Kennedy G A, Butler J, Western R, Morton J, Durrant S, Hill G R
Department of Haematology, Royal Brisbane and Women's Hospital, Brisbane, Queensland 4029, Australia.
Bone Marrow Transplant. 2006 Jun;37(12):1143-7. doi: 10.1038/sj.bmt.1705380. Epub 2006 May 8.
Antitumor necrosis factor-alpha antibodies are increasingly being used for the treatment of steroid-refractory acute graft-versus-host disease (GVHD) complicating allogeneic stem cell transplantation. We retrospectively reviewed the outcomes of 16 patients with refractory acute predominantly visceral GVHD treated with combination antithymocyte globulin (ATG), tacrolimus and etanercept +/- mycophenolate mofetil (MMF) at our institution. Overall response rate (CR+PR) was 81%, with median survival post commencing salvage immunosuppression 224 days (range 20-1216 days). In total, eight patients (50%) died, including from progressive GVHD in two cases (13%), infection in five (31%) and relapse of underlying malignancy in one (6%). In comparison to our previous experience of ATG+tacrolimus as treatment for refractory visceral GVHD, both response rate and overall survival were improved with addition of etanercept, with no apparent increase in infectious complications. As such, use of etanercept in combination with ATG +/- MMF for treatment of steroid refractory acute GVHD appears to be associated with high response rates, significant survival and no unexpected toxicity. Further study of this immunosuppression combination in a larger cohort of patients in this setting is indicated.
抗肿瘤坏死因子-α抗体越来越多地用于治疗异基因干细胞移植后并发的类固醇难治性急性移植物抗宿主病(GVHD)。我们回顾性分析了我院16例以内脏为主的难治性急性GVHD患者,这些患者接受了抗胸腺细胞球蛋白(ATG)、他克莫司和依那西普联合治疗(±霉酚酸酯)。总体缓解率(CR+PR)为81%,开始挽救性免疫抑制后的中位生存期为224天(范围20-1216天)。共有8例患者(50%)死亡,其中2例(13%)死于进行性GVHD,5例(31%)死于感染,1例(6%)死于潜在恶性肿瘤复发。与我们之前使用ATG+他克莫司治疗难治性内脏GVHD的经验相比,添加依那西普后缓解率和总生存期均有所改善,感染并发症无明显增加。因此,依那西普联合ATG(±MMF)治疗类固醇难治性急性GVHD似乎具有高缓解率、显著生存期且无意外毒性。有必要在更大规模的患者队列中对这种免疫抑制联合方案进行进一步研究。