Impact of cytomegalovirus (CMV) seroconversion pre-allogeneic hematopoietic cell transplantation on posttransplant outcomes

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Ayman Sayyed, Leeann Wilson, Vered Stavi, Shiyi Chen, Carol Chen, Jonas Mattsson, Jeffrey H. Lipton, Dennis D. Kim, Auro Viswabandya, Rajat Kumar, Wilson Lam, Arjun D. Law, Armin Gerbitz, Ivan Pasic, Igor Novitzky-Basso, Tony Mazzulli, Fotios V. Michelis
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Abstract

Cytomegalovirus (CMV) reactivation post-allogeneic hematopoietic cell transplantation (post-alloHCT) increases morbidity and mortality. We sought to determine the frequency of CMV seroconversion in patients pre-alloHCT and to investigate the impact on posttransplant outcomes. We retrospectively investigated 752 adult patients who underwent alloHCT at our center from January 2015 to February 2020 before the adoption of letermovir prophylaxis. CMV serology was assessed at consult and pretransplant. The cohort was divided into four groups based on pretransplant CMV seroconversion: negative to positive (Group 1), positive to negative (Group 2), consistently negative (Group 3), and consistently positive (Group 4). Eighty-nine patients (12%) had seroconverted from negative to positive, 17 (2%) from positive to negative, 151 (20%) were consistently seronegative, and 495 (66%) were consistently seropositive pretransplant. For the four CMV serostatus groups, cumulative incidence of CMV reactivation at 6 months posttransplant was 4.5%, 47.1%, 6.6%, and 76.6% for Groups 1, 2, 3, and 4, respectively (p < .0001). No differences between groups were seen regarding Grade III–IV acute graft-versus-host disease (GVHD) (p = .91), moderate/severe chronic GVHD (p = .41), or graft failure (p = .28). On multivariable analysis, there was no impact of CMV serostatus group on overall survival (p = .67), cumulative incidence of relapse (p = .83) or non-relapse mortality. alloHCT patients who demonstrate CMV seroconversion pretransplant from negative to positive have a very low risk of CMV reactivation posttransplant. The observed seroconversion may be due to passive CMV immunity acquired through blood products. Quantitative CMV immunoglobulin G/immunoglobulin M pretransplant may help differentiate between true seroconversion and passively transmitted CMV immunoglobulin.

异基因造血细胞移植前巨细胞病毒(CMV)血清转换对移植后预后的影响。
异基因造血细胞移植(异体HCT)后巨细胞病毒(CMV)再激活会增加发病率和死亡率。我们试图确定异体造血干细胞移植前患者CMV血清转换的频率,并研究其对移植后预后的影响。我们回顾性调查了 2015 年 1 月至 2020 年 2 月在本中心接受alloHCT 的 752 名成年患者,当时尚未采用 Letermovir 预防措施。在就诊时和移植前对 CMV 血清学进行了评估。根据移植前CMV血清转换情况,将患者分为四组:阴性转为阳性(第1组)、阳性转为阴性(第2组)、持续阴性(第3组)和持续阳性(第4组)。89 名患者(12%)血清从阴性转为阳性,17 名患者(2%)血清从阳性转为阴性,151 名患者(20%)血清持续阴性,495 名患者(66%)移植前血清持续阳性。在 CMV 血清状态的四个组别中,移植后 6 个月 CMV 再激活的累积发生率在第 1、2、3 和 4 组分别为 4.5%、47.1%、6.6% 和 76.6%(P<0.05)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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