AI Article Synopsis

  • Cytomegalovirus (CMV) disease can occur before hematopoietic cell transplantation (HCT) and negatively affect post-transplant outcomes, but the effects of reactivation prior to the procedure were previously unclear.
  • A study found that 11% of HCT candidates experienced pre-HCT CMV reactivation, with lymphopenia identified as a strong risk factor.
  • The presence of pre-HCT CMV reactivation was linked to higher risks of further reactivation and related diseases within the first year after HCT, supporting the need for regular surveillance and potential antiviral therapy in high-risk patients.

Article Abstract

Cytomegalovirus (CMV) disease occurs occasionally before allogeneic hematopoietic cell transplantation (HCT) and is associated with poor post-HCT outcomes; however, the impact of pre-HCT CMV reactivation is unknown. Pre-HCT CMV reactivation was assessed in HCT candidates from the preemptive antiviral therapy (2007-2017) and letermovir prophylaxis (2018-2021) eras. CMV DNA polymerase chain reaction (PCR) surveillance was routinely performed during the pre-HCT workup period, and antiviral therapy was recommended according to risk of progression to CMV disease. Risk factors for pre-HCT CMV reactivation were characterized, and the associations of pre-HCT CMV reactivation with post-HCT outcomes were examined using logistic regression and Cox proportional hazard models, respectively. A total of 1694 patients were identified, and 11% had pre-HCT CMV reactivation 14 days (median; interquartile range [IQR], 6-23) before HCT. Lymphopenia (≤0.3 × 103/μL) was the strongest risk factor for pre-HCT CMV reactivation at multiple PCR levels. In the preemptive therapy era, patients with pre-HCT CMV reactivation had a significantly increased risk of CMV reactivation by day 100 as well as CMV disease and death by 1 year after HCT. Clearance of pre-HCT CMV reactivation was associated with a lower risk of post-HCT CMV reactivation. Similar associations with post-HCT CMV end points were observed in a cohort of patients receiving letermovir prophylaxis. Pre-HCT CMV reactivation can be routinely detected in high-risk HCT candidates and is a significant risk factor for post-HCT CMV reactivation and disease. Pre-HCT CMV DNA PCR surveillance is recommended in high-risk HCT candidates, and antiviral therapy may be indicated to prevent post-HCT CMV reactivation.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11399585PMC
http://dx.doi.org/10.1182/bloodadvances.2023012234DOI Listing

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