Management of Patients With Adenocarcinoma or Squamous Cancer of the Esophagus

被引:93
作者
Ilson, David H. [1 ]
van Hillegersberg, Richard [2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, 300 E 66th St,BAIC Room 1031, New York, NY 10065 USA
[2] Univ Utrecht, Utrecht, Netherlands
关键词
Preoperative Therapy; Immune Checkpoint Inhibitors; HER2 Targeted Therapy; VEGF Targeted Therapy; PHASE-III TRIAL; ADVANCED GASTRIC-CANCER; POSTOPERATIVE PULMONARY COMPLICATIONS; PATHOLOGICAL COMPLETE RESPONSE; MINIMALLY INVASIVE ESOPHAGECTOMY; LIMITED TRANSHIATAL RESECTION; CAPECITABINE PLUS OXALIPLATIN; COMBINED-MODALITY THERAPY; NEOADJUVANT CHEMORADIATION; OPEN-LABEL;
D O I
10.1053/j.gastro.2017.09.048
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Esophageal cancer is characterized by early and frequent metastasis. Surgery is the primary treatment for earlystage disease, whereas patients with patients with locally advanced disease receive perioperative chemotherapy or chemoradiotherapy. Squamous cancers can be treated with primary chemoradiotherapy without surgery, depending on their response to therapy and patient tolerance for subsequent surgery. Chemotherapy with a fluorinated pyrimidine and a platinum agent, followed by later treatment with taxanes and irinotecan, provides some benefit. Agents that inhibit the erb-b2 receptor tyrosine kinase 2 (ERBB2 or HER2), or vascular endothelial growth factor, including trastuzumab, ramucirumab, and apatinib, increase response and survival times. Esophageal adenocarcinomas have mutations in tumor protein p53 and mutations that activate receptor-associated tyrosine kinase, vascular endothelial growth factor, and cell cycle pathways, whereas esophageal squamous tumors have a distinct set of mutations. Esophageal cancers develop systems to evade anti-tumor immune responses, but studies are needed to determine how immune checkpoint modification contributes to esophageal tumor development.
引用
收藏
页码:437 / 451
页数:15
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