Treatment Response to Diphenylcyclopropenone in Patients with Alopecia Totalis/Universalis.

Q2 Medicine International Journal of Trichology Pub Date : 2023-07-01 Epub Date: 2024-04-05 DOI:10.4103/ijt.ijt_2_22
Smitha Ancy Varghese, Sandhya S Nair, Anuja Elizabeth George, Induprabha Yadev
{"title":"Treatment Response to Diphenylcyclopropenone in Patients with Alopecia Totalis/Universalis.","authors":"Smitha Ancy Varghese, Sandhya S Nair, Anuja Elizabeth George, Induprabha Yadev","doi":"10.4103/ijt.ijt_2_22","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Alopecia totalis (AT) and Alopecia universalis (AU) are forms of Alopecia areata (AA) which represent the strongest predictor of poor prognosis since spontaneous regrowth is <10%. Topical immunotherapy agent, diphenylcyclopropenone (DPCP) has shown clinical efficacy with limited side effects in severe forms of AA. However, its specific role in AT/AU characterized by complete hair loss over the scalp can help highlight the efficacy of the drug with fewer confounders.</p><p><strong>Methodology: </strong>Data were collected from 18 patients diagnosed with AT/AU and treated with topical immunotherapy with DPCP as per protocol by Happle <i>et al</i>. Baseline Severity of Alopecia Tool (SALT) score and subclass was recorded. In the case of AU, baseline body hair loss score was also recorded. Patients were reassessed after 6 months of treatment in terms of change in SALT score and hair regrowth was assessed using the Global Assessment Score. The side effects during treatment were also assessed and recorded.</p><p><strong>Results: </strong>Eighteen patients of whom eleven (61.1%) were diagnosed as AU and seven (38.9%) as AT were treated. The mean age was 21.6, with a male: female ratio of 3:2. The comorbidities noted were atopy in six (33.3%), atopy and hypothyroidism in one (5.5%), Down's syndrome in two (11.1%), and hypothyroidism alone in one (5.5%) patient. The mean duration of disease at the time of presentation was 3 years and all patients had remained refractory to various other modalities of treatment. All patients had a baseline SALT score of 100 corresponding to S5. After 6 months of treatment, 27.7% of patients did not show any response (SALT score S5), 16.6% had a score of S4, 11.1% had a score of S3, 11.1% had a score of S2, 22.2% had a score of S1, and 11.1% had a score of S0. On assessing improvement in body hair loss score, 36.3% of patients showed no improvement, 36.3% showed partial improvement, and 27.2% of patients showed complete body hair regrowth. About 55.5% of patients developed notable side effects that included severe local reactions, cervical lymphadenopathy, acne and pigmentation at the site of application as well as untreated sites.</p><p><strong>Conclusion: </strong>The AT/AU subtypes of AA, was amenable to treatment with contact immunotherapeutic agent DPCP with a >75% hair regrowth in 33.3% of patients. The castling phenomenon was seen in 63.6% of AU patients. The adverse effects noted were not severe enough to deter treatment.</p>","PeriodicalId":14417,"journal":{"name":"International Journal of Trichology","volume":"15 4","pages":"149-153"},"PeriodicalIF":0.0000,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11098142/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Trichology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/ijt.ijt_2_22","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/4/5 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Alopecia totalis (AT) and Alopecia universalis (AU) are forms of Alopecia areata (AA) which represent the strongest predictor of poor prognosis since spontaneous regrowth is <10%. Topical immunotherapy agent, diphenylcyclopropenone (DPCP) has shown clinical efficacy with limited side effects in severe forms of AA. However, its specific role in AT/AU characterized by complete hair loss over the scalp can help highlight the efficacy of the drug with fewer confounders.

Methodology: Data were collected from 18 patients diagnosed with AT/AU and treated with topical immunotherapy with DPCP as per protocol by Happle et al. Baseline Severity of Alopecia Tool (SALT) score and subclass was recorded. In the case of AU, baseline body hair loss score was also recorded. Patients were reassessed after 6 months of treatment in terms of change in SALT score and hair regrowth was assessed using the Global Assessment Score. The side effects during treatment were also assessed and recorded.

