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

被引:78
作者
Feinstein, LC
Sandmaier, BM
Hegenbart, U
McSweeney, PA
Maloney, DG
Gooley, TA
Maris, MB
Chauncey, TR
Bruno, B
Appelbaum, FR
Niederwieser, DW
Storb, RF
机构
[1] Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
[2] Univ Washington, Seattle, WA 98195 USA
[3] Univ Leipzig, Leipzig, Germany
[4] Univ Colorado, Denver, CO 80202 USA
[5] VA Puget Sound Hlth Care Syst, Seattle, WA USA
[6] Univ Turin, Turin, Italy
关键词
AML; first remission; non-myeloablative; transplant;
D O I
10.1046/j.1365-2141.2003.04057.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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/m(2) 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.
引用
收藏
页码:281 / 288
页数:8
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