Tada Yayoi, Guan Jia, Iwasaki Ryoko, Morita Akimichi
Department of Dermatology, Teikyo University Hospital, Tokyo, Japan.
Boehringer Ingelheim Pharmaceuticals Inc., Ridgefield, Connecticut, USA.
J Dermatol. 2024 Mar;51(3):391-402. doi: 10.1111/1346-8138.17097. Epub 2024 Jan 12.
Generalized pustular psoriasis (GPP) is a potentially life-threatening skin disease. Although several medications are approved for treating GPP in Japan, there are limited data on real-world treatment patterns or drug survival (the number of prescribed days of treatment). This retrospective cohort study describes drug survival and treatment patterns of patients with newly diagnosed GPP (International Classification of Diseases, 10th Revision code L40.1), and ≥1 year of follow-up, using de-identified claims data (Medical Data Vision Co., Ltd.) from January 2016 to August 2021. Most (97.0%) of the 434 Japanese patients received first-line therapy of etretinate (26.4%), topical medications (14.7%), or cyclosporin (14.3%); 80.0% and 60.1% of patients received a second and third line of therapy (LOT), respectively. Use of etretinate (12.6%) and cyclosporin (5.9%) decreased in second-line therapies, whereas use of biologics (interleukin [IL]-17, 14.3%; IL-23 inhibitors, 7.6%) and topical medications (22.1%) increased or remained consistent. Approximately 50% of biologics were prescribed in combination with systemic medications or systemic corticosteroids. Median (range) time to next therapy (TTNT) was 2.8 (0.03-48.07) months for first-line therapy and 3.3 (0.03-52.97) months for all other LOTs. TTNT was longer for combination therapies (up to 16.5 months) compared with monotherapies (up to 7.5 months). Biologics exhibited longer drug survival with fewer treatment episodes compared with non-biologic systemic medications. Among frequently used therapies, the median (95% confidence interval) drug survival was 8.8 (5.8-11.8) months for etretinate, 4.3 (2.2-6.9) months for systemic corticosteroids, and 19.6 (16.1-26.7) months for secukinumab. Treatment patterns varied considerably, highlighting the need for treatment algorithms and effective, well-tolerated medications to support patients to help them remain on long-term therapy.
泛发性脓疱型银屑病(GPP)是一种可能危及生命的皮肤病。尽管在日本有几种药物被批准用于治疗GPP,但关于实际治疗模式或药物生存期(规定治疗天数)的数据有限。这项回顾性队列研究使用2016年1月至2021年8月去识别化的索赔数据(Medical Data Vision Co., Ltd.),描述了新诊断为GPP(国际疾病分类第10版代码L40.1)且随访时间≥1年的患者的药物生存期和治疗模式。434名日本患者中,大多数(97.0%)接受了一线治疗,包括依曲替酯(26.4%)、外用药物(14.7%)或环孢素(14.3%);分别有80.0%和60.1%的患者接受了二线和三线治疗(LOT)。在二线治疗中,依曲替酯(12.6%)和环孢素(5.9%)的使用减少,而生物制剂(白细胞介素[IL]-17,14.3%;IL-23抑制剂,7.6%)和外用药物(22.1%)的使用增加或保持稳定。大约50%的生物制剂与全身用药或全身糖皮质激素联合使用。一线治疗的下次治疗中位(范围)时间(TTNT)为2.8(0.03 - 48.07)个月,所有其他LOT的TTNT为3.3(0.03 - 52.97)个月。与单一疗法(最长7.5个月)相比,联合疗法的TTNT更长(最长16.5个月)。与非生物性全身用药相比,生物制剂的药物生存期更长,治疗次数更少。在常用疗法中,依曲替酯的中位(95%置信区间)药物生存期为8.8(5.8 - 11.8)个月,全身糖皮质激素为4.3(2.2 - 6.9)个月,司库奇尤单抗为19.6(16.1 - 26.7)个月。治疗模式差异很大,这突出表明需要治疗算法以及有效、耐受性良好的药物来支持患者,帮助他们坚持长期治疗。