Shirley K. Chan Sanchez, Samuel V. David, Efstathia Polychronopoulou, Mukaila Raji, Yong-Fang Kuo
{"title":"阿片类药物和阿片类替代品对癌症幸存者疼痛和健康相关生活质量的比较效果","authors":"Shirley K. Chan Sanchez, Samuel V. David, Efstathia Polychronopoulou, Mukaila Raji, Yong-Fang Kuo","doi":"10.1002/cam4.71189","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Introduction</h3>\n \n <p>Chronic pain is a major but modifiable contributor to poor quality of life among long-term cancer survivors. With growing concern over opioid-related risks, gabapentinoids have emerged as a safer alternative, though evidence comparing their effectiveness remains limited.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>We conducted a retrospective cohort study using SEER-MHOS linked data (1998–2021) to examine pain interference and health-related quality of life (HRQoL) among 24,651 cancer survivors. Participants were categorized as opioid-only (OPIOID-only), gabapentinoid-only (GABA-only), both (BOTH), or no medication (NONE). Changes in pain interference and Physical and Mental Component Summary scores (PCS, MCS) were analyzed using paired t-tests and multivariate regression, adjusting for demographic and clinical covariates.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Over a 1 to 3 year follow-up, all groups showed increased pain interference and declines in PCS and MCS scores. PCS declined by −1.01 in the OPIOID-only group and −1.06 in the GABA-only group. The BOTH group had stable PCS (+0.06) and a modest improvement in pain interference (−0.07). Multivariate models showed no significant difference between OPIOID-only and GABA-only for pain interference or PCS, but the BOTH group had significantly less pain worsening (<i>p</i> = 0.0001) and PCS decline (<i>p</i> = 0.004).</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Gabapentinoids demonstrate comparable effectiveness as opioids for pain and HRQoL in cancer survivors, supporting their use as a safer alternative. Combination therapy showed better physical function and pain control, but findings may reflect higher baseline comorbidity and limited decline capacity rather than true superiority. These results underscored the need for personalized, multimodal pain management and further research on the long-term safety of combination therapy.</p>\n </section>\n </div>","PeriodicalId":139,"journal":{"name":"Cancer Medicine","volume":"14 17","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cam4.71189","citationCount":"0","resultStr":"{\"title\":\"Comparative Effectiveness of Opioids and Opioid Substitutes on Pain and Health Related Quality of Life Among Cancer Survivors\",\"authors\":\"Shirley K. Chan Sanchez, Samuel V. 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Changes in pain interference and Physical and Mental Component Summary scores (PCS, MCS) were analyzed using paired t-tests and multivariate regression, adjusting for demographic and clinical covariates.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Over a 1 to 3 year follow-up, all groups showed increased pain interference and declines in PCS and MCS scores. PCS declined by −1.01 in the OPIOID-only group and −1.06 in the GABA-only group. The BOTH group had stable PCS (+0.06) and a modest improvement in pain interference (−0.07). Multivariate models showed no significant difference between OPIOID-only and GABA-only for pain interference or PCS, but the BOTH group had significantly less pain worsening (<i>p</i> = 0.0001) and PCS decline (<i>p</i> = 0.004).</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusion</h3>\\n \\n <p>Gabapentinoids demonstrate comparable effectiveness as opioids for pain and HRQoL in cancer survivors, supporting their use as a safer alternative. Combination therapy showed better physical function and pain control, but findings may reflect higher baseline comorbidity and limited decline capacity rather than true superiority. 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Comparative Effectiveness of Opioids and Opioid Substitutes on Pain and Health Related Quality of Life Among Cancer Survivors
Introduction
Chronic pain is a major but modifiable contributor to poor quality of life among long-term cancer survivors. With growing concern over opioid-related risks, gabapentinoids have emerged as a safer alternative, though evidence comparing their effectiveness remains limited.
Methods
We conducted a retrospective cohort study using SEER-MHOS linked data (1998–2021) to examine pain interference and health-related quality of life (HRQoL) among 24,651 cancer survivors. Participants were categorized as opioid-only (OPIOID-only), gabapentinoid-only (GABA-only), both (BOTH), or no medication (NONE). Changes in pain interference and Physical and Mental Component Summary scores (PCS, MCS) were analyzed using paired t-tests and multivariate regression, adjusting for demographic and clinical covariates.
Results
Over a 1 to 3 year follow-up, all groups showed increased pain interference and declines in PCS and MCS scores. PCS declined by −1.01 in the OPIOID-only group and −1.06 in the GABA-only group. The BOTH group had stable PCS (+0.06) and a modest improvement in pain interference (−0.07). Multivariate models showed no significant difference between OPIOID-only and GABA-only for pain interference or PCS, but the BOTH group had significantly less pain worsening (p = 0.0001) and PCS decline (p = 0.004).
Conclusion
Gabapentinoids demonstrate comparable effectiveness as opioids for pain and HRQoL in cancer survivors, supporting their use as a safer alternative. Combination therapy showed better physical function and pain control, but findings may reflect higher baseline comorbidity and limited decline capacity rather than true superiority. These results underscored the need for personalized, multimodal pain management and further research on the long-term safety of combination therapy.
期刊介绍:
Cancer Medicine is a peer-reviewed, open access, interdisciplinary journal providing rapid publication of research from global biomedical researchers across the cancer sciences. The journal will consider submissions from all oncologic specialties, including, but not limited to, the following areas:
Clinical Cancer Research
Translational research ∙ clinical trials ∙ chemotherapy ∙ radiation therapy ∙ surgical therapy ∙ clinical observations ∙ clinical guidelines ∙ genetic consultation ∙ ethical considerations
Cancer Biology:
Molecular biology ∙ cellular biology ∙ molecular genetics ∙ genomics ∙ immunology ∙ epigenetics ∙ metabolic studies ∙ proteomics ∙ cytopathology ∙ carcinogenesis ∙ drug discovery and delivery.
Cancer Prevention:
Behavioral science ∙ psychosocial studies ∙ screening ∙ nutrition ∙ epidemiology and prevention ∙ community outreach.
Bioinformatics:
Gene expressions profiles ∙ gene regulation networks ∙ genome bioinformatics ∙ pathwayanalysis ∙ prognostic biomarkers.
Cancer Medicine publishes original research articles, systematic reviews, meta-analyses, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented in the paper.