CA19-9-Low&Lewis (+) pancreatic cancer: A unique subtype

被引:23
作者
Luo, Guopei [1 ,2 ,3 ]
Liu, Chen [1 ,2 ,3 ]
Guo, Meng [1 ,2 ,3 ]
Long, Jiang [1 ,2 ,3 ]
Liu, Zuqiang [1 ,2 ,3 ]
Xiao, Zhiwen [1 ,2 ,3 ]
Jin, Kaizhou [1 ,2 ,3 ]
Cheng, He [1 ,2 ,3 ]
Lu, Yu [1 ,2 ,3 ]
Ni, Quanxing [1 ,2 ,3 ]
Yu, Xianjun [1 ,2 ,3 ]
机构
[1] Fudan Univ, Dept Pancreat Surg, Shanghai Canc Ctr, Shanghai 200032, Peoples R China
[2] Fudan Univ, Shanghai Med Coll, Dept Oncol, Shanghai 200032, Peoples R China
[3] Fudan Univ, Pancreat Canc Inst, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
Pancreatic adenocarcinoma; Lewis antigen; Heterogeneity; CA19-9; LONG-TERM SURVIVAL; CA-19-9; CA19-9; LEWIS; GEMCITABINE; STATISTICS; EXPRESSION; CORRELATE; ANTIGENS;
D O I
10.1016/j.canlet.2016.10.046
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The study was performed to identify unique subtype from the long-term survival (>24 months) patients with advanced pancreatic cancer (1039 cases). Long-term survival patients had higher proportion of low secretion of carbohydrate antigen 19-9 (CA19-9) than that of patients with non long-term survival (P < 0.001). Considering the impact of Lewis status on CA19-9 secretion, Lewis genotypes were further determined by Sanger sequencing. The prognosis of CA19-9-Low&Lewis (-) patients was worse than that of CA19-9-Low&Lewis (+) (hazard ratio (HR) = 0.37, P < 0.001). The proportion of epidermal growth factor receptor (EGFR) () cases was lower in the CA19-9-Low&Lewis (+) subgroup than that in other patients (P = 0.047). For the CA19-9-Low&Lewis (+) subgroup, chemotherapy plus radiotherapy but not chemotherapy was found to be an independent prognostic factor (versus best supportive care, chemotherapy, HR = 0.71, P = 0.267; chemotherapy plus radiotherapy, HR = 0.33, P = 0.022). We conclude that CA19-9-Low&Lewis (+) pancreatic cancer is a unique subtype with special biological properties. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:46 / 50
页数:5
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