Cyclosporine and mycophenolate mofetil prophylaxis with fludarabine and melphalan conditioning for unrelated donor transplantation: a prospective study of 22 patients with hematologic malignancies

被引:24
作者
Rodriguez, R
Parker, P
Nademanee, A
Smith, D
O'Donnell, MR
Stein, A
Snyder, DS
Fung, HC
Krishnan, AY
Popplewell, L
Cohen, S
Somlo, G
Angelopoulou, M
Al-Kadhimi, Z
Falk, PM
Spielberger, R
Kogut, N
Sahebi, F
Senitzer, D
Slovak, M
Schriber, J
Forman, SJ
机构
[1] City Hope Natl Med Ctr, Div Hematol & Bone Marrow Transplantat, Duarte, CA 91010 USA
[2] So Calif Permanente Med Grp, Los Angeles, CA 90027 USA
[3] City Hope Good Samaritan Bone Marrow Transplantat, Phoenix, AZ USA
关键词
adult; graft-versus-host disease; hematopoietic cell transplantation; unrelated donor; reduced-intensity conditioning;
D O I
10.1038/sj.bmt.1704493
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In an attempt to decrease toxicity in high-risk patients undergoing unrelated donor hematopoietic stem cell transplantation (URD HSCT), we tested a combination of cyclosporine (CSP) and mycophenolate mofetil (MMF) as graft-versus-host disease (GVHD) prophylaxis with the reduced-intensity conditioning regimen fludarabine/melphalan (Flu/Mel). A total of 22 adult patients with advanced myeloid (n = 15) and lymphoid (n = 7) malignancies were treated. All patients received Flu 25 mg/m(2) for 5 days and Mel 140 mg/m(2), with CSP 3 mg/kg daily and MMF 15 mg/kg three times a day. The median age was 49 years (range 18-66). Durable engraftment was seen in all but one patient with myelobrosis. The 1-year nonrelapse mortality was 32%, 27% from GVHD. The cumulative incidence of acute GVHD grade 2-4 and 3-4 was 63 and 41%, respectively. With a median follow-up of 18 months, the disease-free survival (DFS) and overall survival ( OS) are 55 and 59%, respectively. For patients with AML and MDS (n = 14), the DFS and OS is 71%. For patients undergoing a second transplant ( n 14), the DFS and OS is 57%. In conclusion, this regimen is associated with acceptable toxicity but high rates of GVHD in high-risk patients undergoing URD HSCT. Encouraging disease control for patients with advanced myeloid malignancies was observed.
引用
收藏
页码:1123 / 1129
页数:7
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