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Randomized Controlled Trials to Define Viral Load Thresholds for Cytomegalovirus Pre-Emptive Therapy

BACKGROUND: To help decide when to start and when to stop pre-emptive therapy for cytomegalovirus infection, we conducted two open-label randomized controlled trials in renal, liver and bone marrow transplant recipients in a single centre where pre-emptive therapy is indicated if viraemia exceeds 30...

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Autores principales: Griffiths, Paul D., Rothwell, Emily, Raza, Mohammed, Wilmore, Stephanie, Doyle, Tomas, Harber, Mark, O’Beirne, James, Mackinnon, Stephen, Jones, Gareth, Thorburn, Douglas, Mattes, Frank, Nebbia, Gaia, Atabani, Sowsan, Smith, Colette, Stanton, Anna, Emery, Vincent C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5042415/
https://www.ncbi.nlm.nih.gov/pubmed/27684379
http://dx.doi.org/10.1371/journal.pone.0163722
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author Griffiths, Paul D.
Rothwell, Emily
Raza, Mohammed
Wilmore, Stephanie
Doyle, Tomas
Harber, Mark
O’Beirne, James
Mackinnon, Stephen
Jones, Gareth
Thorburn, Douglas
Mattes, Frank
Nebbia, Gaia
Atabani, Sowsan
Smith, Colette
Stanton, Anna
Emery, Vincent C.
author_facet Griffiths, Paul D.
Rothwell, Emily
Raza, Mohammed
Wilmore, Stephanie
Doyle, Tomas
Harber, Mark
O’Beirne, James
Mackinnon, Stephen
Jones, Gareth
Thorburn, Douglas
Mattes, Frank
Nebbia, Gaia
Atabani, Sowsan
Smith, Colette
Stanton, Anna
Emery, Vincent C.
author_sort Griffiths, Paul D.
collection PubMed
description BACKGROUND: To help decide when to start and when to stop pre-emptive therapy for cytomegalovirus infection, we conducted two open-label randomized controlled trials in renal, liver and bone marrow transplant recipients in a single centre where pre-emptive therapy is indicated if viraemia exceeds 3000 genomes/ml (2520 IU/ml) of whole blood. METHODS: Patients with two consecutive viraemia episodes each below 3000 genomes/ml were randomized to continue monitoring or to immediate treatment (Part A). A separate group of patients with viral load greater than 3000 genomes/ml was randomized to stop pre-emptive therapy when two consecutive levels less than 200 genomes/ml (168 IU/ml) or less than 3000 genomes/ml were obtained (Part B). For both parts, the primary endpoint was the occurrence of a separate episode of viraemia requiring treatment because it was greater than 3000 genomes/ml. RESULTS: In Part A, the primary endpoint was not significantly different between the two arms; 18/32 (56%) in the monitor arm had viraemia greater than 3000 genomes/ml compared to 10/27 (37%) in the immediate treatment arm (p = 0.193). However, the time to developing an episode of viraemia greater than 3000 genomes/ml was significantly delayed among those randomized to immediate treatment (p = 0.022). In Part B, the primary endpoint was not significantly different between the two arms; 19/55 (35%) in the less than 200 genomes/ml arm subsequently had viraemia greater than 3000 genomes/ml compared to 23/51 (45%) among those randomized to stop treatment in the less than 3000 genomes/ml arm (p = 0.322). However, the duration of antiviral treatment was significantly shorter (p = 0.0012) in those randomized to stop treatment when viraemia was less than 3000 genomes/ml. DISCUSSION: The results illustrate that patients have continuing risks for CMV infection with limited time available for intervention. We see no need to alter current rules for stopping or starting pre-emptive therapy.
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spelling pubmed-50424152016-10-27 Randomized Controlled Trials to Define Viral Load Thresholds for Cytomegalovirus Pre-Emptive Therapy Griffiths, Paul D. Rothwell, Emily Raza, Mohammed Wilmore, Stephanie Doyle, Tomas Harber, Mark O’Beirne, James Mackinnon, Stephen Jones, Gareth Thorburn, Douglas Mattes, Frank Nebbia, Gaia Atabani, Sowsan Smith, Colette Stanton, Anna Emery, Vincent C. PLoS One Research Article BACKGROUND: To help decide when to start and when to stop pre-emptive therapy for cytomegalovirus infection, we conducted two open-label randomized controlled trials in renal, liver and bone marrow transplant recipients in a single centre where pre-emptive therapy is indicated if viraemia exceeds 3000 genomes/ml (2520 IU/ml) of whole blood. METHODS: Patients with two consecutive viraemia episodes each below 3000 genomes/ml were randomized to continue monitoring or to immediate treatment (Part A). A separate group of patients with viral load greater than 3000 genomes/ml was randomized to stop pre-emptive therapy when two consecutive levels less than 200 genomes/ml (168 IU/ml) or less than 3000 genomes/ml were obtained (Part B). For both parts, the primary endpoint was the occurrence of a separate episode of viraemia requiring treatment because it was greater than 3000 genomes/ml. RESULTS: In Part A, the primary endpoint was not significantly different between the two arms; 18/32 (56%) in the monitor arm had viraemia greater than 3000 genomes/ml compared to 10/27 (37%) in the immediate treatment arm (p = 0.193). However, the time to developing an episode of viraemia greater than 3000 genomes/ml was significantly delayed among those randomized to immediate treatment (p = 0.022). In Part B, the primary endpoint was not significantly different between the two arms; 19/55 (35%) in the less than 200 genomes/ml arm subsequently had viraemia greater than 3000 genomes/ml compared to 23/51 (45%) among those randomized to stop treatment in the less than 3000 genomes/ml arm (p = 0.322). However, the duration of antiviral treatment was significantly shorter (p = 0.0012) in those randomized to stop treatment when viraemia was less than 3000 genomes/ml. DISCUSSION: The results illustrate that patients have continuing risks for CMV infection with limited time available for intervention. We see no need to alter current rules for stopping or starting pre-emptive therapy. Public Library of Science 2016-09-29 /pmc/articles/PMC5042415/ /pubmed/27684379 http://dx.doi.org/10.1371/journal.pone.0163722 Text en © 2016 Griffiths et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Griffiths, Paul D.
Rothwell, Emily
Raza, Mohammed
Wilmore, Stephanie
Doyle, Tomas
Harber, Mark
O’Beirne, James
Mackinnon, Stephen
Jones, Gareth
Thorburn, Douglas
Mattes, Frank
Nebbia, Gaia
Atabani, Sowsan
Smith, Colette
Stanton, Anna
Emery, Vincent C.
Randomized Controlled Trials to Define Viral Load Thresholds for Cytomegalovirus Pre-Emptive Therapy
title Randomized Controlled Trials to Define Viral Load Thresholds for Cytomegalovirus Pre-Emptive Therapy
title_full Randomized Controlled Trials to Define Viral Load Thresholds for Cytomegalovirus Pre-Emptive Therapy
title_fullStr Randomized Controlled Trials to Define Viral Load Thresholds for Cytomegalovirus Pre-Emptive Therapy
title_full_unstemmed Randomized Controlled Trials to Define Viral Load Thresholds for Cytomegalovirus Pre-Emptive Therapy
title_short Randomized Controlled Trials to Define Viral Load Thresholds for Cytomegalovirus Pre-Emptive Therapy
title_sort randomized controlled trials to define viral load thresholds for cytomegalovirus pre-emptive therapy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5042415/
https://www.ncbi.nlm.nih.gov/pubmed/27684379
http://dx.doi.org/10.1371/journal.pone.0163722
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