Systemic Opioids for Dyspnea in Cancer Patients: A Real-world Observational Study
Although Systemic opioids are recommended as a pharmacological treatment for cancer-related dyspnea, their effectiveness and safety needs to be investigated in a real-world context To evaluate the effectiveness and safety of systemic regular opioids for dyspnea in cancer patients, in the real-world...
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Veröffentlicht in: | Journal of pain and symptom management 2023-05, Vol.65 (5), p.400-408 |
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creator | Yamaguchi, Takashi Matsunuma, Ryo Matsuda, Yoshinobu Tasaki, Junichi Ikari, Tomoo Miwa, Satoru Aiki, Sayo Takagi, Yusuke Kiuchi, Daisuke Suzuki, Kozue Oyamada, Shunsuke Ariyoshi, Keisuke Kihara, Kota Mori, Masanori |
description | Although Systemic opioids are recommended as a pharmacological treatment for cancer-related dyspnea, their effectiveness and safety needs to be investigated in a real-world context
To evaluate the effectiveness and safety of systemic regular opioids for dyspnea in cancer patients, in the real-world palliative care practice.
This was a multicenter prospective observational study. We consecutively enrolled adult cancer patients starting regular opioids (morphine, oxycodone, hydromorphone, or fentanyl) for dyspnea from 12 palliative care services across Japan. We evaluated dyspnea intensity using the Numerical Rating Scale (NRS) and Integrated Palliative Outcome Scale (IPOS) every 24 hours until 72 hours after starting opioids (T1–T3). We also evaluated common opioid-related adverse events (AEs) and other severe AEs.
We enrolled 402 cancer patients. The proportion of responders was 68.8% (95%confidence intervals (CI): 0.63–0.74) at T1, 75.7% (95%CI: 0.70–0.81) at T2, and 82.1% (95%CI: 0.76–0.87) at T3. The mean differences in dyspnea NRS from baseline were 1.73 (95%CI: 1.46–1.99) at T1, 1.99 (95%CI: 1.71–2.28) at T2, and 2.47 (95%CI:2.13–2.82) at T3. The most common treatment-emergent AE was somnolence with an incidence of the severe form of approximately 10% throughout the study period. In the multivariate analysis, baseline dyspnea NRS ≥6 had a positive correlation with dyspnea relief by systemic regular opioids, while liver metastasis, clinician-predicted survival days, and opioid tolerance had a negative correlation.
Regular systemic opioids were effective for dyspnea in real-world cancer patients. |
doi_str_mv | 10.1016/j.jpainsymman.2022.12.146 |
format | Article |
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To evaluate the effectiveness and safety of systemic regular opioids for dyspnea in cancer patients, in the real-world palliative care practice.
This was a multicenter prospective observational study. We consecutively enrolled adult cancer patients starting regular opioids (morphine, oxycodone, hydromorphone, or fentanyl) for dyspnea from 12 palliative care services across Japan. We evaluated dyspnea intensity using the Numerical Rating Scale (NRS) and Integrated Palliative Outcome Scale (IPOS) every 24 hours until 72 hours after starting opioids (T1–T3). We also evaluated common opioid-related adverse events (AEs) and other severe AEs.
We enrolled 402 cancer patients. The proportion of responders was 68.8% (95%confidence intervals (CI): 0.63–0.74) at T1, 75.7% (95%CI: 0.70–0.81) at T2, and 82.1% (95%CI: 0.76–0.87) at T3. The mean differences in dyspnea NRS from baseline were 1.73 (95%CI: 1.46–1.99) at T1, 1.99 (95%CI: 1.71–2.28) at T2, and 2.47 (95%CI:2.13–2.82) at T3. The most common treatment-emergent AE was somnolence with an incidence of the severe form of approximately 10% throughout the study period. In the multivariate analysis, baseline dyspnea NRS ≥6 had a positive correlation with dyspnea relief by systemic regular opioids, while liver metastasis, clinician-predicted survival days, and opioid tolerance had a negative correlation.
