• J Pain Symptom Manage · Feb 2015

    Randomized Controlled Trial Comparative Study

    Morphine or oxycodone for cancer-related pain? A randomized, open-label, controlled trial.

    • Julia Riley, Ruth Branford, Joanne Droney, Sophy Gretton, Hiroe Sato, Alison Kennett, Christina Oyebode, Michael Thick, Athol Wells, John Williams, Ken Welsh, and Joy Ross.
    • Royal Marsden NHS Foundation Trust, London, United Kingdom; National Heart & Lung Institute, Imperial College London, London, United Kingdom. Electronic address: julia.riley@rmh.nhs.uk.
    • J Pain Symptom Manage. 2015 Feb 1;49(2):161-72.

    ContextThere is wide interindividual variation in response to morphine for cancer-related pain; 30% of patients do not have a good therapeutic outcome. Alternative opioids such as oxycodone are increasingly being used, and opioid switching has become common clinical practice.ObjectivesTo compare clinical response to oral morphine vs. oral oxycodone when used as first-line or second-line (after switching) treatment in patients with cancer-related pain.MethodsIn this prospective, open-label, randomized, controlled trial (ISRCTN65155201) with a selected crossover phase, patients with cancer-related pain were randomized to receive either oral morphine or oxycodone as first-line treatment. Dose was individually titrated until the patient reported adequate pain control. Patients who did not respond to the first-line opioid (either because of inadequate analgesia or unacceptable adverse effects) were switched to the alternative opioid.ResultsTwo hundred patients were recruited. On intention-to-treat analysis (n = 198, morphine 98, oxycodone 100), there was no significant difference between the numbers of patients responding to morphine (61/98 = 62%) or oxycodone (67/100 = 67%) when used as a first-line opioid. Similarly, there was no significant difference in subsequent response when patients were switched to either morphine (8/12 = 67%) or oxycodone (11/21 = 52%). Per-protocol analysis demonstrated a 95% response rate when both opioids were available. There was no difference in adverse reaction scores between morphine and oxycodone either in first-line responders or nonresponders.ConclusionIn this population, there was no difference between analgesic response or adverse reactions to oral morphine and oxycodone when used as a first- or second-line opioid. These data provide evidence to support opioid switching to improve outcomes.Copyright © 2015. Published by Elsevier Inc.

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