4.7 Article

Immunoguided Discontinuation of Prophylaxis for Cytomegalovirus Disease in Kidney Transplant Recipients Treated With Antithymocyte Globulin: A Randomized Clinical Trial

Journal

CLINICAL INFECTIOUS DISEASES
Volume 74, Issue 5, Pages 757-765

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciab574

Keywords

cytomegalovirus infection; kidney transplant; CMV-specific cell-mediated immunity; QuantiFERON-CMV assay; antithymocyte globulin

Funding

  1. 2013-2016 National RDI Plan
  2. Carlos III Health Institute [PI15/00402]
  3. Spanish Society of Nephrology
  4. National R&D&I Plan 2013-2016
  5. Carlos III Health Institute, General Sub-Directorate of Networks and Cooperative Research Centres, Ministry of Science and Innovation, Spanish Network for Research in Infectious Diseases [REIPI RD16/0016/000, RD16/0016/0003, RD16/0016/0007, RD16/0016/0008, RD16/0016/0009, RD16/0016/0012]
  6. European Regional Development Fund A way to achieve Europe, Operational Programme Intelligent Growth 2014-2020
  7. Spanish Network for Renal Disease Research (RedInRen) [RD16/0009/0006, RD16/0009/0008, RD16/0009/0013, RD16/0009/0014, RD16/0009/0019, RD16/0009/0027, RD16/0009/0034]
  8. CIBERES [CB06/06/0058]
  9. Spanish Group for the Study of Infection in Transplantation and the Immunosuppressed Host of the Spanish Society of Infectious Diseases and Clinical Microbiology (SEIMC)
  10. Spanish Clinical Research Network - ISCIII-Subdirectorate General for the Evaluation and Promotion of Research integrated in the 2013-2016 National RDI Plan [PT13/0002/0010-PT17/0017/0012, PT13/0002/0014-PT17/0017/0032]
  11. National Plan for Scientific and Technical Research and Innovation (2017-2020)
  12. European Regional Development Fund

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For CMV-seropositive kidney transplant recipients receiving ATG induction, it is safe and effective to discontinue prophylaxis when CMV-CMI is recovered, as there is no significant increase in the incidence of CMV replication or disease. Immunoguided prevention is not inferior to prophylaxis in preventing CMV complications.
Background Antiviral prophylaxis is recommended in cytomegalovirus (CMV)-seropositive kidney transplant (KT) recipients receiving antithymocyte globulin (ATG) as induction. An alternative strategy of premature discontinuation of prophylaxis after CMV-specific cell-mediated immunity (CMV-CMI) recovery (immunoguided prevention) has not been studied. Our aim was to determine whether it is effective and safe to discontinue prophylaxis when CMV-CMI is detected and to continue with preemptive therapy. Methods In this open-label, noninferiority clinical trial, patients were randomized 1:1 to follow an immunoguided strategy, receiving prophylaxis until CMV-CMI recovery or to receive fixed-duration prophylaxis until day 90. After prophylaxis, preemptive therapy (valganciclovir 900 mg twice daily) was indicated in both arms until month 6. The primary and secondary outcomes were incidence of CMV disease and replication, respectively, within the first 12 months. Desirability of outcome ranking (DOOR) assessed 2 deleterious events (CMV disease/replication and neutropenia). Results A total of 150 CMV-seropositive KT recipients were randomly assigned. There was no difference in the incidence of CMV disease (0% vs 2.7%; P = .149) and replication (17.1% vs 13.5%; log-rank test, P = .422) between both arms. Incidence of neutropenia was lower in the immunoguided arm (9.2% vs 37.8%; odds ratio, 6.0; P < .001). A total of 66.1% of patients in the immunoguided arm showed a better DOOR, indicating a greater likelihood of a better outcome. Conclusions Prophylaxis can be prematurely discontinued in CMV-seropositive KT patients receiving ATG when CMV-CMI is recovered since no significant increase in the incidence of CMV replication or disease is observed. In cytomegalovirus (CMV)-seropositive kidney transplant recipients receiving ATG induction, immunoguided prevention is not inferior to prophylaxis to prevent CMV complications. Prophylaxis can be prematurely discontinued after CMV-cell-mediated immunity recovery with no significant increase in the incidence of CMV replication or disease.

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