Journal of Clinical Oncology, Vol 19, Issue 11
(June), 2001: 2898-2904
© 2001 American Society for Clinical Oncology
Switching From Morphine to Methadone to Improve Analgesia and Tolerability in Cancer Patients: A Prospective Study
By Sebastiano Mercadante,
Alessandra Casuccio,
Fabio Fulfaro,
Liliana Groff,
Roberto Boffi,
Patrizia Villari,
Vittorio Gebbia,
Carla Ripamonti
From the Pain Relief and Palliative Care Unit, La Maddalena Cancer Center; Home Care Program, Societé per lAssistenza al Maleto Oncologico Terminale; Department of Hygiene and Microbiology, University of Palermo; and Department of Oncology, La Maddalena Cancer Center, Palermo; and Rehabilitation and Palliative Care Division, National Cancer Institute of Milan, Italy.
Address reprint requests to Sebastiano Mercadante, MD, Pain Relief and Palliative Care Unit, La Maddalena Cancer Center, Via S Lorenzo 312, 90146 Palermo, Italy; email: mercadsa{at}tin.it
PURPOSE: To evaluate the clinical benefits of switching from morphine to oral methadone in patients who experience poor analgesia or adverse effects from morphine.
PATIENTS AND METHODS: Fifty-two consecutive cancer patients receiving oral morphine but with uncontrolled pain and/or moderate to severe opioid adverse effects were switched to oral methadone administered every 8 hours using different dose ratios. Intensity of pain and adverse effects were assessed daily, and the symptom distress score (DS) was calculated before and after switching.
RESULTS: Data were analyzed for 50 patients. Switching was considered effective in 80% of the patients; results were achieved in an average of 3.65 days. In the 10 patients who switched to methadone because of uncontrolled pain, a significant reduction in pain intensity (P < .005) and an average of a 33% increase in methadone doses necessary (P < .01) were found after an average of 3.5 days. DS significantly decreased from an average of 8.4 to 4.5 (P < .0005). In the 32 patients switching because of uncontrolled pain and morphine-related adverse effects, significant improvement was found in pain intensity (P < .0005), nausea and vomiting (P < .03), constipation (P < .001), and drowsiness (P < .01), but a significant increase in the methadone dose of an average of 20% (P < .004) was required.
CONCLUSION: In most patients with cancer pain referred for poor pain control and/or adverse effects, switching to oral methadone is a valid therapeutic option. In the clinical setting of poor pain control, higher doses of methadone are necessary with respect to the equianalgesic calculated dose ratios previously published.
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