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Journal of Clinical Oncology, Vol 23, No 22 (August 1), 2005: pp. 5229-5234
© 2005 American Society of Clinical Oncology.
DOI: 10.1200/JCO.2005.13.128

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Rapid Switching Between Transdermal Fentanyl and Methadone in Cancer Patients

Sebastiano Mercadante, Patrizia Ferrera, Patrizia Villari, Alessandra Casuccio

From the Anesthesia and Intensive Care Unit and Pain Relief and Palliative Care Unit, La Maddalena Cancer Center; and Department of Ophthalmology, University of Palermo, Palermo, Italy

Address reprint requests to Sebastiano Mercadante, MD, Anesthesia and Intensive Care Unit, Pain Relief and Palliative Care Unit, La Maddalena Cancer Center, Via San Lorenzo 312, 90146 Palermo, Italy; e-mail: terapiadeldolore{at}la-maddalena.it

PURPOSE: The aim of this study was to examine the clinical effects of switching from transdermal (TTS) fentanyl to methadone, or vice versa, in patients with a poor response to the previous opioid.

PATIENTS AND METHODS: A prospective study was carried out on 31 patients who switched from TTS fentanyl to oral methadone, or vice versa, because of poor opioid response. A fixed conversion ratio of fentanyl to methadone of 1:20 was started and assisted by rescue doses of opioids, and then doses were changed according to clinical response. Pain and symptom intensity, expressed as distress score, were recorded before switching doses of the two opioids and after subsequent doses. The number of changes of the daily doses, time to achieve stabilization, and hospital stay were also recorded.

RESULTS: Eighteen patients were switched from TTS fentanyl to methadone, and seven patients were switched from methadone to TTS fentanyl. A significant decrease in pain and symptom intensity, expressed as symptom distress score, was found within 24 hours after switching took place in both directions. Unsuccessful switching occurred in six patients, who were subsequently treated with an alternative therapy.

CONCLUSION: A rapid switching using an initial fixed ratio of fentanyl to methadone of 1:20 is an effective method to improve the balance between analgesia and adverse effects in cancer patients with poor response to the previous opioid. No relationship between the final opioid dose and the dose of the previous opioid has been found.

Authors' disclosures of potential conflicts of interest are found at the end of this article.


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