异体造血干细胞移植后HHV-6脑炎预后的最新进展。

IF 3.6 3区 医学 Q2 HEMATOLOGY
Kazuya Kurihara, Daichi Sadato, Takashi Toya, Chizuko Hirama, Kana Kato, Kaori Kondo, Yasutaka Sadaga, Chika Kato, Masashi Shimabukuro, Atsushi Jinguji, Fumihiko Ouchi, Hiroaki Shimizu, Yuho Najima, Yuka Harada, Noriko Doki
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引用次数: 0

摘要

背景:人疱疹病毒6 (HHV-6)脑炎是异基因造血干细胞移植(alloo - hsct)后罕见但致命的并发症。尽管移植结果和支持治疗取得了进展,但关于HHV-6脑炎的临床特征和预后因素的知识仍然有限。目的:本研究旨在阐明同种异体造血干细胞移植受者HHV-6脑炎的临床特征,并确定预后因素。研究设计:这是一项单中心回顾性研究,分析了2004年至2023年在我所接受同种异体造血干细胞移植的HHV-6脑炎患者。通过出现神经系统症状和实时聚合酶链反应检测脑脊液中HHV-6 DNA,证实了HHV-6脑炎的诊断。结果:53例患者纳入本研究。从同种异体造血干细胞移植到HHV-6脑炎发病的中位时间为24天(范围:3-189天)。在53例患者中,38例(71.7%)接受了全身性类固醇治疗,从类固醇开始到脑炎发作的中位间隔为11天(范围:2-46天)。脑炎诊断后的一年总生存率和非复发死亡率(NRM)分别为33.5%和46.5%。虽然HHV-6脑炎直接导致1例死亡,但与HHV-6无关的感染是死亡的主要原因(47.5%)。近期病例从发病到开始抗病毒治疗的间隔时间显著缩短(2018年后0.0天vs. 2017年前1.5天:p = 0.0086),1年NRM显著降低(26.8 vs. 62.1%; = 0.024页)。多因素分析显示,2017年之前的同种异体移植(风险比[HR] 3.13, p = 0.012)和单倍体移植(风险比[HR] 3.07, p = 0.001)是NRM的独立预后因素。在开始HHV-6脑炎治疗后存活超过100天的32例患者中,16例(50.0%)的神经系统后遗症持续存在,包括11例的短期记忆障碍。结论:总的来说,我们的研究表明,最近同种异体造血干细胞移植后HHV-6脑炎预后的改善可能是早期开始抗病毒治疗的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recent Advances in the Prognosis of HHV-6 Encephalitis Following Allogeneic Hematopoietic Stem Cell Transplantation.

Human herpesvirus-6 (HHV-6) encephalitis is a rare but fatal complication following allogeneic hematopoietic stem cell transplantation (allo-HSCT). Despite advancements in transplantation outcomes and supportive care, knowledge regarding the clinical features and prognostic factors of HHV-6 encephalitis remains limited. This study aims to clarify the clinical characteristics of HHV-6 encephalitis in allo-HSCT recipients and to identify prognostic factors. This is a single-center retrospective study that analyzed the patients with HHV-6 encephalitis who underwent allo-HSCT at our institute between 2004 and 2023. The diagnosis of HHV-6 encephalitis was confirmed by the presence of neurological symptoms and the detection of HHV-6 DNA in the cerebrospinal fluid using real-time polymerase chain reaction. Fifty-three patients were included in this study. The median time from allo-HSCT to HHV-6 encephalitis onset was 24 days (range: 3 to 189). Of the 53 patients, 38 (71.7%) received systemic steroids, with a median interval of 11 days (range: 2 to 46) from steroid initiation to encephalitis onset. One-year overall survival and non-relapse mortality (NRM) after encephalitis diagnosis were 33.5% and 46.5%, respectively. While HHV-6 encephalitis directly caused one death, infections unrelated to HHV-6 were the leading cause of mortality (47.5%). The interval from the onset to the initiation of antiviral therapy was significantly shorter in recent cases (0.0 after 2018 versus 1.5 days before 2017: P = .0086), and 1-year NRM was significantly lower (26.8 versus 62.1%; P = .024). Multivariate analysis revealed that allo-HSCT before 2017 (hazard ratio [HR] 3.13, P = .012) and haploidentical transplantation (HR 3.07, P = .001) were independent prognostic factors for NRM. Among the 32 patients who survived for over 100 days after the initiation of HHV-6 encephalitis treatment, neurological sequelae persisted in 16 (50.0%) cases, including short-term memory impairment in 11. Overall, our study indicates that recent improvements in HHV-6 encephalitis outcomes after allo-HSCT likely result from earlier initiation of antiviral treatment.

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CiteScore
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