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Clinical Trials in Germany / NCT07109024
Starting soon Observational

Resistance Profiling Using Functional Imaging and Next Generation Sequencing in Refractory Gastrointestinal Stomal Tumors (GIST)

NCT07109024 · tracked via the Priya Life Science Germany tracker
Phase
Observational
Started
2025-09-01
Last updated
2025-08-19

Condition(s) studied

Gastrointestinal Stromal Tumor (GIST)

Investigational drug(s) / intervention(s)

Generation of a comprehensive and single-lesion resistance profile

Generation of a comprehensive and single-lesion resistance profile: AI-supported image analysis of functional imaging (PET-CT) and previous imaging data and specialized molecular methods (next-generation sequencing) will be combined into a comprehensive resistance profile.

Study summary

Gastrointestinal stromal tumors (GIST) are the most common malignant sarcomas of the gastrointestinal tract. Inhibitors of the mutated driver proteins KIT and PDGFRA can temporarily control disseminated GIST disease but cannot cure it. Recently, the investigators were able to elucidate the two main resistance mechanisms-the coexistence of ATP-binding pocket (AP) and activation loop (AL) mutations, as well as AP/AL combination mutations. Determining these resistance factors requires methods that are not yet established in routine clinical practice. The investigators hypothesize that identifying these factors and creating resistance profiles in the context of the anatomical location of metastatic lesions can open up new, clinically relevant therapeutic options, including local therapies. The aim of this project is to evaluate the practicability of these methods in everyday clinical use. An AI-supported image analysis and specialized molecular methods will be combined into a comprehensive resistance profile and will be provided to the treating physicians to potentially guide treatment decisions.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Advanced gastrointestinal stromal tumors history of exposure and progression or intolerance to imatinib, sunitinib, regorafenib and ripretinib * Clinical indication for PET-CT and tumor biopsy (optional) (sarcoma center tumorboard protocol) * Age 18 years and older * FFPE tumor tissue available * Previous imaging studies available (CT/MRI/PET Abdomen, ideally at baseline, best response and progression) * ECOG ≤ 2 * Progressing tumor lesion(s) of which one is accessible for biopsy Exclusion Criteria: * contraindication for systemic TKI treatment * contraindication for contrast-enhanced both CT and MRI imaging. * GIST without KIT or PDGFRA mutations * pregnant or breastfeeding women * patient that - to the investigator's discretion - are not able or willing to comply with the provided protocol and visit schemes

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
University Hospital Essen Essen Germany
University Hospital Schleswig-Holstein, Dpt. of Hematlogy and Oncology Lübeck Germany

More Universität Duisburg-Essen trials in Germany

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 NCT07109024 on ClinicalTrials.gov ↗ ← All trials in Germany