Department of Dermatology, Haseki Training and Research Hospital, Istanbul, Turkey.
Oncology Department, Haseki Training and Research Hospital, Istanbul, Turkey.
Cutan Ocul Toxicol. 2020 Dec;39(4):380-384. doi: 10.1080/15569527.2020.1833028. Epub 2020 Oct 20.
Epidermal growth factor receptor inhibitors (EGFRs) are chemotherapeutic agents used in multiple solid organ malignity. These medications have common dermatological side effects, particularly papulopustular (PPL) lesions. The management of the diagnosis and treatment processes for such side effects may facilitate the continuation of chemotherapy and enhance the patient's quality of life.
The objective of this study is to report the cutaneous side effects of EGFR inhibitors and to share treatment methods for such side effects.
In this prospective study, 59 patients using EGFR due to breast and colorectal carcinoma at the oncology unit of Haseki Training and Research Hospital were assessed. The patients for whom EGFR was initiated were examined at the beginning of the treatment at weeks 1 and 2, their demographic characteristics were recorded, and the patients who developed a skin rash were followed up from the onset of the lesion. The PPL side effects that developed in the patients and other dermatological findings were recorded. The PPL side effects were graded, and the treatment plans were reported. The study was conducted between February 2016 and February 2018 under the approval of the local ethical committee.
The mean age of the 59 patients (47 females, 12 males) taking EGFR inhibitors was 52.4 ± 12.0 (range: 29-84). Forty-five patients had early stage and 14 patients had advanced stage carcinoma. Fourteen patients had colorectal carcinoma, three patients had renal cancer, and 42 patients had breast cancer. Forty-two patients were using trastuzumab (single therapy in 29 patients and combined therapy in 13 patients), five patients were using cetuximab, three patients were using sunitinib, eight patients were using panitumumab, and six patients were using pertuzumab. In 22 patients, PPL side effects were observed in the skin; it was G1 in 19 patients and G2 in three patients. In seven patients who developed acneiform side effects, systemic doxycycline was used, and in others, topical tetracycline and clindamycin were used. Except for one patient using trastuzumab, all patients has lesions on the face, upper trunk, and back. One patient exhibited an atypical rash, which was diagnosed as a granulomatous follicular reaction. Xerosis was present in two cases, and paronychia, pyogenic granuloma, trichomegaly, and madarosis were observed in one patient each. The patients who developed an acneiform rash were treated with topical and systemic antibiotics, light keratolytics, and emollients. The skin side effects of all patients were mild to moderate, and all patients completed the chemotherapy process. An acneiform skin rash and other dermatological side effects are common with EGFR inhibitors. To treat these side effects, emollients, topical steroids, and local, systemic antibiotics are recommended. Clindamycin may be preferred as a topical treatment, and doxycycline may be preferred as a systematic treatment.
表皮生长因子受体抑制剂(EGFRs)是用于多种实体器官恶性肿瘤的化疗药物。这些药物具有常见的皮肤副作用,特别是丘疹脓疱性(PPL)病变。管理这些副作用的诊断和治疗过程可以促进化疗的继续,并提高患者的生活质量。
本研究旨在报告 EGFR 抑制剂的皮肤副作用,并分享此类副作用的治疗方法。
在这项前瞻性研究中,评估了哈塞基培训与研究医院肿瘤病房因乳腺癌和结直肠癌而使用 EGFR 的 59 名患者。在治疗开始时对开始使用 EGFR 的患者进行检查,在第 1 周和第 2 周进行检查,记录患者的人口统计学特征,并从病变开始时对出现皮疹的患者进行随访。记录患者出现的 PPL 副作用和其他皮肤发现。对 PPL 副作用进行分级,并报告治疗计划。该研究在当地伦理委员会的批准下于 2016 年 2 月至 2018 年 2 月进行。
59 名接受 EGFR 抑制剂治疗的患者(47 名女性,12 名男性)的平均年龄为 52.4±12.0(范围:29-84)。45 名患者为早期,14 名患者为晚期癌症。14 名患者患有结直肠癌,3 名患者患有肾癌,42 名患者患有乳腺癌。42 名患者使用曲妥珠单抗(29 名患者单一治疗,13 名患者联合治疗),5 名患者使用西妥昔单抗,3 名患者使用舒尼替尼,8 名患者使用帕尼单抗,6 名患者使用培妥珠单抗。在 22 名患者中,皮肤出现 PPL 副作用;19 名患者为 G1,3 名患者为 G2。在 7 名出现痤疮样副作用的患者中,使用了全身性多西环素,而在其他患者中,使用了局部四环素和克林霉素。除了一名使用曲妥珠单抗的患者外,所有患者的面部、上躯干和背部均有病变。一名患者出现非典型皮疹,诊断为肉芽肿性滤泡反应。有 2 例出现干燥症,1 例出现甲床炎、化脓性肉芽肿、多毛症和睫毛缺失。出现痤疮样皮疹的患者接受了局部和全身抗生素、光角质松解剂和保湿剂治疗。所有患者的皮肤副作用均为轻度至中度,所有患者均完成了化疗过程。EGFR 抑制剂常引起痤疮样皮疹和其他皮肤副作用。为了治疗这些副作用,建议使用保湿剂、局部类固醇和局部、全身抗生素。克林霉素可能是一种较好的局部治疗药物,多西环素可能是一种较好的系统治疗药物。