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Plasma Morphine and Metabolite Concentrations Are Associated With Clinical Effects of Morphine in Cancer Patients
Abstract Context Morphine is the opioid of choice for cancer-related pain, but for many patients the benefits of morphine are outweighed by its side effect profile. Morphine is metabolized to morphine-3-glucuronide and morphine-6-glucuronide; however, little is known about the contribution of these...
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Published in: | Journal of pain and symptom management 2013-04, Vol.45 (4), p.670-680 |
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creator | Gretton, Sophy K., PhD, MRCP Ross, Joy R., PhD, FRCP Rutter, Dag, MD, MBBS, MRCP Sato, Hiroe, MD, PhD Droney, Joanne M., PhD, MRCP Welsh, Kenneth I., PhD, FRCP (Hons) Joel, Simon, PhD Riley, Julia, MD, MRCGP, FRCP |
description | Abstract Context Morphine is the opioid of choice for cancer-related pain, but for many patients the benefits of morphine are outweighed by its side effect profile. Morphine is metabolized to morphine-3-glucuronide and morphine-6-glucuronide; however, little is known about the contribution of these metabolites to analgesia and morphine-related side effects. Objectives We investigated the association between plasma morphine and metabolite concentrations and the clinical effects of morphine in cancer patients. Methods A prospective study was performed in cancer patients taking oral morphine for moderate-to-severe cancer pain. Subjects who responded well to morphine (responders) and subjects who failed to respond to morphine because of lack of analgesia and/or the presence of intolerable side effects (nonresponders/switchers) were recruited. Pain and toxicity scores were recorded and blood samples were analyzed for plasma morphine, morphine-3-glucuronide, and morphine-6-glucuronide concentrations. Results Results showed that 1) morphine responders have higher plasma morphine and metabolite concentrations compared with nonresponders, 2) lower pain scores are associated with higher plasma morphine and metabolite concentrations, 3) central side effects are associated with a higher metabolite:plasma morphine ratio, and 4) myoclonus is associated with extremely high concentrations of plasma morphine and metabolites. Conclusion This study has shown that plasma morphine and metabolite concentrations are associated with the clinical effects of morphine therapy. These results are important because they demonstrate the relevance of measuring plasma metabolite concentrations in clinical trials and the potential for metabolite data to deepen our understanding of factors that influence an individual's response to morphine. |
doi_str_mv | 10.1016/j.jpainsymman.2012.03.015 |
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Morphine is metabolized to morphine-3-glucuronide and morphine-6-glucuronide; however, little is known about the contribution of these metabolites to analgesia and morphine-related side effects. Objectives We investigated the association between plasma morphine and metabolite concentrations and the clinical effects of morphine in cancer patients. Methods A prospective study was performed in cancer patients taking oral morphine for moderate-to-severe cancer pain. Subjects who responded well to morphine (responders) and subjects who failed to respond to morphine because of lack of analgesia and/or the presence of intolerable side effects (nonresponders/switchers) were recruited. Pain and toxicity scores were recorded and blood samples were analyzed for plasma morphine, morphine-3-glucuronide, and morphine-6-glucuronide concentrations. Results Results showed that 1) morphine responders have higher plasma morphine and metabolite concentrations compared with nonresponders, 2) lower pain scores are associated with higher plasma morphine and metabolite concentrations, 3) central side effects are associated with a higher metabolite:plasma morphine ratio, and 4) myoclonus is associated with extremely high concentrations of plasma morphine and metabolites. Conclusion This study has shown that plasma morphine and metabolite concentrations are associated with the clinical effects of morphine therapy. These results are important because they demonstrate the relevance of measuring plasma metabolite concentrations in clinical trials and the potential for metabolite data to deepen our understanding of factors that influence an individual's response to morphine.