| Literature DB >> 27840089 |
Guopei Luo1, Chen Liu1, Meng Guo1, Jiang Long1, Zuqiang Liu1, Zhiwen Xiao1, Kaizhou Jin1, He Cheng1, Yu Lu1, Quanxing Ni1, Xianjun Yu2.
Abstract
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. Copyright ÂEntities:
Keywords: CA19-9; Heterogeneity; Lewis antigen; Pancreatic adenocarcinoma
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Year: 2016 PMID: 27840089 DOI: 10.1016/j.canlet.2016.10.046
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679