Cytomegalovirus Infection according to Cell Source after Hematopoietic Cell Transplantation in Pediatric Patients.
10.3349/ymj.2012.53.2.393
- Author:
Eun Sang YI
1
;
Yae Jean KIM
Author Information
1. Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. yaejeankim@skku.edu
- Publication Type:Original Article
- Keywords:
CMV;
cord blood;
stem cell transplantation;
leukemia
- MeSH:
Acyclovir/therapeutic use;
Adolescent;
Antiviral Agents/therapeutic use;
Child;
Child, Preschool;
Cyclosporine/therapeutic use;
Cytomegalovirus Infections/*diagnosis/drug therapy/etiology;
Female;
Graft vs Host Disease/diagnosis/drug therapy/etiology;
Hematopoietic Stem Cell Transplantation/*adverse effects;
Humans;
Immunosuppressive Agents/therapeutic use;
Infant;
Leukemia/therapy;
Male;
Retrospective Studies;
Young Adult
- From:Yonsei Medical Journal
2012;53(2):393-400
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: This study was performed in order to evaluate the incidence and characteristics of cytomegalovirus (CMV) infection in children with acute leukemia according to donor source and graft type. MATERIALS AND METHODS: We retrospectively identified children with acute leukemia who had received allogeneic hematopoietic cell transplantation at Samsung Medical Center in Korea from October 1998 to December 2009. RESULTS: In total, 134 recipients were identified. The patients were classified into the following three groups: unrelated cord blood (CB, n=36), related bone marrow or peripheral blood stem cells (RD, n=41), and unrelated bone marrow or peripheral blood stem cells (UD, n=57). The 365-day cumulative incidence of CMV antigenemia was not significantly different among the three groups (CB 67% vs. RD 49% vs. UD 65%, p=0.17). However, CB recipients had the highest median value of peak antigenemia (CB 160/2x10(5) leukocytes vs. RD 7/2x10(5) leukocytes vs. UD 19/2x10(5) leukocytes, p<0.01) and the longest duration of CMV antigenemia than the other stem cell source recipients (CB 87 days vs. RD 17 days vs. UD 28 days, p<0.01). In addition, the 730-day cumulative incidence of CMV disease was the highest in the CB recipients (CB 36% vs. RD 2% vs. UD 5%, p<0.01). Thirteen CB recipients developed CMV disease, in which five of them had more than one organ involvement. Two patients, who were CB recipients, died of CMV pneumonia. CONCLUSION: This study suggests that CB recipients had both longer and higher cumulative incidences of CMV infection. Therefore, a more aggressive and effective strategy of CMV management should be considered in CB recipients.
