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中国异基因造血干细胞移植后巨细胞病毒感染的流行病学、临床结局及治疗模式:一项范围综述和荟萃分析

Epidemiology, clinical outcomes, and treatment patterns of cytomegalovirus infection after allogeneic hematopoietic stem cell transplantation in China: a scoping review and meta-analysis.

作者信息

Lin Ren, Wu Jingyi, Liu Qifa

机构信息

Department of Hematology, Nanfang Hospital, Southern Medical University, Clinical Medical Research Center of Hematological Diseases of Guangdong Province, Guangzhou, China.

Medical Affairs, Takeda (China) International Trading Company, Shanghai, China.

出版信息

Front Microbiol. 2025 Apr 3;16:1518275. doi: 10.3389/fmicb.2025.1518275. eCollection 2025.


DOI:10.3389/fmicb.2025.1518275
PMID:40248426
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12003426/
Abstract

INTRODUCTION: Cytomegalovirus (CMV) infection poses a significant threat to individuals undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT), potentially resulting in substantial morbidity and mortality. This review summarized the epidemiology, clinical outcomes, and treatment patterns of CMV infection among allo-HSCT recipients in China. METHODS: PubMed, EMBASE, the Cochrane Library, Web of Science, China National Knowledge Infrastructure (CNKI), Wanfang and Chinese Biomedical Literature Database (CBM) were systematically searched from 2013 to March 2023. All analyses were performed using R 4.1.1 software with a random effects model. RESULTS: Fifty-six studies, which included 13,882 patients, were reviewed. The pooled overall incidence of CMV infection was 49.99% [95% confidence interval (CI) 43.72-56.26%]. Among post allo-HSCT recipients with CMV infection, 32.03% (95% CI 22.93-41.12%) developed refractory CMV infection. The overall incidence of CMV disease was 13.30% (95% CI 8.99-19.66%). The pooled all-cause mortality rate was 29.25% (95% CI 17.96-40.55%) and the CMV-related mortality rate was 3.46% (95% CI 1.19-5.73%). Results demonstrate that management of CMV has mainly focused on pre-emptive therapy due to the treatment-limiting toxicity of anti-CMV agents. Additionally, CMV infection is continuing to occur after the discontinuation of prophylaxis, highlighting the unmet need for a more effective treatment without treatment-limiting toxicities. CONCLUSION: This review underscores the urgent need for improved therapeutic strategies to effectively manage cytomegalovirus infection in allo-HSCT recipients, particularly in light of the high incidence and associated morbidity, as well as the limitations of current treatment options. SYSTEMATIC REVIEW REGISTRATION: https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42024513908, identifier: CRD42024513908.

摘要

引言:巨细胞病毒(CMV)感染对接受异基因造血干细胞移植(allo-HSCT)的个体构成重大威胁,可能导致严重的发病和死亡。本综述总结了中国allo-HSCT受者中CMV感染的流行病学、临床结局和治疗模式。 方法:系统检索2013年至2023年3月期间的PubMed、EMBASE、Cochrane图书馆、Web of Science、中国知网(CNKI)、万方和中国生物医学文献数据库(CBM)。所有分析均使用R 4.1.1软件并采用随机效应模型进行。 结果:共纳入56项研究,涉及13882例患者。CMV感染的总体合并发生率为49.99%[95%置信区间(CI)43.72 - 56.26%]。在allo-HSCT后发生CMV感染的受者中,32.03%(95%CI 22.93 - 41.12%)发生难治性CMV感染。CMV疾病的总体发生率为13.30%(95%CI 8.99 - 19.66%)。总体全因死亡率为29.25%(95%CI 17.96 - 40.55%),CMV相关死亡率为3.46%(95%CI 1.19 - 5.73%)。结果表明,由于抗CMV药物的治疗限制性毒性,CMV的管理主要集中在抢先治疗上。此外,预防措施停止后CMV感染仍持续发生,凸显了对更有效且无治疗限制性毒性的治疗方法的未满足需求。 结论:本综述强调迫切需要改进治疗策略,以有效管理allo-HSCT受者中的巨细胞病毒感染,特别是鉴于其高发生率和相关发病率,以及当前治疗选择的局限性。 系统评价注册:https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42024513908,标识符:CRD42024513908。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2526/12003426/abdac21b1ff6/fmicb-16-1518275-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2526/12003426/862bd888ce71/fmicb-16-1518275-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2526/12003426/197ab5668a8d/fmicb-16-1518275-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2526/12003426/471fcc402028/fmicb-16-1518275-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2526/12003426/86829a40db88/fmicb-16-1518275-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2526/12003426/8cf552a17eac/fmicb-16-1518275-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2526/12003426/abdac21b1ff6/fmicb-16-1518275-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2526/12003426/862bd888ce71/fmicb-16-1518275-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2526/12003426/197ab5668a8d/fmicb-16-1518275-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2526/12003426/471fcc402028/fmicb-16-1518275-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2526/12003426/86829a40db88/fmicb-16-1518275-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2526/12003426/8cf552a17eac/fmicb-16-1518275-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2526/12003426/abdac21b1ff6/fmicb-16-1518275-g0006.jpg

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Epidemiology, clinical outcomes, and treatment patterns of cytomegalovirus infection after allogeneic hematopoietic stem cell transplantation in China: a scoping review and meta-analysis.

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本文引用的文献

[1]
Highly stable and immunogenic CMV T cell vaccine candidate developed using a synthetic MVA platform.

NPJ Vaccines. 2024-3-30

[2]
Safety and Immunogenicity of a Messenger RNA-Based Cytomegalovirus Vaccine in Healthy Adults: Results From a Phase 1 Randomized Clinical Trial.

J Infect Dis. 2024-9-23

[3]
Cytomegalovirus Infection after Allogeneic Hematopoietic Cell Transplantation under 100-Day Letermovir Prophylaxis: A Real-World 1-Year Follow-Up Study.

Viruses. 2023-9-6

[4]
[Clinical analysis of the usefulness of letermovir for prevention of cytomegalovirus infection after haploidentical hematopoietic stem cell transplantation].

Zhonghua Nei Ke Za Zhi. 2023-7-1

[5]
Epidemiology, treatment patterns, and disease burden of cytomegalovirus in hematopoietic cell transplant recipients in selected countries outside of Europe and North America: A systematic review.

Transpl Infect Dis. 2023-8

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Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2023-4

[7]
The revised JBI critical appraisal tool for the assessment of risk of bias for randomized controlled trials.

JBI Evid Synth. 2023-3-1

[8]
[The Chinese consensus on the management of cytomegalovirus infection in allogeneic hematopoietic stem cell transplantation patients (2022)].

Zhonghua Xue Ye Xue Za Zhi. 2022-8-14

[9]
[Clinical analysis of the efficacies of ganciclovir plus foscarnet and a single antiviral drug for the treatment of cytomegalovirus infection after haploidentical stem cell transplantation].

Zhonghua Nei Ke Za Zhi. 2023-1-1

[10]
Risk factors for CMV infection within 100 days posttransplantation in patients with acute leukemia.

Blood Sci. 2022-7-20

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