RecruitingPhase 4NCT06499415

Combination Therapy of 5-Fluorouracil and CALcipotriol Versus 5-Fluorouracil in the Treatment of Actinic Keratosis

Combination Therapy of 5-Fluorouracil and CALcipotriol Versus 5-Fluorouracil in the Treatment of Actinic Keratosis: a Multicentre Randomized Controlled Clinical Trial


Sponsor

Maastricht University Medical Center

Enrollment

232 participants

Start Date

Sep 4, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

5-Fluorouracil (5FU) is proven to be the most effective therapy in field directed treatment for AK, with Jansen et al. reporting a 1-year probability of treatment success of 74.7%. However, treatment with 5FU is associated with side effects, like erythema, itching, a burning sensation and crusting, and a burdensome dosing regimen of twice daily application for four weeks. This long treatment duration in combination with side-effects and overall lifestyle adjustments during treatment can be the reason for poor adherence and premature termination, and it can also lead to future refusal of 5FU therapy. Therefore, room for improvement lies in increasing the tolerability, in terms of side effects or treatment duration, while maintaining the efficacy of 5FU in the treatment of AK. Addition therapy, which can shorten the duration of treatment, might be the key to success. Calcipotriol (CAL) enhances thymic stromal lymphopoietin (TSLP), an epithelium-derived cytokine, which promotes antitumor immunity. Therefore, it is known to have a synergistic effect when combined with 5FU in the treatment of AK. This suggests that short-term treatment with 5FU-CAL is effective and provides the opportunity to shorten duration of treatment, thereby improving tolerability of treatment and full adherence to the treatment regimen. However, no study compared 5FU-CAL combination therapy with standard 5FU treatment for a duration of 28 days. This study aims to evaluate whether a short course of combination therapy with 5FU-CAL is non-inferior to a full course of 5FU monotherapy with respect to the 1-year probability of treatment success.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called 5-FU 50 MG/ML Topical Cream and a drug called 5FU-Calcipotriol for people with actinic keratoses. The study is currently recruiting participants at 4 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUG5FU-Calcipotriol

topical 5FU-CAL, twice daily, during 4 or 6 consecutive days, depending on the treatment location

DRUG5-FU 50 MG/ML Topical Cream

topical 5FU, twice daily, 7 days a week, during 4 weeks


Locations(4)

Zuyderland Medical Center

Heerlen, Limburg, Netherlands

Maastricht University Medical Center

Maastricht, Limburg, Netherlands

VieCuri Medical Center

Venlo, Limburg, Netherlands

Catharina Hospital Eindhoven

Eindhoven, North Brabant, Netherlands

View Full Details on ClinicalTrials.gov

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NCT06499415


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