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Updated: Jun 24, 2026

Robotic Duodenal Sleeve Resection for Gastrointestinal Stromal Tumor with Rare Exon 8 KIT Mutation Following Neoadjuvant Imatinib
Published on: April 3, 2026
Does imatinib turn recurrent and/or metastasized gastrointestinal stromal tumors into a chronic disease? - single
Thomas Armbrust1, Michael Sobotta, Bastian Gunawan
1Department of Gastroenterology and Endocrinology, Georg-August-University of Göttingen, Germany.
Background:
Gastrointestinal stromal tumors (GIST) are mesenchymal tumors of the gastrointestinal tract supposed to arise from the cells of Cajal because of gain-of-function mutations of the tyrosine receptor kinases c-kit or platelet-derived growth factor receptor A. Imatinib selectively inhibits the kinase activity of both receptors. Despite this breakthrough in the treatment of GIST, resistance against imatinib has been reported to be as high as 50% after the first 2 years of treatment.
Aim:
Outcome of 13 consecutive patients with relapsed or metastasized GIST who were treated with imatinib was analyzed.
Results:
Mean duration of treatment was 53.5 months. Four patients developed progressive disease and died after a mean treatment time of 31 months in spite of increase of imatinib dosages to 800 mg daily. Two patients (23%) developed a progressive disease after 46 months or 52 months of treatment. Two patients had a stable disease and five had a partial response. The overall progression rate was 46%, the mean survival time since primary diagnosis was 85.8 months.
Conclusion:
From our experience, frequency of resistance development to imatinib may be below that given in the literature (50% after 2 years). Individual treatment in specialized centers may improve compliance.
Insights
This study on gastrointestinal stromal tumors (GIST) found that imatinib treatment resistance may be lower than previously reported. Specialized care may improve patient outcomes and compliance with imatinib therapy.
Area of Science:
- Oncology
- Gastroenterology
- Pharmacology
Background:
- Gastrointestinal stromal tumors (GIST) are mesenchymal tumors often driven by c-kit or PDGFRA mutations.
- Imatinib is a targeted therapy inhibiting these mutations but resistance is a significant clinical challenge.
- Reported imatinib resistance rates in GIST reach up to 50% within two years of treatment.
Purpose of the Study:
- To analyze the treatment outcomes of 13 patients with relapsed or metastatic GIST receiving imatinib.
- To evaluate the efficacy and resistance patterns of imatinib in a real-world clinical setting.
Main Methods:
- Retrospective analysis of 13 consecutive GIST patients treated with imatinib.
- Dosage adjustments (up to 800 mg daily) were made for some patients.
- Outcomes including progression, stable disease, partial response, and overall survival were recorded.
Main Results:
- The overall progression rate was 46% over a mean treatment duration of 53.5 months.
- Four patients progressed and died despite dose escalation.
- Two patients showed progressive disease late (46 and 52 months), while seven achieved stable disease or partial response.
Conclusions:
- Imatinib resistance in GIST may occur less frequently than the reported 50% at 2 years.
- Individualized treatment strategies in specialized centers could enhance patient compliance and potentially improve outcomes.
- Long-term treatment with imatinib can be effective for a significant proportion of GIST patients.
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