</description><identifier>ISSN: 0885-3924</identifier><identifier>EISSN: 1873-6513</identifier><identifier>DOI: 10.1016/j.jpainsymman.2012.03.015</identifier><identifier>PMID: 22995672</identifier><identifier>CODEN: JSPME2</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Analgesia ; Analgesics, Opioid - blood ; Analgesics, Opioid - therapeutic use ; Anesthesia & Perioperative Care ; Biological and medical sciences ; Biomarkers - blood ; Blood ; Cancer ; Causality ; Comorbidity ; Female ; Humans ; Male ; Medical sciences ; metabolite ; Middle Aged ; Morphine ; Morphine - blood ; Morphine - therapeutic use ; Multiple tumors. Solid tumors. Tumors in childhood (general aspects) ; Neoplasms - blood ; Neoplasms - epidemiology ; Neoplasms - nursing ; opioid ; Opioid-Related Disorders - blood ; Opioid-Related Disorders - epidemiology ; Pain ; Pain - blood ; Pain - epidemiology ; Pain - prevention & control ; Pain Measurement - drug effects ; Pain Measurement - statistics & numerical data ; Pain Medicine ; Pharmacology. Drug treatments ; Prevalence ; responder ; Risk Factors ; Side effects ; Statistics as Topic ; switcher ; Treatment Outcome ; Tumors ; United Kingdom - epidemiology</subject><ispartof>Journal of pain and symptom management, 2013-04, Vol.45 (4), p.670-680</ispartof><rights>U.S. Cancer Pain Relief Committee</rights><rights>2013 U.S. Cancer Pain Relief Committee</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2013 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c579t-9d31cb52a56069dd40b775e6e90a6196891c561c4bc3f935a42f79052a25bc8a3</citedby><cites>FETCH-LOGICAL-c579t-9d31cb52a56069dd40b775e6e90a6196891c561c4bc3f935a42f79052a25bc8a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925,31000</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27251047$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22995672$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gretton, Sophy K., PhD, MRCP</creatorcontrib><creatorcontrib>Ross, Joy R., PhD, FRCP</creatorcontrib><creatorcontrib>Rutter, Dag, MD, MBBS, MRCP</creatorcontrib><creatorcontrib>Sato, Hiroe, MD, PhD</creatorcontrib><creatorcontrib>Droney, Joanne M., PhD, MRCP</creatorcontrib><creatorcontrib>Welsh, Kenneth I., PhD, FRCP (Hons)</creatorcontrib><creatorcontrib>Joel, Simon, PhD</creatorcontrib><creatorcontrib>Riley, Julia, MD, MRCGP, FRCP</creatorcontrib><title>Plasma Morphine and Metabolite Concentrations Are Associated With Clinical Effects of Morphine in Cancer Patients</title><title>Journal of pain and symptom management</title><addtitle>J Pain Symptom Manage</addtitle><description>Abstract Context Morphine is the opioid of choice for cancer-related pain, but for many patients the benefits of morphine are outweighed by its side effect profile. Morphine is metabolized to morphine-3-glucuronide and morphine-6-glucuronide; however, little is known about the contribution of these metabolites to analgesia and morphine-related side effects. Objectives We investigated the association between plasma morphine and metabolite concentrations and the clinical effects of morphine in cancer patients. Methods A prospective study was performed in cancer patients taking oral morphine for moderate-to-severe cancer pain. Subjects who responded well to morphine (responders) and subjects who failed to respond to morphine because of lack of analgesia and/or the presence of intolerable side effects (nonresponders/switchers) were recruited. Pain and toxicity scores were recorded and blood samples were analyzed for plasma morphine, morphine-3-glucuronide, and morphine-6-glucuronide concentrations. Results Results showed that 1) morphine responders have higher plasma morphine and metabolite concentrations compared with nonresponders, 2) lower pain scores are associated with higher plasma morphine and metabolite concentrations, 3) central side effects are associated with a higher metabolite:plasma morphine ratio, and 4) myoclonus is associated with extremely high concentrations of plasma morphine and metabolites. Conclusion This study has shown that plasma morphine and metabolite concentrations are associated with the clinical effects of morphine therapy. These results are important because they demonstrate the relevance of measuring plasma metabolite concentrations in clinical trials and the potential for metabolite data to deepen our understanding of factors that influence an individual's response to morphine.