Skip Navigation



Japanese Journal of Clinical Oncology Advance Access published online on November 30, 2007

Japanese Journal of Clinical Oncology, doi:10.1093/jjco/hym130
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
37/12/969    most recent
hym130v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Request Permissions
Google Scholar
Right arrow Articles by Nonami, A.
Right arrow Articles by Nagafuji, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nonami, A.
Right arrow Articles by Nagafuji, K.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 2007 Foundation for Promotion of Cancer Research

Successful Treatment of Primary Plasma Cell Leukaemia by Allogeneic Stem Cell Transplantation from Haploidentical Sibling

Atsushi Nonami1,, Toshihiro Miyamoto1,2, Mika Kuroiwa3, Yuya Kunisaki1, Kenjiro Kamezaki1, Katsuto Takenaka1, Naoki Harada1, Takanori Teshima2, Mine Harada1 and Koji Nagafuji1

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


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.