Division of Bone Marrow Transplantation and Immune Deficiency, Cancer and Blood Disease Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.
Blood. 2024 Mar 21;143(12):1112-1123. doi: 10.1182/blood.2023022526.
High-risk, complement mediated, untreated transplant-associated thrombotic microangiopathy (hrTMA) has dismal outcomes due to multi-organ dysfunction syndrome (MODS). The complement C5 blocker eculizumab shows promising results in hrTMA, but has not been prospectively studied in hematopoietic stem cell transplant (HCT) recipients. We performed the first multi-institutional prospective study in children and young adults to evaluate eculizumab as an early targeted intervention for hrTMA/MODS. We hypothesized that eculizumab would more than double survival in HCT recipients with hrTMA, compared to our prior study of prospectively screened, untreated hrTMAs serving as historical controls. HrTMA features (elevated terminal complement (sC5b-9) and proteinuria measured by random urine protein/creatinine ratio (≥1mg/mg)) were required for inclusion. The primary endpoint was survival at 6 six-months from hrTMA diagnosis. Secondary endpoints were cumulative incidence of MODS 6 months after hrTMA diagnosis and 1-year posttransplant survival. Eculizumab dosing included intensive loading, induction, and maintenance phases for up to 24 weeks of therapy. All 21 evaluated study subjects had MODS. Primary and secondary study endpoints were met by demonstrating survival of 71% (P < .0001) 6 months after hrTMA diagnosis and 62% 1 year after transplant. Of fifteen survivors, 11 (73%) fully recovered organ function and are well. Our study demonstrates significant improvement in survival and recovery of organ function in hrTMA using an intensified eculizumab dosing and real time biomarker monitoring. This study serves as a benchmark for planning future studies that should focus on preventative measures or targeted therapy to be initiated prior to organ injury. This trial was registered at www.clinicaltrials.gov as #NCT03518203.
高危、补体介导、未经治疗的移植相关血栓性微血管病(hrTMA)由于多器官功能障碍综合征(MODS)而预后不良。补体 C5 抑制剂依库珠单抗在 hrTMA 中显示出良好的效果,但尚未在造血干细胞移植(HCT)受者中进行前瞻性研究。我们进行了第一项针对儿童和年轻成人的多机构前瞻性研究,以评估依库珠单抗作为 hrTMA/MODS 的早期靶向干预措施。我们假设,与我们之前前瞻性筛选、未经治疗的 hrTMA 作为历史对照的研究相比,依库珠单抗将使 HCT 受者的生存率提高一倍以上。hrTMA 的特征(通过随机尿蛋白/肌酐比值(≥1mg/mg)测量的终末补体(sC5b-9)升高和蛋白尿)需要纳入。主要终点是从 hrTMA 诊断后 6 个月的生存率。次要终点是 hrTMA 诊断后 6 个月和移植后 1 年的 MODS 累积发生率。依库珠单抗的剂量包括强化负荷、诱导和维持期,最长可达 24 周的治疗。所有 21 例评估的研究对象均有 MODS。通过证明 71%(P<0.0001)的生存率达到 hrTMA 诊断后 6 个月和移植后 1 年的主要和次要研究终点。在 15 名幸存者中,11 名(73%)完全恢复了器官功能且状况良好。本研究表明,通过强化依库珠单抗剂量和实时生物标志物监测,在使用依库珠单抗治疗 hrTMA 方面,生存率和器官功能恢复均显著提高。该研究为计划未来研究提供了基准,未来研究应侧重于在器官损伤前启动预防措施或靶向治疗。该试验在 www.clinicaltrials.gov 上注册为 #NCT03518203。