AI Article Synopsis

  • Actinic keratosis (AK) is a pre-cancerous skin condition that often appears as thick, scaly patches on sun-exposed areas, commonly treated with photodynamic therapy or diclofenac plus hyaluronic acid gel.
  • A study compared the effectiveness of a new type of photodynamic therapy (MAL DL-PDT) with diclofenac, finding that MAL DL-PDT significantly increased the likelihood of complete lesion response within 12 weeks.
  • This research highlights MAL DL-PDT's potential as a more effective and less painful treatment option for AK but suggests that more studies are needed to evaluate long-term effects and patient experiences.

Article Abstract

Actinic keratosis (AK) is a pre-cancerous condition characterised by patches of thick, scaly skin developing on sun-exposed areas of the body. When multiple AKs develop on severely photodamaged skin, commonly used treatments include photodynamic therapy and diclofenac plus hyaluronic acid gel (DHA). Methyl aminolevulinate daylight photodynamic therapy (MAL DL-PDT) is an alternative to conventional photodynamic therapy (MAL c-PDT). Trials have indicated that MAL DL-PDT is as effective as MAL c-PDT but reduces treatment-related pain and dermatological side effects. To indirectly compare between MAL DL-PDT and DHA in patients with AK. A total of three randomised trials were collected using a systematic literature review. An adjusted indirect comparison was conducted on complete lesion response rate at 12 weeks. The data indicated that mild lesions, moderate lesions, and mild and moderate lesions treated with MAL DL-PDT were more than four times more likely to undergo a complete response than lesions treated with DHA at 12 weeks, with ORs ranging from 4.23 to 4.81. Results were all statistically significant. This is the first indirect comparison demonstrating the effectiveness of MAL-PDT over DHA for the treatment of AK, and further research is needed to assess the long-term efficacy of these interventions (i.e. six months and beyond), as well as safety and patient-reported outcomes.

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http://dx.doi.org/10.1684/ejd.2016.2822DOI Listing

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