Prediction of Postoperative Treatment Efficacy and Recurrence Risk of High-risk GIST Based on Minimal Residual Disease Detected by Liquid Biopsy

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

So far, MRD assessment by liquid biopsy (ctDNA) has not been used to predict postoperative treatment efficacy and recurrence risk of GIST patients because of special disease characteristics and technological limitations. Therefore, we conducted this prospective multi-center, single-arm observational study to collect 45 operable patients with locally advanced, suspected high-risk GIST. NGS genetic testing platform is used to detect tumour tissues and peripheral ctDNA will also be dectected. we try to explore the correlation between PFS/OS and MRD in high-risk GIST patients by analyzing the relationship between dynamic changes in ctDNA mutation spectrum and postoperative adjuvant therapy efficacy, and to evaluate MRD-based genomic characteristics to guide further treatment.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Patients aged between 18 and 80

• Patients suspected for high-risk GIST by preoperative imaging examinations or diagnosed with high-risk GIST by pathological biopsy, who have not received preoperative neoadjuvant treatment

• Patients must have not received any treatment including radiotherapy, chemotherapy or surgery

• The function of other organs including liver and kidneys is good enough so that the patients could tolerate targeted therapy and surgery

• Postoperative pathology conformed the diagnosis of high-risk GIST

• Patients and their families could understand the protocol of this study and voluntarily agree to participate in. Signed informed consents are required

Locations
Other Locations
China
Peking University People'S Hospital
RECRUITING
Beijing
Time Frame
Start Date: 2022-01-01
Estimated Completion Date: 2028-04
Participants
Target number of participants: 45
Sponsors
Leads: Peking University People's Hospital

This content was sourced from clinicaltrials.gov