在SARS-CoV-2 Omicron变异体和COVID-19疗法时代,造血细胞移植和嵌合抗原受体T细胞受者的COVID-19疗效。

IF 3.6 3区 医学 Q2 HEMATOLOGY
Emily A. Rosen , Elizabeth M. Krantz , Denise J. McCulloch , Marie H. Wilson , Frank Tverdek , Zahra Kassamali Escobar , Darra Drucker , Eduardo Sanchez , Masumi Ueda Oshima , Marco Mielcarek , Jordan Gauthier , Steven A. Pergam , Joshua A. Hill , Catherine Liu
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引用次数: 0

摘要

背景:细胞疗法(包括造血细胞移植(HCT)和嵌合抗原受体 T 细胞疗法(CART))的受者有可能因冠状病毒病 2019(COVID-19)而导致不良后果。在多种抗病毒疗法广泛应用的奥米克龙时代,描述细胞疗法前后早期患者预后的数据非常有限:研究设计:这是一项单中心回顾性队列研究,研究对象是2022年1月1日至2023年3月1日期间在本癌症中心确诊为细胞治疗前后早期COVID-19阳性的成年HCT和CART受者。主要结果是 30 天 COVID-19 相关住院和死亡。次要结果是出现持续性 COVID-19,即在确诊 COVID-19 后 31-90 天内 SARS-CoV-2 聚合酶链反应 (PCR) 呈阳性:在纳入的 65 名患者中,52 人(80%)接受了至少一种 COVID-19 治疗。初次确诊 COVID-19 后最常见的治疗方法是尼马瑞韦/利托那韦(29%),其次是单克隆抗体疗法(26%)和雷米地韦(11%)。在随访至少 30 天的 64 名患者中,有 8 名患者(12%)至少有一次与 COVID-19 相关的住院治疗,其中一名患者死亡,但死因并非 COVID-19。在因 COVID-19 而住院的 8 名患者中,1 人病情严重,7 人有轻度或中度感染。13/65(20%)名患者出现了持续的 COVID-19,其中 4 名患者需要额外的抗病毒治疗。3名接受细胞疗法前的患者因COVID-19持续存在而延迟接受细胞疗法:结论:在 Omicron 时代,30 天 COVID-19 相关住院率和死亡率在这批接受肝移植前和肝移植后早期以及 CART 治疗的患者中相对较低,其中大多数患者接受了至少一种抗病毒药物的治疗。每 5 例患者中就有 1 例在细胞治疗期间出现了持续的 COVID-19,并导致数例患者的细胞治疗延迟,这凸显了对新的 COVID-19 治疗策略的需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
COVID-19 Outcomes Among Hematopoietic Cell Transplant and Chimeric Antigen Receptor T-Cell Recipients in the Era of SARS-CoV-2 Omicron Variants and COVID-19 Therapeutics
Recipients of cellular therapies, including hematopoietic cell transplant (HCT) and chimeric antigen receptor T-cell (CART) therapy, are at risk for poor outcomes from coronavirus disease 2019 (COVID-19). There are limited data describing outcomes among patients in the pre- and early post-cellular therapy period during the Omicron era when multiple antiviral therapeutics were widely available. The objective of this study is to describe COVID-19 treatment and outcomes in patients diagnosed with COVID-19 during the pre- or early post-cellular therapy period. This is a single-center retrospective cohort study of adult HCT and CART recipients diagnosed with COVID-19 in the pre- and early post-cellular therapy period who tested positive for COVID-19 at our cancer center between January 1, 2022 and March 1, 2023. Primary outcomes were 30-day COVID-19-related hospitalization and death. A secondary outcome was development of persistent COVID-19, defined by a positive SARS-CoV-2 polymerase chain reaction (PCR) 31 to 90 days after COVID-19 diagnosis. Among 65 patients included, 52 (80%) received at least one COVID-19 therapeutic. The most common treatment after initial COVID-19 diagnosis was nirmatrelvir/ritonavir (29%), followed by monoclonal antibody therapy (26%) and remdesivir (11%). Of the 64 patients with at least 30 days of follow-up, 8 (12%) had at least one COVID-19-related hospitalization and one patient died, though cause of death was not due to COVID-19. Of the 8 patients hospitalized for COVID-19, one had severe disease and 7 had mild or moderate infection. Persistent COVID-19 was observed in 13/65 (20%) patients, with 4 patients requiring additional antiviral therapy. Three pre-cellular therapy patients had delays in receiving cellular therapy due to persistent COVID-19. During the Omicron era, rates of 30-day COVID-19-related hospitalization and death were relatively low in this cohort of pre- and early post-HCT and CART recipients, the majority of whom received treatment with at least one antiviral agent. Persistent COVID-19 occurred in 1 in 5 patients in the peri-cellular therapy period and led to cellular therapy treatment delays in several patients, highlighting the need for new COVID-19 treatment strategies.
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CiteScore
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