Correlation between efficacy and skin rash occurrence following treatment with the epidermal growth factor receptor inhibitor cetuximab: A single institution retrospective analysis

被引:44
作者
Orditura, Michele [1 ]
De Vita, Ferdinando
Galizia, Gennaro [2 ]
Lieto, Eva [2 ]
Vecchione, Loredana
Vitiello, Fabiana
Martinelli, Erika
Ciardiello, Fortunato
机构
[1] Univ Naples 2, Sch Med, F Magrassi A Lanzara Dept Clin & Expt Med, Div Med Oncol,Policlin 2, I-80131 Naples, Italy
[2] Univ Naples 2, Sch Med, F Magrassi A Lanzara Dept Clin & Expt Med, Div Gen Surg, I-80131 Naples, Italy
关键词
epidermal growth factor receptor; cetuximab; skin rash; predictive factor; METASTATIC COLORECTAL-CANCER; CURATIVE SURGERY; PLUS IRINOTECAN; MUTATION STATUS; PHASE-II; EXPRESSION; THERAPY; OXALIPLATIN; SURVIVAL; ANTIBODY;
D O I
10.3892/or_00000319
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Several trials show a relationship between skin toxicity, response rate, and overall survival in cetuximab-treated patients. We analyzed our database to evaluate the importance of skin rash as a surrogate marker of favorable outcome in cancer patients referred to our institution in the last three years. We retrospectively analyzed 90 cetuximab-treated patients: 57 colon cancer patients, 10 NSCLC patients, 14 locally advanced esophageal cancer patients, and 9 miscellaneous. A significant correlation was observed between skin rash and response to therapy. Skin rash was experienced by 93% of PR and 100% of CR patients. The mean TTP was 184 days in patients showing skin rash and 94 days in patients without skin rash, respectively. On multivariate analysis, skin rash was demonstrated to be the only independent prognostic variable with regard to TTP. Patients who did not develop skin rash had a 2-fold greater likelihood to manifest tumor progression significantly earlier than patients who developed skin rash. In our series, a statistically significant correlation between rash, response rate, and TTP was demonstrated in 90 cetuximab-treated patients. Skin toxicity was confirmed as the only clinical variable able to predict the response to cetuximab.
引用
收藏
页码:1023 / 1028
页数:6
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