</description><subject>Analgesia</subject><subject>Analgesics, Opioid - blood</subject><subject>Analgesics, Opioid - therapeutic use</subject><subject>Anesthesia & Perioperative Care</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>Blood</subject><subject>Cancer</subject><subject>Causality</subject><subject>Comorbidity</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>metabolite</subject><subject>Middle Aged</subject><subject>Morphine</subject><subject>Morphine - blood</subject><subject>Morphine - therapeutic use</subject><subject>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</subject><subject>Neoplasms - blood</subject><subject>Neoplasms - epidemiology</subject><subject>Neoplasms - nursing</subject><subject>opioid</subject><subject>Opioid-Related Disorders - blood</subject><subject>Opioid-Related Disorders - epidemiology</subject><subject>Pain</subject><subject>Pain - blood</subject><subject>Pain - epidemiology</subject><subject>Pain - prevention & control</subject><subject>Pain Measurement - drug effects</subject><subject>Pain Measurement - statistics & numerical data</subject><subject>Pain Medicine</subject><subject>Pharmacology. Drug treatments</subject><subject>Prevalence</subject><subject>responder</subject><subject>Risk Factors</subject><subject>Side effects</subject><subject>Statistics as Topic</subject><subject>switcher</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><subject>United Kingdom - epidemiology</subject><issn>0885-3924</issn><issn>1873-6513</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>7QJ</sourceid><recordid>eNqNkl2L1DAYhYso7rj6FyReCN605qNJmxthKOsH7OKCipchTd-yqW0ym7cjzL83w4yueOVVbp5zEp6conjFaMUoU2-natpZH_CwLDZUnDJeUVFRJh8VG9Y2olSSicfFhratLIXm9UXxDHGilEqhxNPignOtpWr4pri_nS0ultzEtLvzAYgNA7mB1fZx9iuQLgYHYU129TEg2SYgW8TovF1hIN_9eke62Qfv7EyuxhHciiSOD3U-kM7mikRuc0VuwufFk9HOCC_O52Xx7f3V1-5jef35w6due1062ei11INgrpfcSkWVHoaa9k0jQYGmVjGtWs2cVMzVvROjFtLWfGw0zQEue9dacVm8OfXuUrzfA65m8ehgnm2AuEfDRCNqTWtdZ1SfUJciYoLR7JJfbDoYRs3RuJnMX8bN0bihwmTjOfvyfM2-X2D4k_ytOAOvz4DFbGlMWYfHB67hktG6yVx34iBL-ekhGXRZmIPBp6zVDNH_13Pe_dPizt_zAw6AU9ynkK0bZjBnzJfjRI4LYZxSkechfgENhbo7</recordid><startdate>20130401</startdate><enddate>20130401</enddate><creator>Gretton, Sophy K., PhD, MRCP</creator><creator>Ross, Joy R., PhD, FRCP</creator><creator>Rutter, Dag, MD, MBBS, MRCP</creator><creator>Sato, Hiroe, MD, PhD</creator><creator>Droney, Joanne M., PhD, MRCP</creator><creator>Welsh, Kenneth I., PhD, FRCP (Hons)</creator><creator>Joel, Simon, PhD</creator><creator>Riley, Julia, MD, MRCGP, FRCP</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QJ</scope></search><sort><creationdate>20130401</creationdate><title>Plasma Morphine and Metabolite Concentrations Are Associated With Clinical Effects of Morphine in Cancer Patients</title><author>Gretton, Sophy K., PhD, MRCP ; Ross, Joy R., PhD, FRCP ; Rutter, Dag, MD, MBBS, MRCP ; Sato, Hiroe, MD, PhD ; Droney, Joanne M., PhD, MRCP ; Welsh, Kenneth I., PhD, FRCP (Hons) ; Joel, Simon, PhD ; Riley, Julia, MD, MRCGP, FRCP</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c579t-9d31cb52a56069dd40b775e6e90a6196891c561c4bc3f935a42f79052a25bc8a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Analgesia</topic><topic>Analgesics, Opioid - blood</topic><topic>Analgesics, Opioid - therapeutic use</topic><topic>Anesthesia & Perioperative Care</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - blood</topic><topic>Blood</topic><topic>Cancer</topic><topic>Causality</topic><topic>Comorbidity</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>metabolite</topic><topic>Middle Aged</topic><topic>Morphine</topic><topic>Morphine - blood</topic><topic>Morphine - therapeutic use</topic><topic>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</topic><topic>Neoplasms - blood</topic><topic>Neoplasms - epidemiology</topic><topic>Neoplasms - nursing</topic><topic>opioid</topic><topic>Opioid-Related Disorders - blood</topic><topic>Opioid-Related Disorders - epidemiology</topic><topic>Pain</topic><topic>Pain - blood</topic><topic>Pain - epidemiology</topic><topic>Pain - prevention & control</topic><topic>Pain Measurement - drug effects</topic><topic>Pain Measurement - statistics & numerical data</topic><topic>Pain Medicine</topic><topic>Pharmacology. Drug treatments</topic><topic>Prevalence</topic><topic>responder</topic><topic>Risk Factors</topic><topic>Side effects</topic><topic>Statistics as Topic</topic><topic>switcher</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><topic>United