Could Efinaconazole 10% Have An Impact For Onychomycosis?
- Volume 26 - Issue 2 - February 2013
- 10567 reads
- 0 comments
Can an emerging topical hold promise for onychomycosis? This author takes a closer look in this case study of a 24-year-old patient with distal lateral subungual onychomycosis.
Onychomycosis is the most frequent nail disease affecting some 35 million people in the United States.1,2 It is the number one diagnosed and treated disease by podiatrists today.3
Although oral treatment is generally required, patients express concerns about oral therapies. In addition, few podiatrists use these modalities routinely.4,5 Not only are there safety concerns (such as hepatotoxicity) but oral antifungals can also cause rashes and hypogeusia. Potential drug interactions limit the use of oral therapies in many patients, especially the elderly in whom onychomycosis and the use of concomitant medications are most common.6,7
Our onychomycosis patients would prefer a topical treatment. However, reported cure rates of available topical therapies are much lower than those with systemic treatments.8 To date, ciclopirox nail lacquer (Penlac, Sanofi-Aventis) is the only topical treatment approved by the Food and Drug Administration (FDA) for the treatment of onychomycosis in the United States.10 Unfortunately, ciclopirox nail lacquer has reported complete cure rates of 5.5-8.5 percent, requires frequent nail debridement and patients have to use alcohol to remove excess buildup of lacquer from the ventral aspect of the nail plate to avoid additional infection.9,10
The main challenge in the development of topicals for onychomycosis has been to formulate a drug that can penetrate through the nail plate and reach the site of infection in the nail bed in a high enough concentration.
Accordingly, I would like to present a clinical case of distal lateral subungual onychomycosis and effective topical treatment with efinaconazole 10% solution, the first topical triazole antifungal developed specifically for the treatment of onychomycosis. The patient was enrolled in one of 2 phase 3 multicenter, randomized, double-blind studies on efinaconazole 10% solution, the full details of which are reported elsewhere.11
When A Patient Presents With Distal Lateral Subungual Onychomycosis Of The Great Toenail
A 24 year-old man presented at our clinic with distal lateral subungual onychomycosis of the great toenail. He had suffered from the disease for over 10 years. Forty-five percent of the great toenail was affected and laboratory results from the baseline fungal culture were positive for Trichophyton rubrum. The patient had five infected toenails.
The patient used efinaconazole 10% solution once a day for 48 weeks. The patient applied efinaconazole 10% solution to the clean, dry nail plate surface, lateral and proximal nail folds, hyponychium, and the undersurface of the nail plate. The patient was assessed for efficacy and safety at 12-week intervals post-baseline (i.e., Weeks 12, 24, 36. 48) and at follow-up (Week 52). I noted progressive improvement over the treatment period and at follow-up. By Week 12, the percentage of the affected nail had decreased to 30 percent and down to 10 percent at Week 24. The KOH was positive and the fungal culture was negative at this visit.
By Week 48 (the end of treatment), the great toenail had 0 percent involvement. Three other toenails were still affected. Both KOH and fungal cultures were negative from Week 36. At the week 52 follow-up visit, the patient’s onychomycosis was not completely cleared (5 percent involvement). However, the KOH and fungal cultures were still negative, and one of the other affected toenails was clear.
Any new topical product for onychomycosis must not cause irritation or contact dermatitis. The patient reported no redness, swelling, burning, itching or vesiculation during treatment. There were no adverse events relating to efinaconazole use.