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Cancer pain therapy with a fixed combination of prolonged-release oxycodone/naloxone: results from a non-interventional study
BACKGROUND: Strong opioids, including oxycodone, are the most effective analgesics used to combat moderate to severe cancer pain, but opioid-induced bowel dysfunction is a relevant problem associated with the therapy. Clinical studies have demonstrated equivalent analgesic efficacy and improved bowe...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045016/ https://www.ncbi.nlm.nih.gov/pubmed/27774024 http://dx.doi.org/10.2147/POR.S49793 |
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author | Nolte, Thomas Schutter, Ulf Loewenstein, Oliver |
author_facet | Nolte, Thomas Schutter, Ulf Loewenstein, Oliver |
author_sort | Nolte, Thomas |
collection | PubMed |
description | BACKGROUND: Strong opioids, including oxycodone, are the most effective analgesics used to combat moderate to severe cancer pain, but opioid-induced bowel dysfunction is a relevant problem associated with the therapy. Clinical studies have demonstrated equivalent analgesic efficacy and improved bowel function in treatment with a fixed combination of prolonged-release (PR) oxycodone and PR naloxone compared to oxycodone alone in patients with nonmalignant pain. Here, we report of a prospective, non-interventional study evaluating the effectiveness and safety of PR oxycodone/PR naloxone in a subgroup of patients with severe cancer pain. PATIENTS AND METHODS: Within the non-interventional multicenter study, 1,178 cancer patients with severe chronic pain received PR oxycodone/PR naloxone, dosed according to pain intensity, for 4 weeks. Recorded variables included pain intensity, patient-reported bowel function (Bowel Function Index), and pain-related functional impairment as a measure of quality of life (QoL). RESULTS: During treatment with PR oxycodone/PR naloxone, clinically relevant improvements in pain intensity were observed in opioid-naïve patients and in patients pretreated with weak or strong opioids, as reflected by reductions in pain scores of 51%, 53%, and 33%, respectively. Improvement in analgesia was paralleled by a significant reduction of opioid-induced bowel dysfunction in opioid-pretreated patients. The reductions in the mean Bowel Function Index of −20.5 and −36.5 in patients pretreated with weak and strong opioids, respectively, represent clinically relevant improvements in bowel function. Pain-related functional impairment decreased consistently across all seven domains, which is equivalent to a substantial improvement in QoL. CONCLUSION: This subgroup analysis of cancer patients within a large non-interventional study demonstrates that treatment with PR oxycodone/PR naloxone provides effective analgesia with minimization of bowel dysfunction and improved QoL. These data extend our knowledge of the effectiveness and tolerability of PR oxycodone/PR naloxone to the population of patients with cancer under real-life conditions. |
format | Online Article Text |
id | pubmed-5045016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50450162016-10-21 Cancer pain therapy with a fixed combination of prolonged-release oxycodone/naloxone: results from a non-interventional study Nolte, Thomas Schutter, Ulf Loewenstein, Oliver Pragmat Obs Res Original Research BACKGROUND: Strong opioids, including oxycodone, are the most effective analgesics used to combat moderate to severe cancer pain, but opioid-induced bowel dysfunction is a relevant problem associated with the therapy. Clinical studies have demonstrated equivalent analgesic efficacy and improved bowel function in treatment with a fixed combination of prolonged-release (PR) oxycodone and PR naloxone compared to oxycodone alone in patients with nonmalignant pain. Here, we report of a prospective, non-interventional study evaluating the effectiveness and safety of PR oxycodone/PR naloxone in a subgroup of patients with severe cancer pain. PATIENTS AND METHODS: Within the non-interventional multicenter study, 1,178 cancer patients with severe chronic pain received PR oxycodone/PR naloxone, dosed according to pain intensity, for 4 weeks. Recorded variables included pain intensity, patient-reported bowel function (Bowel Function Index), and pain-related functional impairment as a measure of quality of life (QoL). RESULTS: During treatment with PR oxycodone/PR naloxone, clinically relevant improvements in pain intensity were observed in opioid-naïve patients and in patients pretreated with weak or strong opioids, as reflected by reductions in pain scores of 51%, 53%, and 33%, respectively. Improvement in analgesia was paralleled by a significant reduction of opioid-induced bowel dysfunction in opioid-pretreated patients. The reductions in the mean Bowel Function Index of −20.5 and −36.5 in patients pretreated with weak and strong opioids, respectively, represent clinically relevant improvements in bowel function. Pain-related functional impairment decreased consistently across all seven domains, which is equivalent to a substantial improvement in QoL. CONCLUSION: This subgroup analysis of cancer patients within a large non-interventional study demonstrates that treatment with PR oxycodone/PR naloxone provides effective analgesia with minimization of bowel dysfunction and improved QoL. These data extend our knowledge of the effectiveness and tolerability of PR oxycodone/PR naloxone to the population of patients with cancer under real-life conditions. Dove Medical Press 2013-12-19 /pmc/articles/PMC5045016/ /pubmed/27774024 http://dx.doi.org/10.2147/POR.S49793 Text en © 2014 Nolte et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Nolte, Thomas Schutter, Ulf Loewenstein, Oliver Cancer pain therapy with a fixed combination of prolonged-release oxycodone/naloxone: results from a non-interventional study |
title | Cancer pain therapy with a fixed combination of prolonged-release oxycodone/naloxone: results from a non-interventional study |
title_full | Cancer pain therapy with a fixed combination of prolonged-release oxycodone/naloxone: results from a non-interventional study |
title_fullStr | Cancer pain therapy with a fixed combination of prolonged-release oxycodone/naloxone: results from a non-interventional study |
title_full_unstemmed | Cancer pain therapy with a fixed combination of prolonged-release oxycodone/naloxone: results from a non-interventional study |
title_short | Cancer pain therapy with a fixed combination of prolonged-release oxycodone/naloxone: results from a non-interventional study |
title_sort | cancer pain therapy with a fixed combination of prolonged-release oxycodone/naloxone: results from a non-interventional study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045016/ https://www.ncbi.nlm.nih.gov/pubmed/27774024 http://dx.doi.org/10.2147/POR.S49793 |
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