Kingdom - epidemiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gretton, Sophy K., PhD, MRCP</creatorcontrib><creatorcontrib>Ross, Joy R., PhD, FRCP</creatorcontrib><creatorcontrib>Rutter, Dag, MD, MBBS, MRCP</creatorcontrib><creatorcontrib>Sato, Hiroe, MD, PhD</creatorcontrib><creatorcontrib>Droney, Joanne M., PhD, MRCP</creatorcontrib><creatorcontrib>Welsh, Kenneth I., PhD, FRCP (Hons)</creatorcontrib><creatorcontrib>Joel, Simon, PhD</creatorcontrib><creatorcontrib>Riley, Julia, MD, MRCGP, FRCP</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Applied Social Sciences Index & Abstracts (ASSIA)</collection><jtitle>Journal of pain and symptom management</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gretton, Sophy K., PhD, MRCP</au><au>Ross, Joy R., PhD, FRCP</au><au>Rutter, Dag, MD, MBBS, MRCP</au><au>Sato, Hiroe, MD, PhD</au><au>Droney, Joanne M., PhD, MRCP</au><au>Welsh, Kenneth I., PhD, FRCP (Hons)</au><au>Joel, Simon, PhD</au><au>Riley, Julia, MD, MRCGP, FRCP</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasma Morphine and Metabolite Concentrations Are Associated With Clinical Effects of Morphine in Cancer Patients</atitle><jtitle>Journal of pain and symptom management</jtitle><addtitle>J Pain Symptom Manage</addtitle><date>2013-04-01</date><risdate>2013</risdate><volume>45</volume><issue>4</issue><spage>670</spage><epage>680</epage><pages>670-680</pages><issn>0885-3924</issn><eissn>1873-6513</eissn><coden>JSPME2</coden><abstract>Abstract Context Morphine is the opioid of choice for cancer-related pain, but for many patients the benefits of morphine are outweighed by its side effect profile. Morphine is metabolized to morphine-3-glucuronide and morphine-6-glucuronide; however, little is known about the contribution of these metabolites to analgesia and morphine-related side effects. Objectives We investigated the association between plasma morphine and metabolite concentrations and the clinical effects of morphine in cancer patients. Methods A prospective study was performed in cancer patients taking oral morphine for moderate-to-severe cancer pain. Subjects who responded well to morphine (responders) and subjects who failed to respond to morphine because of lack of analgesia and/or the presence of intolerable side effects (nonresponders/switchers) were recruited. Pain and toxicity scores were recorded and blood samples were analyzed for plasma morphine, morphine-3-glucuronide, and morphine-6-glucuronide concentrations. Results Results showed that 1) morphine responders have higher plasma morphine and metabolite concentrations compared with nonresponders, 2) lower pain scores are associated with higher plasma morphine and metabolite concentrations, 3) central side effects are associated with a higher metabolite:plasma morphine ratio, and 4) myoclonus is associated with extremely high concentrations of plasma morphine and metabolites. Conclusion This study has shown that plasma morphine and metabolite concentrations are associated with the clinical effects of morphine therapy. These results are important because they demonstrate the relevance of measuring plasma metabolite concentrations in clinical trials and the potential for metabolite data to deepen our understanding of factors that influence an individual's response to morphine.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>22995672</pmid><doi>10.1016/j.jpainsymman.2012.03.015</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analgesia Analgesics, Opioid - blood Analgesics, Opioid - therapeutic use Anesthesia & Perioperative Care Biological and medical sciences Biomarkers - blood Blood Cancer Causality Comorbidity Female Humans Male Medical sciences metabolite Middle Aged Morphine Morphine - blood Morphine - therapeutic use Multiple tumors. Solid tumors. Tumors in childhood (general aspects) Neoplasms - blood Neoplasms - epidemiology Neoplasms - nursing opioid Opioid-Related Disorders - blood Opioid-Related Disorders - epidemiology Pain Pain - blood Pain - epidemiology Pain - prevention & control Pain Measurement - drug effects Pain Measurement - statistics & numerical data Pain Medicine Pharmacology. Drug treatments Prevalence responder Risk Factors Side effects Statistics as Topic switcher Treatment Outcome Tumors United Kingdom - epidemiology |
title | Plasma Morphine and Metabolite Concentrations Are Associated With Clinical Effects of Morphine in Cancer Patients |
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