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Systematic Review of Intralesional Therapies for Cutaneous Warts. | LitMetric

AI Article Synopsis

  • Intralesional therapies for warts lack FDA approval and consensus on the best treatment, prompting a systematic review of 62 randomized controlled trials (RCTs).
  • The most commonly studied therapies included the MMR vaccine, PPD, vitamin D3, and Candida antigen, with MMR showing a complete response rate of 27-90%.
  • Common side effects included injection-site reactions and flu-like symptoms, and the review underscores a gap in large multi-center RCTs despite the high prevalence of warts.

Article Abstract

Intralesional therapies are used for recalcitrant warts, but no Food and Drug Administration-approved treatment exists nor is there consensus regarding the most efficacious therapy. Therefore, this systematic review aims to summarize efficacy and adverse events reported in 62 randomized controlled trials (RCTs) of intralesional therapies for cutaneous warts. The most studied intralesional therapies included measles, mumps, rubella (MMR) vaccine (n = 24 studies), purified protein derivative (PPD) (n = 19 studies), vitamin D3 (n = 15 studies), and Candida antigen (n = 14 studies). Most studies included adult and pediatric patients or adults alone, with only 4 studies on pediatric patients alone. MMR vaccine was the most studied treatment (n = 853 patients). MMR had a complete response rate of 27-90%. The next most common treatment, PPD, had a complete response rate of 45-87%. Other treatments included Candida antigen and vitamin D3, with complete response rates of 25-84% and 40-96%, respectively. The most frequent side effects were injection-site reactions and flu-like symptoms. This systematic review represents a useful summary of intralesional therapy RCTs for clinician reference. This study also highlights the lack of large multi-institutional RCTs, despite many patients being treated for this widespread problem.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10990969PMC
http://dx.doi.org/10.1016/j.xjidi.2024.100264DOI Listing

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