Japanese Journal of Clinical Oncology Advance Access published online on November 30, 2007
Japanese Journal of Clinical Oncology, doi:10.1093/jjco/hym130
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© 2007 Foundation for Promotion of Cancer Research
Successful Treatment of Primary Plasma Cell Leukaemia by Allogeneic Stem Cell Transplantation from Haploidentical Sibling
1 Medicine and Biosystemic Science
2 Center for Cellular and Molecular Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan
3 Department of Hematology, National Fukuoka-Higashi Medical Center, Fukuoka, Japan
For reprints and all correspondence: Atsushi Nonami, First Department of Internal Medicine, Graduate School of Medicine, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan; E-mail: anonamin{at}yahoo.co.jp
Received July 25, 2007; accepted September 2, 2007
Primary plasma cell leukaemia (PCL) is a rare, aggressive neoplasm of plasma cell dyscrasia. Conventional chemotherapy is usually ineffective, with an overall survival of only 8 months. Here, we describe a 42-year-old man with primary PCL, who was successfully treated with haploidentical (2-HLA loci mismatched) haematopoietic stem-cell transplantation (HSCT). To overcome the human leukocyte antigen (HLA) disparity, in vivo T-cell purging by the pre-transplant administration of antithymocyte globulin followed by a conventional prophylactic treatment against graft-versus-host disease (GVHD) resulted in an avoidance of severe GVHD as well as infectious complications. The patient has maintained complete remission for 13 months after haploidentical HSCT, indicating that a graft-versus-PCL effect might be preserved. Haploidentical HSCT can be a potentially curative treatment for patients with primary PCL who do not have an HLA-identical donor.
Key Words: plasma cell leukaemia haploidentical stem cell transplantation ATG