Controlled-release oxycodone compared with controlled-release morphine in the treatment of cancer pain: a randomized, double-blind, parallel-group study

被引:127
|
作者
Mucci-LoRusso, P
Berman, BS
Silberstein, PT
Citron, ML
Bressler, L
Weinstein, SM
Kaiko, RF
Buckley, BJ
Reder, RF
机构
[1] Harper Grace Hosp, Div Hematol & Oncol, Detroit, MI 48201 USA
[2] Karmanos Canc Inst, Detroit, MI USA
[3] Treatment Ctr Canc & Blood Disorders PA, Kissimmee, FL USA
[4] N Iowa Mercy Hlth Ctr, Mercy Canc Ctr, Mason City, IA USA
[5] Long Isl Jewish Med Ctr, New Hyde Park, NY 11042 USA
[6] Univ Illinois Hosp, Chicago, IL USA
[7] Vet Adm Med Ctr, Chicago, IL USA
[8] Univ Texas, Md Anderson Canc Ctr, Houston, TX USA
[9] Purdue Pharma LP, Norwalk, CT USA
来源
EUROPEAN JOURNAL OF PAIN-LONDON | 1998年 / 2卷 / 03期
关键词
D O I
10.1016/S1090-3801(98)90020-9
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Controlled-release oral formulations of oxycodone and morphine are both suitable analgesics for moderate to severe pain. They were compared in cancer-pain patients randomized to double-blind treatment with controlled-release oxycodone (n = 48) or controlled-release morphine (n = 52) every 12 h for up to 12 days. Stable analgesia was achieved by 83% of controlled-release oxycodone and 81% of controlled-release morphine patients in 2 days (median). Following titration to stable analgesia, pain intensity (0 = none to 3 = severe) decreased from baseline within each group (p less than or equal to 0.005), from 1.9 (0.1) to 1.3 (0.1), mean (SE), with controlled-release oxycodone, and from 1.6 (0.1) to 1.0 (0.1) with controlled-release morphine (no significant between-group differences). Typical opioid adverse experiences were reported in both groups. Hallucinations were reported only with controlled-release morphine (n = 2). Visual analog scores (VAS) for 'itchy' and 'scratching' were lower with controlled-release oxycodone (p less than or equal to 0.044), as was peak-to-trough fluctuation in steady-state plasma concentration (p = 0.004). The correlation between plasma concentration and dose was stronger (p = 0.026) for oxycodone (0.7) than morphine (0.3). The relationship between pain intensity (VAS) and plasma concentration was more positive for oxycodone (p = 0.046). There was a positive relationship between morphine-6-glucuronide concentrations and urea nitrogen and creatinine levels (p = 0.0001). Controlled-release oxycodone was as effective as controlled-release morphine in relieving chronic cancer-related pain, and as easily titrated to the individual's need for pain control. While adverse experiences were similar, controlled-release oxycodone was associated with less itching and no hallucinations. Controlled-release oxycodone provides a rational alternative to controlled-release morphine for the management of moderate to severe cancer-related pain.
引用
收藏
页码:239 / 249
页数:11
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