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Allogeneic Hematopoietic Cell Transplantation for Adult T Cell Acute Lymphoblastic Leukemia.

Authors :
Hamilton, Betty Ky
Rybicki, Lisa
Abounader, Donna
Adekola, Kehinde
Advani, Anjali
Aldoss, Ibrahim
Bachanova, Veronika
Bashey, Asad
Brown, Stacey
DeLima, Marcos
Devine, Steven
Flowers, Christopher R.
Ganguly, Siddharth
Jagasia, Madan
Kennedy, Vanessa E.
Kim, Dennis Dong Hwan
McGuirk, Joseph
Pullarkat, Vinod
Romee, Rizwan
Sandhu, Karamjeet
Source :
Biology of Blood & Marrow Transplantation. Jul2017, Vol. 23 Issue 7, p1117-1121. 5p.
Publication Year :
2017

Abstract

Allogeneic hematopoietic cell transplantation (HCT) is recommended for patients with T cell acute lymphoblastic leukemia (T-ALL) in second or later complete remission (CR) and high-risk patients in first CR. Given its relative rarity, data on outcomes of HCT for T-ALL are limited. We conducted a multicenter retrospective cohort study using data from 208 adult patients who underwent HCT between 2000 and 2014 to describe outcomes of allogeneic HCT for T-ALL in the contemporary era. The median age at HCT was 37 years, and the majority of patients underwent HCT in CR, using total body irradiation (TBI)-based myeloablative conditioning regimens. One-quarter of the patients underwent alternative donor HCT using a mismatched, umbilical cord blood, or haploidentical donor. With a median follow up of 38 months, overall survival at 5 years was 34%. The corresponding cumulative incidence of non-relapse mortality and relapse was 26% and 41%, respectively. In multivariable analysis, factors significantly associated with overall survival were the use of TBI (HR, 0.57; P  = .021), age >35 years (HR, 1.55; P  = .025), and disease status at HCT (HR, 1.98; P  = .005 for relapsed/refractory disease compared with CR). Relapse was the most common cause of death (58% of patients). Allogeneic HCT remains a potentially curative option in selected patients with adult T-ALL, although relapse is a major cause of treatment failure. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10838791
Volume :
23
Issue :
7
Database :
Academic Search Index
Journal :
Biology of Blood & Marrow Transplantation
Publication Type :
Academic Journal
Accession number :
123506099
Full Text :
https://doi.org/10.1016/j.bbmt.2017.04.003