Effects of KIR ligand incompatibility on clinical outcomes of umbilical cord blood transplantation without ATG for acute leukemia in complete ... View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2013-11-29

AUTHORS

J Tanaka, Y Morishima, Y Takahashi, T Yabe, K Oba, S Takahashi, S Taniguchi, H Ogawa, Y Onishi, K Miyamura, H Kanamori, N Aotsuka, K Kato, S Kato, Y Atsuta, Y Kanda

ABSTRACT

To clarify the effect of killer cell immunoglobulin-like receptor (KIR) ligand incompatibility on outcomes of acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL) patients in complete remission after single cord blood transplantation (CBT), we assessed the outcomes of CBT registered in the Japan Society for Hematopoietic Cell Transplantation (JSHCT) database. A total of 643 acute leukemia (357 AML and 286 ALL) patient and donor pairs were categorized according to their KIR ligand incompatibility by determining whether or not they expressed HLA-C, Bw4 or A3/A11 by DNA typing. A total of 128 patient–donor pairs were KIR ligand-incompatible in the graft-versus-host (GVH) direction and 139 patient–donor pairs were incompatible in the host-versus-graft (HVG) direction. Univariate and multivariate analyses showed no significant differences between the KIR ligand-incompatible and compatible groups in the GVH direction for both AML and ALL patients of overall survival, disease-free survival, relapse incidence, non-relapse mortality and acute GVH disease. However, KIR incompatibility in the HVG direction ameliorated engraftment in ALL patients (hazard ratio 0.66, 95% confidence interval 0.47–0.91, P=0.013). Therefore, there were no effects of KIR ligand incompatibility in the GVH direction on single CBT outcomes for acute leukemia patients without anti-thymocyte globulin use. However, it is necessary to pay attention to KIR incompatibility in the HVG direction for engraftment. More... »

PAGES

e164-e164

Journal

TITLE

Blood Cancer Journal

ISSUE

11

VOLUME

3

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/bcj.2013.62

DOI

http://dx.doi.org/10.1038/bcj.2013.62

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1013157959

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/24292416


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