Haematology Department, Royal North Shore Hospital, Sydney, Australia.
National Centre for Infection in Cancer, Peter MacCallum Cancer Centre, Melbourne, Australia.
Transpl Infect Dis. 2021 Jun;23(3):e13548. doi: 10.1111/tid.13548. Epub 2021 Jan 5.
Cytomegalovirus (CMV) reactivation is a frequent complication after allogeneic hematopoietic cell transplant (alloHCT).
We analyzed 159 alloHCT recipients with 4409 quantitative CMV viral loads to determine pre-transplant predictors of CMV reactivation, clinically significant CMV infection (cs-CMVi, defined as CMV viral load >1000 IU/mL), CMV disease, kinetics of spontaneous clearance of CMV, and survival using a standardized pre-emptive therapy approach to identify at-risk groups to target prevention strategies.
Cs-CMVi was most common in D-/R+ unrelated donor transplants (URD). Spontaneous CMV clearance occurred in 26% of patients who reached a viral load of 56-137 IU/mL, 6% at 138-250 IU/mL and in one patient >250 IU/mL. Median time between the first CMV reactivation (>56 IU/mL) and a viral load >250 IU/mL was 13 days, whereas the time from the first viral load >250 IU/mL to reach a vial load >1000 IU/mL was 4 days. Cs-CMVi was associated with a significant increase in non-relapse mortality (NRM) on multivariate analysis.
Overall, this study indicates that D-/R+ URD recipients are at high-risk for cs-CMVi- and CMV-related mortality, and are potential candidates for targeted CMV prophylaxis. Spontaneous clearance of CMV beyond a viral load of 250 IU/mL is uncommon, suggesting that this could be used as an appropriate threshold to initiate pre-emptive therapy.
巨细胞病毒(CMV)再激活是异基因造血细胞移植(alloHCT)后常见的并发症。
我们分析了 159 例 alloHCT 受者的 4409 份定量 CMV 病毒载量,以确定 CMV 再激活、临床显著 CMV 感染(cs-CMVi,定义为 CMV 病毒载量>1000 IU/mL)、CMV 疾病、CMV 自发性清除动力学和生存的移植前预测因子,采用标准化的先发制人治疗方法确定高危人群,以确定预防策略的目标。
D-/R+无关供体移植(URD)中最常见 cs-CMVi。26%达到 56-137 IU/mL 病毒载量的患者出现自发性 CMV 清除,6%达到 138-250 IU/mL 的患者出现自发性 CMV 清除,1 例患者>250 IU/mL。首次 CMV 再激活(>56 IU/mL)与病毒载量>250 IU/mL 之间的中位时间为 13 天,而从首次病毒载量>250 IU/mL 到病毒载量>1000 IU/mL 的时间为 4 天。多变量分析显示,cs-CMVi 与非复发死亡率(NRM)显著增加相关。
总体而言,本研究表明 D-/R+URD 受者 cs-CMVi 和与 CMV 相关的死亡率风险高,是靶向 CMV 预防的潜在候选者。病毒载量>250 IU/mL 后 CMV 的自发性清除并不常见,这表明这可能作为启动先发制人治疗的适当阈值。