AI Article Synopsis

  • Chemotherapy-induced peripheral neuropathy (CIPN) is a common and limiting side effect of chemotherapy, and while many trials have investigated drugs for its prevention or treatment, previous reviews haven't proven their effectiveness.
  • The article outlines a protocol for a systematic review and network meta-analysis (NMA) aimed at assessing the efficacy and safety of various drugs, including vitamins and analgesics, in preventing and treating CIPN.
  • The research will involve a comprehensive literature search for relevant studies and will utilize statistical methods to analyze the effectiveness of treatments, with findings expected to be published in a peer-reviewed journal.

Article Abstract

Introduction: Chemotherapy-induced peripheral neuropathy (CIPN) is one of the most common dose-limiting side effects of chemotherapeutic drugs. Numerous clinical trials of various targeted drugs for the prevention or treatment of CIPN have been conducted; however, previous systematic reviews with direct comparisons have failed to demonstrate the efficacy of these drugs in the prevention or treatment of CIPN. In addition, no systematic reviews have indirectly compared CIPN prevention and treatment. This article describes a protocol for evaluating the efficacy and safety of drug therapy for the prevention and treatment of CIPN. The results of the proposed systematic review with network meta-analysis (NMA) will provide new insights into the prevention and treatment of CIPN.

Methods And Analysis: We will conduct a literature search in MEDLINE, PubMed, Embase, Cochrane Central Register of Controlled Trials and ClinicalTrials.gov to find relevant articles published through January 2023. We will include studies that investigated the efficacy and safety of vitamin B, goshajinkigan, non-steroidal anti-inflammatory analgesics, opioids, calcium and magnesium, antidepressants and anticonvulsants on CIPN. Two authors will individually screen the retrieved reports and review the full text based on the selection criteria. The primary outcome is the incidence and severity of CIPN. The risk of bias will be assessed using V.2.0 of the Cochrane risk-of-bias tool. We will apply a frequentist random-effects NMA model to pool effect sizes across trials using risk ratios and mean differences with their 95% CIs. Competing interventions will be ranked using the surface under cumulative ranking probabilities. Heterogeneity will be assessed using the heterogeneity variance τ, Cochran's Q test and I² statistic.

Ethics And Dissemination: This review does not require ethical approval. The research will be published in a peer-reviewed journal.

Prospero Registration Number: CRD42022371829.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10503317PMC
http://dx.doi.org/10.1136/bmjopen-2022-070645DOI Listing

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