This study is aimed: * to evaluate the dynamic monitoring value of MRD detection for postoperative recurrence in high-risk GIST patients; * to evaluate the effect of drug holiday mode based on MRD detection on progression-free Survival (PFS) and/or overall survival (OS) after drug withdrawal for high-risk GIST patients who have achieved disease control after long-term use of imatinib; ③ to investigate the response rate of imatinib re-use in patients who developed disease progression after drug withdrawal; ④ to explore whether the "drug holiday" treatment mode based on MRD detection could delay the occurrence of secondary imatinib resistance mutations for high-risk GIST patients with long-term use of imatinib after surgery.
Gastrointestinal stromal tumor (GIST) is the most common mesenchymal tumor of the gastrointestinal tract, and surgery is the preferred treatment method for primary resectable GIST. The guidelines recommend that patients at high risk of recurrence should be treated with tyrosine kinase inhibitors (TKI) such as imatinib for at least 3 years after surgery. However, in actual clinical practice, some patients face the situation of early withdrawal or prolonged medication, so the timing of drug withdrawal needs to be further studied. Recent studies have reported that some GIST patients who have achieved disease control through long-term use of imatinib can still achieve a long progression-free survival after drug withdrawal, and those who relapse after drug withdrawal can still achieve disease control after re-use of imatinib. This suggests that for some selected patients, a "drug holiday" treatment mode could be possible, in which drugs are discontinued when appropriate and restarted if necessary. How to select patients suitable for this mode of treatment needs further exploration. Liquid biopsy of peripheral blood circulating tumor DNA (ctDNA) to detect minimal residual disease (MRD) can be used for the diagnosis, efficacy evaluation, recurrence and drug resistance monitoring of a variety of malignant tumors. Existing studies have explored the "drug holiday" treatment mode based on MRD detection assisting patients with advanced non-small cell lung cancer to use TKI. Therefore, this one-arm prospective observational clinical study will assist some high-risk GIST patients who have been treated with imatinib for 3 years after surgery and have achieved disease control to adopt the treatment mode of "drug holiday" based MRD detection, aiming to evaluate the value of MRD detection in monitoring postoperative recurrence of high-risk GIST, investigate the effect of "drug holiday" treatment mode based on MRD detection on disease recurrence and patient survival, and to explore whether it can delay the occurrence of drug-resistant mutations.
Study Type
OBSERVATIONAL
Enrollment
40
Peking University People's Hospital
Beijing, Beijing Municipality, China
RECRUITINGProgress-free Survival
Progression-free survival after patients first enter the drug holiday
Time frame: From date when patients first enter the drug holiday until the date of imaging examinations confirmed disease progression up to 3 years
Drug re-use rate
The proportion of patients who take drug re-use due to disease progression within 3 years after first entering drug holiday
Time frame: 3 years from the time when patients first enter the drug holiday
Drug retreatment response rate
Drug response rate among patients who take drug re-use due to disease progression within 3 years after first entering drug holiday
Time frame: 3 years from the time when patients first enter the drug holiday
Overall Survival
Overall survival after patients first enter the drug holiday
Time frame: From date when patients first enter the drug holiday until the date of death up to 3 years
genetic mutation profiling of ctDNA-MRD
Results of genetic mutations in patients after the conversion of MRD from negative to positive, especially the detection of secondary imatinib resistance mutations
Time frame: 3 years from the time when patients first enter the drug holiday
MRD versus imaging examination
compare the time of MRD conversion and the time of disease progression assessed by imaging examination
Time frame: 3 years from the time when patients first enter the drug holiday
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