Implication of early lymphocyte recovery after allogeneic hematopoietic stem cell transplantation in children with leukemia.

Yonsei Med J

Department of Pediatrics, Environmental Health Center for Childhood Leukemia and Cancer, Chonnam National University Hwasun Hospital, Chonnam National University Medical School, Hwasun, Korea.

Published: January 2013

Purpose: The repopulating lymphocytes after allogeneic hematopoietic stem cell transplantation have an important role not only on the prevention of serious infections in the early transplantation period, but also on the killing of residual leukemic cells by graft-versus-leukemia effect. The aim of this study was to analyze the impact of lymphocyte recovery after allogeneic stem cell transplantation in children with hematologic malignancies.

Materials And Methods: We evaluated 69 children transplanted for acute lymphoblastic leukemia (ALL) (n=34), acute myeloid leukemia (AML) (n=26), chronic leukemia (n=7) and juvenile myelomonocytic leukemia (n=2) between 1996 and 2008 at the Chonnam National University Hospital, Korea. The patients were grouped based on absolute lymphocyte counts (ALC) <500/μL or ≥ 500/μL at D+21 and D+30 after transplant.

Results: Patients with a High ALC at D+21 and D+30 had a faster neutrophil and platelet engraftment. The High at D+30 group had a better 5 year overall survival (71% vs. 53%, p=0.043) and event-free survival (72% vs. 53%, p=0.065) than the Low at D+30 group. The incidence of grade II-IV acute and chronic graft-versus-host disease (GVHD), and relapse rate did not differ by the ALC counts. However, the Low at D+30 group had a significantly increased risk for transplant-related mortality (p=0.019). The univariate analysis showed that the factors associated with decreased survival were a Low ALC at D+30, patients with high risk ALL, and grade II-IV aGVHD in patients with ALL and AML.

Conclusion: Early posttransplant serial lymphocyte measurement would be a simple but useful method for predicting transplant outcomes.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3521273PMC
http://dx.doi.org/10.3349/ymj.2013.54.1.62DOI Listing

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