
Valganciclovir Preferred to Prevent Cytomegalovirus After Allogeneic Hematopoietic Cell Transplantation
Investigators at Memorial Sloan Kettering Cancer Center determined valganciclovir was the preferred first-line preemptive therapy to prevent cytomegalovirus in patients following an allogeneic hematopoietic cell transplantation.
Patients undergoing allogeneic hematopoietic cell transplantation (HCT) are susceptible to developing cytomegalovirus after the procedure, and current antiviral preemptive therapy (PET) is often stunted by toxicity concerns.
A new real-world study at Memorial Sloan Kettering Cancer Center sought to analyze PET and associated toxicities in 232 HCT recipients, some considered high risk (HR) and some low risk (LR) for CMV, through day 100 post-HCT.
In a poster presented at the
A total of 121 (52%; 40 low risk and 81 high risk) patients received PET, which was started at a median 35-day post-HCT [HR vs. LR: 32 vs. 39, P<0.0001].
“CMV viral load (VL) at PET initiation was <137 IU/mL in 23 patients; and median of 475 IU/ml in 98 patients. Valganciclovir was the most common 1st PET (55%), followed by foscarnet (26%) and ganciclovir (19%),” investigators wrote in the abstract. “Sixty-five patients completed planned 1st PET regimen; 33.1% discontinued 1st PET due to either clinical toxicity (20.7%) or lack of virologic response (12.4%). Subsequently, 2nd and 3rd PET agents were administered to 46.1% and 20.7% of patients respectively. Median duration of PET was 37 days [HR vs. LR: 41 vs. 30.5, P = 0.011].”
The team concluded that valganciclovir was the preferred first-line PET agent, with the first PET discontinuation or change made due to clinical or laboratory-defined toxicity occurring with similar frequency between HR and LR patients.
The poster, “
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