发明名称 |
Method of determining administration effect in cancer chemotherapy with S-1 |
摘要 |
Provided is a method of determining a therapeutic effect of cancer chemotherapy with an anticancer drug obtained by blending three ingredients, i.e., tegafur, gimeracil, and oteracil potassium as active ingredients (hereinafter abbreviated as S-1) quickly, simply, and accurately before carrying out the cancer chemotherapy. Specifically, provided is a method of determining an administration effect in chemotherapy with S-1, the method comprising: a step (a) of measuring expression level of a decorin gene in a biological sample collected from a subject to be diagnosed; and a step (b) of determining an administration effect of S-1 based on the expression level of the gene obtained from the measurement. |
申请公布号 |
US9494594(B2) |
申请公布日期 |
2016.11.15 |
申请号 |
US201313853137 |
申请日期 |
2013.03.29 |
申请人 |
National University Corporation Chiba University |
发明人 |
Tanzawa Hideki;Kasamatsu Atsushi;Uzawa Katsuhiro |
分类号 |
C12Q1/68;G01N33/68 |
主分类号 |
C12Q1/68 |
代理机构 |
Kilyk & Bowersox, P.L.L.C. |
代理人 |
Kilyk & Bowersox, P.L.L.C. |
主权项 |
1. A method of administering chemotherapy with S-1 for a subject in need of chemotherapy, the method comprising:
a step (a) of collecting a biological sample from a subject before carrying out chemotherapy with S-1, wherein S-1 is obtained by blending tegafur, gimeracil, and oteracil potassium as active ingredients, the biological sample comprises a cancer tissue, and the biological sample is from a head and neck squamous cell carcinoma patient or an oral squamous cell carcinoma patient; a step (b) of measuring expression level of a decorin gene in the biological sample collected from the subject before carrying out the chemotherapy with S-1; a step (c) of predicting an administration effect of S-1 using a predetermined reference value wherein the subject is assessed to have resistance to S-1 when the expression level of the decorin gene in the biological sample is high as compared to the predetermined reference value, while the subject is assessed to have sensitivity to S-1 when the expression level of the decorin gene is low as compared to the predetermined reference value; a step (d) of identifying the subject as having the sensitivity to S-1; and a step (e) administering said chemotherapy with S-1 to the subject assessed to have the sensitivity to S-1. |
地址 |
Chiba JP |