Objective
To summarize the literature on the use of quantitative sensory testing (QST) in the assessment of pain in people with cancer and to describe which QST parameters consistently demonstrate abnormal sensory processing in patients with cancer pain.
Databases and Data Treatment
Medline, EMBASE, AMED, CINAHL, SCOPUS and CENTRAL were searched for observational or experimental studies using QST in patients with a cancer diagnosis and reporting pain. Search strategies were based on the terms âquantitative sensory testingâ, âcancerâ, âpainâ, âcancer painâ and âassessmentâ. Databases were searched from inception to January 2019. Data were extracted and synthesized narratively, structured around the different QST modalities and subâgrouped by cancer pain aetiology (tumourâ or treatmentârelated pain).
Results
Searches identified 286 records of which 18 met the eligibility criteria for inclusion. Three studies included patients with tumourârelated pain, and 15 studies included patients with pain from chemotherapyâinduced peripheral neuropathy (CIPN). Across all studies, 50% (9/18) reported sensory abnormities using thermal detection thresholds (cool and warm), 44% (8/18) reported abnormal mechanical detection thresholds using vonâFrey filaments and 39% (7/18) found abnormal pinprick thresholds. Abnormal vibration and thermal pain (heat/cold) thresholds were each reported in a third of included studies.
Conclusion
This systematic review highlights the lack of published data characterizing the sensory phenotype of tumourârelated cancer pain. This has implications for our understanding of the underlying pathophysiological mechanisms of cancer pain. Understanding the multiple mechanisms driving cancer pain will help to move towards rational individualized analgesic treatment choices.
Significance
This systematic review found that pain in cancer patients is associated with abnormal sensory responses to thermal, mechanical and pinprick stimuli. However, these findings are based primarily on studies of chemotherapyâinduced peripheral neuropathy and data on tumourârelated pain are lacking, warranting further research.