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Placebo response in trials of drug treatments for cancer-related fatigue: a systematic review, meta-analysis and meta-regression

BACKGROUND: Cancer-related fatigue (CRF) is one of the most distressing symptoms experienced by patients. There is no gold standard treatment, although multiple drugs have been tested with little evidence of efficacy. Randomised controlled trials (RCTs) of these drugs have commented on the existence...

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Autores principales: Roji, Rocio, Stone, Patrick, Ricciardi, Federico, Candy, Bridget
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691807/
https://www.ncbi.nlm.nih.gov/pubmed/32046962
http://dx.doi.org/10.1136/bmjspcare-2019-002163
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author Roji, Rocio
Stone, Patrick
Ricciardi, Federico
Candy, Bridget
author_facet Roji, Rocio
Stone, Patrick
Ricciardi, Federico
Candy, Bridget
author_sort Roji, Rocio
collection PubMed
description BACKGROUND: Cancer-related fatigue (CRF) is one of the most distressing symptoms experienced by patients. There is no gold standard treatment, although multiple drugs have been tested with little evidence of efficacy. Randomised controlled trials (RCTs) of these drugs have commented on the existence or size of the placebo response (PR). The objective of this systematic review was to establish the magnitude of the PR in RCTs of drugs to relieve CRF and to identify contributing factors. METHOD: RCTs were included in which the objective was to treat CRF. A meta-analysis was conducted using the standardised mean change (SMC) between baseline and final measurement in the placebo group. To explore factors that may be associated with the PR (eg, population or drug), a meta-regression was undertaken. Risk of bias was assessed using the revised Cochrane tool. RESULTS: From 3916 citations, 30 relevant RCTs were identified. All had limitations that increased their risk of bias. The pooled SMC in reduction in fatigue status in placebo groups was −0.23 (95% confidence intervals −0.42 to −0.04). None of the variables analysed in the meta-regression were statistically significant related to PR. CONCLUSION: There is some evidence, based on trials with small samples, that the PR in trials testing drugs for CRF is non-trivial in size and statistically significant. We recommend that researchers planning drug studies in CRF should consider implementing alternative trial designs to better account for PR and decrease impact on the study results.
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spelling pubmed-76918072020-12-09 Placebo response in trials of drug treatments for cancer-related fatigue: a systematic review, meta-analysis and meta-regression Roji, Rocio Stone, Patrick Ricciardi, Federico Candy, Bridget BMJ Support Palliat Care Review BACKGROUND: Cancer-related fatigue (CRF) is one of the most distressing symptoms experienced by patients. There is no gold standard treatment, although multiple drugs have been tested with little evidence of efficacy. Randomised controlled trials (RCTs) of these drugs have commented on the existence or size of the placebo response (PR). The objective of this systematic review was to establish the magnitude of the PR in RCTs of drugs to relieve CRF and to identify contributing factors. METHOD: RCTs were included in which the objective was to treat CRF. A meta-analysis was conducted using the standardised mean change (SMC) between baseline and final measurement in the placebo group. To explore factors that may be associated with the PR (eg, population or drug), a meta-regression was undertaken. Risk of bias was assessed using the revised Cochrane tool. RESULTS: From 3916 citations, 30 relevant RCTs were identified. All had limitations that increased their risk of bias. The pooled SMC in reduction in fatigue status in placebo groups was −0.23 (95% confidence intervals −0.42 to −0.04). None of the variables analysed in the meta-regression were statistically significant related to PR. CONCLUSION: There is some evidence, based on trials with small samples, that the PR in trials testing drugs for CRF is non-trivial in size and statistically significant. We recommend that researchers planning drug studies in CRF should consider implementing alternative trial designs to better account for PR and decrease impact on the study results. BMJ Publishing Group 2020-12 2020-02-11 /pmc/articles/PMC7691807/ /pubmed/32046962 http://dx.doi.org/10.1136/bmjspcare-2019-002163 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
spellingShingle Review
Roji, Rocio
Stone, Patrick
Ricciardi, Federico
Candy, Bridget
Placebo response in trials of drug treatments for cancer-related fatigue: a systematic review, meta-analysis and meta-regression
title Placebo response in trials of drug treatments for cancer-related fatigue: a systematic review, meta-analysis and meta-regression
title_full Placebo response in trials of drug treatments for cancer-related fatigue: a systematic review, meta-analysis and meta-regression
title_fullStr Placebo response in trials of drug treatments for cancer-related fatigue: a systematic review, meta-analysis and meta-regression
title_full_unstemmed Placebo response in trials of drug treatments for cancer-related fatigue: a systematic review, meta-analysis and meta-regression
title_short Placebo response in trials of drug treatments for cancer-related fatigue: a systematic review, meta-analysis and meta-regression
title_sort placebo response in trials of drug treatments for cancer-related fatigue: a systematic review, meta-analysis and meta-regression
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691807/
https://www.ncbi.nlm.nih.gov/pubmed/32046962
http://dx.doi.org/10.1136/bmjspcare-2019-002163
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