AI Article Synopsis

  • Patients with cancer receiving chemotherapeutics often experience adverse effects like erectile dysfunction (ED), leading researchers to investigate the link between anticancer drugs and impaired erectile function in rats.
  • The study used data from the FDA Adverse Event Reporting System (AERS) to calculate the association strength between specific drugs and ED, with significant findings for drugs like melphalan, vincristine, and docetaxel.
  • The results suggest that certain anticancer agents increase the risk of ED, highlighting the need for ongoing monitoring of erectile function in cancer survivors to guide potential treatment strategies.

Article Abstract

Background: Patients with cancer are treated with chemotherapeutics that cause adverse effects, including erectile dysfunction (ED).

Objectives: We investigated erectile function in rats after the administration of anticancer agents based on data retrieved through mining of the US Food and Drug Administration (FDA) Adverse Event Reporting System (AERS) database.

Materials And Methods: The statistical signal strength for the association between anticancer drugs and ED was calculated using the reporting odds ratio (ROR). A drug-event combination was detected when the lower limit of the 95% confidence interval (CI) of the ROR exceeded 1.00. Rats were administered anticancer agents detected in the FDA AERS analysis. Erectile function was assessed using intracavernous pressure (ICP) and mean arterial pressure (MAP) analysis after electrical stimulation of the cavernous nerve. Statistical significance was determined using Welch's t-test or two-way ANOVA.

Results: Melphalan (L-PAM; ROR = 4.72, 95% CI = 2.78-8.00), vincristine (VCR; ROR = 2.47, 95% CI = 1.54-3.97), docetaxel (DTX; ROR = 2.25, 95% CI = 1.28-3.95), methotrexate (MTX; ROR = 1.96, 95% CI = 1.39-2.75), and doxorubicin (DOX; ROR = 1.82, 95% CI = 1.07-3.19) enhanced ED risk. L-PAM and MTX decreased the ICP/MAP ratio 1 week after administration. VCR and DOX decreased erectile function 4 weeks after administration. DTX decreased erectile function at all assessed time points.

Discussion And Conclusion: Certain anticancer agents should be considered risk factors for ED. Our results provide possible treatment strategies for maintaining erectile function in cancer survivors, including careful erectile function monitoring after treatment.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291990PMC
http://dx.doi.org/10.1111/andr.13094DOI Listing

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