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Nonopioid drug combinations for cancer pain: a systematic review
Pain is highly prevalent in patients with cancer—nearly 40% report moderate-severe pain, which is commonly treated with opioids. Increasing cancer survivorship, opioid epidemics in some regions of the world, and limited opioid access in other regions have focused attention on nonopioid treatments. G...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8893303/ https://www.ncbi.nlm.nih.gov/pubmed/35261931 http://dx.doi.org/10.1097/PR9.0000000000000995 |
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author | Sohi, Gursharan Lao, Nicholas Caraceni, Augusto Moulin, Dwight E. Zimmermann, Camilla Herx, Leonie Gilron, Ian |
author_facet | Sohi, Gursharan Lao, Nicholas Caraceni, Augusto Moulin, Dwight E. Zimmermann, Camilla Herx, Leonie Gilron, Ian |
author_sort | Sohi, Gursharan |
collection | PubMed |
description | Pain is highly prevalent in patients with cancer—nearly 40% report moderate-severe pain, which is commonly treated with opioids. Increasing cancer survivorship, opioid epidemics in some regions of the world, and limited opioid access in other regions have focused attention on nonopioid treatments. Given the limitations of monotherapy, combining nonopioids—such as antiepileptics and antidepressants—have shown promise in noncancer pain. This review seeks to evaluate efficacy of nonopioid combinations for cancer-related pain. Systematic searches of PubMed, EMBASE, and Cochrane CENTRAL were conducted for double-blind, randomized, controlled trials comparing a nonopioid combination with at least one of its components and/or placebo. This search yielded 4 randomized controlled trials, published between 1998 and 2019 involving studies of (1) imipramine + diclofenac; (2) mitoxantrone + prednisone + clodronate; (3) pentoxifylline + tocopherol + clodronate; and (4) duloxetine + pregabalin + opioid. In the first 3 of these trials, trends favouring combination efficacy failed to reach statistical significance. However, in the fourth trial, duloxetine + pregabalin + opioid was superior to pregabalin + opioid. This review illustrates recognition for the need to evaluate nonopioid drug combinations in cancer pain, although few trials have been published to date. Given the growing practice of prescribing more than 1 nonopioid for cancer pain and the need to expand the evidence base for rational combination therapy, more high-quality trials in this area are needed. |
format | Online Article Text |
id | pubmed-8893303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
spelling | pubmed-88933032022-03-07 Nonopioid drug combinations for cancer pain: a systematic review Sohi, Gursharan Lao, Nicholas Caraceni, Augusto Moulin, Dwight E. Zimmermann, Camilla Herx, Leonie Gilron, Ian Pain Rep Cancer and Palliative Pain is highly prevalent in patients with cancer—nearly 40% report moderate-severe pain, which is commonly treated with opioids. Increasing cancer survivorship, opioid epidemics in some regions of the world, and limited opioid access in other regions have focused attention on nonopioid treatments. Given the limitations of monotherapy, combining nonopioids—such as antiepileptics and antidepressants—have shown promise in noncancer pain. This review seeks to evaluate efficacy of nonopioid combinations for cancer-related pain. Systematic searches of PubMed, EMBASE, and Cochrane CENTRAL were conducted for double-blind, randomized, controlled trials comparing a nonopioid combination with at least one of its components and/or placebo. This search yielded 4 randomized controlled trials, published between 1998 and 2019 involving studies of (1) imipramine + diclofenac; (2) mitoxantrone + prednisone + clodronate; (3) pentoxifylline + tocopherol + clodronate; and (4) duloxetine + pregabalin + opioid. In the first 3 of these trials, trends favouring combination efficacy failed to reach statistical significance. However, in the fourth trial, duloxetine + pregabalin + opioid was superior to pregabalin + opioid. This review illustrates recognition for the need to evaluate nonopioid drug combinations in cancer pain, although few trials have been published to date. Given the growing practice of prescribing more than 1 nonopioid for cancer pain and the need to expand the evidence base for rational combination therapy, more high-quality trials in this area are needed. Wolters Kluwer 2021-03-02 /pmc/articles/PMC8893303/ /pubmed/35261931 http://dx.doi.org/10.1097/PR9.0000000000000995 Text en Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The International Association for the Study of Pain. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Cancer and Palliative Sohi, Gursharan Lao, Nicholas Caraceni, Augusto Moulin, Dwight E. Zimmermann, Camilla Herx, Leonie Gilron, Ian Nonopioid drug combinations for cancer pain: a systematic review |
title | Nonopioid drug combinations for cancer pain: a systematic review |
title_full | Nonopioid drug combinations for cancer pain: a systematic review |
title_fullStr | Nonopioid drug combinations for cancer pain: a systematic review |
title_full_unstemmed | Nonopioid drug combinations for cancer pain: a systematic review |
title_short | Nonopioid drug combinations for cancer pain: a systematic review |
title_sort | nonopioid drug combinations for cancer pain: a systematic review |
topic | Cancer and Palliative |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8893303/ https://www.ncbi.nlm.nih.gov/pubmed/35261931 http://dx.doi.org/10.1097/PR9.0000000000000995 |
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