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Published in 2019 at "Clinical Cancer Research"
DOI: 10.1158/1078-0432.ccr-19-2150
Abstract: Purpose: Polyclonal emergence of KIT secondary mutations is a main mechanism of imatinib progression in gastrointestinal stromal tumor (GIST). Approved KIT inhibitors sunitinib and regorafenib have complementary activity against KIT resistance mutations. Preclinical evidence suggests…
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Keywords:
rapid alternation;
treatment;
sunitinib regorafenib;
gastrointestinal stromal ... See more keywords
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Published in 2017 at "Journal of Clinical Oncology"
DOI: 10.1200/jco.2017.35.15_suppl.11038
Abstract: 11038Background: We retrospectively collected data from metastatic Italian GIST patients treated with imatinib or sunitinib reintroduction after progression to conventional three or four lines of t...
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Keywords:
sunitinib regorafenib;
imatinib sunitinib;
advanced gist;
gist progressing ... See more keywords
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Published in 2018 at "Journal of Clinical Oncology"
DOI: 10.1200/jco.2018.36.15_suppl.11510
Abstract: 11510Background: Polyclonal emergence of KIT secondary mutations (muts) is the main mechanism of imatinib (IM) progression in GIST. Although approved KIT inhibitors SU and RE each suppress only a s...
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Keywords:
rapid alternation;
alternation sunitinib;
study rapid;
gist ... See more keywords