| Literature DB >> 26271192 |
Hiroyuki Ishida1, Motohiro Kato2, Kazuko Kudo3, Takashi Taga4, Daisuke Tomizawa5, Takako Miyamura6, Hiroaki Goto7, Jiro Inagaki8, Katsuyoshi Koh9, Kiminori Terui10, Atsushi Ogawa11, Yoshifumi Kawano12, Masami Inoue13, Akihisa Sawada13, Koji Kato14, Yoshiko Atsuta15, Takuya Yamashita16, Souichi Adachi17.
Abstract
Pediatric patients with acute myeloid leukemia (AML) mainly receive myeloablative conditioning regimens based on busulfan (BU) or total body irradiation (TBI) before allogeneic hematopoietic cell transplantation (allo-HCT); however, the optimal conditioning regimen remains unclear. To identify which of these regimens is better for pediatric patients, we performed a retrospective analysis of nationwide registration data collected in Japan between 2006 and 2011 to assess the outcomes of patients receiving these regimens before a first allo-HCT. Myeloablative conditioning regimens based on i.v. BU (i.v. BU-MAC) (n = 69) or TBI (TBI-MAC) (n = 151) were compared in pediatric AML patients in first or second complete remission (CR1/CR2). The incidences of sinusoid obstruction syndrome, acute and chronic graft-versus-host disease, and early nonrelapse mortality (NRM) before day 100 were similar for both conditioning groups; however, the incidence of bacterial infection during the acute period was higher in the TBI-MAC group (P = .008). Both groups showed a similar incidence of NRM, and there was no significant difference in the incidence of relapse between the groups. Univariate and multivariate analyses revealed no significant differences in the 2-year relapse-free survival rates for the i.v. BU-MAC and TBI-MAC groups in the CR1/CR2 setting (71% versus 67%, P = .36; hazard ratio, .73; 95% CI, .43 to 1.24, respectively). TBI-MAC was no better than i.v. BU-MAC for pediatric AML patients in remission. Although this retrospective registry-based analysis has several limitations, i.v. BU-MAC warrants further evaluation in a prospective trial.Entities:
Keywords: Acute myeloid leukemia; Busulfan; Children; Hematopoietic stem cell transplantation; Total body irradiation
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Year: 2015 PMID: 26271192 DOI: 10.1016/j.bbmt.2015.08.011
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742