Ph-like acute lymphoblastic leukemia: a high-risk subtype in adults

Author:

Jain Nitin1,Roberts Kathryn G.2,Jabbour Elias1,Patel Keyur3,Eterovic Agda Karina4,Chen Ken4,Zweidler-McKay Patrick5,Lu Xinyan3,Fawcett Gloria4,Wang Sa A.3,Konoplev Sergej3,Harvey Richard C.6,Chen I-Ming6,Payne-Turner Debbie2,Valentine Marcus2,Thomas Deborah1,Garcia-Manero Guillermo1,Ravandi Farhad1,Cortes Jorge1,Kornblau Steven1,O’Brien Susan7,Pierce Sherry1,Jorgensen Jeffrey3,Shaw Kenna R. Mills4,Willman Cheryl L.6,Mullighan Charles G.2,Kantarjian Hagop1,Konopleva Marina1

Affiliation:

1. Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX;

2. Department of Pathology, St. Jude Children’s Research Hospital, Memphis, TN;

3. Department of Hematopathology,

4. Institute for Personalized Cancer Therapy, and

5. Department of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, TX;

6. Department of Pathology, University of New Mexico Comprehensive Cancer Center, Albuquerque, NM; and

7. Division of Hematology/Oncology, Chao Family Comprehensive Cancer Center, University of California Irvine Medical Center, Orange, CA

Abstract

Key Points Approximately 20% to 25% of adults with B-ALL have Ph-like ALL with increased frequency of Ph-like ALL in adults with Hispanic ethnicity. Adult patients with CRLF2+ ALL have poor long-term outcomes; novel strategies are needed to improve the outcomes.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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