Department of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, Binghamton University, State University of New York, PO Box 6000, Binghamton, NY, 13902-6000, USA.
Department of Pharmacy Practice, School of Pharmacy and Pharmaceutical Sciences, Binghamton University, State University of New York, PO Box 6000, Binghamton, NY, 13902-6000, USA.
Clin Drug Investig. 2021 Sep;41(9):751-755. doi: 10.1007/s40261-021-01068-9. Epub 2021 Aug 5.
We review here the pharmacology, pharmacokinetics, efficacy, dosage and administration, and place in therapy of tirbanibulin for the treatment of actinic keratosis (AK). A literature search using PubMed was conducted using the terms tirbanibulin (tirbanibulin) and actinic keratosis from September 2014 to February 2021. All English-language articles evaluating tirbanibulin were analyzed for this review. Tirbanibulin was granted approval for the treatment of AK of the face or scalp as a first-line therapy. It is administered at a dose of 2.5 mg in 250 mg of white or off-white ointment for a 25 cm contiguous treatment surface for 5 consecutive days. Adverse effects include flaking/scaling, crusting, swelling, vesiculation/pustulation, and erosion/ulceration. This article discusses the clinical trials that led to the approval of tirbanibulin and comparison with other approved topical ointments indicated for the treatment of AK. In the clinical trials, all participants experienced a decrease in lesion size or saw complete clearance with minimal adverse effects.
我们在此回顾了替比嘧啶的药理学、药代动力学、疗效、剂量和给药以及在光化性角化病(AK)治疗中的地位。使用 PubMed 进行了文献检索,使用的术语是替比嘧啶(tirbanibulin)和光化性角化病(actinic keratosis),检索时间为 2014 年 9 月至 2021 年 2 月。对所有评估替比嘧啶的英文文章进行了分析,以供本综述使用。替比嘧啶被批准用于面部或头皮 AK 的一线治疗。它的剂量为 2.5mg,在 250mg 的白色或灰白色软膏中,用于 25cm 连续治疗表面,连续使用 5 天。不良反应包括片状/鳞屑、结痂、肿胀、水疱/脓疱、糜烂/溃疡。本文讨论了导致替比嘧啶批准的临床试验,并与其他批准用于治疗 AK 的局部软膏进行了比较。在临床试验中,所有参与者的病变面积均有所缩小,或完全清除,不良反应最小。