Lei-ming Guo, Cheng-zhe Yang, Chun-yu He, Ke Li, L. Qiao, Shuning Xu, Xiaoyuan Wu, Y. Liu
{"title":"Clinical Evidence on Apatinib in Treating Chemotherapy-Refractory Metastatic Esophageal Squamous Cell Carcinoma","authors":"Lei-ming Guo, Cheng-zhe Yang, Chun-yu He, Ke Li, L. Qiao, Shuning Xu, Xiaoyuan Wu, Y. Liu","doi":"10.31487/j.cor.2020.03.08","DOIUrl":null,"url":null,"abstract":"Majority Chinese esophageal cancer patients have squamous cell carcinoma (ESCC) and with metastasis at\ninitial diagnosis. Treatment for metastatic ESCC where first-line chemotherapy failed is an unmet medical\nneed. Targeting human epidermal growth factor receptor 2 (HER2) and vascular endothelial growth factor\nreceptor 2 (KDR) have been approved to be effective for esophageal adenocarcinoma (EAC). We explored\nthe clinical relevance of these molecular signaling in ESCC cohorts and collected clinical evidence on\napplying apatinib, a Chinese FDA-approved KDR inhibitor for late-stage gastric carcinoma, in 26 patients\nwith chemotherapy-refractory metastatic ESCC. The clinical response rate and disease control rate of these\npatients to apatinib 500mg once daily regimen was 12% and 60%, respectively. The patients’ median\nprogression-free survival time (PFS) was 3.2 months (95% CI, 2.23-4.17 months) and overall survival time\n(OS) was 5.3 months (95% CI, 4.46-6.14 months). The most common grade 3-4 treatment-related adverse\nevents included leukopenia (7.7%) and anemia (7.7%). No drug-related death occurred. In conclusion,\napatinib has favorable activity and acceptable safety, and could be a new treatment option for patients with\nchemotherapy refractory metastatic ESCC.","PeriodicalId":10487,"journal":{"name":"Clinical Oncology and Research","volume":"2 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Oncology and Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31487/j.cor.2020.03.08","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Majority Chinese esophageal cancer patients have squamous cell carcinoma (ESCC) and with metastasis at
initial diagnosis. Treatment for metastatic ESCC where first-line chemotherapy failed is an unmet medical
need. Targeting human epidermal growth factor receptor 2 (HER2) and vascular endothelial growth factor
receptor 2 (KDR) have been approved to be effective for esophageal adenocarcinoma (EAC). We explored
the clinical relevance of these molecular signaling in ESCC cohorts and collected clinical evidence on
applying apatinib, a Chinese FDA-approved KDR inhibitor for late-stage gastric carcinoma, in 26 patients
with chemotherapy-refractory metastatic ESCC. The clinical response rate and disease control rate of these
patients to apatinib 500mg once daily regimen was 12% and 60%, respectively. The patients’ median
progression-free survival time (PFS) was 3.2 months (95% CI, 2.23-4.17 months) and overall survival time
(OS) was 5.3 months (95% CI, 4.46-6.14 months). The most common grade 3-4 treatment-related adverse
events included leukopenia (7.7%) and anemia (7.7%). No drug-related death occurred. In conclusion,
apatinib has favorable activity and acceptable safety, and could be a new treatment option for patients with
chemotherapy refractory metastatic ESCC.