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Anti-inflammatory vs. inflammatory treatments for actinic keratoses
1Department of Dermatology, University of Nice-Sophia Antipolis, France. ortonne@unice.fr
Abstract:
The treatment of actinic keratoses (AKs) provides an important opportunity to prevent the development of squamous cell carcinoma. The recent discovery that cyclo-oxygenase-2 (COX-2) is a potential pharmacological target for skin tumours has prompted interest in using topical nonsteroidal anti-inflammatory drugs (NSAIDs) as a treatment for AKs. Topical 3% diclofenac in 2.5% hyaluronic acid gel (Solaraze) is currently the only NSAID licensed for the treatment of AKs. In randomised, double-blind studies, this therapy was effective in clearing AKs, with the efficacy increasing in proportion to the duration of treatment. Topical 3% diclofenac in 2.5% hyaluronic acid gel was well tolerated, with the vast majority of adverse events rated as mild or moderate. Older treatments, such as fluorouracil, which promotes an inflammatory response, are also effective in treating AKs, but are not acceptable to many patients because of severe irritation. Imiquimod is an alternative inflammatory treatment, which, although highly effective, is expensive and produces severe erythema, erosion and flaking in a large proportion of patients. Topical anti-inflammatory agents, such as 3% diclofenac in 2.5% hyaluronic acid gel, can facilitate the early treatment of AKs without the level of severe side-effects observed with some of the other therapies.
Insights
Topical diclofenac gel effectively treats actinic keratoses (AKs), a precursor to skin cancer. This nonsteroidal anti-inflammatory drug (NSAID) offers a well-tolerated option with fewer side effects than older treatments.
Area of Science:
- Dermatology
- Oncology
- Pharmacology
Background:
- Actinic keratoses (AKs) are common pre-cancerous skin lesions that can progress to squamous cell carcinoma.
- Cyclo-oxygenase-2 (COX-2) is a validated pharmacological target for skin tumors.
- Topical nonsteroidal anti-inflammatory drugs (NSAIDs) are being investigated for AK treatment.
Purpose of the Study:
- To evaluate the efficacy and tolerability of topical 3% diclofenac in 2.5% hyaluronic acid gel for treating AKs.
- To compare the safety and effectiveness of this NSAID treatment with other AK therapies.
Main Methods:
- Randomized, double-blind studies were conducted.
- The study involved topical application of 3% diclofenac in 2.5% hyaluronic acid gel.
- Efficacy was assessed based on AK clearance and duration of treatment.
Main Results:
- Topical 3% diclofenac in 2.5% hyaluronic acid gel demonstrated efficacy in clearing AKs.
- Treatment efficacy increased with longer treatment durations.
- The gel formulation was well-tolerated, with most adverse events being mild to moderate.
Conclusions:
- Topical diclofenac gel is an effective and well-tolerated treatment for AKs.
- It presents a favorable alternative to treatments like fluorouracil and imiquimod, which have more severe side effects.
- This NSAID facilitates early intervention for AKs, potentially preventing squamous cell carcinoma development.
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