Management of skin toxicities during panitumumab treatment in metastatic colorectal cancer
皮毒性的管理在在变形 colorectal 癌症的 panitumumab 治疗期间作者机构：Department of Gastroenterology and Digestive OncologyHopital Robert Debre CHU ReimsReims 51000France Oncology DepartmentCentre Paul StraussStrasbourg 67000France Oncology DepartmentCentre HospitalierCarcassonne 11000France Medical DepartmentAMGEN FranceBoulogne-Billancourt 92100France Radiation OncologyCentre de Haute EnergieNice 06000France Dermatology DepartmentHopital Saint-Andre CHU de BordeauxBordeaux 33000France Oncology DepartmentAvicenne HospitalBobigny 93000France
出 版 物：《World Journal of Gastroenterology》 (世界胃肠病学杂志（英文版）)
年 卷 期：2019年第25卷第29期
页 面：4007-4018页
核心收录：
学科分类：10[医学]
主 题：Metastatic colorectal cancer Epidermal growth factor receptor inhibitors Panitumumab Skin toxicity Quality of life
摘 要：BACKGROUND Anti-epidermal growth factor receptor therapy is associated with skin adverse events not previously reported with conventional chemotherapy. Prophylactic actions are recommended, but routine clinical management of these toxicities and their impact on quality of life remain unknown. AIM To assess the dermatological toxicities reported after panitumumab initiation, their impact on the quality of life and the clinical practices for their management. METHODS Patients included in this prospective multicenter observational study were over 18 years of age and began treatment with panitumumab for wild-type KRAS metastatic colorectal cancer. The incidence of dermatological toxicities, clinical practices for their management and impact on quality of life were recorded during a 6-mo follow-up. RESULTS Overall, 229 patients (males, 57.6%;mean age, 66.2 years) were included. At day 15, 59.3% of patients had dermatological toxicity;the rate peaked at month 2 (74.7%) and decreased at month 6 (46.5%). The most frequent dermatological toxicities were rash/acneiform rash, xerosis and skin cracks. At least one preventive treatment was administered to 65.9% of patients (oral antibiotics, 84.1%;emollients, 75.5%;both, 62.9%). The rates of patients who received at least one curative treatment peaked at month 2 (63.4%) and decreased at month 6 (44.8%). The impact of the dermatological toxicities on quality of life was limited as assessed with Dermatology Life Quality Index scores and inconvenience visual analogic scale score. The rates of topical corticosteroids administration and visits to specialists were low. CONCLUSION The rates of the different skin toxicities peaked at various times and were improved at the end of follow-up. Nevertheless, their clinical management could be optimized with a better adherence to current recommendations. The impact of skin toxicities on patient’s quality of life appeared to be limited.
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