Suppr超能文献

成人脐带血移植后延长疗程更昔洛韦预防巨细胞病毒感染。

Extended-duration letermovir prophylaxis for cytomegalovirus infection after cord blood transplantation in adults.

机构信息

Adult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Department of Medicine, Weill Cornell Medical College, New York, NY.

出版信息

Blood Adv. 2022 Dec 27;6(24):6291-6300. doi: 10.1182/bloodadvances.2022008047.

Abstract

Cord blood transplantation (CBT) can be complicated by a high incidence of clinically significant cytomegalovirus infection (csCMVi). We have investigated the efficacy of extended letermovir prophylaxis in seropositive adult CBT recipients. The aim was to continue prophylaxis for ≥6 months (insurance permitting). By day 100, the incidence of csCMVi was 0% in 28 patients who received letermovir prophylaxis. Moreover, of 24 patients alive at day 100, none had csCMVi by day 180, having continued prophylaxis for all (n = 20) or part (n = 4) of that period. Overall, 20 patients stopped letermovir at a median of 354 days (range, 119-455 days) posttransplant, with only 5 requiring 1 (n = 4) or 2 (n = 1) courses of valganciclovir (median total duration, 58 days; range, 12-67 days) for postprophylaxis viremia, with no subsequent csCMVi. There were no toxicities attributable to letermovir. Of the 62 historic control subjects who received acyclovir only, 51 developed csCMVi (median onset, 34 days; range, 5-74 days), for a day 100 incidence of 82% (95% confidence interval, 73-92). Seven patients developed proven/probable CMV disease, and 6 died before day 100 (3 with proven/probable CMV pneumonia). Forty-five patients required extended therapy during the first 6 months for 1 (n = 10), 2 (n = 14), or 3/persistent (n = 21) csCMVi, with 43 (84%) of 51 developing significant treatment toxicities. Letermovir is a highly effective, well-tolerated prophylaxis that mitigates CMV infection, CMV-related mortality, and antiviral therapy toxicities in CBT recipients. Our data support prophylaxis duration of at least 6 months after CBT.

摘要

脐带血移植(CBT)可能会出现临床显著巨细胞病毒感染(csCMVi)的高发病率。我们研究了延长洛韦预防在血清阳性成人 CBT 受者中的疗效。目的是在保险允许的情况下继续预防治疗≥6 个月。在 28 例接受洛韦预防的患者中,第 100 天 csCMVi 的发生率为 0%。此外,在第 100 天存活的 24 例患者中,在继续预防治疗(n=20)或部分预防治疗(n=4)的所有患者中,在第 180 天均未出现 csCMVi。总体而言,20 例患者在移植后中位数 354 天(范围 119-455 天)停止使用洛韦,只有 5 例需要 1(n=4)或 2(n=1)个疗程更昔洛韦(中位数总疗程 58 天;范围 12-67 天)用于预防后病毒血症,随后无 csCMVi。没有归因于洛韦的毒性。在仅接受阿昔洛韦的 62 例历史对照中,51 例发生 csCMVi(中位发病时间 34 天;范围 5-74 天),第 100 天的发生率为 82%(95%置信区间,73-92)。7 例患者发生明确/可能的 CMV 疾病,6 例在第 100 天前死亡(3 例明确/可能的 CMV 肺炎)。45 例患者在前 6 个月需要延长治疗,1(n=10)、2(n=14)或 3/持续(n=21)csCMVi,51 例中有 43 例(84%)发生显著治疗毒性。洛韦是一种高效、耐受性良好的预防药物,可减轻 CBT 受者的 CMV 感染、CMV 相关死亡率和抗病毒治疗毒性。我们的数据支持 CBT 后至少 6 个月的预防治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5d8/9806329/0d5bc5673b4c/BLOODA_ADV-2022-008047-fx1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验