Abstract

Simple SummaryThe assessment of actinic keratoses (AKs) in prevention and therapeutic trials, as well as clinical practice, could significantly benefit from the incorporation of non-invasive imaging technology. Such technology has the potential to enhance the objective evaluation of clinical and subclinical AKs with the added advantage of sequential monitoring. In vivo reflectance confocal microscopy (RCM) allows for the non-invasive imaging of AKs at a cellular level. We aimed to establish an in in vivo RCM protocol for AK response monitoring, ultimately leading to more reliable characterization of longitudinal responses and therapy optimization.Reflectance confocal microscopy (RCM) presents a non-invasive method to image actinic keratosis (AK) at a cellular level. However, RCM criteria for AK response monitoring vary across studies and a universal, standardized approach is lacking. We aimed to identify reliable AK response criteria and to compare the clinical and RCM evaluation of responses across AK severity grades. Twenty patients were included and randomized to receive either cryotherapy (n = 10) or PDT (n = 10). Clinical assessment and RCM evaluation of 12 criteria were performed in AK lesions and photodamaged skin at baseline, 3 and 6 months. We identified the RCM criteria that reliably characterize AK at baseline and display significant reduction following treatment. Those with the highest baseline odds ratio (OR), good interobserver agreement, and most significant change over time were atypical honeycomb pattern (OR: 12.7, CI: 5.7–28.1), hyperkeratosis (OR: 13.6, CI: 5.3–34.9), stratum corneum disruption (OR: 7.8, CI: 3.5–17.3), and disarranged epidermal pattern (OR: 6.5, CI: 2.9–14.8). Clinical evaluation demonstrated a significant treatment response without relapse. However, in grade 2 AK, 10/12 RCM parameters increased from 3 to 6 months, which suggested early subclinical recurrence detection by RCM. Incorporating standardized RCM protocols for the assessment of AK may enable a more meaningful comparison across clinical trials, while allowing for the early detection of relapses and evaluation of biological responses to therapy over time.

Highlights

  • Actinic keratoses are common skin lesions with the risk to evolve into squamous cell carcinoma (SCC)

  • We observed significant reductions in many of the Reflectance confocal microscopy (RCM) criteria, our results suggest that atypical honeycomb patterns, hyperkeratosis, disarranged epidermal patterns, and stratum corneum disruptions are the most reliable criteria for assessing actinic keratosis (AK) treatment response

  • By studying and analyzing Grade 1 AK (G1) and Grade 2 AK (G2) AK separately, we found that the baseline odds ratios were higher in thicker (G2) AKs than thinner (G1) AKs, suggesting that pathologic RCM criteria are more detected in higher-grade AKs

Read more

Summary

Introduction

Actinic keratoses are common skin lesions with the risk to evolve into squamous cell carcinoma (SCC). It is currently not possible to predict which AK lesions will progress and various sources differ on the potential rate of progression. A landmark paper from Callen et al approximated a 0.25–20% annual transformation rate for a single AK [1]. Treatment options for AK are abundant and include photodynamic therapy (PDT), cryotherapy, 5-fluorouracil, diclofenac gel, imiquimod, and chemical peels, among others. Cryotherapy represents a lesion-directed therapy while PDT is a field-directed therapy that requires a photosensitizer, light, and oxygen. Photosensitizing agents include topical methyl aminolevulinate (MAL), 5-aminolevulinic acid (ALA), or BF-200 ALA, a nanoemulsion-based gel that optimizes epidermal penetration [3]. While light sources typically include red or blue light, daylight PDT has been demonstrated to be effective [4,5]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call