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Significance of minimal residual disease in pediatric mixed phenotype acute leukemia: a multicenter cohort study

The rarity of mixed phenotype acute leukemia (MPAL) has precluded adequate data to incorporate minimal residual disease (MRD) monitoring into therapy. Fluidity in MPAL classification systems further complicates understanding its biology and outcomes; this includes uncertainty surrounding the impact...

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Bibliographic Details
Published in:Leukemia 2020-07, Vol.34 (7), p.1741-1750
Main Authors: Oberley, Matthew J, Raikar, Sunil S, Wertheim, Gerald B, Malvar, Jemily, Sposto, Richard, Rabin, Karen R, Punia, Jyotinder N, Seif, Alix E, Cahen, Viviane C, Schore, Reuven J, Luca, Dragos C, Guinipero, Terri, Woods, William G, O'Gorman, Maurice R G, Orgel, Etan
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Language:English
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Summary:The rarity of mixed phenotype acute leukemia (MPAL) has precluded adequate data to incorporate minimal residual disease (MRD) monitoring into therapy. Fluidity in MPAL classification systems further complicates understanding its biology and outcomes; this includes uncertainty surrounding the impact of shifting diagnostic requirements even between iterations of the World Health Organization (WHO) classification. Our primary objective was to address these knowledge gaps. To do so, we analyzed clinicopathologic features, therapy, MRD, and survival in a centrally-reviewed, multicenter cohort of MPAL uniformly diagnosed by the WHO classification and treated with acute lymphoblastic leukemia (ALL) regimens. ALL induction therapy achieved an EOI MRD negative (
ISSN:0887-6924
1476-5551
DOI:10.1038/s41375-020-0741-0