Efficacy and safety of tirbanibulin 1% ointment in actinic keratoses: Data from two phase‐III trials and the real‐life clinical practice presented at the European Academy of Dermatology and Venereology Congress 2022

Author:

Pellacani G.1,Schlesinger T.2,Bhatia N.3,Berman B.4ORCID,Lebwohl M.5,Cohen J. L.67,Patel G. K.8,Kunstfeld R.9,Hadshiew I.10,Lear J. T.1112

Affiliation:

1. Department of Clinical Internal, Anesthesiological, and Cardiovascular Sciences La Sapienza University Rome Italy

2. Clinical Research Center of the Carolinas Charleston South Carolina USA

3. Therapeutics Clinical Research San Diego California USA

4. Department of Dermatology and Cutaneous Surgery University of Miami Miller School of Medicine Miami Florida USA

5. Icahn School of Medicine at Mount Sinai New York New York USA

6. Department of Dermatology University of California Irvine California USA

7. AboutSkin Dermatology and DermSurgery Greenwood Village Colorado USA

8. Welsh Institute of Dermatology University Hospital Wales Cardiff UK

9. Dermatology Department Medical University Vienna Vienna Austria

10. Derma Koeln Cologne Germany

11. Mid Cheshire Hospitals NHS Foundation Trust Crewe UK

12. MAHSC, Manchester University Manchester UK

Abstract

AbstractBackgroundThe 31st European Academy of Dermatology and Venereology (EADV) Congress took place between 7th and 10th of September 2022 in Milan, Italy.ObjectivesWe report presented clinical data on the efficacy/effectiveness, safety and tolerability of tirbanibulin 1% ointment that has recently been licensed for actinic keratosis (AK) of the face or scalp in adults.MethodsSummary of presentations given at the EADV Congress.ResultsProf. Pellacani presented two post hoc analyses from two phase‐III trials with AK patients (NCT03285477 [N = 351] and NCT03285490 [N = 351]): A descriptive analysis of medical history, concomitant medications, and safety results confirming a favourable profile for tirbanibulin showing that number of baseline AK lesions was not correlated to severity of local skin reactions. The latter analysis showed that cases of tirbanibulin application site pain or pruritus were few, and most were found to be mild. Prof. Kunstfeld reported six real‐life clinical cases in Austria showing good tirbanibulin effectiveness, safety and tolerability for the treatment of new or recurring AK lesions. Results demonstrated that after 2‐ to 4‐month follow‐up, tirbanibulin was well tolerated and effective in AK patients. Presentations by Dr. Patel confirmed good outcomes and tolerability of tirbanibulin in Olsen grade 1–2 AK (N = 12) and porokeratosis patients (N = 4) treated once daily for 5 consecutive days in the United Kingdom. Furthermore, real‐world experience in solid organ transplant recipients (N = 2) demonstrated effectiveness of tirbanibulin in skin field cancerization treatment. A symposium sponsored by Almirall was conducted during the congress in which Dr. Hadshiew and Dr. Lear brought together their clinical experience in Germany and the United Kingdom respectively. Interesting clinical cases of 5 consecutive days of tirbanibulin treatment compared to other treatments were discussed with attendees, as well as current treatment needs of AK patients.ConclusionsThis article provides an overview of presentations and symposium discussions, summarizing key phase‐III results and real‐life clinical experience with tirbanibulin shared by dermatologists across Europe.

Funder

Almirall

Publisher

Wiley

Subject

Infectious Diseases,Dermatology

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