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CMV viral load kinetics as surrogate endpoints after allogeneic transplantation
Elizabeth R. Duke, … , Joshua T. Schiffer, Michael Boeckh
Elizabeth R. Duke, … , Joshua T. Schiffer, Michael Boeckh
Published September 24, 2020
Citation Information: J Clin Invest. 2021;131(1):e133960. https://doi.org/10.1172/JCI133960.
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Clinical Research and Public Health Infectious disease

CMV viral load kinetics as surrogate endpoints after allogeneic transplantation

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Abstract

BACKGROUND Viral load (VL) surrogate endpoints transformed development of HIV and hepatitis C therapeutics. Surrogate endpoints for CMV-related morbidity and mortality could advance development of antiviral treatments. Although observational data support using CMV VL as a trial endpoint, randomized controlled trials (RCTs) demonstrating direct associations between virological markers and clinical endpoints are lacking.METHODS We performed CMV DNA PCR on frozen serum samples from the only placebo-controlled RCT of ganciclovir for early treatment of CMV after hematopoietic cell transplantation (HCT). We used established criteria to assess VL kinetics as surrogates for CMV disease or death by weeks 8, 24, and 48 after randomization and quantified antiviral effects captured by each marker. We used ensemble-based machine learning to assess the predictive ability of VL kinetics and performed this analysis on a ganciclovir prophylaxis RCT for validation.RESULTS VL suppression with ganciclovir reduced cumulative incidence of CMV disease and death for 20 years after HCT. Mean VL, peak VL, and change in VL during the first 5 weeks of treatment fulfilled the Prentice definition for surrogacy, capturing more than 95% of ganciclovir’s effect, and yielded highly sensitive and specific predictions by week 48. In the prophylaxis trial, the viral shedding rate satisfied the Prentice definition for CMV disease by week 24.CONCLUSIONS Our results support using CMV VL kinetics as surrogates for CMV disease, provide a framework for developing CMV preventative and therapeutic agents, and support reductions in VL as the mechanism through which antivirals reduce CMV disease.FUNDING Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.

Authors

Elizabeth R. Duke, Brian D. Williamson, Bhavesh Borate, Jonathan L. Golob, Chiara Wychera, Terry Stevens-Ayers, Meei-Li Huang, Nicole Cossrow, Hong Wan, T. Christopher Mast, Morgan A. Marks, Mary E. Flowers, Keith R. Jerome, Lawrence Corey, Peter B. Gilbert, Joshua T. Schiffer, Michael Boeckh

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Figure 1

CONSORT diagram and study designs for the early treatment trial.

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CONSORT diagram and study designs for the early treatment trial.
Study d...
Study design for Goodrich et al. RCT (A and B) and for VL kinetic analysis (C). (A) The reconstructed CONSORT diagram for the original RCT. (B) The original study design with surveillance and screening beginning at HCT and randomization beginning at the time of first positive surveillance culture. (C) The VL kinetics study design with analysis beginning at randomization (receipt of study drug) and ending at day 100 after HCT or a study endpoint of CMV disease or death, whichever occurred first.

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