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Volume 16, Issue 2, Pages 231-238 (February 2010)


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Outcome of 125 Children with Chronic Myelogenous Leukemia Who Received Transplants from Unrelated Donors: The Japan Marrow Donor Program

Hideki Muramatsu1, Seiji Kojima1, Ayami Yoshimi2, Yoshiko Atsuta2, Koji Kato3, Yoshihisa Nagatoshi4, Masami Inoue5, Kazutoshi Koike6, Takakazu Kawase7, Masaki Ito8, Hidemitsu Kurosawa9, Akihiko Tanizawa10, Chikako Tono11, Kazuko Hamamoto12, Noriko Hotta13, Akihiro Watanabe14, Yasuo Morishima15, Keisei Kawa5, Hiroyuki Shimada16Corresponding Author Informationemail address

Received 18 July 2009; accepted 24 September 2009. published online 05 October 2009.

Because of a small number of patients, only a few studies have addressed the outcome of bone marrow transplantation (BMT) in children with Philadelphia chromosome–positive (Ph+) chronic myelogenous leukemia (CML), who receive graft from a volunteer-unrelated donor (VUD), especially after practical application of imatinib mesylate. The outcomes of BMT from a VUD in 125 children with Ph+ CML were retrospectively reviewed. Patients were identified through the Japan Marrow Donor Program as having undergone BMT between 1993 and 2005 and were aged 1-19 years at the time of transplant (median age, 14 years). The probabilities of 5-year overall survival (OS) and leukemia-free survival (LFS) were 59.3% and 55.5%, respectively. Multivariate analysis identified the following unfavorable survival factors: infused total nucleated cell dose<314×106 /kg (relative risk [RR]=2.43; 95% confidence interval [CI]=1.33-4.44; P=.004), advanced phase (RR=2.43; 95% CI=1.37-4.31; P=.004), and no major cytogenetic response (MCyR) at the time of BMT (RR=6.55; 95% CI=1.98-21.6; P=.002). Of the 17 patients treated with imatinib, 15 (88%) achieved MCyR at the time of BMT, and this group had an excellent 5-year OS of 81.9%. Disease phase, infused total nucleated cell dose, and cytogenetic response were independent risk factors for survival of unrelated BMT. These findings provide important information for assessing the indications for and improving outcome in unrelated BMT for the treatment of pediatric CML.

1 Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan

2 Department of Hematopoietic Stem Cell Transplantation Data Management, Nagoya University School of Medicine, Nagoya, Japan

3 Division of Pediatric Hematology/Oncology, Children's Medical Center, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan

4 Section of Pediatrics, National Kyushu Cancer Center, Fukuoka, Japan

5 Department of Hematology/Oncology, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan

6 Department of Pediatrics, Ibaraki Children's Hospital, Ibaraki, Japan

7 Division of Epidemiology and Prevention, Aichi Cancer Center Research Institute, Nagoya, Japan

8 Department of Pediatrics, Fukushima Medical University School of Medicine, Fukushima, Japan

9 Department of Pediatrics, Dokkyo Medical University, Tokyo, Japan

10 Department of Pediatrics, University of Fukui Faculty of Medical Sciences, Fukui, Japan

11 Department of Pediatrics, Aomori Rosai Hospital, Aomori, Japan

12 Department of Pediatrics, Hiroshima Red Cross Hospital & Atomic-Bomb Survivors Hospital, Hiroshima, Japan

13 Department of Pediatrics, Tokuyama Central Hospital, Tokuyama, Japan

14 Department of Pediatrics, Niigata Cancer Center Hospital, Niigata, Japan

15 Department of Hematology and Cell Therapy, Aichi Cancer Center Hospital, Nagoya, Japan

16 Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan

Corresponding Author InformationCorrespondence and reprint requests: Hiroyuki Shimada, MD, PhD, Department of Pediatrics, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, Tokyo, 160-8582, Japan.

 Financial disclosure: See Acknowledgments on page 237.

PII: S1083-8791(09)00445-5

doi:10.1016/j.bbmt.2009.09.022


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