Impact of kidney function on 200 days of antiviral prophylaxis for cytomegalovirus disease in CMV-seronegative recipients of CMV-seropositive donor kidneys Post hoc analysis of a randomized, phase 3 trial of letermovir versus valganciclovir prophylaxis.
Academic Article
Overview
abstract
This post-hoc analysis was conducted to understand the impact of kidney function on 200 days of cytomegalovirus (CMV) prophylaxis in CMV donor-positive/recipient-negative (D+R-) kidney transplant recipients (KTRs). Adult CMV D+R- KTRs were randomized (1:1) post-transplant to letermovir 480 mg (with acyclovir and valganciclovir placebo) or valganciclovir 900 mg (with acyclovir and letermovir placebos) daily for 28-weeks (NCT03443869). Valganciclovir and acyclovir doses were modified for kidney function (Cockcroft-Gault creatinine clearance [CrCl]). Dose frequency, adherence, CMV DNAemia, and discontinuations were evaluated at week 28. 480 CMV D+R- KTRs had a median CrCl of 67 mL/min. All participants taking letermovir (or letermovir placebo) received daily dosing (i.e., no intermittent dosing), whereas approximately 50% of participants receiving valganciclovir (or valganciclovir placebo) received intermittent dosing (i.e., every 2 days or twice weekly titrated to CrCl). Kidney function did not impact adherence, quantifiable CMV DNAemia, or prophylaxis discontinuation in the letermovir group; however, adherence was lower, and quantifiable CMV DNAemia and discontinuation occurred more frequently in the valganciclovir group, particularly among those with lower kidney function post-transplant. In CMV D+R- KTRs, letermovir prophylaxis was associated with less CMV DNAemia compared to valganciclovir in participants with low kidney function during the 200-day prophylaxis period. CLINICAL TRIALS REGISTRATION: ClinicalTrials.gov: NCT03443869, EudraCT: 2017-001055-30.
