Unmanipulated haploidentical hematopoietic stem cell transplantation for mixed phenotype acute leukemia: a single center study

Author:

Huang Junbin1ORCID,Feng Bo2,Cheng Yifei3,Xu Lanping4,Zhang Xiao-hui5ORCID,Huang Xiao-Jun6ORCID,Wang Yu7ORCID

Affiliation:

1. the seventh affiliated hospital, Sun Yat-sen University

2. Jiujiang First People's Hospital

3. Peking University People’s Hospital

4. Peking University Institute of Hematology

5. Peking University People's Hospital

6. Peking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease

7. Peking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing Key Laboratory of Hematopoietic Stem Cell Tr

Abstract

Abstract Mixed-phenotype acute leukemia (MPAL), which is categorized as a rare subtype of acute leukemia with a generally dismal prognosis. Hemopoietic stem cell transplantation (HSCT) is traditionally considered a curative treatment for MPAL. Thirty-three MPAL patients undergoing HSCT at the Peking University Institute of Hematology, Peking University People’s Hospital (Beijing, China) between December 2017 and April 2022 were enrolled in this study. The 2-year overall survival (OS) rate was 84.4% (95% confidence interval [95% CI], 69.9–98.9%), and the event-free survival (EFS) rate was 86.3% (95% CI, 73.8–98.8%) in MPAL patients undergoing HSCT in first complete remission (CR1). The median time to relapse after HSCT was 7.2 months (range: 0.8–12 months). The 2-year cumulative incidence of relapse (CIR) was 13.7% (95% CI, 4.2–28.9%). No patients died due to non-relapsed mortality (NRM) events. This study suggested that haplo-HSCT is a feasible and safe strategy for patients with MPAL patients in CR1. The outcomes were promising; however, they need to be confirmed by further research.

Publisher

Research Square Platform LLC

Reference36 articles.

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3. Borowitz, M.J., et al., Acute leukemias of ambiguous lineage. In WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. 2008.

4. Swerdlow, S.H.C.E., et al., WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, Revised, 4th ed.. 2017.

5. Survival of patients with mixed phenotype acute leukemias: A large population-based study;Shi R;Leuk Res,2015

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