Prediction of Postoperative Treatment Efficacy and Recurrence Risk of High-risk GIST Based on Liquid Biopsy MRD
NCT ID: NCT05408897
Last Updated: 2022-09-21
Study Results
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Basic Information
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RECRUITING
45 participants
OBSERVATIONAL
2022-01-01
2028-04-30
Brief Summary
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Detailed Description
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In this study, a prospective multi-center, single-arm observational study is conducted to collect operable patients with locally advanced GIST. According to results of preoperative imaging examinations or pathological biopsy, 45 high-risk GIST patients will be screened and enrolled. Next-Generation Sequencing (NGS) genetic testing platform (Burning Rock Oncoscreen Plus TM) is used to detect the baseline tumour tissues (detection depth 1000X) of these patients. And peripheral ctDNA (detection depth 30000X) of multiple pre/postoperative time points will be detected. The genetic profile and clinical information of each patient will be collected. Combining all the information, bioinformatics analysis will be carried out on the gene detection results of these patients at each time point, and the correlation between the postoperative recurrence time and the ctDNA positive rate/postoperative clearance rate of patients will be compared. The characteristics changes and dynamic changes of tumor release degree will also be analyzed. To explore the correlation between PFS/OS and MRD in high-risk GIST patients, we plan to analyze 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.
Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Interventions
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liquid biopsy
A test that enables the diagnosis or analysis of tumors using only a blood or fluid sample rather than a solid tissue biopsy.
Eligibility Criteria
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Inclusion Criteria
* 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
Exclusion Criteria
* Emergent surgery because of bowel obstruction, perforation or bleeding
* Pregnant or lactant women
* Medical history of severe mental illness
* Patients with contraindication for targeted therapy and surgery
* Non-R0 resection
* Postoperative pathology conformed the diagnosis of non-high-risk GIST
* Patients with distant metastasis
* Other situations in which researchers consider that the patient is unsuitable for this study
ALL
No
Sponsors
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Peking University People's Hospital
OTHER
Responsible Party
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YE Yingjiang
Director of the department of gastrointestinal surgery
Principal Investigators
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Yingjiang Ye
Role: PRINCIPAL_INVESTIGATOR
Peking University People's Hospital
Locations
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Peking University People'S Hospital
Beijing, Beijing Municipality, China
Countries
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Facility Contacts
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References
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Abbosh C, Birkbak NJ, Wilson GA, Jamal-Hanjani M, Constantin T, Salari R, Le Quesne J, Moore DA, Veeriah S, Rosenthal R, Marafioti T, Kirkizlar E, Watkins TBK, McGranahan N, Ward S, Martinson L, Riley J, Fraioli F, Al Bakir M, Gronroos E, Zambrana F, Endozo R, Bi WL, Fennessy FM, Sponer N, Johnson D, Laycock J, Shafi S, Czyzewska-Khan J, Rowan A, Chambers T, Matthews N, Turajlic S, Hiley C, Lee SM, Forster MD, Ahmad T, Falzon M, Borg E, Lawrence D, Hayward M, Kolvekar S, Panagiotopoulos N, Janes SM, Thakrar R, Ahmed A, Blackhall F, Summers Y, Hafez D, Naik A, Ganguly A, Kareht S, Shah R, Joseph L, Marie Quinn A, Crosbie PA, Naidu B, Middleton G, Langman G, Trotter S, Nicolson M, Remmen H, Kerr K, Chetty M, Gomersall L, Fennell DA, Nakas A, Rathinam S, Anand G, Khan S, Russell P, Ezhil V, Ismail B, Irvin-Sellers M, Prakash V, Lester JF, Kornaszewska M, Attanoos R, Adams H, Davies H, Oukrif D, Akarca AU, Hartley JA, Lowe HL, Lock S, Iles N, Bell H, Ngai Y, Elgar G, Szallasi Z, Schwarz RF, Herrero J, Stewart A, Quezada SA, Peggs KS, Van Loo P, Dive C, Lin CJ, Rabinowitz M, Aerts HJWL, Hackshaw A, Shaw JA, Zimmermann BG; TRACERx consortium; PEACE consortium; Swanton C. Phylogenetic ctDNA analysis depicts early-stage lung cancer evolution. Nature. 2017 Apr 26;545(7655):446-451. doi: 10.1038/nature22364.
Other Identifiers
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WCJZL202103
Identifier Type: -
Identifier Source: org_study_id
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