Volume 120, Issue 2 pp. 281-288

Non-myeloablative allografting from human leucocyte antigen-identical sibling donors for treatment of acute myeloid leukaemia in first complete remission

Lyle C. Feinstein

Lyle C. Feinstein

Fred Hutchinson Cancer Research Center,

University of Washington, Seattle, WA, USA

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Brenda M. Sandmaier

Brenda M. Sandmaier

Fred Hutchinson Cancer Research Center,

University of Washington, Seattle, WA, USA

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Ute Hegenbart

Ute Hegenbart

University of Leipzig, Leipzig, Germany,

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Peter A. McSweeney

Peter A. McSweeney

University of Colorado, Denver, CO,

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David G. Maloney

David G. Maloney

Fred Hutchinson Cancer Research Center,

University of Washington, Seattle, WA, USA

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Theodore A. Gooley

Theodore A. Gooley

Fred Hutchinson Cancer Research Center,

University of Washington, Seattle, WA, USA

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Michael B. Maris

Michael B. Maris

Fred Hutchinson Cancer Research Center,

University of Washington, Seattle, WA, USA

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Thomas R. Chauncey

Thomas R. Chauncey

Fred Hutchinson Cancer Research Center,

University of Washington, Seattle, WA, USA

VA Puget Sound Health Care System, Seattle, WA, USA, and

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Benedetto Bruno

Benedetto Bruno

University of Torino, Torino, Italy

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Frederick R. Appelbaum

Frederick R. Appelbaum

Fred Hutchinson Cancer Research Center,

University of Washington, Seattle, WA, USA

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Dietger W. Niederwieser

Dietger W. Niederwieser

University of Leipzig, Leipzig, Germany,

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Rainer F. Storb

Rainer F. Storb

Fred Hutchinson Cancer Research Center,

University of Washington, Seattle, WA, USA

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First published: 24 January 2003
Citations: 83
Rainer Storb, MD, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue N., D1-100, PO Box 19024, Seattle, WA 98109–1024, USA. E-mail: [email protected]

Abstract

Summary. Many patients with acute myeloid leukaemia (AML) in first complete remission (CR1) are ineligible for allogeneic transplantation as a result of age or medical problems other than leukaemia. Eighteen patients (median age 59 years, range 36–73 years) with de novo (n = 13) and secondary (n = 5) AML in morphological CR1, who were not candidates for conventional allografting, received non-myeloablative peripheral blood stem cell transplants from human leucocyte antigen identical sibling donors after conditioning with 2 Gy total body irradiation (TBI; n = 10) or 2 Gy TBI and 90 mg/m2 of fludarabine (n = 8). Postgrafting immunosuppression was with cyclosporine and mycophenolate mofetil. Two rejections were observed in patients not given fludarabine and one died with relapse. Overall, 10 patients died between 77 and 841 d, seven from relapse and three from non-relapse mortality (NRM). Day +100 NRM was 0% with a 1-year estimated NRM of 17%[95% confidence interval (CI) 0–35%]. The median follow-up among the eight survivors was 766 d (range, 188–1141 d). Seven of these eight survivors remain in complete remission (CR). One-year estimates of overall and progression-free survivals were 54% (95% CI 31–78%) and 42% (95% CI 19–66%) respectively. While follow-up is short, this analysis demonstrates that the procedure is sufficiently safe to be studied in a wider group of patients.

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