Translating genomic profiling to gastrointestinal cancer treatment

被引:7
|
作者
Harada, Kazuto [1 ,2 ]
Kaya, Dilsa Mizrak [1 ]
Shimodaira, Yusuke [1 ]
Song, Shumei [1 ]
Baba, Hideo [2 ]
Ajani, Jaffer A. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, 1515 Holcombe Blvd, Houston, TX 77030 USA
[2] Kumamoto Univ, Grad Sch Med Sci, Dept Gastroenterol Surg, 1-1-1 Honjo, Kumamoto 8608556, Japan
基金
日本学术振兴会;
关键词
gastrointestinal cancer; genome sequencing; translational research; METASTATIC COLORECTAL-CANCER; ADVANCED GASTRIC-CANCER; CIRCULATING TUMOR-CELLS; MULTICENTER PHASE-II; DOUBLE-BLIND; 1ST-LINE TREATMENT; OPEN-LABEL; ESOPHAGEAL ADENOCARCINOMA; JUNCTION ADENOCARCINOMA; EGFR BLOCKADE;
D O I
10.2217/fon-2016-0422
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Next-generation sequencing enables faster, cheaper and more accurate whole-genome sequencing, allowing genome profiling and discovery of molecular features. As molecular targeted drugs are developed, treatment can be tailored according to molecular subtype. Gastric and colorectal cancers have each been divided into four subtypes according to molecular features. Profiling of the esophageal cancer genome is underway and its classification is anticipated. To date, identification of HER2 expression in gastric adenocarcinoma and KRAS, NRAS and BRAF mutations in colon cancer have proved essential for treatment decisions. However, to overcome therapy resistance and improve prognosis, further individualized therapy is required. Here, we summarize the treatment options for gastrointestinal cancer according to genomic profiling and discuss future directions.
引用
收藏
页码:919 / 934
页数:16
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