Genetic Variants Associated with Cancer Pain and Response to Opioid Analgesics: Implications for Precision Pain Management.
Gee Su Yang, Natalie M Barnes, Debra E Lyon and 1 others
PMID 31085105WHAT IT FOUND
Gene variants have been linked to cancer pain risk and opioid dose, but most links are not confirmed and are not ready for clinical use.
Do not change pain care based on these associations.
Key findings
01The OPRM1 118A>G variant was reported to be associated with needing more opioid for cancer pain relief.
02COMT Val/Val genotype was associated with higher morphine dose than Val/Met or Met/Met genotypes in cancer pain.
03In a European study of 2,294 cancer patients treated with opioids, no association was found between opioid dose and 112 SNPs across 25 genes, including OPRM1, COMT and ABCB1.
STILL TO COME
How it was doneWhat they foundWhat it means for RNs
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What it does not show
Most included studies were in non-Hispanic white patients with solid tumors, so the results may not apply to patients with other cancers or ethnic backgrounds. Most genetic associations have not been replicated, so they are not confirmed for clinical use. The studies did not use one consistent way to define or measure cancer pain. The review selected polymorphisms already reported to have significant associations, so negative or inconclusive findings may be under-represented. The paper describes associations, not tested interventions, so it cannot show that genetic testing improves care.
Declared interests
No conflicts-of-interest or funding declaration is present in the supplied text. The publication types list NIH extramural research support.
The easy way to misread this
Do not conclude that genetic testing can guide opioid choice or dose for cancer pain. The paper reports associations from published studies, many of which need replication, and it says such tests would need to be clinically available before patients could benefit.