Efficacy and Tolerability of Oxycodone Hydrochloride Controlled-Release Tablets in Moderate to Severe Cancer Pain
Authors: Pan, Hongming1; Zhang, Zaiyun2; Zhang, Yiping3; Xu, Nong4; Lu, Liqin5; Dou, Chunfeng6; Guo, Yong7; Wu, Shixiu8; Yue, Jianhua9; Wu, Dongping10; Dai, Yuechu11
Source: Clinical Drug Investigation, Volume 27, Number 4, 2007 , pp. 259-267(9)
Publisher: Adis International
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Abstract:
Background and objective: Oxycodone is a semisynthetic opioid analgesic drug classed as a strong opioid. The controlled-release oxycodone tablet formulation (OCRT) was approved in China in 2004 for management of moderate to severe cancer pain. Few data about the efficacy of OCRT and clinical outcomes in Chinese patients taking this drug are available. The purpose of this study was to evaluate the efficacy and tolerability of this drug for relief of moderate to severe cancer pain in Chinese patients.Methods: This was a prospective, open-label, multicentre clinical trial carried out in ten hospitals in Zhejiang Province, China. Patients with cancer pain with a score ≥4 (numerical rating scale) were enrolled. They received oral OCRT at an initial dosage of 5mg every 12 hours for patients scoring 4-6 and 10mg every 12 hours for patients scoring ≥7. Doses were then titrated on an individual basis. Onset of analgesic action, pain score and quality-of-life (QOL) scores - including items measuring family understanding and support, sleep, mental state, appetite, fatigue, and activities of daily life - were evaluated. Adverse effects were also documented.Results: 216 patients (126 males and 90 females) aged 22-84 years were enrolled. The total mean OCRT dosage was 445.2 ± 361.6mg (range 130-2320mg). The daily dosages of the vast majority of cases (89%) were between 10mg and 30mg. Onset of analgesic action occurred within 1 hour in 198 cases (91.7%) following administration of OCRT. 82.4% of cases were titrated to a steady dosage level within 2 days following administration of the first dose of medication. Pain score decreased significantly (p < 0.01) from 7.1 ± 1.2 at baseline to 2.3 ± 1.2 one week after starting medication and 1.8 ± 0.9 four weeks after starting medication. Scores on all six QOL items increased significantly (p < 0.01) compared with baseline but showed varying rates of improvement. Adverse events included constipation, nausea, vomiting, drowsiness and dysuria. These were noted most frequently in the first week (25.5% of patients) and lessened over time. No severe adverse events were noted.Conclusion: We conclude that OCRT is well tolerated and effective in controlling moderate to severe cancer pain in Chinese patients.Keywords: Cancer pain; Opioid analgesics; Oxycodone
Document Type: Research article
Affiliations: 1: 1 Medical Oncology Department, Sir Run Run Shaw Hospital, Medical School of Zhejiang University, Hangzhou, China 2: 2 Oncology Department, Sir Run Run Shaw Hospital, Medical School of Zhejiang University, Hangzhou, China 3: 3 Chemotherapy Department, Zhejiang Cancer Hospital, Hangzhou, China 4: 4 Chemotherapy Department, The First Hospital Affiliated to Medical School of Zhejiang University, Zhejiang, China 5: 5 Oncology Department, Zhejiang Provincial Hospital, Hangzhou, China 6: 6 Oncology Department, Zhejiang Hospital, Hangzhou, China 7: 7 Oncology Department, Zhejiang Provincial Traditional Chinese Medicine Hospital, Hangzhou, China 8: 8 Oncology Department, The First Hospital Affiliated to Wenzhou Medical College, Wenzhou, China 9: 9 Oncology Department, Hangzhou Armed Police Hospital, Hangzhou, China 10: 10 Oncology Department, The People's Hospital of Shaoxing City, Shaoxing, China 11: 11 Oncology Department, Central Hospital of Taizhou City, Taizhou, China
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