Table 1.
Clinical | Pathologic | Molecular/Genetic |
---|---|---|
Sex | Stage (many systems)
AJCC/pTNM Lauren/Ming MI Borrman |
VEGF/VEGF-C expression |
Primary Site | DNA-repair error | |
Antrum or pyloric | K-ras mutation | |
Body or middle 1/3 | c-met amplification | |
GE junction | K-sam | |
Depth | Histological type
Diffuse Intestinal Mixed Not available |
C-erb B-2 amplification |
Tumor localization | EGFR | |
Lymph nodes | EGF | |
Venous invasion | TGF alpha | |
Neovascularization | VEGF | |
Size | Differentiation (grade) | p53 LOH |
Presence of bone marrow micro-metastases | p53 (mutation) | |
Presence of Helicobacter pylori | APC LOH | |
R classification | uPA system | |
L/V classification | E-cadherin | |
Disseminated epithelial cells |
Abbreviations: AJCC = American Joint Committee on Cancer; APC = adenomatous polyposis coli gene; EGF = epidermal growth factor; EGFR = EGF receptor; GE = gastroesophageal; LOH = loss of heterozygosity; L/V = lymphatic/vascular; MI = Maruyama Index; pTNM = pathologic tumor-node-metastasis stage; R = resection; TGF = transforming growth factor; uPA = urokinase-type plasminogen activator; VEGF = vascular endothelial growth factor.