دورية أكاديمية

Radiotherapy may exacerbated anti‐programmed cell death 1 treatment induced vitiligo: A case report

التفاصيل البيبلوغرافية
العنوان: Radiotherapy may exacerbated anti‐programmed cell death 1 treatment induced vitiligo: A case report
المؤلفون: Chengqian Chen, Qihang Chang, Bo Wang, Yaqi Wang, Zhen Zhang, Xiuli Wang
المصدر: Skin Health and Disease, Vol 4, Iss 1, Pp n/a-n/a (2024)
بيانات النشر: Wiley, 2024.
سنة النشر: 2024
المجموعة: LCC:Dermatology
مصطلحات موضوعية: Dermatology, RL1-803
الوصف: Abstract Immunotherapy with programmed cell death 1 (PD‐1) checkpoint inhibitors combined with chemoradiotherapy shows great potential for cancer treatment and is getting extensively researched. However, a plethora of immune‐related adverse events (irAEs) has been observed during anti‐PD‐1 treatment, including cutaneous adverse events, such as vitiligo and pruritus. These adverse events may lead to treatment discontinuation. When anti‐PD‐1 treatment is combined with radiotherapy (RT), irAEs may be exacerbated. Here we present a case report of an elderly patient with stage IIIb rectal cancer, who developed PD‐1 inhibitor‐associated vitiligo. After a session of RT, vitiligo lesions enlarged shortly thereafter. After discontinuation of anti‐PD‐1 treatment, vitiligo lesions and pruritus quickly improved with appropriate treatment. The rectal cancer achieved clinical complete response with no sign of recurrence or metastasis during follow‐up. Considering the similar mechanism of anti‐PD‐1 treatment in targeting cancer and in inducing irAEs, cutaneous adverse events may be associated with favourable clinical response. Additionally, cutaneous irAEs aggravated by RT in this patient may suggested significant immune activation, which may occasionally contribute to tumour regression and favourable clinical outcome.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2690-442X
Relation: https://doaj.org/toc/2690-442X
DOI: 10.1002/ski2.287
URL الوصول: https://doaj.org/article/0c743b0439f340f0811d597e53ad83bd
رقم الأكسشن: edsdoj.0c743b0439f340f0811d597e53ad83bd
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:2690442X
DOI:10.1002/ski2.287