DOI: 10.1111/papr.13292 ISSN:

Finding predictors for successful opioid response in cancer patients: An analysis of data from four randomized controlled trials

Maike S. Imkamp, Maurice Theunissen, Sander M. van Kuijk, Johan Haumann, Oscar Corli, Cristina Bosetti, Wojciech Leppert, Cinzia Brunelli, Ernesto Zecca, Marieke H. van den Beuken‐van Everdingen
  • Anesthesiology and Pain Medicine

Abstract

Context

There is no consensus on which “strong” (or step 3 WHO analgesic ladder) opioid to prescribe to a particular patient with cancer‐related pain. A better understanding of opioid and patient characteristics on treatment response will contribute to a more personalized opioid treatment.

Objectives

Assessment of potential predictors for successful opioid treatment response in patients with cancer pain.

Methods

An international partnership between four cancer pain research groups resulted in a combined individual‐level database from four relevant randomized controlled trials (RCTs; n = 881). Together, these RCTs investigated the short‐term (1 week) and medium‐term (4 or 5 weeks) treatment responses for morphine, buprenorphine, methadone, oxycodone, and fentanyl. Candidate predictors for treatment response were sex, age, pain type, pain duration, depression, anxiety, Karnofsky performance score, opioid type, and use of anti‐neuropathic drug.

Results

Opioid type and pain type were found statistically significant predictors of short‐term treatment success. Sex, age, pain type, anxiety, and opioid type were statistically, significantly associated with medium‐term treatment success. However, these models showed low discriminative power.

Conclusion

Fentanyl and methadone, and mixed pain were found to be statistically significant predictors of treatment success in patients with cancer‐related pain. With the predictors currently assessed our data did not allow for the creation of a clinical prediction model with good discriminative power. Additional – unrevealed – predictors are necessary to develop a future prediction model.

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