Safety and efficacy of low-dose methotrexate for pediatric patients with steroid-refractory acute graft-versus-host disease after hematopoietic stem cell transplantation

被引:10
作者
Inagaki, Jiro [1 ]
Fukano, Reiji [1 ]
Kodama, Yuichi [1 ]
Nishimura, Miho [1 ]
Shimokawa, Mototsugu [2 ]
Okamura, Jun [1 ]
机构
[1] Kyushu Natl Canc Ctr, Dept Pediat, Minami Ku, Fukuoka 8111395, Japan
[2] Kyushu Natl Canc Ctr, Inst Clin Res, Minami Ku, Fukuoka 8111395, Japan
关键词
Low-dose methotrexate; Acute graft-versus-host disease; Opportunistic infection; Children; BONE-MARROW-TRANSPLANTATION; NECROSIS-FACTOR-ALPHA; THERAPY; CYCLOSPORINE; PROPHYLAXIS; MTX;
D O I
10.1007/s00277-013-1923-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Low-dose methotrexate (LD-MTX) has long been included in prophylaxis regimens for acute graft-versus-host disease (aGVHD). In addition, LD-MTX is expected as a treatment option to control aGVHD by regulating the cytokine network. In this study, we retrospectively evaluated 35 patients with steroid-refractory acute GVHD to evaluate the safety and efficacy of LD-MTX as a salvage treatment. LD-MTX was administered weekly at a dose of 10 mg/m(2). Overall, 13 patients (37 %) achieved complete response and three (9 %) achieved partial response within 4 weeks after LD-MTX was initiated without any additional agents. Resolution of manifestations of aGVHD in each evaluable organ was observed in 12 of the 23 cases (52 %) with skin aGVHD and in eight of the 23 cases (35 %) with GI aGVHD. Neutropenia and thrombocytopenia (grades III and IV) were observed in nine (26 %) and 17 patients (49 %), respectively. Fatal infectious complications occurred in only three patients (9 %) after LD-MTX treatment. Of the 35 patients studied, 22 were alive with a median follow-up of 60 months and an overall survival rate (Kaplan-Meier estimate) was 62 %. LD-MTX seems suitable for salvage therapy and will not increase risk of infection. Further evaluation of the use of LD-MTX as salvage therapy for steroid-refractory acute GVHD is warranted.
引用
收藏
页码:645 / 651
页数:7
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