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在接受 PTCy 的无 CMV 暴露的异基因造血干细胞移植人群中,来特莫韦暴露后发生出血性膀胱炎的危险因素。

Risk factors for hemorrhagic cystitis after allogeneic hematopoietic stem cell transplantation in a letermovir-exposed CMV-free population receiving PTCy.

机构信息

UOC Ematologia e Trapianto di cellule staminali emopoietiche, Dipartimento di Diagnostica per Immagini, Radioterapia Oncologica ed Ematologia, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

UOC Clinica Urologica, Dipartimento di Scienze Mediche e Chirurgiche Addominali ed Endocrino Metaboliche, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

出版信息

Eur J Haematol. 2024 Apr;112(4):577-584. doi: 10.1111/ejh.14147. Epub 2024 Jan 6.

Abstract

Hemorrhagic cystitis (HC) is a highly impacting complication in allogeneic hematopoietic stem cell transplantation (HSCT), occurring in 12%-37% of patients. The impact of transplant- and patient-specific variables has been described, with a possible role for JCV and BKV, which may be cooperating with cytomegalovirus (CMV). Here, we analyze 134 letermovir-exposed, CMV-free patients, treated with the same cyclophosphamide-based graft-versus-host disease (GVHD) prophylaxis, describing risk factors for HC. The overall incidence of HC was 23%. Patients with HLA mismatched transplant, higher comorbidity score, and receiving three alkylating agents with TBF (thiotepa, busulfan, and fludarabine) conditioning regimen had a higher risk of HC in multivariate analysis (OR: 4.48, 6.32, and 1.32, respectively). A HC-score including male gender, TBF conditioning, and HLA-mismatch stratifies the risk of HC in the first 100 days after HSCT. The role of BKV and JCV was not highly impacting in those patients, suggesting a possible synergistic effect between CMV and JCV in causing HC. HC can be interpreted as the combination of patient-related factors, chemotherapy-related toxicities-especially due to alkylating agents-and immunological elements.

摘要

出血性膀胱炎 (HC) 是异基因造血干细胞移植 (HSCT) 中一种具有高度影响的并发症,发生于 12%-37%的患者中。已经描述了与移植和患者相关的变量的影响,JC 病毒和 BK 病毒可能具有作用,它们可能与巨细胞病毒 (CMV) 协同作用。在这里,我们分析了 134 例接受来特莫韦暴露、无 CMV 的患者,他们接受了相同的基于环磷酰胺的移植物抗宿主病 (GVHD) 预防方案,描述了 HC 的危险因素。HC 的总发生率为 23%。在多变量分析中,具有 HLA 错配移植、更高的合并症评分以及接受包含三烷化剂(噻替哌、白消安和氟达拉滨)的 TBF(thiotepa,busulfan,and fludarabine)预处理方案的患者发生 HC 的风险更高(OR:4.48、6.32 和 1.32)。在 HSCT 后 100 天内,包含男性、TBF 预处理和 HLA 错配的 HC 评分可对 HC 风险进行分层。在这些患者中,BK 病毒和 JC 病毒的作用并不显著,表明 CMV 和 JC 病毒在引起 HC 方面可能具有协同作用。HC 可以被解释为患者相关因素、与化疗相关的毒性(特别是由于烷化剂)和免疫因素的综合作用。

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