Low dose valganciclovir as cytomegalovirus prophylaxis in post-renal transplant recipients induced with alemtuzumab: A single-center study.
Adult
Aged
Alemtuzumab
/ adverse effects
Antiviral Agents
/ therapeutic use
CD52 Antigen
/ immunology
Cytomegalovirus
/ physiology
Cytomegalovirus Infections
/ etiology
Drug Dosage Calculations
Graft Rejection
/ drug therapy
Humans
Kidney Transplantation
Lymphocyte Depletion
Middle Aged
Postoperative Period
Retrospective Studies
Risk
Steroids
/ therapeutic use
Transplantation, Homologous
Treatment Outcome
Valganciclovir
/ therapeutic use
Alemtuzumab
CMV
Renal transplantation
Valganciclovir
Journal
Transplant immunology
ISSN: 1878-5492
Titre abrégé: Transpl Immunol
Pays: Netherlands
ID NLM: 9309923
Informations de publication
Date de publication:
10 2019
10 2019
Historique:
received:
14
05
2019
revised:
18
07
2019
accepted:
21
07
2019
pubmed:
26
7
2019
medline:
4
4
2020
entrez:
26
7
2019
Statut:
ppublish
Résumé
Alemtuzumab (Ale) is a recombinant monoclonal antibody which binds to CD52 causing profound lymphodepletion, thus allowing its use in renal transplantation induction therapy. However, patients may be at increased risk for opportunistic infections, such as Cytomegalovirus (CMV). We analyzed CMV infection in renal allograft recipients administered low-dose valganciclovir (VGCV) prophylaxis with alemtuzumab induction and steroid minimization. In this retrospective analysis, 678 kidney transplant recipients were evaluated, with 606 included for analysis. Patients were excluded for receiving induction therapy other than Ale, or for lack of follow-up within 1 year. VGCV prophylaxis was stratified by recipient CMV risk status and low-dose (450 mg) VGCV was given 3 times a week to low and moderate risk patients and daily to high risk individuals. Subject records were examined for recipient demographics, donor and recipient CMV serostatus, CMV viremia, and invasive infection. Of the 606 recipients, 154 were defined as low risk for CMV infection (donor and recipient both negative, or D-/R-), 236 as moderate risk without mismatch (D+/R+), 122 as moderate risk with mismatch (D-/R+), and 94 as high risk (D+/R-). Twenty-nine (29) individuals (4.8%) tested positive by PCR for CMV viremia and 10 (1.7%) patients developed invasive CMV disease, including colitis (n = 4), esophagitis (n = 1), enteritis (n = 1), nephritis (n = 1), and pneumonia (n = 3). High risk recipients (D+/R-) accounted for the majority of invasive CMV disease (n = 5), followed by moderate risk (n = 4). CMV viremia was also more common in high risk and moderate risk (D+/R+) individuals. Overall rejection rate for our study population was 27%. In this institution's experience, CMV incidence was reduced compared to historically reported data by using low-dose (450 mg) VGCV prophylaxis in combination with Ale induction and steroid minimization. However, overall rejection rate was significantly higher in our population, possibly influenced by the degree of steroid minimization.
Identifiants
pubmed: 31344441
pii: S0966-3274(19)30067-X
doi: 10.1016/j.trim.2019.101226
pii:
doi:
Substances chimiques
Antiviral Agents
0
CD52 Antigen
0
Steroids
0
Alemtuzumab
3A189DH42V
Valganciclovir
GCU97FKN3R
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
101226Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.