Center for International Blood and Marrow Transplant Research, Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Department of Pediatrics, Duke University, Durham, North Carolina.
Biol Blood Marrow Transplant. 2017 Oct;23(10):1714-1721. doi: 10.1016/j.bbmt.2017.06.023. Epub 2017 Jul 3.
The Blood and Marrow Transplant Clinical Trials Network (BMT CTN 0501) randomized children with hematologic malignancies to transplantation with 1 or 2 cord blood units (UCB) between 2006 and 2012. While the trial concluded that survival was similar regardless of number of units infused, survival was better than previously reported. This prompted a comparison of survival of trial versus nontrial patients to determine the generalizability of trial results and whether survival was better because of the trial treatment regimen. During the trial period, 396 recipients of a single UCB unit met trial eligibility but were not enrolled. Trial patients (n = 100) received total body irradiation (TBI) 1320 cGy, cyclophosphamide 120 mg/kg, and fludarabine 75 mg/m (TCF). Nontrial patients either received the same regimen (n = 62; nontrial TCF) or alternative regimens (n = 334; nontrial regimens). Five-year survival between trial and nontrial patients conditioned with TCF was similar (70% versus 62%). However, 5-year survival was significantly lower with nontrial TBI-containing (47%; hazard ratio [HR], 1.97; P = .001) and chemotherapy-only regimens (49%; HR, 1.87; P = .007). The results of BMT CTN 0501 appear generalizable to the population of trial-eligible patients. The survival difference between the trial-specified regimen and other regimens indicate the importance of conditioning regimen for UCB transplantation.
2006 年至 2012 年期间,血液和骨髓移植临床试验网络(BMT CTN 0501)将血液恶性肿瘤患儿随机分为接受 1 或 2 个脐带血单位(UCB)移植。虽然该试验的结论是输注的单位数量对生存率没有影响,但生存率却好于之前的报道。这促使人们比较了试验和非试验患者的生存率,以确定试验结果的普遍性,以及生存率的提高是否是由于试验治疗方案。在试验期间,396 名符合单份 UCB 单位入选条件但未入选的受者。试验患者(n=100)接受全身照射(TBI)1320cGy、环磷酰胺 120mg/kg 和氟达拉滨 75mg/m2(TCF)。非试验患者接受相同的方案(n=62;非试验 TCF)或替代方案(n=334;非试验方案)。TCF 预处理的试验和非试验患者的 5 年生存率相似(70%与 62%)。然而,非试验 TBI 方案(47%;风险比 [HR],1.97;P=.001)和化疗方案(49%;HR,1.87;P=.007)的 5 年生存率明显较低。BMT CTN 0501 的结果似乎可推广至符合入选条件的患者人群。试验规定方案与其他方案之间的生存差异表明 UCB 移植的预处理方案对生存的重要性。