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Updated: Aug 17, 2026

Orthotopic Implantation and Peripheral Immune Cell Monitoring in the II-45 Syngeneic Rat Mesothelioma Model
Published on: October 2, 2015
Limited efficacy of imatinib mesylate in malignant mesothelioma: a phase II trial
Alexandre Mathy1, Paul Baas, Otilia Dalesio
1Biometrics Department, Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands. a.mathy@nki.nl
Abstract:
Twenty-five patients with histologically proven malignant mesothelioma participated in a trial of imatinib mesylate (Glivec) with a starting dose of 400 mg per day taken orally, up to a maximal dose of 800 mg. No responses were observed in the patient group, while three patients showed prolonged (>6 months) stabilization of disease. The median survival time was 398 days (range 88-840); the median time to progression was 63 days (range 29-275). Side effects of the medication were mild and included edema, nausea, constipation and diarrhea. We conclude that further investigation with monotherapy imatinib in mesothelioma is not warranted.
Insights
Imatinib mesylate (Glivec) showed no significant response in malignant mesothelioma patients. While some experienced disease stabilization, further research into imatinib monotherapy for this cancer is not recommended.
Area of Science:
- Oncology
- Medical Research
Background:
- Malignant mesothelioma is a rare and aggressive cancer.
- Treatment options for malignant mesothelioma are limited, necessitating novel therapeutic approaches.
Purpose of the Study:
- To evaluate the efficacy and safety of imatinib mesylate as a monotherapy for patients with malignant mesothelioma.
Main Methods:
- A clinical trial involving 25 patients with histologically confirmed malignant mesothelioma.
- Patients received oral imatinib mesylate, starting at 400 mg/day, with a maximum dose of 800 mg/day.
Main Results:
- No objective responses were observed in any of the patients.
- Three patients (12%) achieved prolonged disease stabilization for over 6 months.
- Median survival time was 398 days; median time to progression was 63 days.
- Reported side effects were mild, including edema, nausea, constipation, and diarrhea.
Conclusions:
- Imatinib mesylate monotherapy did not demonstrate significant efficacy in malignant mesothelioma.
- Further clinical investigation of imatinib as a single agent for this indication is not warranted based on these findings.
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