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Clinical benefit of sunitinib in gastrointestinal stromal tumors with different exon 11 mutation genotypes
Author(s) -
Zhi Dong,
Jing Gao,
Jifang Gong,
Jie Li,
Yanyan Li,
Lin Shen,
Jian Li
Publication year - 2017
Publication title -
future oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.857
H-Index - 72
eISSN - 1744-8301
pISSN - 1479-6694
DOI - 10.2217/fon-2017-0252
Subject(s) - sunitinib , medicine , genotype , exon , stromal cell , gist , mutation , cancer research , gastrointestinal cancer , oncology , stromal tumor , genetics , cancer , colorectal cancer , gene , biology
Aim: To assess the efficacy of second-line sunitinib therapy in gastrointestinal stromal tumor patients with different exon 11 mutation genotypes. Patients & methods: Thirty eight of the 75 patients received imatinib (IM) dose escalation followed by sunitinib (IM escalation group), while 37 were switched to sunitinib directly after the failure of first-line IM treatment (sunitinib group). Progression-free survival and overall survival were compared. Results: The median progression-free survival in the sunitinib group was significantly longer than in the IM escalation group (14 vs 4 months; p < 0.001), so was in patients with exon 11 deletions (16 vs 3 months; p < 0.001). Conclusion: Patients who have an exon 11 deletion mutation are more likely to benefit from switching to sunitinib directly than from IM dose escalation.

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