Results: Eighteen patients of whom eleven (61.1%) were diagnosed as AU and seven (38.9%) as AT were treated. The mean age was 21.6, with a male: female ratio of 3:2. The comorbidities noted were atopy in six (33.3%), atopy and hypothyroidism in one (5.5%), Down's syndrome in two (11.1%), and hypothyroidism alone in one (5.5%) patient. The mean duration of disease at the time of presentation was 3 years and all patients had remained refractory to various other modalities of treatment. All patients had a baseline SALT score of 100 corresponding to S5. After 6 months of treatment, 27.7% of patients did not show any response (SALT score S5), 16.6% had a score of S4, 11.1% had a score of S3, 11.1% had a score of S2, 22.2% had a score of S1, and 11.1% had a score of S0. On assessing improvement in body hair loss score, 36.3% of patients showed no improvement, 36.3% showed partial improvement, and 27.2% of patients showed complete body hair regrowth. About 55.5% of patients developed notable side effects that included severe local reactions, cervical lymphadenopathy, acne and pigmentation at the site of application as well as untreated sites.

Conclusion: The AT/AU subtypes of AA, was amenable to treatment with contact immunotherapeutic agent DPCP with a >75% hair regrowth in 33.3% of patients. The castling phenomenon was seen in 63.6% of AU patients. The adverse effects noted were not severe enough to deter treatment.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
二苯基环丙酮对完全性/泛发型脱发患者的治疗反应。
导言:全秃(AT)和普秃(AU)是斑秃(AA)的一种形式,是预后不良的最有力的预测指标,因为自发再生是方法学的一种:根据 Happle 等人的方案,收集了 18 名被诊断为 AT/AU 并接受 DPCP 局部免疫疗法治疗的患者的数据。对于AU患者,还记录了基线体毛脱落评分。治疗 6 个月后,根据 SALT 评分的变化对患者进行重新评估,并使用总体评估评分对毛发再生情况进行评估。此外,还对治疗期间的副作用进行了评估和记录:18名患者接受了治疗,其中11人(61.1%)被诊断为AU,7人(38.9%)被诊断为AT。平均年龄为 21.6 岁,男女比例为 3:2。6名患者(33.3%)患有过敏症,1名患者(5.5%)患有过敏症和甲状腺功能减退症,2名患者(11.1%)患有唐氏综合征,1名患者(5.5%)仅患有甲状腺功能减退症。患者发病时的平均病程为 3 年,所有患者均对其他各种治疗方法无效。所有患者的基线 SALT 评分均为 100 分,相当于 S5。治疗 6 个月后,27.7% 的患者没有任何反应(SALT 评分为 S5),16.6% 的患者评分为 S4,11.1% 的患者评分为 S3,11.1% 的患者评分为 S2,22.2% 的患者评分为 S1,11.1% 的患者评分为 S0。在评估体毛脱落评分的改善情况时,36.3% 的患者没有改善,36.3% 的患者有部分改善,27.2% 的患者体毛完全再生。约 55.5%的患者出现了明显的副作用,包括严重的局部反应、颈部淋巴结病、痤疮和用药部位及未治疗部位的色素沉着:结论:AT/AU 亚型 AA 适合使用接触性免疫治疗剂 DPCP 治疗,33.3% 的患者毛发再生率大于 75%。63.6%的AU患者出现了秃顶现象。不良反应并不严重,不足以阻止治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
1.50
自引率
0.00%
发文量
38
期刊最新文献
A Cross-sectional Observational Study to Correlate the Trichoscopic Findings of Female Pattern Hair Loss with the Disease Severity and Underlying Histopathological Changes. A Study of Serum Ferritin and Thyroid-Stimulating Hormone Levels in Male Patients with Androgenetic Alopecia. Alopecia Areata with Renal Dysgenesis. Graham-Little-Piccardi-Lassueur Syndrome with Mucosal Involvement: A Rare Case. Mucinous Lupus Alopecia with Papulonodular Mucinosis as a Sole Cutaneous Manifestation of Systemic Lupus Erythematosus.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1