Imkamp Maike S V, Theunissen Maurice, Viechtbauer Wolfgang, van Kuijk Sander M J, van den Beuken-van Everdingen Marieke H J
Center of Expertise for Palliative Care; (M.S.V.I., M.T., M.H.J.V.D.B.); Maastricht University Medical Center+ (MUMC+); Maastricht; Netherlands; Department of Clinical Epidemiology and Medical Technology; (M.S.V.I., S.M.J.V.K.); Maastricht University Medical Center+ (MUMC+); Maastricht; Netherlands.
Center of Expertise for Palliative Care; (M.S.V.I., M.T., M.H.J.V.D.B.); Maastricht University Medical Center+ (MUMC+); Maastricht; Netherlands.
J Pain Symptom Manage. 2024 Sep;68(3):223-236. doi: 10.1016/j.jpainsymman.2024.05.022. Epub 2024 Jun 4.
Strong opioids are the cornerstone in the treatment of cancer-related pain.
This study aims to compare analgesic effectiveness of different strong opioids for the treatment of cancer-related pain.
PubMed and Embase were searched for RCTs that compared strong opioids for treatment of cancer-related pain against one another. A network meta-analysis was conducted and the related Surface Under the Cumulative RAnking (SUCRA)-based treatment ranks were calculated. Primary outcome was pain intensity (numerical rating scale (NRS)) and/or the percentage of patients with ≥50% pain reduction, after 1 and 2-4 weeks.
Sixteen RCTs (1813 patients) were included. Methadone showed, with a high certainty of evidence, increased ORs for treatment success at 1 week, compared with morphine, buprenorphine, fentanyl, and oxycodone, range 3.230-36.833. Methadone had the highest likelihood to be the treatment of preference (ToP) (SUCRA 0.9720). For fentanyl, ORs were lower, however significant and with high certainty. After 2-4 weeks, methadone again showed the highest likelihood for ToP, however, with moderate certainty and nonsignificant ORs. The combination of morphine/methadone, compared with morphine, buprenorphine, fentanyl, hydromorphone, methadone, and oxycodone achieved a treatment effect of mean NRS difference after 2-4 weeks between -1.100 and -1.528 and had the highest likelihood for ToP.
The results suggest that methadone possibly deserves further promotion as first-line treatment for the treatment of cancer-related pain.
强效阿片类药物是治疗癌症相关疼痛的基石。
本研究旨在比较不同强效阿片类药物治疗癌症相关疼痛的镇痛效果。
检索PubMed和Embase数据库,查找比较强效阿片类药物治疗癌症相关疼痛效果的随机对照试验(RCT)。进行网状Meta分析,并计算基于累积排序曲线下面积(SUCRA)的相关治疗排名。主要结局指标为1周以及2 - 4周后疼痛强度(数字评分量表(NRS))和/或疼痛减轻≥50%的患者百分比。
纳入16项RCT(1813例患者)。与吗啡、丁丙诺啡、芬太尼和羟考酮相比,美沙酮在1周时治疗成功的优势比(OR)增加,证据确定性高,范围为3.230 - 36.833。美沙酮最有可能成为首选治疗药物(ToP)(SUCRA 0.9720)。对于芬太尼,OR较低,但具有显著性且证据确定性高。在2 - 4周后,美沙酮再次显示出成为ToP的可能性最高,但证据确定性中等且OR无显著性差异。吗啡/美沙酮联合用药与吗啡、丁丙诺啡、芬太尼、氢吗啡酮、美沙酮和羟考酮相比,在2 - 4周后的平均NRS差异治疗效果在 - 1.100至 - 1.528之间,且成为ToP的可能性最高。
结果表明,美沙酮可能值得进一步推广作为治疗癌症相关疼痛的一线治疗药物。