Multicenter phase II study of an opioid-based pain control program for head and neck cancer patients receiving chemoradiotherapy

Radiother Oncol. 2011 Dec;101(3):410-4. doi: 10.1016/j.radonc.2011.09.016. Epub 2011 Oct 14.

Abstract

Background: The aim of this multi-center phase II study was to clarify the clinical benefit of an opioid-based pain control program for head and neck cancer patients during chemoradiotherapy.

Patients and methods: Head and neck cancer patients who were to receive definitive or postoperative chemoradiotherapy were enrolled. The opioid-based pain control program consisted of a three-step ladder, with basic regimens of: The primary endpoint of this study was compliance with radiotherapy.

Results: A total of 101 patients from 10 institutions were registered between February 2008 and May 2009 and included in the analysis. The major combination chemotherapy regimen was cisplatin alone (76%). The rate of completion of radiotherapy was 99% and the rate of unplanned breaks in radiotherapy was 13% (13/101, 90% confidence interval: 9.9-16.5%). Median maximum quantity of morphine used per day was 35 mg (range 0-150 mg).

Conclusions: Use of a systematic pain control program may improve compliance with CRT.

Publication types

  • Clinical Trial, Phase II
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Analgesics, Opioid / therapeutic use*
  • Chemoradiotherapy / adverse effects*
  • Cisplatin / therapeutic use
  • Female
  • Head and Neck Neoplasms / therapy*
  • Humans
  • Male
  • Middle Aged
  • Morphine / therapeutic use*
  • Pain Management*

Substances

  • Analgesics, Opioid
  • Morphine
  • Cisplatin