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A single-centre, non-randomised, single-arm clinical study: evaluating the efficacy and safety of radiotherapy in combination with ripretinib for unresectable advanced GIST

A single-centre, non-randomised, single-arm clinical study: evaluating the efficacy and safety of radiotherapy in combination with ripretinib for unresectable advanced GIST

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082253
Enrollment
Unknown
Registered
2024-03-25
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastrointestinal Stromal Tumors

Interventions

Test group:Radiotherapy combined with oral ripretinib

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Voluntarily participate and sign an informed consent form in writing; 2. Age range from 18 to 75 years old, regardless of gender; 3. Patients histologically diagnosed with GIST; 4. The subject's ECOG physical condition score is 0-2; 5. Disease progression or intolerance to first-line, second-line, and third-line treatments; 6. Based on imaging evidence, the lesion was assessed by MDT as unresectable and suitable for local radiotherapy; 7. No severe abnormalities in the hematologic, cardiac, pulmonary, hepatic, renal functions, or immune deficiency; 8. Expected survival of more than 3 months.

Exclusion criteria

Exclusion criteria: 1. Patients with resectable GIST; 2. Patients who have previously received radiotherapy at the intended site, or have a high tumor activity and poor tolerance to radiotherapy in adjacent organs, and are deemed unsuitable for radiotherapy after MDT discussion; 3. Patients with other serious illnesses such as severe infections, severe bone marrow suppression, and mental disorders , etc., deemed ineligible for enrollment by the researchers;; 4. Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Progression-Free Survival;

Secondary

MeasureTime frame
Overall Survival;Objective Response Rate;Disease Control Rate;

Countries

China

Contacts

Public ContactJun Zhang

The First Affiliated Hospital of Chongqing Medical University

zjun2323@sina.cn+86 136 1766 6067

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026