Heppt Markus V, Dykukha Igor, Graziadio Sara, Salido-Vallejo Rafael, Chapman-Rounds Matt, Edwards Mary
Department of Dermatology, Universitätsklinikum Erlangen, Friedrich-Alexander-University Erlangen-Nürnberg (FAU), Ulmenweg 18, 91054 Erlangen, Germany.
Comprehensive Cancer Center Erlangen-European Metropolitan Area of Nuremberg (CCC ER-EMN), 91054 Erlangen, Germany.
J Clin Med. 2022 Mar 16;11(6):1654. doi: 10.3390/jcm11061654.
Actinic keratosis (AK) is a chronic skin condition that may progress to cutaneous squamous cell carcinoma. We conducted a systematic review of efficacy and safety for key treatments for AK of the face and scalp, including the novel 5-day tirbanibulin 1% ointment. MEDLINE, PubMed, Embase, Cochrane Library, clinical trial registries and regulatory body websites were searched. The review included 46 studies, of which 35 studies included interventions commonly used in Europe and were sufficiently homogenous to inform a Bayesian network meta-analysis of complete clearance against topical placebo or vehicle. The network meta-analysis revealed the following odds ratios and 95% credible intervals: cryosurgery 13.4 (6.2-30.3); diclofenac 3% 2.9 (1.9-4.3); fluorouracil 0.5% + salicylic acid 7.6 (4.6-13.5); fluorouracil 4% 30.3 (9.1-144.7); fluorouracil 5% 35.0 (10.2-164.4); imiquimod 3.75% 8.5 (3.5-22.4); imiquimod 5% 17.9 (9.1-36.6); ingenol mebutate 0.015% 12.5 (8.1-19.9); photodynamic therapy with aminolevulinic acid 24.1 (10.9-52.8); photodynamic therapy with methyl aminolevulinate 11.7 (6.0-21.9); tirbanibulin 1% 11.1 (6.2-20.9). Four sensitivity analyses, from studies assessing efficacy after one treatment cycle only, for ≤25 cm treatment area, after 8 weeks post-treatment, and with single placebo/vehicle node confirmed the findings from the base case. Safety outcomes were assessed qualitatively. These results suggest that tirbanibulin 1% offers a novel treatment for AK, with a single short treatment period, favourable safety profile and efficacy, in line with existing topical treatments available in Europe.
光化性角化病(AK)是一种慢性皮肤疾病,可能会发展为皮肤鳞状细胞癌。我们对脸部和头皮AK的关键治疗方法的疗效和安全性进行了系统评价,包括新型的1%替拉替尼软膏,为期5天。检索了MEDLINE、PubMed、Embase、Cochrane图书馆、临床试验注册库和监管机构网站。该评价纳入了46项研究,其中35项研究纳入了欧洲常用的干预措施,且具有足够的同质性,可用于针对局部安慰剂或赋形剂的完全清除率进行贝叶斯网络荟萃分析。网络荟萃分析显示了以下优势比和95%可信区间:冷冻疗法13.4(6.2 - 30.3);3%双氯芬酸2.9(1.9 - 4.3);0.5%氟尿嘧啶 + 7%水杨酸7.6(4.6 - 13.5);4%氟尿嘧啶30.3(9.1 - 144.7);5%氟尿嘧啶35.0(10.2 - 164.4);3.75%咪喹莫特8.5(3.5 - 22.4);5%咪喹莫特17.9(9.1 - 36.6);鬼臼毒素0.015%12.5(8.1 - 19.9);氨基酮戊酸光动力疗法24.1(10.9 - 52.8);甲基氨基酮戊酸光动力疗法11.7(6.0 - 21.9);1%替拉替尼11.1(6.2 - 20.9)。四项敏感性分析,分别来自仅评估一个治疗周期后的疗效、治疗面积≤25平方厘米、治疗后8周以及单一安慰剂/赋形剂节点的研究,证实了基础病例的结果。对安全性结果进行了定性评估。这些结果表明,1%替拉替尼为AK提供了一种新的治疗方法,治疗周期短,安全性良好且有效,与欧洲现有的局部治疗方法相当。