A Prospective Multicentre Study to Evaluate the Efficacy and Tolerability of Osmotic Release Oral System (Oros®) Hydromorphone in Opioid-Naive Cancer Patients: Results of the Korean South West Oncology Group Study

Author:

Song Eun-Kee1,Shim Hyunjeong2,Han Hye-Suk3,Sun DerSheng4,Lee Soon-Il5,Kang Myung Hee6,Lee KyuTaek7,Cho DoYeun8,Cho In Sung9,Park Suk Young10,Kim Samyong11,Yim Chang-Yeol1

Affiliation:

1. Department of Internal Medicine, Chonbuk National University Medical School and Research Institute of Clinical Medicine of Chonbuk National University – Biomedical Research Institute of Chonbuk National University Hospital, Jeonju, Republic of Korea

2. Department of Internal Medicine, Chonnam National University Hwasun Hospital, Gwangju, Republic of Korea

3. Department of Internal Medicine, College of Medicine, Chungbuk National University, Cheongju, Republic of Korea

4. Department of Internal Medicine, St. Mary’s Hospital, Cheongju, Republic of Korea

5. Department of Internal Medicine, Dankook University Hospital, Choenan, Republic of Korea

6. Department of Internal Medicine, Gyeongsang National University Hospital, Jinju, Republic of Korea

7. Department of Internal Medicine, Soon Chun Hyang University Cheonan Hospital, Cheonan, Republic of Korea

8. Department of Internal Medicine, Konyang University Hospital, Nonsan, Republic of Korea

9. Department of Internal Medicine, Eulji University Hospital, Republic of Korea

10. Department of Internal Medicine, The Catholic University Korea Daejeon St Mary’s Hospital, Republic of Korea

11. Department of Internal Medicine, Chungnam National University Hospital, Deajeon, Republic of Korea

Abstract

BACKGROUND: Osmotic release oral system (OROS®) hydromorphone is a potent, long-acting opioid analgesic, effective and safe for controlling cancer pain in patients who have received other strong opioids. To date, few studies have examined the efficacy of hydromorphone for pain relief in opioid-naive cancer patients.OBJECTIVES: A prospective, open-label, multicentre trial was conducted to determine the efficacy and tolerability of OROS hydromorphone as a single and front-line opioid therapy for patients experiencing moderate to severe cancer pain.METHODS: OROS hydromorphone was administered to patients who had not previously received strong, long-acting opioids. The baseline evaluation (visit 1) was followed by two evaluations (visits 2 and 3) performed two and 14 weeks later, respectively. The starting dose of OROS hydromorphone was 4 mg/day and was increased every two days when pain control was insufficient. Immediate-release hydromorphone was the only accepted alternative strong opioid for relief of breakthrough pain. The efficacy, safety and tolerability of OROS hydromorphone, including the effects on quality of life, and patients’ and investigators’ global impressions on pain relief were evaluated. The primary end point was pain intensity difference (PID) at visit 2 relative to visit 1 (expressed as %PID).RESULTS: A total of 107 patients were enrolled in the present study. An improvement in pain intensity of >50% (≥50% PID) was observed in 51.0% of the full analysis set and 58.6% of the per-protocol set. The mean pain score, measured using a numerical rating scale, was significantly reduced after two weeks of treatment, and most adverse events were manageable. Quality of life also improved, and >70% of patients and investigators were satisfied with the treatment.CONCLUSIONS: OROS hydromorphone provided effective pain relief and improved quality of life in opioid-naive cancer patients. As a single and front-line treatment, OROS hydromorphone delivered rapid pain control.

Publisher

Hindawi Limited

Subject

Anesthesiology and Pain Medicine,Neurology

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