Allogeneic bone marrow transplantation for high-risk acute lymphoblastic leukemia during first complete remission

Author:

Chao NJ1,Forman SJ1,Schmidt GM1,Snyder DS1,Amylon MD1,Konrad PN1,Nademanee AP1,O'Donnell MR1,Parker PM1,Stein AS1

Affiliation:

1. Department of Medicine and Pediatrics, Stanford University Medical Center, CA 94305.

Abstract

Abstract Fifty-three patients with high-risk acute lymphoblastic leukemia (ALL) under age 50 with a histocompatible sibling donor received high-dose radiochemotherapy followed by allogeneic bone marrow transplantation (BMT). The high-risk factors used to identify the patients were: white blood cell count at initial presentation, cytogenetic abnormalities, age, extramedullary leukemic infiltration, and time from initial therapy to complete remission. Patients with one or more of the above risk factors who received BMT have a disease-free survival of 61% with a median follow-up of 66 months (range 11 months to 10.6 years), and an actuarial relapse rate of 10%. This study demonstrates that patients with high-risk ALL achieve a significant disease-free survival and cure rate with the use of allogeneic fully matched sibling BMT. However, a properly designed prospective study comparing the outcome of BMT with the best currently available chemotherapy data is required to define the ultimate role of BMT in this group of patients.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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