Blood online
Home About Blood Authors Subscriptions Permission Advertising Public Access contact us
 

 
Advanced
Current Issue
First Edition
Archives
Submit to Blood
Search
American Society of Hematology
Meeting Abstracts
Email Alerts
Blood, 1 February 2008, Vol. 111, No. 3, pp. 1054-1059.
Prepublished online as a Blood First Edition Paper on November 7, 2007; DOI 10.1182/blood-2007-08-099168.


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental Appendix
Right arrow All Versions of this Article:
blood-2007-08-099168v1
111/3/1054    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
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 Download to citation manager
Right arrow reprints & permissions
Right arrow Rights and Permissions
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kosaka, Y.
Right arrow Articles by Kojima, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kosaka, Y.
Right arrow Articles by Kojima, S.
Related Collections
Right arrow Clinical Trials and Observations
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

arrow to previous article Previous Article  |  Table of Contents  |  Next Article next article arrow

CLINICAL TRIALS AND OBSERVATIONS

Prospective multicenter trial comparing repeated immunosuppressive therapy with stem-cell transplantation from an alternative donor as second-line treatment for children with severe and very severe aplastic anemia

Yoshiyuki Kosaka1, Hiroshi Yagasaki2, Kimihiko Sano3, Ryoji Kobayashi4, Hiroshi Ayukawa5, Takashi Kaneko6, Hiromasa Yabe7, Masahiro Tsuchida8, Hideo Mugishima9, Akira Ohara10, Akira Morimoto11, Yoshitoshi Otsuka12, Shouichi Ohga13, Fumio Bessho14, Tatsutoshi Nakahata15, Ichiro Tsukimoto16, Seiji Kojima, on behalf of the Japan Childhood Aplastic Anemia Study Group2

1 Department of Pediatrics, Hyogo Children Hospital, Hyogo; 2 Department of Pediatrics, Nagoya University Graduate School of Medicine, Aichi; 3 Department of Pediatrics, Kobe University Graduate School of Medicine, Hyogo; 4 Department of Pediatrics, Hokkaido University Graduate School of Medicine, Hokkaido; 5 Department of Pediatrics, Yamaguchi University School of Medicine, Yamaguchi; 6 Department of Pediatrics, Kiyose Children's Hospital, Tokyo; 7 Specialized Clinical Science, Pediatrics, Tokai University School of Medicine, Kanagawa; 8 Department of Pediatrics, Ibaraki Children's Hospital, Ibaraki; 9 Department of Pediatrics, Nihon University School of Medicine, Tokyo; 10 Department of Transfusion, Toho University School of Medicine, Tokyo; 11 Department of Pediatrics, Kyoto Prefectural University of Medicine, Kyoto; 12 Department of Pediatrics, Hyogo College of Medicine, Hyogo; 13 Department of Pediatrics, Kyushu University Graduate School of Medicine, Fukuoka; 14 Department of Pediatrics, Kyorin University School of Medicine, Tokyo; 15 Department of Pediatrics, Kyoto University Graduate School of Medicine, Kyoto; and 16 Department of Pediatrics, Toho University School of Medicine, Tokyo, Japan

We conducted a prospective multicenter study to compare the efficacy of repeated immunosuppressive therapy (IST) with stem-cell transplantation (SCT) from an alternative donor in children with acquired aplastic anemia (AA) who failed to respond to an initial course of IST. Patients with severe (n = 86) and very severe disease (n = 119) received initial IST consisting of antithymocyte globulin (ATG) and cyclosporine. Sixty patients failed to respond to IST after 6 months from the initial IST and were eligible for second-line treatment. Among them, 21 patients lacking suitable donors received a second course of IST. Three patients developed an anaphylactoid reaction to ATG and could not complete the second IST. A trilineage response was seen in only 2 of 18 (11%) evaluable patients after 6 months. Thirty-one patients received SCT from an alternative donor. At 5 years from the initiation of second-line therapy, the estimated failure-free survival (FFS), defined as survival with response, was 83.9% (± 16.1%, SD) in the SCT group compared with 9.5% (± 9.0%) in the IST group (P = .001). These results suggest that SCT from an alternative donor offers a better chance of FFS than a second IST in patients not responding to an initial IST.


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




 click for free articles
home about blood authors subscriptions permissions advertising public access contact us
Sponsor: Genentech BioOncology and and Biogen Idec
Blood Online is supported in part by
Genentech BioOncology and Biogen Idec
  Copyright © 2008 by American Society of Hematology         Online ISSN: 1528-0020