Letermovir Rescue Therapy in Kidney Transplant Recipients with Refractory/Resistant CMV Disease

Author:

von Hoerschelmann Ellen1ORCID,Münch Johannes1ORCID,Gao Linde1,Lücht Christian1,Naik Marcel G.1ORCID,Schmidt Danilo1ORCID,Pitzinger Paul2,Michel Detlef3,Avaniadi Parthenopi1,Schrezenmeier Eva1ORCID,Choi Mira1ORCID,Halleck Fabian1,Budde Klemens1ORCID

Affiliation:

1. Department of Nephrology and Medical Intensive Care, Charité Universitätsmedizin Berlin, 10117 Berlin, Germany

2. Institute of Virology, Charité Universitätsmedizin Berlin, Labor Berlin-Charité-Vivantes GmbH, 10117 Berlin, Germany

3. Institute of Virology, Universitätsklinikum Ulm, 89081 Ulm, Germany

Abstract

(1) Background: CMV infections remain a problem after kidney transplantation, particularly if patients are refractory or resistant (r/r) to treatment with valganciclovir (VGCV) or ganciclovir (GCV). (2) Methods: In a single-center retrospective study, kidney transplant recipients (KTR) receiving letermovir (LTV) as rescue therapy for VGCV-/GCV-r/r CMV disease were analyzed regarding CMV history, immunosuppression, and outcomes. (3) Results: Of 201 KTR treated for CMV between 2017 and 2022, 8 patients received LTV following treatment failure with VGCV/GCV. All patients received CMV prophylaxis with VGCV according to the center’s protocol, and 7/8 patients had a high-risk (D+/R−) CMV constellation. In seven of eight cases, rising CMV levels occurred during prophylaxis. In seven of eight patients, a mutation in UL97 associated with a decreased response to VGCV/GCV was detected. In four of eight patients, LTV resulted in CMV clearance after 24 ± 10 weeks (16–39 weeks), two of eight patients stabilized at viral loads <2000 cop/mL (6–20 weeks), and two of eight patients developed LTV resistance (range 8–10 weeks). (4) Conclusion: LTV, which is currently evaluated for CMV prophylaxis in kidney transplantation, also shows promising results for the treatment of patients with VGCV/GCV resistance despite the risk of developing LTV resistance. Additional studies are needed to further define its role in the treatment of patients with CMV resistance.

Publisher

MDPI AG

Subject

General Medicine

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