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Journal of Clinical Oncology, Vol 26, No 26 (September 10), 2008: pp. 4326-4332
© 2008 American Society of Clinical Oncology.
DOI: 10.1200/JCO.2008.16.4442

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Unrelated Donor Bone Marrow Transplantation for Children With Acute Myeloid Leukemia Beyond First Remission or Refractory to Chemotherapy

Nancy J. Bunin, Stella M. Davies, Richard Aplenc, Bruce M. Camitta, Kenneth B. DeSantes, Rakesh K. Goyal, Neena Kapoor, Nancy A. Kernan, Joseph Rosenthal, Franklin O. Smith, Mary Eapen

From the Children's Hospital of Philadelphia, Philadelphia; Children's Hospital of Pittsburgh, Pittsburgh, PA; Cincinnati Children's Hospital Medical Center, Cincinnati, OH; Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee; University of Wisconsin Hospital and Clinics, Madison, WI; Children's Hospital of Los Angeles, Los Angeles; City of Hope National Medical Center, Duarte, CA; and Memorial Sloan-Kettering Cancer Center, New York, NY

Corresponding author: Mary Eapen, MBBS, MS, Statistical Center, Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, 8701 Watertown Plank Rd, Milwaukee, WI; e-mail: meapen{at}mcw.edu

Purpose Identify prognostic factors that influence outcome after unrelated donor bone marrow transplantation in children with acute myeloid leukemia (AML).

Patients and Methods Included are 268 patients (age ≤ 18 years) with AML in second complete remission (n = 142), relapse (n = 90), or primary induction failure (n = 36) at transplantation. All patients received bone marrow grafts from an unrelated donor and a myeloablative conditioning regimen. Cox regression models were constructed to identify risk factors that influence outcome after transplantation.

Results In this analysis, the only risk factor that predicted leukemia recurrence and overall and leukemia-free survival was disease status at transplantation. The 5-year probabilities of leukemia-free survival were 45%, 20%, and 12% for patients who underwent transplantation at second complete remission, relapse, and primary induction failure, respectively. As expected, risk of acute but not chronic graft-versus-host disease (GVHD) was lower with T-cell–depleted bone marrow grafts; T-cell–depleted grafts were not associated with higher risks of leukemia recurrence. We observed similar risks of leukemia relapse in patients with and without acute and chronic GVHD.

Conclusion Children who underwent transplantation in remission had a superior outcome compared with children who underwent transplantation during relapse or persistent disease. Nevertheless, 20% of children who underwent transplantation in relapse are long-term survivors, suggesting that unrelated donor bone marrow transplantation is an effective therapy in a significant proportion of children with recurrent or primary refractory AML.

The views expressed in this article do not reflect the official policy or position of the National Institute of Health, the Department of the Navy, the Department of Defense, or any other agency of the US Government.

Authors’ disclosures of potential conflicts of interest and author contributions are found at the end of this article.


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Copyright © 2008 by the American Society of Clinical Oncology, Online ISSN: 1527-7755. Print ISSN: 0732-183X
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