New Genetic Mutations Linked to Subset of Gastrointestinal Stromal Tumors

Sicklick and colleagues are leading efforts to diagnose and treat GIST, which originates in special cells that signal muscles to contract, moving food and liquid through the digestive system. Many current therapies for GIST are ineffective in patients (About 10–15% of adult and most pediatric cases) whose tumors lack mutations in the classic oncogenic drivers of GIST. Ultimately, over 95% of patients eventually succumb to drug-resistant GIST, highlighting the necessity for alternative therapeutic targets.

Treatment with imatinib (marketed as Gleevec) has proven effective in many GIST cases associated with KIT oncogene mutations, the most common driver of the disease. Building upon that success and approach, the research team used broad genomic sequencing of GIST patients without KIT – or other documented mutations – to identify alterations in at least two new genes: FGFR1 and NTRK3.

“Broad genomic sequencing was critical to expand our search beyond the KIT mutations streetlight,” said Olivier Harismendy, PhD, head of the oncogenomics laboratory at Moores Cancer Center, referring to observational bias of previous studies.

“These findings provide novel insights into the biology of the disease and new potential genetic drivers,” said Prof. Sicklick, “With further studies, we can build an even more complete genetic profile of GIST, which in turn can lead to new individualized treatments and better outcomes for more GIST patients. For example, one patient in this study had an ETV6-NTRK3 mutant GIST and responded to a matched therapy with Loxo-101, a highly selective TRK inhibitor, after progressing on several earlier lines of FDA-approved therapies for GIST.

The study, by Shi E et al, was published December 14, 2016, in the Journal of Translational Medicine.

Related Links:
University of Californai San Diego School of Medicine
Moores Cancer Center at UCSD Health