Endoscopic Ultrasound as a Pretreatment Clinical Staging Tool for Gastric Cancer: Association with Pathology and Outcome

被引:15
|
作者
Merkow, Ryan P. [1 ]
Herrera, Gabriel [1 ]
Goldman, Debra A. [2 ]
Gerdes, Hans [3 ]
Schattner, Mark A. [3 ]
Markowitz, Arnold J. [3 ]
Strong, Vivian E. [1 ]
Brennan, Murray F. [1 ]
Coit, Daniel G. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Surg, 1275 York Ave, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Epidemiol & Biostat, 1275 York Ave, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Serv Gastroenterol & Nutr, 1275 York Ave, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
ADJUVANT CHEMOTHERAPY USE; POSTOPERATIVE COMPLICATIONS; PERIOPERATIVE CHEMOTHERAPY; NEOADJUVANT CHEMOTHERAPY; GUIDE TREATMENT; ULTRASONOGRAPHY; ADENOCARCINOMA; RESECTION; TOMOGRAPHY; ACCURACY;
D O I
10.1245/s10434-017-6050-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Endoscopic ultrasound (EUS) is a guideline-recommended diagnostic test to estimate pretreatment clinical stage in gastric cancer. The impact of EUS to discriminate long-term outcomes has not been established. The objectives of our study were to (1) evaluate the association between EUS and pathologic stage; (2) evaluate the ability of EUS to predict disease-specific survival (DSS); and (3) determine how neoadjuvant chemotherapy (NCT) affects these relationships. A prospective gastric cancer database at a tertiary care cancer center identified 734 patients who underwent curative intent resection. Patients were separated into EUS low-risk (T1-2, N0) and EUS high-risk (T3-4 Nany, or Tany N+) groups. Agreement statistics and 5-year DSS were estimated stratified by NCT. Between 1987 and 2015, 68% (502/734) of patients were not treated with NCT. Among these patients, percentage agreement between EUS and pathology was moderate (individual T stage: 52%; N stage: 70%; risk group: 73%). EUS accurately estimated pathologic risk group in 73% (365/502) of patients, whereas it overestimated pathologic risk group in 19% (93/502) of patients and underestimated risk in 8% (41/502) of patients. EUS in non-NCT staging was able to discriminate DSS for T stage (hazard ratio [HR] 5.07, p < 0.05), N stage (HR 3.58, p < 0.05), and risk group (HR 6.35, p < 0.05). Among patients treated with NCT, EUS was unable to discriminate DSS for T stage (HR 0.94, p > 0.05), N stage (HR 1.46, p > 0.05) and risk group (HR 0.50, p > 0.05). Pretreatment clinical staging based on EUS alone could lead to over- or under treatment in 27% of patients and can discriminate DSS in NCT-naive patients. EUS should be used in the context of other validated clinical risk tools.
引用
收藏
页码:3658 / 3666
页数:9
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