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Clinical Trials in Taiwan / NCT07724626
Starting soon Observational

Hyperpolarized MRI for GIST on Imatinib

NCT07724626 · tracked via the Priya Life Science Taiwan tracker
Phase
Observational
Started
2027-01-01
Last updated
2026-07-24

Condition(s) studied

Imatinib Therapy ResponseGastrointestinal Stromal Tumor (GIST)

Investigational drug(s) / intervention(s)

Hyperpolarized 13C-MRI →

Hyperpolarized 13C-MRI: Metabolic MRI using IV injection of hyperpolarized \[1-13C\]pyruvate.

Study summary

Conventional imaging methods, such as CT and MRI, are limited in evaluating GIST response to imatinib, as they mainly reflect tumor size and fail to capture early metabolic or molecular changes. This study investigates GISTs from a metabolic perspective by integrating hyperpolarized (HP) 13C-MRI, metabolomics, and radiomics. HP 13C-MRI enables real-time monitoring of metabolic flux in vivo, while NMR-based metabolomics provides systemic insights. In this single-center, prospective observational cohort study, 30 GIST patients receiving imatinib will undergo pre-treatment CT, HP 13C-MRI, metabolomics, and biopsy. Early response will be assessed at one month, with routine evaluation at four months. Patients will be categorized as responders or non-responders, and multi-omics data will be analyzed using machine learning. The study hypothesizes that metabolic changes detected by HP 13C-MRI can predict treatment response, offering reproducible, quantifiable metrics to improve evaluation and patient care.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: 1. Patients with biopsy proved GIST. 2. Patents will undergo imatinib. 3. Patients have measurable disease on imaging study. 4. Patients more than 18-year-old. Exclusion Criteria: 1. Pregnant or breast-feeding women. 2. Contraindication to MRI study (e.g., claustrophobia or non-removable devices or implants that are incompatible with MRI). 3. Intercurrent illness that will affect the compliance of the patient during the MRI study (e.g., active infection, symptomatic congestive heart failure, uncontrollable angina, arrhythmia, psychiatric disorders, dyspnea, or diarrhea). 4. Severe hepatic dysfunction (alkaline phosphatase/aspartate aminotransferase/alanine aminotransferase \>20 × upper limit of normal \[ULN\] or bilirubin \> 10 × ULN). 5. Severe renal impairment (eGFR \<30 ml/min/1.73m2).

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Chang Gung Memorial hospital Taoyuan Taiwan

More Chang Gung Memorial Hospital trials in Taiwan

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07724626 on ClinicalTrials.gov ↗ ← All trials in Taiwan