Regular systemic opioids were effective for dyspnea in real-world cancer patients.</description><identifier>ISSN: 0885-3924</identifier><identifier>EISSN: 1873-6513</identifier><identifier>DOI: 10.1016/j.jpainsymman.2022.12.146</identifier><identifier>PMID: 36641006</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Analgesics, Opioid - adverse effects ; cancer ; Drug Tolerance ; Dyspnea ; Dyspnea - drug therapy ; Dyspnea - etiology ; Humans ; Morphine - therapeutic use ; Neoplasms - complications ; Neoplasms - drug therapy ; opioid ; Oxycodone - therapeutic use ; palliative care ; real-world</subject><ispartof>Journal of pain and symptom management, 2023-05, Vol.65 (5), p.400-408</ispartof><rights>2023</rights><rights>Copyright © 2023. Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c487t-c6ee970670b721ddade87de63de04f783dcff6a785096117ee0295ada003d7263</citedby><cites>FETCH-LOGICAL-c487t-c6ee970670b721ddade87de63de04f783dcff6a785096117ee0295ada003d7263</cites><orcidid>0000-0002-8130-6815 ; 0000-0003-3060-0245 ; 0000-0001-5092-9377 ; 0000-0002-0305-1597 ; 0000-0002-5489-9395</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0885392423000040$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36641006$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yamaguchi, Takashi</creatorcontrib><creatorcontrib>Matsunuma, Ryo</creatorcontrib><creatorcontrib>Matsuda, Yoshinobu</creatorcontrib><creatorcontrib>Tasaki, Junichi</creatorcontrib><creatorcontrib>Ikari, Tomoo</creatorcontrib><creatorcontrib>Miwa, Satoru</creatorcontrib><creatorcontrib>Aiki, Sayo</creatorcontrib><creatorcontrib>Takagi, Yusuke</creatorcontrib><creatorcontrib>Kiuchi, Daisuke</creatorcontrib><creatorcontrib>Suzuki, Kozue</creatorcontrib><creatorcontrib>Oyamada, Shunsuke</creatorcontrib><creatorcontrib>Ariyoshi, Keisuke</creatorcontrib><creatorcontrib>Kihara, Kota</creatorcontrib><creatorcontrib>Mori, Masanori</creatorcontrib><title>Systemic Opioids for Dyspnea in Cancer Patients: A Real-world Observational Study</title><title>Journal of pain and symptom management</title><addtitle>J Pain Symptom Manage</addtitle><description>Although Systemic opioids are recommended as a pharmacological treatment for cancer-related dyspnea, their effectiveness and safety needs to be investigated in a real-world context
To evaluate the effectiveness and safety of systemic regular opioids for dyspnea in cancer patients, in the real-world palliative care practice.
This was a multicenter prospective observational study. We consecutively enrolled adult cancer patients starting regular opioids (morphine, oxycodone, hydromorphone, or fentanyl) for dyspnea from 12 palliative care services across Japan. We evaluated dyspnea intensity using the Numerical Rating Scale (NRS) and Integrated Palliative Outcome Scale (IPOS) every 24 hours until 72 hours after starting opioids (T1–T3). We also evaluated common opioid-related adverse events (AEs) and other severe AEs.
We enrolled 402 cancer patients. The proportion of responders was 68.8% (95%confidence intervals (CI): 0.63–0.74) at T1, 75.7% (95%CI: 0.70–0.81) at T2, and 82.1% (95%CI: 0.76–0.87) at T3. The mean differences in dyspnea NRS from baseline were 1.73 (95%CI: 1.46–1.99) at T1, 1.99 (95%CI: 1.71–2.28) at T2, and 2.47 (95%CI:2.13–2.82) at T3. The most common treatment-emergent AE was somnolence with an incidence of the severe form of approximately 10% throughout the study period. In the multivariate analysis, baseline dyspnea NRS ≥6 had a positive correlation with dyspnea relief by systemic regular opioids, while liver metastasis, clinician-predicted survival days, and opioid tolerance had a negative correlation.
