Avapritinib in the treatment of PDGFRA exon 18 mutated gastrointestinal stromal tumors

Author:

Smrke Alannah1ORCID,Gennatas Spyridon1ORCID,Huang Paul2ORCID,Jones Robin L12ORCID

Affiliation:

1. Sarcoma Unit, Royal Marsden Hospital, 203 Fulham Road, London, SW36JJ, UK

2. Department of Pathology, Molecular & Systems Oncology, The Institute of Cancer Research, 237 Fulham Road, London, SW3 6JB, UK

Abstract

Gastrointestinal stromal tumors (GIST) can be molecularly classified based on different subtypes including mutations in KIT and PDGFRA. Patients with PDGFRA mutations are an important subgroup that commonly arise in the stomach and are associated with a more indolent disease course. Importantly, the most common PDGFRA molecular subtype, the D842V mutation in exon 18 of the gene which alters the activation loop, is imatinib insensitive in in vitro studies. Poor responses to imatinib have been seen clinically compared with PDGFRA exon 18 non-D842V-mutated GIST. Avapritinib (BLU-285) is a potent KIT and PDGFRA-specific tyrosine kinase inhibitor which has shown >90% response rates in patients with PDGFRA exon 18 D842V-mutated GIST. Results from the Phase I trial of avapritinib have indicated that this drug should be the standard of care for patients with PDGFRA exon 18 D842V-mutated GIST.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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