Clinical Outcomes and Treatment Strategies of Adult Transplant‐Associated Thrombotic Microangiopathy: External Validation of Harmonizing Definitions and High‐Risk Criteria

血栓性微血管病 医学 内科学 中止 伊库利珠单抗 队列 移植 相伴的 胃肠病学 钙调神经磷酸酶 造血干细胞移植 入射(几何) 外科 疾病 免疫学 物理 补体系统 抗体 光学
作者
Aldo A. Acosta‐Medina,Meera Sridharan,Ronald S. Go,Ann M. Moyer,Nelson Leung,Maria Alice V. Willrich,Robert Christian Wolf,Rabee Kassis,AlMothana Manasrah,Mira A. Kohorst,Urshila Durani,Aasiya Matin,Mehrdad Hefazi,Saad S. Kenderian,Abhishek A. Mangaonkar,Mithun Vinod Shah,Mark R. Litzow,William J. Hogan,David Dingli,Hassan B. Alkhateeb
出处
期刊:American Journal of Hematology [Wiley]
标识
DOI:10.1002/ajh.27651
摘要

Transplant-associated thrombotic microangiopathy (TA-TMA) is an endothelial dysfunction syndrome observed after allogeneic hematopoietic cell transplant (alloHCT). Our aim was to externally validate the impact of high-risk features on the clinical outcomes of adult patients meeting the updated TA-TMA harmonizing criteria. Between 2005 and 2022, 99 patients were diagnosed with TA-TMA at Mayo Clinic Rochester (incidence 6.2%) after a median of 137 days post alloHCT (IQR: 34-283 days). The development of TA-TMA was associated with an inferior overall survival posttransplant (HR: 3.8, 95% CI: 2.97-4.72). High-risk features, including concomitant infection, acute graft-versus-host disease (GVHD), and organ dysfunction, were associated with poor survival, while LDH elevation was not associated with inferior outcomes. The most common treatment strategy for TA-TMA was discontinuation of calcineurin or mTOR inhibitors in 80 (81%) patients. Thirty (37.5%) patients experienced worsening of GVHD with this strategy, of which 26 (86.7%) patients had died at last follow-up. The most common cause of death among these patients was worsening GVHD (69%; n = 18), followed by infection (11%; n = 3), disease relapse (8%; n = 2), other/unknown causes (8%; n = 2), or TA-TMA (4%; n = 1). Objective response rate (ORR) to initial treatment for the cohort was 56.6%. Eculizumab was used in 11 patients with an observed ORR of 70%, including 5 complete responses. In conclusion, TA-TMA remains a significant contributor to non-relapse mortality and is associated with worse survival following alloHCT. Not all high-risk features, particularly LDH elevation, have consistently demonstrated a negative impact in adult cohorts. Patients with TA-TMA may benefit from immune suppression dose adjustment, rather than a discontinuation, and the addition of complement-directed therapy, particularly among high-risk patients.
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