Conditioning with targeted busulfan and cyclophosphamide for hemopoietic stem cell transplantation from related and unrelated donors in patients with myelodysplastic syndrome

被引:215
作者
Deeg, HJ
Storer, B
Slattery, JT
Anasetti, C
Doney, KC
Hansen, JA
Kiem, HP
Martin, PJ
Petersdorf, E
Radich, JP
Sanders, JE
Shulman, HM
Warren, EH
Witherspoon, RP
Bryant, EM
Chauncey, TR
Getzendaner, L
Storb, R
Appelbaum, FR
机构
[1] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98109 USA
[2] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98109 USA
[3] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
[4] Univ Washington, Dept Med, Seattle, WA 98195 USA
[5] Univ Washington, Dept Pathol, Seattle, WA 98195 USA
[6] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[7] Univ Washington, Dept Pharmaceut, Seattle, WA 98195 USA
[8] Vet Adm Med Ctr, Seattle, WA 98108 USA
关键词
D O I
10.1182/blood-2002-02-0527
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A total of 109 patients (aged 6-66 years; median, 46 years) with myelodysplastic syndrome (MDS) were treated with busulfan (BU) targeted to plasma concentrations of 800 to 900 ng/mL plus cyclophosphamide (CY), 2 x 60 mg/kg, and hemopoietic stem cell (HSC) transplantation from related (n = 45) or unrelated donors (n = 64). At the time of transplantation, 69 patients had less than 5% myeloblasts in the marrow, and 40 patients had more advanced disease. All but 2 evaluable patients had engraftment. The Kaplan-Meier estimates of 3-year relapse-free survival (RFS) were 56% for related and 59% for unrelated recipients. The cumulative incidences of relapse were 16% for related and 11% for unrelated recipients. Nonrelapse mortality (NRM) at 100 days (3 years) was 12% (28%) for related and 13% (30%) for unrelated recipients. The only factor significant for RFS was the etiology of MDS (de novo better than treatment related; P = .03). Factors significantly correlated with relapse were advanced French-American-British classification (P = .002) and International Prognostic Scoring System score (P = .009), poor-risk cytogenetics (P = .03), and treatment-related etiology (P = .03). None of the factors examined was statistically significant for NRM. Patient age and donor type had no significant impact on outcome. RFS tended to be superior in patients receiving transplants with peripheral blood rather than marrow stem cells. Thus, a targeted BUCY regimen provided effective transplant conditioning for patients with MDS receiving transplants from HILA-identical siblings or alternative donors. Although there was still considerable non-relapse morbidity and mortality, the present regimen was used successfully even in patients older than 60 years of age. (C) 2002 by The American Society of Hematology.
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收藏
页码:1201 / 1207
页数:7
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