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Article

Tirbanibulin 1% Ointment Significantly Reduces the Actinic Keratosis Area and Severity Index in Patients with Actinic Keratosis: Results from a Real-World Study

by
Michael Constantin Kirchberger
1,2,3,*,
Michael Gfesser
1,
Michael Erdmann
2,3,
Stefan Schliep
2,3,
Carola Berking
2,3 and
Markus Vincent Heppt
2,3
1
Hautarztzentrum Ingolstadt, Schlüterstr. 3a, 85057 Ingolstadt, Germany
2
Department of Dermatology, Uniklinikum Erlangen, Friedrich-Alexander-University Erlangen-Nürnberg (FAU), Ulmenweg 18, 91054 Erlangen, Germany
3
Comprehensive Cancer Center Erlangen-European Metropolitan Area of Nuremberg (CCC ER-EMN), 91054 Erlangen, Germany
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2023, 12(14), 4837; https://doi.org/10.3390/jcm12144837
Submission received: 24 June 2023 / Revised: 15 July 2023 / Accepted: 19 July 2023 / Published: 22 July 2023
(This article belongs to the Section Dermatology)

Abstract

Background: Actinic keratosis (AK) is a cutaneous lesion resulting from the proliferation of atypical epidermal keratinocytes caused by long-term exposure to ultraviolet radiation. AK may progress to cutaneous squamous cell carcinoma (cSCC) and therefore is often treated with topical agents such as 5-fluorouracil, diclofenac, imiquimod, and photodynamic therapy. Tirbanibulin has been approved based on two phase III trials in the USA. However, real-world evidence for tirbanibulin is absent. Methods: This was a single-centre study of adult patients with clinically typical, visible AK on the face or scalp treated with tirbanibulin 1% ointment. Treatment was administered as per label once daily for 5 consecutive days on the same lesions or field. Treatment outcomes were assessed 4 weeks after treatment, with additional optional assessments conducted at later time points. Efficacy was measured using the actinic keratosis area and severity index (AKASI) and digital dermoscopy. Results: A total of 33 patients were treated of whom 30 were analysed. The median AKASI score was 5.6 (1.4–11) pre-treatment and 1.2 (0–7.4) post-treatment (p < 0.0001). Complete clearance as defined by AKASI scores less than 1 was achieved in 47% (n = 14) and 57% (n = 13) at the first and second follow-up, respectively. All local reactions resolved spontaneously and without sequelae. The most common local reactions were erythema (80%, n = 26) and flaking or scaling (43%, n = 13). Conclusions: Tirbanibulin 1% ointment significantly and rapidly reduced the AKASI score in a real-world setting. The complete clearance rates were in line with those observed in the two pivotal trials.
Keywords: actinic keratosis; Klisyri; AKASI score actinic keratosis; Klisyri; AKASI score

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MDPI and ACS Style

Kirchberger, M.C.; Gfesser, M.; Erdmann, M.; Schliep, S.; Berking, C.; Heppt, M.V. Tirbanibulin 1% Ointment Significantly Reduces the Actinic Keratosis Area and Severity Index in Patients with Actinic Keratosis: Results from a Real-World Study. J. Clin. Med. 2023, 12, 4837. https://doi.org/10.3390/jcm12144837

AMA Style

Kirchberger MC, Gfesser M, Erdmann M, Schliep S, Berking C, Heppt MV. Tirbanibulin 1% Ointment Significantly Reduces the Actinic Keratosis Area and Severity Index in Patients with Actinic Keratosis: Results from a Real-World Study. Journal of Clinical Medicine. 2023; 12(14):4837. https://doi.org/10.3390/jcm12144837

Chicago/Turabian Style

Kirchberger, Michael Constantin, Michael Gfesser, Michael Erdmann, Stefan Schliep, Carola Berking, and Markus Vincent Heppt. 2023. "Tirbanibulin 1% Ointment Significantly Reduces the Actinic Keratosis Area and Severity Index in Patients with Actinic Keratosis: Results from a Real-World Study" Journal of Clinical Medicine 12, no. 14: 4837. https://doi.org/10.3390/jcm12144837

APA Style

Kirchberger, M. C., Gfesser, M., Erdmann, M., Schliep, S., Berking, C., & Heppt, M. V. (2023). Tirbanibulin 1% Ointment Significantly Reduces the Actinic Keratosis Area and Severity Index in Patients with Actinic Keratosis: Results from a Real-World Study. Journal of Clinical Medicine, 12(14), 4837. https://doi.org/10.3390/jcm12144837

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