Validation of histomolecular classification utilizing histological subtype, MUC1, and CDX2 for prognostication of resected ampullary adenocarcinoma

被引:43
作者
Schueneman, A. [1 ]
Goggins, M. [2 ,3 ,4 ]
Ensor, J. [5 ]
Saka, B. [6 ]
Neishaboori, N. [7 ]
Lee, S. [7 ]
Maitra, A. [7 ]
Varadhachary, G. [8 ]
Rezaee, N. [9 ]
Wolfgang, C. [9 ]
Adsay, V. [6 ]
Wang, H. [7 ]
Overman, M. J. [8 ]
机构
[1] Univ Texas Houston, MD Anderson Canc Ctr, Dept Grad Med Educ, Div Canc Med, Houston, TX 77030 USA
[2] Johns Hopkins Univ Hosp, Dept Pathol, Baltimore, MD 21287 USA
[3] Johns Hopkins Univ Hosp, Dept Med, Baltimore, MD 21287 USA
[4] Johns Hopkins Univ Hosp, Dept Oncol, Baltimore, MD 21287 USA
[5] Univ Texas Houston, MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[6] Emory Univ, Sch Med, Dept Pathol, Atlanta, GA 30322 USA
[7] Univ Texas Houston, MD Anderson Canc Ctr, Dept Pathol, Div Pathol Lab Med, Houston, TX 77030 USA
[8] Univ Texas Houston, MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Div Canc Med, Houston, TX 77030 USA
[9] Johns Hopkins Univ Hosp, Dept Surg, Baltimore, MD 21287 USA
关键词
ampullary adenocarcinoma; MUC1; CDX2; histomolecular phenotype; prognostic; PERIAMPULLARY ADENOCARCINOMA; ADJUVANT CHEMOTHERAPY; GENE-EXPRESSION; INTESTINAL-TYPE; CARCINOMA; SURVIVAL; VATER; IMMUNOHISTOCHEMISTRY; GEMCITABINE; CANCER;
D O I
10.1038/bjc.2015.172
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Outcomes for ampullary adenocarcinomas are heterogeneous, and numerous methods of categorisation exist. A histomolecular phenotype based on histology, caudal-type homeodomain transcription factor 2 (CDX2) staining and Mucin 1 (MUC1) staining has recently been tested and validated in two cohorts. We attempt to validate this classification in a large patient population. Methods: Tissue samples from 163 patients with resected ampullary adenocarcinoma were classified based on histology and immunohistochemical expression of CDX2 and MUC1. A pancreaticobiliary histomolecular classification (PB) was defined as a sample with pancreaticobiliary histology, positive MUC1 and negative CDX2 expression. Results: There were 82 deaths; median follow-up of 32.4 months; and median overall survival of 87.7 (95% CI 42.9-109.5) months. PB comprised 28.2% of the cases. Factors associated with overall survival were histological subtype (P = 0.0340); T1/2 vs T3/4 (P = 0.001); perineural (P<0.0001) and lymphovascular (P = 0.0203) invasion; and histomolecular intestinal histomolecular phenotype (INT) vs PB phenotype (106.4 vs 21.2 months, P<0.0001). Neither MUC1 nor CDX2 was statistically significant, although MUC1 positivity defined as >= 10% staining was significant (P = 0.0023). In multivariate analysis, age (HR 1.03), PB phenotype (HR 2.26) and perineural invasion (PNI; HR 2.26) were associated with poor survival. Conclusions: The prognostic ability of histomolecular phenotype has been validated in an independent cohort of ampullary adenocarcinoma patients.
引用
收藏
页码:64 / 68
页数:5
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