Breast Cancer Clinical Trial
Official title:
Chemotherapy - Induced Peripheral Neuropathy (CIPN). Could There be a Role for Physical Therapy Treatment?
The cause of Chemotherapy-Induced Peripheral Neuropathy (CIPN) is still unknown. An estimated 55-60% of patients will experience lasting symptoms affecting function for years post-treatment. Physical therapy is an established, effective treatment for entrapped nerves and neuropathic pain. This study sought to identify additional risk factors and provide evidence for the role of physical therapy in the treatment of CIPN.
A common side effect is chemotherapy induced peripheral neuropathy (CIPN). CIPN is a small
fibre sensory neuropathy that develops in the hands/feet and worsens with increasing dose and
duration of treatment. It impacts the Aβ, Aδ, and C-Fiber function involved in light touch
and vibration sense, thermal detection and thermal pain. This results in a variety of
positive and/or negative sensory symptoms including hypoesthesia, dysesthesias, hyperalgesia,
allodynia and neuropathic pain. Quantitative sensory testing (QST) are a variety of
non-invasive tests aimed at quantifying sensory perceptions used in research to clinically
assess neuropathy. It is used for sensory detection and pain thresholds for both mechanical
and thermal stimuli. QST provides information on large myelinated (Aβ), small thinly
myelinated (Aδ) and unmyelinated (C-fiber) function or dysfunction. Deep pressure threshold
measured by a pressure algometry stimulates intramuscular afferents, and can be used as a
measure of central sensitization when used at a distant site from the site of pain. Aδ fibres
transmit cool detection threshold, while warm detection threshold is transmitted by C-fibers.
Both noxious heat and noxious cold transmit via C-fiber and Aδ fibers. An increased
sensitivity to thermal pain thresholds, results in thermal hyperalgesia.
Physical therapy treatment for nerve disorders is well established in orthopedics and plastic
surgery for entrapment neuropathies, neuropathic pain, post-operative nerve repair and
regeneration. Nerve gliding exercises are frequently used exercises in physical therapy to
improve neural excursion across joints, improve pain and decrease inflammation. Patient
reported symptoms (patient questionnaires NPRS, S-LANSS and DASH) and quantitative sensory
testing (QST) specifically pain pressure thresholds and vibration were used for the primary
purpose in evaluating the role for an upper extremity nerve mobilization physical therapy
home program during chemotherapy for the prevention and management of CIPN.
Primary Outcome Measures was the NPRS and reported as those having no vs no pain. Grip
strength, Vibration, DASH and S-LANSS were identified outcome measures prior to the trial
that would best describe sensory impairment and function for the physical therapy question
Additional QST measures collected included warm/cool, Hot/Cold Pain thresholds that were used
with the vibration data to compare quantitative data on the right and left side to evaluate
possible a possible dual nerve disorder when combined with surgery as well as identifying
different sensory profiles of QST data between those reporting neuropathic pain and
non-neuropathic pain using the S-LANSS
A sub analysis of data was completed dividing participants that remained active throughout
compared to less active participants to evaluate the effect of exercise on sensory
preservation. This was not an intended analysis at the beginning of the trial and these
participants were not randomized.
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