The goal of this observational study is to explore the quantitative relationship between in vivo exposure and efficacy, and the relationship between in vivo exposure and the risk of adverse reactions after adjuvant treatment of imatinib in patients with intermediate and high-risk GIST in the real world, so as to determine the optimal treatment window for imatinib .
Study Type
OBSERVATIONAL
Enrollment
328
RFS
From patient enrollment to tumor recurrence or death for any reason
Time frame: ten years
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