Case Report and Literature Review on Skin Toxicity Induced by PD-1 Inhibitor in a Penile Cancer with Massive Ulceration of Chemoradiotherapy-Resistant and Successful Treatment by Immunotherapy

被引:0
作者
Zhu, Yanyan [1 ]
Cai, Daxia [2 ]
Jiang, Jiangle [3 ]
Tu, Jianfei [2 ]
Tian, Zhifeng [4 ]
Zhang, Xiayan [1 ]
Luo, Songmei [1 ]
Wang, Yonghui [2 ]
机构
[1] Wenzhou Med Univ, Lishui Municipal Cent Hosp, Affiliated Hosp 5, Dept Pharm, Lishui 323000, Peoples R China
[2] Wenzhou Med Univ, Lishui Municipal Cent Hosp, Affiliated Hosp 5, Thorac Oncol Ctr, Lishui 323000, Peoples R China
[3] Wenzhou Med Univ, Lishui Municipal Cent Hosp, Affiliated Hosp 5, Dept Pathol, Lishui 323000, Peoples R China
[4] Wenzhou Med Univ, Lishui Municipal Cent Hosp, Affiliated Hosp 5, Head & Neck Oncol Ctr, Lishui 323000, Peoples R China
关键词
penile cancer; immune checkpoint inhibitors; sintilimab; skin toxicity; immunotherapy; case report; ADVERSE EVENTS; EFFICACY;
D O I
10.2147/CCID.S505045
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Penile cancer is a rare malignant tumor with a poor prognosis in advanced stages. Immune checkpoint inhibitors (ICIs) have demonstrated promising efficacy in patients with advanced penile cancer, but it can also induce immune-related adverse events (irAEs). This article reports a patient who achieved almost a complete response to the PD-1 inhibitor sintilimab as third-line treatment for advanced penile squamous cell cancer with massive ulceration of chemoradiotherapy-resistant, and successful treatment by immunotherapy. One year into maintenance therapy with sintilimab, skin toxicity in the form or grade-2 skin rashes and grade-3 pruritus occurred. Sintilimab was permanently discontinued. The skin toxicity was effectively controlled by oral prednisone at a daily dosage of 15 mg. At the last follow-up of 16 months after sintilimab discontinuation, the patient remained in partial response, with total progression-free survival exceeding 30 months. We also conducted a comprehensive literature search, and summarized skin toxicity of ICIs administration. These articles suggested that immune-related skin toxicity may be indicative of good treatment response.
引用
收藏
页码:699 / 707
页数:9
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