Genomic and clinical characterization of B/T mixed phenotype acute leukemia reveals recurrent features and T-ALL like mutations

Author:

Mi Xiaoli12,Griffin Gabriel3,Lee Winston3,Patel Sanjay3,Ohgami Robert4,Ok Chi Young5,Wang Sa5,Geyer Julia T.6ORCID,Xiao Wenbin7,Roshal Mikhail7,Garcia Jacqueline S.3,Silverman Lewis B.89,Sallan Stephen E.89,Aster Jon C.3,Harris Marian H.2,Weinberg Olga K.2ORCID

Affiliation:

1. Harvard-MIT Division of Health Sciences and Technology; Harvard Medical School; Boston Massachusetts

2. Department of Pathology; Boston Children's Hospital; Boston Massachusetts

3. Department of Pathology; Brigham and Women's Hospital; Boston Massachusetts

4. Department of Pathology; Stanford University Medical Center; California

5. Department of Hematopathology, Division of Pathology and Laboratory Medicine; The University of Texas MD Anderson Cancer Center; Houston Texas

6. Division of Hematopathology; New York-Presbyterian/Weill Cornell Medical College; New York New York

7. Hematopathology Service, Department of Pathology, Memorial Sloan Kettering Cancer Center; New York New York

8. Department of Pediatric Oncology; Dana-Farber Cancer Institute; Boston Massachusetts

9. Division of Pediatric Hematology-Oncology; Boston Children's Hospital; Boston Massachusetts

Publisher

Wiley

Subject

Hematology

Reference35 articles.

1. Mixed-phenotype acute leukemia: historical overview and a new definition;Weinberg;Leukemia,2010

2. Mixed phenotype acute leukemia;Weinberg;Am J Clin Pathol,2014

3. Mixed-phenotype acute leukemia: diagnostic criteria and pitfalls;Charles;Arch Pathol Lab Med,2017

4. Proposals for the immunological classification of acute leukemias. European Group for the Immunological Characterization of Leukemias (EGIL);Bene;Leukemia,1995

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