Department of Chemotherapy, Zhejiang Cancer Hospital, Hangzhou, Zhejiang, China (mainland).
Key Laboratory Diagnosis and Treatment Technology on Thoracic Oncology, Hangzhou, Zhejiang, China (mainland).
Med Sci Monit. 2018 Sep 19;24:6750-6755. doi: 10.12659/MSM.909691.
BACKGROUND Opioid analgesics are used to relieve pain in patients with cancer and can improve their quality of life. This study aimed to investigate the efficacy and tolerability of high-dose (>150 mg/day) controlled-release oxycodone for the control of pain in patients with advanced solid malignant tumors. MATERIAL AND METHODS A retrospective clinical study was undertaken to include patients with advanced cancer treated at the Zhejiang Cancer Hospital who had treatment that included high-dose controlled-release oxycodone. The subjective numeric rating scale (NRS) for assessment of pain intensity (scores between 0-10) was used in all cases. RESULTS The study included 131 patients with advanced solid tumors with moderate to severe cancer pain. The mean NRS score before commencing high-dose controlled-release oxycodone was 7.10. The effective rate of relief pain was achieved in 90.1% (118/131) of patients, with an average effective dose of controlled-release oxycodone of 177.18±11.71 mg/day, resulting in a mean NRS of 2.15. There were 51 patients who achieved pain relief with mean treatment duration of 49.98±11.71 days. Combination therapy was required in 79 patients. Additional drugs included gabapentin (43 patients), pregabalin (10 patients) and non-steroidal anti-inflammatory drugs (NSAIDS) (26 patients). The main side effects of high-dose controlled-release oxycodone included constipation, nausea, vomiting, dysuria, dizziness, and drowsiness, but no patients discontinued treatment because of these. CONCLUSIONS This study showed that high-dose controlled-release oxycodone could effectively relieve moderate to severe cancer pain, without side effects that were severe enough to result in discontinuation of treatment.
阿片类镇痛药用于缓解癌症患者的疼痛,并能提高他们的生活质量。本研究旨在探讨高剂量(>150mg/天)控释羟考酮治疗晚期实体恶性肿瘤患者疼痛的疗效和耐受性。
对浙江省肿瘤医院收治的使用高剂量控释羟考酮治疗的晚期癌症患者进行回顾性临床研究。所有患者均采用主观数字评分量表(NRS)评估疼痛强度(评分 0-10 分)。
本研究纳入 131 例中重度癌痛的晚期实体瘤患者。起始高剂量控释羟考酮前,NRS 评分均值为 7.10。90.1%(118/131)的患者疼痛缓解有效,平均控释羟考酮有效剂量为 177.18±11.71mg/天,NRS 评分为 2.15。51 例患者疼痛缓解,平均治疗持续时间为 49.98±11.71 天。79 例患者需要联合治疗,包括加巴喷丁(43 例)、普瑞巴林(10 例)和非甾体抗炎药(NSAIDs)(26 例)。高剂量控释羟考酮的主要副作用包括便秘、恶心、呕吐、排尿困难、头晕和嗜睡,但没有患者因这些副作用而停止治疗。
本研究表明,高剂量控释羟考酮能有效缓解中重度癌痛,且无严重不良反应导致治疗中断。