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PMID: 18664621 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Impact of prior imatinib mesylate on the outcome of hematopoietic cell transplantation for chronic myeloid leukemia.

Blood ·Vol. 112 ·No. 8 ·2008-10-15 ·Pages 3500-7

Lee SJ, Kukreja M, Wang T, Giralt SA, Szer J, Arora M, Woolfrey AE, Cervantes F, Champlin RE, Gale RP, Halter J, Keating A, Marks DI, McCarthy PL, Olavarria E, Stadtmauer EA, Abecasis M, Gupta V, Khoury HJ, George B, Hale GA, Liesveld JL, Rizzieri DA, Antin JH, Bolwell BJ, Carabasi MH, Copelan E, Ilhan O, Litzow MR, Schouten HC, Zander AR, Horowitz MM, Maziarz RT

Abstract

Imatinib mesylate (IM, Gleevec) has largely supplanted allogeneic hematopoietic cell transplantation (HCT) as first line therapy for chronic myeloid leukemia (CML). Nevertheless, many people with CML eventually undergo HCT, raising the question of whether prior IM therapy impacts HCT success. Data from the Center for International Blood and Marrow Transplant Research on 409 subjects treated with IM before HCT (IM(+)) and 900 subjects who did not receive IM before HCT (IM(-)) were analyzed. Among patients in first chronic phase, IM therapy before HCT was associated with better survival but no statistically significant differences in treatment-related mortality, relapse, and leukemia-free survival. Better HLA-matched donors, use of bone marrow, and transplantation within one year of diagnosis were also associated with better survival. A matched-pairs analysis was performed and confirmed a higher survival rate among first chronic phase patients receiving IM. Among patients transplanted with advanced CML, use of IM before HCT was not associated with treatment-related mortality, relapse, leukemia-free survival, or survival. Acute graft-versus-host disease rates were similar between IM(+) and IM(-) groups regardless of leukemia phase. These results should be reassuring to patients receiving IM before HCT.

MeSH Terms
Adolescent Adult Aged Antineoplastic Agents/therapeutic use Benzamides Child Child, Preschool Disease-Free Survival Female HLA Antigens/metabolism Hematopoietic Stem Cell Transplantation/methods Humans Imatinib Mesylate Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy,therapy Male Middle Aged Piperazines/therapeutic use Pyrimidines/therapeutic use Registries Treatment Outcome
Chemicals
Antineoplastic Agents Benzamides HLA Antigens Piperazines Pyrimidines Imatinib Mesylate
Authors & Affiliations
33 authors, click to expand affiliations / ORCID
Lee Stephanie J
Fred Hutchinson Cancer Research Center, Seattle, WA, USA. [email protected]
Kukreja Manisha
Wang Tao
Giralt Sergio A
Szer Jeffrey
Arora Mukta
Woolfrey Ann E
Cervantes Francisco
Champlin Richard E
Gale Robert Peter
Halter Joerg
Keating Armand
Marks David I
McCarthy Philip L
Olavarria Eduardo
Stadtmauer Edward A
Abecasis Manuel
Gupta Vikas
Khoury H Jean
George Biju
Hale Gregory A
Liesveld Jane L
Rizzieri David A
Antin Joseph H
Bolwell Brian J
Carabasi Matthew H
Copelan Edward
Ilhan Osman
Litzow Mark R
Schouten Harold C
Zander Axel R
Horowitz Mary M
Maziarz Richard T
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Article Info
Journal
Blood
Abbr.
Blood
ISSN
1528-0020
Published
2008-10-15
Epub
2008-00-29
Pages
3500-7
Language
English
Region
United States
NLM ID
7603509
PMCID
PMC2954751
Subset
IM
Grants
NCI NIH HHS · U24 CA076518 · United States
NCI NIH HHS · U24-CA76518 · United States
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