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Predictors of relapse and overall survival in Philadelphia chromosome–positive acute lymphoblastic leukemia after transplantation

Authors :
Eileen Bryant
Kris Doney
Ted Gooley
Derek L. Stirewalt
Frederick R. Appelbaum
Lan Beppu
Jerald P. Radich
Katherine A. Guthrie
Source :
Biology of Blood and Marrow Transplantation. 9:206-212
Publication Year :
2003
Publisher :
Elsevier BV, 2003.

Abstract

Allogeneic transplantation offers a potential cure for patients with Philadelphia chromosome–positive acute lymphoblastic leukemia (Ph+ ALL). We performed a retrospective analysis examining pretransplantation and posttransplantation prognostic factors in 90 patients with Ph+ ALL. The median age of the patients was 33 years, with slightly more than half of the patients (58%) in clinical remission at the time of transplantation. Overall, patients had a nonrelapse mortality rate of 30%, a relapse percentage of 34%, and an estimated 5-year disease-free survival rate of 30%. Pretransplantation risk factors for relapse included the expression of the p190 transcript (relative risk [RR] = 5.1; P = .037), evidence of morphologic disease at the time of transplantation (RR = 3.9; P < .001), and type of donor (RR = 2.5; P = .015), with patients receiving autologous or matched related transplants having the highest risk of relapse. The detection of minimal residual disease by reverse transcription polymerase chain reaction for bcr-abl transcripts was a significant posttransplantation risk factor for relapse (RR = 4.4; P = .001), with posttransplantation patients expressing the p190 transcript having the highest risk of relapse (RR = 8.7; P = .0001). In addition, patients with chronic extensive graft-versus-host disease showed a significantly lower risk of relapse (RR = 0.33; P = .038). Thus, these findings indicate that several pretransplantation and posttransplantation risk factors exist for patients with Ph+ ALL. Together, these factors can be used to improve our risk stratification of patients with Ph+ ALL who undergo transplantation, which will greatly enhance our ability to counsel these patients and potentially lead to the development of more specific treatment plans for them. © 2003 American Society for Blood and Marrow TransplantationBiology of Blood and Marrow Transplantation 9:206-212 (2003)

Details

ISSN :
10838791
Volume :
9
Database :
OpenAIRE
Journal :
Biology of Blood and Marrow Transplantation
Accession number :
edsair.doi.dedup.....d57e58ccdf9ecbe588b5f9c511ca56de
Full Text :
https://doi.org/10.1016/s1083-8791(03)70011-1