{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,5]],"date-time":"2026-10-05T15:41:47Z","timestamp":1791214907128,"version":"4.1.0"},"reference-count":35,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2014,12,22]],"date-time":"2014-12-22T00:00:00Z","timestamp":1419206400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"Department of Health of Guangxi Zhuang Autonomous Region, People's Republic of China"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Asia-Pac J Clncl Oncology"],"published-print":{"date-parts":[[2017,4]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Aim<\/jats:title>\n                    <jats:p>\n                      To evaluate the efficacy and the safety of pregabalin (\n                      <jats:styled-content style=\"fixed-case\">PGB<\/jats:styled-content>\n                      )\u2010morphine combination for the treatment of neuropathic cancer pain (\n                      <jats:styled-content style=\"fixed-case\">NCP<\/jats:styled-content>\n                      ).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      <jats:styled-content style=\"fixed-case\">I<\/jats:styled-content>\n                      n this double\u2010blind, randomized, placebo (\n                      <jats:styled-content style=\"fixed-case\">PL<\/jats:styled-content>\n                      )\u2010controlled crossover study, 40 cancer patients with severe\n                      <jats:styled-content style=\"fixed-case\">NCP<\/jats:styled-content>\n                      were randomized into two groups (20 per group):\n                      <jats:styled-content style=\"fixed-case\">PGB\u2010PL<\/jats:styled-content>\n                      and\n                      <jats:styled-content style=\"fixed-case\">PL\u2010PGB<\/jats:styled-content>\n                      . Patients in the\n                      <jats:styled-content style=\"fixed-case\">PGB\u2010PL<\/jats:styled-content>\n                      group received\n                      <jats:styled-content style=\"fixed-case\">PGB<\/jats:styled-content>\n                      plus oral morphine in phase\n                      <jats:styled-content style=\"fixed-case\">I<\/jats:styled-content>\n                      , and\n                      <jats:styled-content style=\"fixed-case\">PL<\/jats:styled-content>\n                      plus oral morphine in phase\n                      <jats:styled-content style=\"fixed-case\">II<\/jats:styled-content>\n                      . The treatment sequence for the\n                      <jats:styled-content style=\"fixed-case\">PL\u2010PGB<\/jats:styled-content>\n                      group was\n                      <jats:styled-content style=\"fixed-case\">PL<\/jats:styled-content>\n                      plus oral morphine in phase\n                      <jats:styled-content style=\"fixed-case\">I<\/jats:styled-content>\n                      , and\n                      <jats:styled-content style=\"fixed-case\">PGB<\/jats:styled-content>\n                      plus oral morphine in phase\n                      <jats:styled-content style=\"fixed-case\">II<\/jats:styled-content>\n                      . These 2\u2010week treatment periods were separated by a 1\u2010week washout period. The primary outcome measure was the decrements in morphine dose; secondary outcomes included quantitative assessments of sleep (rated according to the Medical Outcomes Study Sleep Scale), the Constipation Assessment Scale and adverse effects.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      The mean minimal effective dose of morphine was 184.4\u2009\u00b1\u200969.9\u2009mg\/day in the period of\n                      <jats:styled-content style=\"fixed-case\">PGB<\/jats:styled-content>\n                      treatments, which was significantly lower than that of\n                      <jats:styled-content style=\"fixed-case\">PL<\/jats:styled-content>\n                      \u2010controls (228.7\u2009\u00b1\u200966.9\u2009mg\/day;\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u20090.001) and baseline (247.5\u2009\u00b1\u200980.0\u2009mg\/day;\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u20090.001). Compared with\n                      <jats:styled-content style=\"fixed-case\">PL<\/jats:styled-content>\n                      ,\n                      <jats:styled-content style=\"fixed-case\">PGB<\/jats:styled-content>\n                      resulted in a significant sleep improvement as measured by sleep disturbance, sleep quantity, and sleep problems index (\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u20090.001), as well as a Constipation Assessment Scale reduction (\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u20090.001).\n                      <jats:styled-content style=\"fixed-case\">PGB<\/jats:styled-content>\n                      resulted in a higher frequency of dry mouth and somnolence than\n                      <jats:styled-content style=\"fixed-case\">PL<\/jats:styled-content>\n                      (\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u20090.05).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      <jats:styled-content style=\"fixed-case\">PGB<\/jats:styled-content>\n                      enhances the efficacy of oral morphine and reduces dose\u2010related adverse reactions. The\n                      <jats:styled-content style=\"fixed-case\">PGB<\/jats:styled-content>\n                      \u2010morphine combination is an effective approach to controlling\n                      <jats:styled-content style=\"fixed-case\">NCP<\/jats:styled-content>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/ajco.12311","type":"journal-article","created":{"date-parts":[[2014,12,22]],"date-time":"2014-12-22T05:47:10Z","timestamp":1419227230000},"source":"Crossref","is-referenced-by-count":27,"title":["Efficacy and safety of pregabalin in patients with neuropathic cancer pain undergoing morphine therapy"],"prefix":"10.1111","volume":"13","author":[{"given":"Zhi","family":"Dou","sequence":"first","affiliation":[{"name":"Department of Pain Management First Affiliated Hospital of Guangxi Medical University Nanning Guangxi Province 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