Why the study?
Chemoinduced polyneuropathy from platinum drugs is unpredictable, lacks early indicators for dose reduction, and has no drugs that effectively prevent or alleviate its course.
This review highlights the mechanisms, risk factors, and clinical features of platinum-induced peripheral neuropathy, a major and unpredictable complication of cancer treatment.
Platinum regimens require CIPNP monitoring to limit disability; leaves open effective prevention strategies in common cancers.
Chemoinduced polyneuropathy (CIPNP) is a common side-effect of chemotherapy, significantly impairing quality of life in patients treated for cancer. Platinum preparations are the most commonly used chemotherapeutic agents used in the treatment of ovarian, testicular, breast, lung and colon cancers. Clinical examination reveals restrictions on the motor, sensory and autonomic functions of the upper and lower extremities, which occur at different stages of antitumor treatment, seriously complicating the treatment of the underlying disease. Pain and sensory disturbances may persist for months or even years after chemotherapy is completed. Thus, CIPNP is a major problem because it is impossible to predict which patients will develop neurological symptoms, to estimate their timing of manifestation, which can occur at any time during the course of chemotherapy, there is no early indication to reduce the dose of the cytotoxic drug, and there are no drugs that effectively prevent or alleviate the course of neuropathy. This review focuses on neurotoxicity with the use of platinum drugs, including the frequency of occurrence, risk factors, cumulative doses, various pathogenetic mechanisms for the development of CIPNP, clinical features and variants of the neurophysiological picture.
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Chubykina et al. (2023) studied this question.
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