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Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
Published on: July 19, 2019
Presenting features and treatment outcome of acute promyelocytic leukemia arising after multiple sclerosis
Emanuele Ammatuna1, Pau Montesinos, Syed Khizer Hasan
1Department of Biopathology, University Tor Vergata, Rome, Italy.
Abstract:
We report the clinical features and treatment outcome of 33 patients with multiple sclerosis who developed acute promyelocytic leukemia. Thirty patients were previously exposed to mitoxantrone. The median latency period between treatment initiation and acute promyelocytic leukemia diagnosis was 32 months. The PML-RARA bcr1 iso-form was identified in 87% of cases. Twenty-nine (90%) patients achieved hematologic remission after all-trans retinoic acid and chemotherapy (n = 31) or arsenic trioxide and all-trans retinoic acid. Consolidation included modified chemotherapy or arsenic trioxide. At a median follow up of 26 months, 23 patients are in complete remission, 4 relapsed and one developed secondary leukemia. The 5-year cumulative incidence of relapse and overall survival were 23% and 68%, respectively. Although treatment heterogeneity and suboptimal post-remission therapy must be taken into account, overall results and development of secondary leukemia in one patient suggest that effective and less toxic agents like arsenic trioxide warrants further investigation in this context.
Insights
Multiple sclerosis patients developing acute promyelocytic leukemia (APL) showed good remission rates with all-trans retinoic acid and chemotherapy or arsenic trioxide. Further investigation of less toxic agents like arsenic trioxide is warranted.
Area of Science:
- Hematology
- Oncology
- Neurology
Background:
- Multiple sclerosis (MS) patients treated with mitoxantrone have a risk of developing acute promyelocytic leukemia (APL).
- Understanding the clinical features and treatment outcomes in this specific patient cohort is crucial for improving management.
Purpose of the Study:
- To report the clinical characteristics and treatment outcomes of 33 patients with multiple sclerosis who developed acute promyelocytic leukemia.
- To evaluate the efficacy of different treatment regimens, including all-trans retinoic acid and arsenic trioxide.
Main Methods:
- Retrospective analysis of 33 patients with MS and APL.
- Review of treatment protocols including all-trans retinoic acid, chemotherapy, and arsenic trioxide.
- Assessment of hematologic remission, relapse rates, and overall survival.
Main Results:
- A median latency of 32 months was observed between mitoxantrone treatment and APL diagnosis.
- The PML-RARA bcr1 iso-form was identified in 87% of cases.
- 90% of patients achieved hematologic remission; 5-year cumulative incidence of relapse was 23% and overall survival was 68%.
Conclusions:
- All-trans retinoic acid and chemotherapy or arsenic trioxide are effective in achieving remission for MS patients with APL.
- Arsenic trioxide shows promise as a less toxic agent warranting further investigation in this context.
- Long-term follow-up is essential to monitor for relapses and secondary malignancies.
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