AI Article Synopsis

  • * A study involving 120 patients explored the potential neuroprotective effects of renin-angiotensin system (RAS) inhibitors during chemotherapy, revealing that those on RAS inhibitors had lower severity of sensory neuropathy compared to those not on the inhibitor.
  • * The study was observational, and while RAS inhibitors showed promise, further randomized controlled trials are needed to validate their effectiveness in preventing CIPN during platinum-based chemotherapy regimens.

Article Abstract

Chemotherapy-induced peripheral neuropathy (CIPN) is a frequent and dose-limiting adverse side effect of treatment. CIPN affects the oncological prognosis of patients, as well as their quality of life. To date, no specific pharmacological therapy has demonstrated effectiveness in preventing CIPN. Accumulating preclinical evidence suggests that renin-angiotensin system (RAS) inhibitors may have neuroprotective effects. One hundred and twenty patients were included in this observational study and were followed from the beginning of their neurotoxic chemotherapy schedule until their final assessment, at least one month after its cessation. The National Cancer Institute's common toxicity criteria 4.0 (NCI-CTC 4.0) were used to grade the severity of adverse events. Follow-ups also included electrochemical skin conductance and scales for pain, quality of life and disability. Among patients receiving a platinum-based regimen, the mean grade of sensory neuropathy (NCI-CTC 4.0) was significantly lower in the RAS inhibitor group after the end of their anticancer treatment schedule. Because of the observational design of the study, patients in the RAS inhibitor group cumulated comorbidities at risk of developing CIPN. Randomized controlled trials in platinum-based regimens would be worth conducting in the future to confirm the neuroprotective potential of RAS inhibitors during chemotherapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9144468PMC
http://dx.doi.org/10.3390/jcm11102939DOI Listing

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