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Reduced intensity conditioning is superior to nonmyeloablative conditioning for older chronic myelogenous leukemia patients undergoing hematopoietic cell transplant during the tyrosine kinase inhibitor era.

Authors :
Warlick E
Ahn KW
Pedersen TL
Artz A
de Lima M
Pulsipher M
Akpek G
Aljurf M
Cahn JY
Cairo M
Chen YB
Cooper B
Deol A
Giralt S
Gupta V
Khoury HJ
Kohrt H
Lazarus HM
Lewis I
Olsson R
Pidala J
Savani BN
Seftel M
Socié G
Tallman M
Ustun C
Vij R
Vindeløv L
Weisdorf D
Source :
Blood [Blood] 2012 Apr 26; Vol. 119 (17), pp. 4083-90. Date of Electronic Publication: 2012 Mar 09.
Publication Year :
2012

Abstract

Tyrosine kinase inhibitors (TKIs) and reduced intensity conditioning (RIC)/nonmyeloablative (NMA) conditioning hematopoietic cell transplants (HCTs) have changed the therapeutic strategy for chronic myelogenous leukemia (CML) patients. We analyzed post-HCT outcomes of 306 CML patients reported to the Center for International Blood and Marrow Transplant Research aged 40 years and older undergoing RIC/NMA HCT from 2001 to 2007: 117 (38%) aged 40 to 49 years, 119 (39%) 50 to 59 years, and 70 (23%) 60 years or older. The majority (74%) had treatment with imatinib before HCT. At HCT, most patients aged 40 to 49 years were in chronic phase (CP) 1 (74%), compared with 31% aged 60 years or older. Siblings were donors for 56% aged 40 to 49 years; older cohorts had more unrelated donors. The majority received peripheral blood grafts and RIC across all age groups. 3 year overall survival (54%, 52%, and 41%), day + 100 grade II-IV acute GVHD (26%, 32%, and 32%), chronic GVHD (58%, 51%, and 43%), and 1-year treatment-related mortality (18%, 20%, and 13%) were similar across ages. The 3-year relapse incidence (36%, 43%, and 66%) and disease-free survival (35%, 32%, and 16%) were inferior in the oldest cohort. Importantly, for CP1 patients, relapse and disease-free survival were similar across age cohorts. Allogeneic RIC HCT for older patients with CML can control relapse with acceptable toxicity and survival in TKI-exposed CML, especially if still in CP1.

Details

Language :
English
ISSN :
1528-0020
Volume :
119
Issue :
17
Database :
MEDLINE
Journal :
Blood
Publication Type :
Academic Journal
Accession number :
22408257
Full Text :
https://doi.org/10.1182/blood-2012-02-409763