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Morphine versus oxycodone in pancreatic cancer pain: a randomized controlled study.
Sebastiano Mercadante1, Walter Tirelli, Fabrizio David
1Anesthesia and Intensive Care Unit & Pain Relief and Palliative Care Unit, La Maddalena Cancer Center, Via san Lorenzo 312, 90146 Palermo, Italy. terapiadeldolore@lamaddalenanet.it
The Clinical Journal of Pain
|October 26, 2010
Summary
Oxycodone and morphine offer similar pain relief and side effects for pancreatic cancer patients. The study did not confirm oxycodone
Area of Science:
- Oncology
- Pain Management
- Pharmacology
Background:
- Pancreatic cancer pain is a significant clinical challenge.
- Oxycodone (OX) has shown potential advantages over morphine (MO) in visceral pain models.
- Previous research suggests OX may offer benefits in managing cancer pain.
Purpose of the Study:
- To investigate the efficacy and dose escalation of oxycodone (OX) compared to morphine (MO) in patients with pancreatic cancer pain.
- To test the hypothesis that OX is superior to MO in this patient population.
- To evaluate pain and symptom intensity, as well as opioid dose requirements.
Main Methods:
- A randomized study involving 60 patients with pancreatic cancer and moderate pain.
- Patients received either sustained-release oral morphine (30 mg/d) or oxycodone (20 mg/d).
- Opioid doses were adjusted based on clinical need, with assessments at baseline and up to 8 weeks.
Main Results:
- No significant differences were observed between oxycodone and morphine groups in terms of age, Karnofsky scores, or opioid escalation indexes.
- Pain and symptom intensity showed no statistical differences between the two treatment groups.
- Both oxycodone and morphine provided comparable analgesia and adverse effect profiles.
Conclusions:
- Oxycodone and morphine demonstrate similar efficacy and safety profiles for managing pancreatic cancer pain.
- The hypothesis that oxycodone would be superior to morphine in this context was not supported by the study findings.
- These results align with observations in the broader cancer pain population.
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