Dasatinib as Salvage Therapy for Steroid Refractory and Imatinib Resistant or Intolerant Sclerotic Chronic Graft-versus-Host Disease

被引:18
作者
Sanchez-Ortega, Isabel [1 ,2 ]
Servitje, Octavio [3 ,4 ]
Arnan, Montserrat [1 ,4 ]
Orti, Guillermo [1 ,4 ]
Peralta, Teresa [1 ,4 ]
Manresa, Federico [4 ,5 ]
Duarte, Rafael F. [1 ,4 ]
机构
[1] Hosp Duran & Reynals, Catalan Inst Oncol, Dept Clin Hematol, Barcelona, Spain
[2] Univ Autonoma Barcelona, E-08193 Barcelona, Spain
[3] Hosp Univ Bellvitge, Dept Dermatol, Barcelona, Spain
[4] Bellvitge Biomed Res Inst IDIBELL, Barcelona, Spain
[5] Hosp Univ Bellvitge, Barcelona, Spain
关键词
Tirosine kinase inhibitors; Dasatinnib; Sclerotic chronic GVHD; PDGF RECEPTOR; STIMULATORY AUTOANTIBODIES; CHRONIC GVHD; MESYLATE; LEUKEMIA; SURVIVAL; EFFICACY; KINASES;
D O I
10.1016/j.bbmt.2011.10.042
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sclerotic chronic graft-versus-host disease (scGVHD) is a severe form of this disease that resembles systemic sclerosis and has limited and disappointing treatment options. Tyrosine kinase inhibitors (TKI) targeting up-regulated profibrotic pathways, such as imatinib mesylate, have been proposed as a potential therapeutic approach for patients with scGVHD. Dasatinib, a second-generation TKI with a well-established safety and efficacy profile in chronic myeloid leukemia patients, who are refractory or intolerant to imatinib, has also shown potent antifibrotic effects. We present here the first direct clinical evidence, from 3 patients treated in a small single-center series, suggesting that dasatinib can be a therapeutic option for patients with severe scGVHD resistant or intolerant to imatinib. All patients achieved partial response, with improvement in scGHVD target organs severity, joint mobility, lung impairment, and deep fibrotic lesions. This clinical response has remained stable or continued to improve after a median of 22 months (20-25) on dasatinib treatment, with very good tolerance. In addition, corticosteroids could be discontinued or significantly reduced in all patients. This clinical evidence suggests that dasatinib could be a safe and effective alternative for scGVHD patients refractory to corticosteroids and resistant or intolerant to imatinib. Based on these preliminary findings, and in order to address appropriate patient selection, time of intervention, and choice of drug, future larger studies should more formally establish the efficacy and safety of second-generation TKI for the treatment of scGVHD.
引用
收藏
页码:318 / 323
页数:6
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