Pediatric Blood and Marrow Transplantation Program, Duke University Medical Center, Durham, North Carolina.
The Emmes Corporation, Rockville, Maryland.
Biol Blood Marrow Transplant. 2014 Mar;20(3):326-36. doi: 10.1016/j.bbmt.2013.11.021. Epub 2013 Dec 1.
Reduced-intensity conditioning (RIC) regimens have the potential to decrease transplantation-related morbidity and mortality. However, engraftment failure has been prohibitively high after RIC unrelated umbilical cord blood transplantation (UCBT) in chemotherapy-naïve children with nonmalignant diseases (NMD). Twenty-two children with a median age of 2.8 years, many with severe comorbidities and prior viral infections, were enrolled in a novel RIC protocol consisting of hydroxyurea, alemtuzumab, fludarabine, melphalan, and thiotepa followed by single UCBT. Patients underwent transplantation for inherited metabolic disorders (n = 8), primary immunodeficiencies (n = 9), hemoglobinopathies (n = 4) and Diamond Blackfan anemia (n = 1). Most umbilical cord blood (UCB) units were HLA-mismatched with median infused total nucleated cell dose of 7.9 × 10(7)/kg. No serious organ toxicities were attributable to the regimen. The cumulative incidence of neutrophil engraftment was 86.4% (95% confidence interval [CI], 65% to 100%) in a median of 20 days, with the majority sustaining > 95% donor chimerism at 1 year. Cumulative incidence of acute graft-versus-host disease (GVHD) grades II to IV and III to IV by day 180 was 27.3% (95% CI, 8.7% to 45.9%) and 13.6% (95 CI, 0% to 27.6%), respectively. Cumulative incidence of extensive chronic GVHD was 9.1% (95% CI, 0% to 20.8%). The primary causes of death were viral infections (n = 3), acute GVHD (n = 1) and transfusion reaction (n = 1). One-year overall and event-free survivals were 77.3% (95% CI, 53.7% to 89.8%) and 68.2% (95% CI, 44.6% to 83.4%) with 31 months median follow-up. This is the first RIC protocol demonstrating durable UCB engraftment in children with NMD. Future risk-based modifications of this regimen could decrease the incidence of viral infections. (www.clinicaltrials.gov/NCT00744692).
减强度预处理(RIC)方案有可能降低移植相关的发病率和死亡率。然而,在未接受预处理的无关脐血造血干细胞移植(UCBT)后,RIC 方案在化疗初治的非恶性疾病(NMD)儿童中导致植活失败率极高。
22 例中位年龄为 2.8 岁的儿童,其中许多人合并严重合并症和既往病毒感染,接受了一种新的 RIC 方案治疗,该方案包括羟基脲、阿仑单抗、氟达拉滨、美法仑和噻替哌,随后进行单 UCBT。患者因遗传性代谢疾病(n=8)、原发性免疫缺陷(n=9)、血红蛋白病(n=4)和 Diamond Blackfan 贫血(n=1)而接受移植。大多数脐血(UCB)单位与 HLA 不合,中位数输注的总核细胞剂量为 7.9×10(7)/kg。该方案无严重的器官毒性。中性粒细胞植入的累积发生率为 86.4%(95%CI,65%至 100%),中位数时间为 20 天,大多数患者在 1 年内维持>95%的供者嵌合状态。180 天时急性移植物抗宿主病(GVHD)Ⅱ至Ⅳ级和Ⅲ至Ⅳ级的累积发生率分别为 27.3%(95%CI,8.7%至 45.9%)和 13.6%(95%CI,0%至 27.6%)。广泛慢性 GVHD 的累积发生率为 9.1%(95%CI,0%至 20.8%)。主要死亡原因为病毒感染(n=3)、急性 GVHD(n=1)和输血反应(n=1)。1 年总生存率和无事件生存率分别为 77.3%(95%CI,53.7%至 89.8%)和 68.2%(95%CI,44.6%至 83.4%),中位随访时间为 31 个月。这是首例在 NMD 儿童中显示出持久的 UCB 植活的 RIC 方案。对该方案进行基于风险的修改,可能会降低病毒感染的发生率。(www.clinicaltrials.gov/NCT00744692)。