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Volume 15, Issue 11, Pages 1431-1438 (November 2009)


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Quantifying the Survival Benefit for Allogeneic Hematopoietic Stem Cell Transplantation in Relapsed Acute Myelogenous Leukemia

Paul M. Armistead1Corresponding Author Informationemail address, Marcos de Lima1, Sherry Pierce2, Wei Qiao3, Xuemei Wang3, Peter F. Thall3, Sergio Giralt1, Farhad Ravandi2, Hagop Kantarjian2, Richard Champlin1, Elihu Estey4

Received 27 May 2009; accepted 9 July 2009. published online 02 September 2009.

Allogeneic hematopoietic stem cell transplantation (HSCT) is the recommended therapy for patients with relapsed acute myelogenous leukemia (AML), despite little evidence showing a survival benefit in patients who undergo HSCT versus chemotherapy alone. Because a prospective randomized trial addressing this issue is unlikely, we retrospectively reviewed all patients receiving initial salvage therapy for AML at M.D. Anderson Cancer Center between 1995 and 2004, focusing on patients undergoing HSCT or chemotherapy without HSCT as second salvage after first salvage failed to produce complete remission (CR) (group A) and patients in first salvage–induced CR (group B). Median survival was 5.1 months for HSCT (n=84) versus 2.3 months for chemotherapy (n = 200; P = .004) in group A and 11.7 months for HSCT (n = 46) versus 5.6 months for chemotherapy (n = 66; P < . 001) in group B. HSCT was associated with a survival benefit in each of 8 subgroups defined by age </≥ 50, high-risk cytogenetics or not, and treatment in first salvage–induced CR or second salvage, and also in 5 of 6 subgroups defined by age </≥ 50 years and duration of first CR (CR1) (primary refractory, CR1 ≤ 36 weeks, CR1 > 36 weeks). Our data suggest that HSCT is preferable to chemotherapy alone in these patients with poor prognoses, with particular benefits noted in patients under age 50 years.

1 Department of Stem Cell Transplantation and Cellular Therapy, M.D. Anderson Cancer Center, Houston Texas

2 Department of Leukemia, M.D. Anderson Cancer Center, Houston Texas

3 Department of Biostatistics, M.D. Anderson Cancer Center, Houston Texas

4 Fred Hutchinson Cancer Research Center, Seattle, Washington

Corresponding Author InformationCorrespondence and reprint requests: Paul Armistead, MD, PhD, Lineberger Comprehensive Cancer Center, 21-244, University of North Carolina, 450 West Road, Chapel Hill, NC 27599.

 Financial disclosure: See Acknowledgments on page 1437.

PII: S1083-8791(09)00338-3

doi:10.1016/j.bbmt.2009.07.008


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