Regular systemic opioids were effective for dyspnea in real-world cancer patients.</description><subject>Adult</subject><subject>Analgesics, Opioid - adverse effects</subject><subject>cancer</subject><subject>Drug Tolerance</subject><subject>Dyspnea</subject><subject>Dyspnea - drug therapy</subject><subject>Dyspnea - etiology</subject><subject>Humans</subject><subject>Morphine - therapeutic use</subject><subject>Neoplasms - complications</subject><subject>Neoplasms - drug therapy</subject><subject>opioid</subject><subject>Oxycodone - therapeutic use</subject><subject>palliative care</subject><subject>real-world</subject><issn>0885-3924</issn><issn>1873-6513</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEtLxDAQx4Mouj6-gsSbl66Tpk1Sb7I-QVif55BNppClL5PuSr-9XVbFozAwh_nN_JkfIWcMpgyYuFhOl53xTRzq2jTTFNJ0ysbKxA6ZMCV5InLGd8kElMoTXqTZATmMcQkAORd8nxxwITIGICbk-XWIPdbe0nnnW-8iLdtAr4fYNWiob-jMNBYDfTK9x6aPl_SKvqCpks82VI7OFxHDepy1janoa79ywzHZK00V8eS7H5H325u32X3yOL97mF09JjZTsk-sQCwkCAkLmTLnjEMlHQruELJSKu5sWQojVQ6FYEwiQlrkxhkA7mQq-BE5397tQvuxwtjr2keLVWUabFdRp1LkUirFYESLLWpDG2PAUnfB1yYMmoHeGNVL_ceo3hjVbKxsE3P6HbNa1Oh-N38UjsBsC-D47Npj0NGOqiw6H9D22rX-HzFf-fmNuQ</recordid><startdate>202305</startdate><enddate>202305</enddate><creator>Yamaguchi, Takashi</creator><creator>Matsunuma, Ryo</creator><creator>Matsuda, Yoshinobu</creator><creator>Tasaki, Junichi</creator><creator>Ikari, Tomoo</creator><creator>Miwa, Satoru</creator><creator>Aiki, Sayo</creator><creator>Takagi, Yusuke</creator><creator>Kiuchi, Daisuke</creator><creator>Suzuki, Kozue</creator><creator>Oyamada, Shunsuke</creator><creator>Ariyoshi, Keisuke</creator><creator>Kihara, Kota</creator><creator>Mori, Masanori</creator><general>Elsevier Inc</general><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>7X8</scope><orcidid>https://orcid.org/0000-0002-8130-6815</orcidid><orcidid>https://orcid.org/0000-0003-3060-0245</orcidid><orcidid>https://orcid.org/0000-0001-5092-9377</orcidid><orcidid>https://orcid.org/0000-0002-0305-1597</orcidid><orcidid>https://orcid.org/0000-0002-5489-9395</orcidid></search><sort><creationdate>202305</creationdate><title>Systemic Opioids for Dyspnea in Cancer Patients: A Real-world Observational Study</title><author>Yamaguchi, Takashi ; 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To evaluate the effectiveness and safety of systemic regular opioids for dyspnea in cancer patients, in the real-world palliative care practice.
This was a multicenter prospective observational study. We consecutively enrolled adult cancer patients starting regular opioids (morphine, oxycodone, hydromorphone, or fentanyl) for dyspnea from 12 palliative care services across Japan. We evaluated dyspnea intensity using the Numerical Rating Scale (NRS) and Integrated Palliative Outcome Scale (IPOS) every 24 hours until 72 hours after starting opioids (T1–T3). We also evaluated common opioid-related adverse events (AEs) and other severe AEs.
We enrolled 402 cancer patients. The proportion of responders was 68.8% (95%confidence intervals (CI): 0.63–0.74) at T1, 75.7% (95%CI: 0.70–0.81) at T2, and 82.1% (95%CI: 0.76–0.87) at T3. The mean differences in dyspnea NRS from baseline were 1.73 (95%CI: 1.46–1.99) at T1, 1.99 (95%CI: 1.71–2.28) at T2, and 2.47 (95%CI:2.13–2.82) at T3. The most common treatment-emergent AE was somnolence with an incidence of the severe form of approximately 10% throughout the study period. In the multivariate analysis, baseline dyspnea NRS ≥6 had a positive correlation with dyspnea relief by systemic regular opioids, while liver metastasis, clinician-predicted survival days, and opioid tolerance had a negative correlation.
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subjects | Adult Analgesics, Opioid - adverse effects cancer Drug Tolerance Dyspnea Dyspnea - drug therapy Dyspnea - etiology Humans Morphine - therapeutic use Neoplasms - complications Neoplasms - drug therapy opioid Oxycodone - therapeutic use palliative care real-world |
title | Systemic Opioids for Dyspnea in Cancer Patients: A Real-world Observational Study |
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