Department of Hematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.
Blood and Marrow Transplant Program, Cleveland Clinic, Cleveland, Ohio.
Biol Blood Marrow Transplant. 2018 Oct;24(10):1961-1964. doi: 10.1016/j.bbmt.2018.06.025. Epub 2018 Jun 25.
Systemic sclerosis is a progressive inflammatory disease that is frequently fatal and has limited treatment options. High-dose chemotherapy with autologous hematopoietic cell transplantation (AHCT) has been evaluated as treatment for this disease in observational studies, multicenter randomized controlled clinical trials, and meta-analyses. On behalf of the American Society for Blood and Marrow Transplantation (ASBMT), a panel of experts in transplantation and rheumatology was convened to review available evidence and make a recommendation on AHCT as an indication for systemic sclerosis. Three randomized trials have compared the efficacy of AHCT with cyclophosphamide only, and all demonstrated benefit for the AHCT arm for their primary endpoint (improvement in the American Scleroderma Stem Cell versus Immune Suppression Trial, event-free survival in Autologous Stem Cell Transplantation International Scleroderma trial, and change in global rank composite score in Scleroderma: Cyclophosphamide or Transplantation trial). AHCT recipients also had better overall survival and a lower rate of disease progression. These findings have been confirmed in subsequent meta-analyses. Based on this high-quality evidence, the ASBMT recommends systemic sclerosis should be considered as a "standard of care" indication for AHCT. Close collaboration between rheumatologists and transplant clinicians is critical for optimizing patient selection and patient outcomes. Transplant centers in the United States are strongly encouraged to report patient and outcomes data to the Center for International Blood and Marrow Transplant Research on their patients receiving AHCT for this indication.
系统性硬化症是一种进行性炎症性疾病,常导致死亡,且治疗选择有限。高剂量化疗联合自体造血细胞移植(AHCT)已在观察性研究、多中心随机对照临床试验和荟萃分析中被评估为该疾病的治疗方法。代表美国血液和骨髓移植学会(ASBMT),一个移植和风湿病学专家小组被召集来审查现有证据,并就 AHCT 作为系统性硬化症的适应证提出建议。三项随机试验比较了 AHCT 与环磷酰胺单独治疗的疗效,所有试验均表明 AHCT 组在其主要终点(美国硬皮病干细胞与免疫抑制试验的改善、自体干细胞移植国际硬皮病试验的无事件生存、硬皮病:环磷酰胺或移植试验的全球排名综合评分变化)方面具有获益。AHCT 受者的总生存率更高,疾病进展率更低。这些发现已在随后的荟萃分析中得到证实。基于这一高质量证据,ASBMT 建议系统性硬化症应被视为 AHCT 的“标准治疗”适应证。风湿病学家和移植临床医生之间的密切合作对于优化患者选择和患者结局至关重要。强烈鼓励美国的移植中心报告接受 AHCT 治疗该适应证的患者的患者和结局数据给国际血液和骨髓移植研究中心。