Deeg H Joachim
Fred Hutchinson Cancer Research Center, Seattle, WA 98109-1024, USA.
Blood. 2007 May 15;109(10):4119-26. doi: 10.1182/blood-2006-12-041889. Epub 2007 Jan 18.
Graft-versus-host disease (GVHD) after allogeneic hematopoietic cell transplantation (HCT) is associated with considerable morbidity and mortality, particularly in patients who do not respond to primary therapy, which usually consists of glucocorticoids (steroids). Approaches to therapy of acute GVHD refractory to "standard" doses of steroids have ranged from increasing the dose of steroids to the addition of polyclonal or monoclonal antibodies, the use of immunotoxins, additional immunosuppressive/chemotherapeutic interventions, phototherapy, and other means. While many pilot studies have yielded encouraging response rates, in most of these studies long-term survival was not improved in comparison with that seen with the use of steroids alone. A major reason for failure has been the high rate of infections, including invasive fungal, bacterial, and viral infections. It is difficult to conduct controlled prospective trials in the setting of steroid-refractory GVHD, and a custom-tailored therapy dependent upon the time after HCT, specific organ manifestations of GVHD, and severity is appropriate. All patients being treated for GVHD should also receive intensive prophylaxis against infectious complications.
异基因造血细胞移植(HCT)后的移植物抗宿主病(GVHD)与相当高的发病率和死亡率相关,尤其是在对通常由糖皮质激素(类固醇)组成的初始治疗无反应的患者中。对于对“标准”剂量类固醇难治的急性GVHD的治疗方法包括增加类固醇剂量、添加多克隆或单克隆抗体、使用免疫毒素、额外的免疫抑制/化疗干预、光疗及其他方法。虽然许多初步研究取得了令人鼓舞的缓解率,但在大多数这些研究中,与单独使用类固醇相比,长期生存率并未提高。失败的一个主要原因是感染率高,包括侵袭性真菌、细菌和病毒感染。在类固醇难治性GVHD的情况下进行对照前瞻性试验很困难,根据HCT后的时间、GVHD的特定器官表现和严重程度进行定制治疗是合适的。所有接受GVHD治疗的患者也应接受针对感染性并发症的强化预防。