4.5 Review

Chemotherapy and peripheral neuropathy

Journal

NEUROLOGICAL SCIENCES
Volume 42, Issue 10, Pages 4109-4121

Publisher

SPRINGER-VERLAG ITALIA SRL
DOI: 10.1007/s10072-021-05576-6

Keywords

Chemotherapy-induced peripheral neuropathy; Features; Mechanisms; Risk factors; Treatment; Prevention

Funding

  1. Cancer Institute NSW Program Grant [14/TPG/1-05]
  2. National Health and Medical Research Council of Australia (NHMRC) [1080521]
  3. NHMRC Career Development Fellowship [1148595]
  4. NHMRC Program Grant [1132524, 1153439]
  5. NHMRC Practitioner Fellowship [1156093]
  6. National Health and Medical Research Council of Australia [1153439, 1132524] Funding Source: NHMRC

Ask authors/readers for more resources

Chemotherapy-induced peripheral neurotoxicity (CIPN) is a dose-limiting side effect of many anti-cancer agents, impacting long-term function and quality of life for cancer survivors. Dose reduction is currently the main strategy to prevent severe neuropathy, but it poses a challenge in balancing treatment efficacy and minimizing long-lasting side effects. Ongoing research focuses on understanding the mechanisms of nerve damage and identifying risk factors for CIPN development, with the goal of improving management strategies.
Chemotherapy-induced peripheral neurotoxicity (CIPN) is a major dose-limiting side effect of many anti-cancer agents, including taxanes, platinums, vinca alkaloids, proteasome inhibitors, immunomodulatory drugs, and antibody-drug conjugates. The resultant symptoms often persist post treatment completion and continue to impact on long-term function and quality of life for cancer survivors. At present, dose reduction remains the only strategy to prevent severe neuropathy, often leading clinicians to the difficult decision of balancing maximal treatment exposure and minimal long-lasting side effects. This review examines the clinical presentations of CIPN with each class of neurotoxic treatment, describing signs, symptoms, and long-term outcomes. We provide an update on the proposed mechanisms of nerve damage and review current data on clinical and genetic risk factors contributing to CIPN development. We also examine recent areas of research in the treatment and prevention of CIPN, with specific focus on current clinical trials and consensus recommendations for CIPN management.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available