Zhu Huiling, Zhu Zhe, Huang Weining, Cheng Xiping, He Jiaxi, Xiong Chunping, Han Jiande
a Department of Dermatology , the First Affiliated Hospital of Guangzhou Medical University , Guangzhou , P. R. China.
b Department of Stem Cell Biology and Regenerative Medicine , Lerner Research Institute, Cleveland Clinic , Cleveland , OH , USA.
Cutan Ocul Toxicol. 2018 Mar;37(1):96-99. doi: 10.1080/15569527.2017.1355316. Epub 2017 Aug 7.
This study presented common lesions with systemic toxicities and uncommon adverse cutaneous reactions such as anaphylactic dermatitis in patients undergoing treatment with erlotinib for the benefit of practicing dermatologists and oncologists.
Adverse cutaneous reactions associated with erlotinib were reported in 20 Chinese patients with cancer.
Adverse cutaneous reactions reported included six cases of anaphylactic dermatitis, 12 cases of acneiform rash, nine cases of xerosis, five cases of nail changes and four cases of hair changes. One case of anaphylactic dermatitis manifested as erythema with swelling on the face and neck, and others as erosive and scaly erythema on the fold of skin, or red macules, papules, plaques and pigmentation on the whole body. Clinical details indicated anaphylactic reactions, including a high percentage of eosinophils in the peripheral blood, eosinophilic infiltration in the dermis layer and good response to antihistamines and topical steroids. Systemic toxicities accompanied by cutaneous reactions occurred in five patients including one case of anaphylactic dermatitis and four cases of acneiform rash. Elevated hepatic enzymes were observed among all the patients with grade-3 or grade-4 acneiform rashes. One patient with anaphylactic dermatitis and one with acneiform rash discontinued erlotinib administration due to severe lesions, high fever or severe elevation of hepatic enzymes.
Anaphylactic cutaneous reactions caused by erlotinib are rarely described hitherto. Systemic toxicities should be emphasized especially in cases with severe skin disorders. Timely detection and appropriate early intervention in patients who develop severe cutaneous reaction while on erlotinib therapy should be considered clinically.
本研究呈现了接受厄洛替尼治疗的患者出现的伴有全身毒性的常见病变以及罕见的不良皮肤反应,如过敏性皮炎,以造福皮肤科医生和肿瘤内科医生。
报告了20例中国癌症患者中与厄洛替尼相关的不良皮肤反应。
报告的不良皮肤反应包括6例过敏性皮炎、12例痤疮样皮疹、9例皮肤干燥、5例指甲改变和4例毛发改变。1例过敏性皮炎表现为面部和颈部红斑伴肿胀,其他表现为皮肤褶皱处糜烂性和鳞屑性红斑,或全身红色斑疹、丘疹、斑块及色素沉着。临床细节显示存在过敏反应,包括外周血中嗜酸性粒细胞比例高、真皮层嗜酸性粒细胞浸润以及对抗组胺药和外用类固醇反应良好。5例患者出现伴有皮肤反应的全身毒性,包括1例过敏性皮炎和4例痤疮样皮疹。所有3级或4级痤疮样皮疹患者均观察到肝酶升高。1例过敏性皮炎患者和1例痤疮样皮疹患者因严重病变、高热或肝酶严重升高而停用厄洛替尼。
厄洛替尼引起的过敏性皮肤反应迄今鲜有描述。应特别强调全身毒性,尤其是在严重皮肤疾病的情况下。临床上应考虑对接受厄洛替尼治疗时出现严重皮肤反应的患者进行及时检测和适当的早期干预。