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巨细胞病毒再激活在急性淋巴细胞白血病异基因造血干细胞移植后复发中的作用

Role of cytomegalovirus reactivation on relapse after allogeneic hematopoietic stem cell transplantation in acute lymphoblastic leukemia.

作者信息

Mekni Sabrine, Ben Abdeljelil Nour, Ouerghi Rihab, Kanoun Rimmel Yosra, Frigui Siwar, Belloumi Dorra, Ben Yaiche Insaf, Turki Ines, Chabaane Anna, Torjemane Lamia, Ben Othman Tarek

机构信息

Hematology Tunis El Manar University.

hematology Tunis El Manar University.

出版信息

Clin Hematol Int. 2024 Dec 5;6(4):125912. doi: 10.46989/001c.125912. eCollection 2024.

DOI:10.46989/001c.125912
PMID:39655058
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11626770/
Abstract

Cytomegalovirus reactivation (CMV-R) is a frequent complication post-allogeneic hematopoietic stem cell transplantation (allo-HSCT), associated with poor outcomes. Previous studies have demonstrated the protective effect of CMV-R against relapse after allo-HSCT for acute myeloblastic leukemia (AML). However, this impact remains unclear in acute lymphoblastic leukemia (ALL). We conducted a retrospective study on 81 patients with ALL who received allo-HSCT after myeloablative conditioning regimen from matched sibling donors between 2016 and 2022. All patients underwent weekly monitoring for CMV-R by quantitative polymerase chain reaction assay from engraftment until day +100 post allo-HSCT, and received antiviral prophylaxis with acyclovir from day +1 to 6 months after allo-HSCT. Preemptive treatment was initiated when a viremia was higher than 150 copies/mL. The median age was 20 years (range, 5-50 years). After allo-HSCT, 35% of patients developed CMV-R after a median of 39 days (range, 19-100 days). After a median follow-up of 30 months (range, 1-93 months), CMV-R was an independent factor associated with lower cumulative incidence of relapse (CIR) (OR: 0.17; 95% CI [0.03 - 0.98], p = 0.04) without survival benefit. Further studies are needed to validate the protective effect of CMV-R on ALL relapse.

摘要

巨细胞病毒再激活(CMV-R)是异基因造血干细胞移植(allo-HSCT)后常见的并发症,与不良预后相关。既往研究已证实CMV-R对急性髓细胞白血病(AML)异基因造血干细胞移植后复发具有保护作用。然而,在急性淋巴细胞白血病(ALL)中,这种影响尚不清楚。我们对2016年至2022年间接受来自匹配同胞供者的清髓性预处理方案后进行allo-HSCT的81例ALL患者进行了一项回顾性研究。所有患者从植入开始至allo-HSCT后第100天每周通过定量聚合酶链反应检测监测CMV-R,并在allo-HSCT后第1天至6个月接受阿昔洛韦抗病毒预防。当病毒血症高于150拷贝/mL时开始进行抢先治疗。中位年龄为20岁(范围5-50岁)。allo-HSCT后,35%的患者在中位39天(范围19-100天)后发生CMV-R。在中位随访30个月(范围1-93个月)后,CMV-R是与较低的累积复发率(CIR)相关的独立因素(OR:0.17;95%CI[0.03-0.98],p=0.04),但无生存获益。需要进一步研究来验证CMV-R对ALL复发的保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0bc/11626770/b6463832aa6d/chi_2024_6_4_125912_253597.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0bc/11626770/2f579795bfe7/chi_2024_6_4_125912_253592.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0bc/11626770/4143a4ecca63/chi_2024_6_4_125912_253593.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0bc/11626770/9964e3e9e8f0/chi_2024_6_4_125912_253594.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0bc/11626770/8c950361e9fa/chi_2024_6_4_125912_253595.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0bc/11626770/6f82a5c31d6b/chi_2024_6_4_125912_253596.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0bc/11626770/b6463832aa6d/chi_2024_6_4_125912_253597.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0bc/11626770/2f579795bfe7/chi_2024_6_4_125912_253592.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0bc/11626770/4143a4ecca63/chi_2024_6_4_125912_253593.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0bc/11626770/9964e3e9e8f0/chi_2024_6_4_125912_253594.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0bc/11626770/8c950361e9fa/chi_2024_6_4_125912_253595.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0bc/11626770/6f82a5c31d6b/chi_2024_6_4_125912_253596.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0bc/11626770/b6463832aa6d/chi_2024_6_4_125912_253597.jpg

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本文引用的文献

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Ann Hematol. 2024 Mar;103(3):917-933. doi: 10.1007/s00277-023-05509-7. Epub 2024 Jan 16.
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CMV reactivation after allogeneic HCT is associated with a reduced risk of relapse in acute lymphoblastic leukemia.异基因造血干细胞移植后 CMV 再激活与急性淋巴细胞白血病复发风险降低相关。
Blood Adv. 2023 Jun 27;7(12):2699-2708. doi: 10.1182/bloodadvances.2022009376.
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New trends in the management of cytomegalovirus infection after allogeneic hematopoietic cell transplantation: a survey of the Infectious Diseases Working Pary of EBMT.
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Bone Marrow Transplant. 2023 Feb;58(2):203-208. doi: 10.1038/s41409-022-01863-8. Epub 2022 Nov 17.
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Outcomes of Refractory Cytomegalovirus Infection in the First Year after Allogeneic Hematopoietic Cell Transplantation.异基因造血细胞移植后第一年难治性巨细胞病毒感染的结果。
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