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

Author:

Chen Chengqian1,Chang Qihang1,Wang Bo2,Wang Yaqi3456,Zhang Zhen3456,Wang Xiuli1ORCID

Affiliation:

1. Institute of Photomedicine Shanghai Skin Disease Hospital School of Medicine Tongji University Shanghai China

2. Department of Dermatology University of Michigan Ann Arbor Michigan USA

3. Department of Radiation Oncology Fudan University Shanghai Cancer Center Shanghai China

4. Department of Oncology Shanghai Medical College Fudan University Shanghai China

5. Shanghai Clinical Research Center for Radiation Oncology Shanghai China

6. Shanghai Key Laboratory of Radiation Oncology Shanghai China

Abstract

AbstractImmunotherapy 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.

Publisher

Wiley

Subject

Dermatology

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