Sense-checking the approach to quantitative sensory testing to detect chemotherapy-induced peripheral neuropathy

People with chemotherapy-induced peripheral neuropathy (CIPN) have abnormalities in Quantitative Sensory Test (QST) findings. However, the predictive utility of QST for the early detection of CIPN in individuals has not been demonstrated. This will require longitudinal QST during chemotherapy treatments. However, QST is time-consuming, requires expertise and complex, costly equipment which has largely prevented its adoption in routine clinical practice. We aimed to assess approaches to develop a reliable, straightforward, time efficient and sensitive sensory testing method. Guided by patient partner input and previous literature, we selected thermal and vibration detection thresholds as target QST parameters. A series of iterative experiments was conducted to determine the optimal body test site and to develop a novel vibration testing protocol. The thenar eminence emerged as the best candidate due to higher sensitivity to all stimulus modalities, lower variance and less age-related change compared to the feet. We demonstrated significant differences in thermal thresholds between healthy participants and people with CIPN measured at the thenar but not the feet. The vibration testing protocol, employing a linear resonant actuator, performed better than a calibrated tuning fork being sufficiently sensitive to identify age-related and body site differences in sensory function well as tracking sensory loss induced by local anaesthetic nerve block. These findings establish a testing framework to deliver QST at a single convenient body site with a reduced set of modalities to efficiently track multifibre sensory function for patients at risk of developing neuropathy.

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Publication Details

Journal
PLoS ONE
Published
2025-12-05
DOI
https://doi.org/10.1371/journal.pone.0338105
Citations
1
Primary Topic
Cancer Treatment and Pharmacology
Type
article
Field-Weighted Citation Impact
1.05
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article

Sense-checking the approach to quantitative sensory testing to detect chemotherapy-induced peripheral neuropathy

James Dunham, A.G. O’Neill, Christian R. Burgess, Marin Dujmović et al.
1 citations
PLoS ONE
Cancer Treatment and Pharmacology
1.05
article

Sense-checking the approach to quantitative sensory testing to detect chemotherapy-induced peripheral neuropathy

James Dunham, A.G. O’Neill, Christian R. Burgess, Marin Dujmović, Johannes Gausden, Lesley Colvin, Anthony E. Pickering, Roger G. Whittaker, Betsy McAlister Groves, Bhushan Thakkar, A. Grant, Alan R. Young, Lynne M. Adams, Nisla Maharjan, Elizabeth Anne Cottuli de Cothi, Chris Geddie
article en
1 citations

Abstract

People with chemotherapy-induced peripheral neuropathy (CIPN) have abnormalities in Quantitative Sensory Test (QST) findings. However, the predictive utility of QST for the early detection of CIPN in individuals has not been demonstrated. This will require longitudinal QST during chemotherapy treatments. However, QST is time-consuming, requires expertise and complex, costly equipment which has largely prevented its adoption in routine clinical practice. We aimed to assess approaches to develop a reliable, straightforward, time efficient and sensitive sensory testing method. Guided by patient partner input and previous literature, we selected thermal and vibration detection thresholds as target QST parameters. A series of iterative experiments was conducted to determine the optimal body test site and to develop a novel vibration testing protocol. The thenar eminence emerged as the best candidate due to higher sensitivity to all stimulus modalities, lower variance and less age-related change compared to the feet. We demonstrated significant differences in thermal thresholds between healthy participants and people with CIPN measured at the thenar but not the feet. The vibration testing protocol, employing a linear resonant actuator, performed better than a calibrated tuning fork being sufficiently sensitive to identify age-related and body site differences in sensory function well as tracking sensory loss induced by local anaesthetic nerve block. These findings establish a testing framework to deliver QST at a single convenient body site with a reduced set of modalities to efficiently track multifibre sensory function for patients at risk of developing neuropathy.

PLoS ONEVol. 20(12)
University of Dundee (GB), At Bristol (GB), University of Bristol (GB), Genomics (United Kingdom) (GB), Newcastle University (GB)
Openalex Percentile: Top 15%
Cancer Treatment and Pharmacology
1.05
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