_primary_10_1200_JCO_21_00217&context=PC&vid=ULSAN&lang=ko_KR&search_scope=default_scope&adaptor=primo_central_multiple_fe&tab=default_tab&query=any,contains,Avapritinib%20Versus%20Regorafenib%20in%20Locally%20Advanced%20Unresectable%20or%20Metastatic%20GI%20Stromal%20Tumor:%20A%20Randomized,%20Open-Label%20Phase%20III%20Study&offset=0&pcAvailability=true
Publisher
JOURNAL OF CLINICAL ONCOLOGY
Location
미국
Language
영어
ISSN
0732-183X
Citation Volume
39
Citation Number
28
Citation Start Page
3128
Citation End Page
3128
Appears in Collections:
Medicine > Medicine
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