Division of Bone Marrow Transplantation and Immune Deficiency, Cancer and Blood Disease Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Division of Bone Marrow Transplantation and Immune Deficiency, Cancer and Blood Disease Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Transplant Cell Ther. 2022 Jul;28(7):392.e1-392.e9. doi: 10.1016/j.jtct.2022.04.019. Epub 2022 Apr 29.
Transplantation-associated thrombotic microangiopathy (TA-TMA) can range from a self-limiting condition to a lethal transplantation complication. It is important to identify TA-TMA patients at risk for severe multiorgan endothelial injury to implement targeted therapies in a timely manner. Current therapeutic approaches with complement blockade have improved survival markedly in high-risk TA-TMA patients, yet one-third of these patients respond inadequately to eculizumab therapy. Poor response may indicate that substantial endothelial injury has already occurred and raises the possibility that earlier intervention may improve outcomes. The goal of this study was to identify additional TA-TMA patients who would benefit from early targeted intervention and update TA-TMA risk stratification methods to reflect these findings. We studied 130 HSCT recipients with a diagnosis of TA-TMA who were screened prospectively and stratified into 3 TA-TMA risk groups (high-risk, n = 64; moderate-risk, n = 48; 18 low-risk, n = 18). We specifically examined TA-TMA biomarkers and clinical outcomes in subjects who were not offered complement blocking therapy (moderate-risk and low-risk TA-TMA subjects) and compared them with those who received TA-TMA-targeted therapy (high-risk TA-TMA subjects). One-year post-HSCT survival for subjects with untreated moderate-risk TA-TMA was similar to those with high-risk TA-TMA receiving eculizumab therapy (71% versus 66%; P = .40), indicating that a subset of moderate-risk patients may benefit from therapy. A detailed analysis of moderate-risk subjects highlighted the importance of relative as well as absolute complement pathway activation in determining organ injury. We demonstrated that activated terminal complement (measured by elevated blood sC5b-9) alone is a valuable indicator of reduced survival. Moderate-risk TA-TMA subjects with elevated sC5b-9 levels had a nearly 3-fold higher risk of mortality that was statistically significant in multivariant analyses (P = .01). A "dose effect" also was observed, and higher sC5b-9 levels were associated with worse outcomes. Furthermore, all moderate-risk patients with sustained sC5b-9 elevation for >2 weeks ultimately developed multiorgan dysfunction syndrome (MODS). This indicates that scheduled sC5b-9 measurements could promptly identify patients at risk for poor outcomes and would facilitate early TA-TMA-directed therapy to prevent organ injury. Untreated low-risk TA-TMA patients had a 1-year post-HSCT survival of 94% and should be observed without targeted interventions. Routine TA-TMA screening and complement-blocking therapies have markedly improved the outcomes for high-risk TA-TMA patients, and our study suggests that additional patients may benefit from TA-TMA treatment. This study provides further support for prospective TA-TMA screening as an integral tool for identifying patients at greatest risk for organ injury and death from TA-TMA. An updated TA-TMA risk algorithm that incorporates relevant laboratory biomarkers, clinical findings, and comorbid conditions was generated using this study's findings, and we propose clinical implementation of this algorithm for the management of TA-TMA.
移植相关血栓性微血管病(TA-TMA)可从自限性疾病发展为致命的移植并发症。及时识别有严重多器官内皮损伤风险的 TA-TMA 患者,并实施靶向治疗非常重要。目前,使用补体阻断的治疗方法显著提高了高危 TA-TMA 患者的生存率,但其中三分之一的患者对依库珠单抗治疗反应不足。反应不佳可能表明已经发生了实质性的内皮损伤,并提出了更早干预可能改善结局的可能性。本研究的目的是确定更多可能从早期靶向干预中获益的 TA-TMA 患者,并更新 TA-TMA 风险分层方法以反映这些发现。我们前瞻性研究了 130 名接受 HSCT 并诊断为 TA-TMA 的患者,并将其分层为 3 个 TA-TMA 风险组(高危,n=64;中危,n=48;低危,n=18)。我们特别研究了未接受补体阻断治疗的 TA-TMA 生物标志物和临床结局(中危和低危 TA-TMA 患者),并将其与接受 TA-TMA 靶向治疗的患者(高危 TA-TMA 患者)进行了比较。未接受治疗的中危 TA-TMA 患者在 HSCT 后 1 年的生存率与接受依库珠单抗治疗的高危 TA-TMA 患者相似(71%比 66%;P=0.40),这表明一部分中危患者可能受益于治疗。对中危患者的详细分析强调了相对和绝对补体途径激活在确定器官损伤中的重要性。我们证明,单独升高的末端补体(通过升高的血 sC5b-9 测量)是降低生存率的一个有价值的指标。中危 TA-TMA 患者 sC5b-9 水平升高,其死亡风险几乎增加了 3 倍,在多变量分析中具有统计学意义(P=0.01)。还观察到“剂量效应”,并且更高的 sC5b-9 水平与更差的结局相关。此外,所有持续 sC5b-9 升高超过 2 周的中危患者最终都发展为多器官功能障碍综合征(MODS)。这表明定期的 sC5b-9 测量可以迅速识别预后不良的患者,并有助于早期进行 TA-TMA 靶向治疗以预防器官损伤。未接受治疗的低危 TA-TMA 患者在 HSCT 后 1 年的生存率为 94%,无需进行靶向干预。常规的 TA-TMA 筛查和补体阻断治疗显著改善了高危 TA-TMA 患者的结局,我们的研究表明,更多的患者可能受益于 TA-TMA 治疗。这项研究进一步支持前瞻性 TA-TMA 筛查作为识别有发生 TA-TMA 相关器官损伤和死亡风险的高危患者的重要工具。使用本研究的结果生成了一个包含相关实验室生物标志物、临床发现和合并症的更新的 TA-TMA 风险算法,并提出了该算法在 TA-TMA 管理中的临床实施。