• Neal E Slatkin, Michelle I Rhiner, Errol M Gould, Tina Ma, and Harry Ahdieh.
• Department of Supportive Care, Pain & Palliative Medicine, City of Hope Medical Group (California Cancer Specialists Medical Group), Pasadena, California, USA.
• J Opioid Manag. 2010 May 1;6(3):181-91.

ObjectiveTo evaluate the long-term safety, tolerability, and effectiveness of oxymorphone extended release (ER) in patients with cancer-related pain.DesignPost hoc analysis of two-1-year open-label extension studies.SettingMultiple US cancer treatment facilities.PatientsPatients with cancer pain who had participated in two short-term crossover comparator trials of oxymorphone ER: one open-label and one double-blind randomized.InterventionsPatients who had been taking oxymorphone ER continued the dose established in the previous study. Patients who had been taking a comparator opioid were switched to an equianalgesic dose of oxymorphone ER. All patients underwent individualized oxymorphone ER dose titration to optimize effectiveness and tolerability.AssessmentsCurrent, average, worst, and least pain scores were normalized to a 100-point scale. Patients rated treatment on a five-point global assessment of study medication (Poor = 1 to Excellent = 5). All adverse events (AEs) were recorded.ResultsOf the 80 patients who entered the extension trials, 26 completed 52 weeks, 7 discontinued owing to loss of effectiveness, and 20 discontinued owing to AEs, most of which were unrelated to study drug. No significant increase in mean (standard deviation [SDD average pain intensity was observed from baseline (30.5 [19.6], 100-point scale) to final visit (35.9 [21.1], p = 0.37). The most common AEs were concomitant disease progression (28.8 percent, n=23), nausea (22.5 percent, n=18), dyspnea (16.3 percent, n=13), fatigue (16.3 percent, n=13), and edema of the lower limb (15 percent, n=12).ConclusionsIn these patients with pain related to cancer, oxymorphone ER was generally well tolerated and provided stable long-term pain control.

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