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Volume 16, Issue 2, Pages 223-230 (February 2010)


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Hematopoietic Stem Cell Transplantation for Refractory or Recurrent Non-Hodgkin Lymphoma in Children and Adolescents

Thomas G. Gross1Corresponding Author Informationemail address, Gregory A. Hale2, Wensheng He3, Bruce M. Camitta4, Jean E. Sanders5, Mitchell S. Cairo6, Robert J. Hayashi7, Amanda M. Termuhlen1, Mei-Jie Zhang3, Stella M. Davies8, Mary Eapen34

Received 27 August 2009; accepted 24 September 2009. published online 01 October 2009.

We examined the role of hematopoietic stem cell transplantation (HSCT) for patients aged18 years with refractory or recurrent Burkitt (n=41), lymphoblastic (n=53), diffuse large B cell (DLBCL; n=52), and anaplastic large cell lymphoma (n=36), receiving autologous (n=90) or allogeneic (n=92; 43 matched sibling and 49 unrelated donor) HSCT in 1990-2005. Risk factors affecting event-free survival (EFS) were evaluated using stratified Cox regression. Characteristics of allogeneic and autologous HSCT recipients were similar. Allogeneic donor HSCT was more likely to use irradiation-containing conditioning regimens, bone marrow (BM) stem cells, be performed in more recent years, and for lymphoblastic lymphoma. EFS rates were lower for patients not in complete remission at HSCT, regardless of donor type. After adjusting for disease status, 5-year EFS were similar after allogeneic and autologous HSCT for DLBCL (50% vs 52%), Burkitt (31% vs 27%), and anaplastic large cell lymphoma (46% vs 35%). However, EFS was higher for lymphoblastic lymphoma, after allogeneic HSCT (40% vs 4%; P < .01). Predictors of EFS for progressive or recurrent disease after HSCT included disease status at HSCT and use of allogeneic donor for lymphoblastic lymphoma. These data were unable to demonstrate a difference in outcome by donor type for the other histological subtypes.

1 Department of Pediatrics, Nationwide Children's Hospital, Ohio State University, Columbus, Ohio

2 Department of Pediatrics, St. Jude Children's Research Hospital, Memphis, Tennessee

3 Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin

4 Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin

5 Department of Pediatrics, Fred Hutchinson Cancer Research Center, Seattle, Washington

6 Department of Pediatrics, New York Presbyterian Hospital, New York, New York

7 Department of Pediatrics, St. Louis Children's Hospital, St. Louis, Missouri

8 Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio

Corresponding Author InformationCorrespondence and reprint requests: Thomas G. Gross, MD, PhD, Department of Pediatrics, Nationwide Children's Hospital, 700 Children's Drive, Columbus, OH 43205.

 Financial disclosure: See Acknowledgments on page 228.

PII: S1083-8791(09)00444-3

doi:10.1016/j.bbmt.2009.09.021


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