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Published on: October 17, 2025
Acute lymphoblastic leukemia-like treatment regimen provides better response in mixed phenotype acute leukemia: a
Eman O Rasekh1, Randa Osman1, Dalia Ibraheem2
1Clinical Pathology Department, National Cancer Institute, Cairo University, Foum elkhalig Sq., Cairo, Egypt.
Abstract:
Mixed phenotype acute leukemia (MPAL) is a rare type of leukemia with a limited number of studies conducted to characterize its clinical spectrum and most importantly the best treatment modality. MPAL blasts show more than one phenotype either myeloid/monocytic with T- or B-lymphoid or extremely rare triple lineage associated phenotypic markers. This study aimed to characterize MPAL cases with special emphasis on comparing adult and pediatric age groups, exploring treatment regimens, and clinical outcome. Among 2571 acute leukemia patients, 102 MPAL cases fulfilling the 2008/2016 WHO diagnostic criteria of MPAL were recruited in the study. The incidence of MPAL was 4% of acute leukemia patients. Pediatric cases were 54 (53%) while adults were 48/102 (47%). Myeloid/B-lymphoid phenotype was found in 86/102 (84%), with BCR-ABL fusion gene transcript detected in 14/102(13.7%) patients. ALL-like treatment showed better response rates as compared with the myeloid based regimen (p = 0.001). MPAL behaves in a manner that resembles in clinical features, their lymphoid progenitor counterpart leukemias both in adults and pediatric patients with superior treatment response to ALL-like regimen, especially in adults.
Insights
Mixed phenotype acute leukemia (MPAL) is rare. Patients responded better to acute lymphoblastic leukemia (ALL)-like treatment, particularly adults, suggesting a lymphoid-driven approach for MPAL.
Area of Science:
- Hematology
- Oncology
- Leukemia Research
Background:
- Mixed phenotype acute leukemia (MPAL) is a rare hematologic malignancy characterized by myeloid and lymphoid lineage markers.
- Limited research exists on MPAL's clinical spectrum and optimal treatment strategies.
- MPAL diagnosis requires adherence to specific World Health Organization (WHO) criteria.
Purpose of the Study:
- To characterize the clinical features of MPAL.
- To compare outcomes between adult and pediatric MPAL patient groups.
- To evaluate the efficacy of different treatment regimens in MPAL.
Main Methods:
- Retrospective analysis of 102 MPAL cases diagnosed between 2008-2016.
- Comparison of clinical characteristics and treatment responses across age groups.
- Evaluation of treatment regimens, including ALL-like and myeloid-based therapies.
Main Results:
- MPAL accounted for 4% of acute leukemia cases (102/2571).
- The myeloid/B-lymphoid phenotype was most common (84%), with BCR-ABL detected in 13.7%.
- ALL-like treatment yielded significantly better response rates than myeloid-based regimens (p=0.001).
Conclusions:
- MPAL exhibits clinical features similar to lymphoid leukemias in both adults and pediatric patients.
- An ALL-like treatment approach appears superior for MPAL, especially in adult populations.
- Further research is warranted to refine MPAL treatment protocols.
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