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Gastric cancer
EPIDEMIOLOGY
Worldwide, gastric carcinoma represents the third or fourth most common
malignancy. The frequency of gastric carcinoma occurrence at different sites within
the stomach has changed in the United States over recent decades. The incidence of
cancer of the distal half of the stomach has been decreasing in the United States
since the 1930s.
RISK FACTORS
1)Average age at onset is fifth decade
2)Male-to-female ratio is 1.7:1
3)African American-to-white ratio is 1.8:1
4)Precursor conditions include chronic atrophic gastritis and intestinal metaplasia,
pernicious anemia (10% to 20% incidence), partial gastrectomy for benign disease,
Helicobacter pylori infection (especially childhood exposure—three- to fivefold
increase), Ménétrier’s disease, and gastric adenomatous polyps. These precursor
lesions are largely linked to distal (intestinal-type) gastric carcinoma
5) Family history: first degree (two- to threefold); the family of Napoléon Bonaparte is
an example; familial clustering; patients with hereditary nonpolyposis colorectal
cancer (Lynch syndrome II) are at increased risk; germline mutations of E-cadherin
(CDH1 gene) have been linked to familial diffuse gastric cancer and associated
lobular breast cancer
6) Tobacco use results in a 1.5- to 3-fold increased risk for cancer
7)High salt and nitrosamine food content from fermenting and smoking process
8)Deficiencies of vitamins A, C, and E; β-carotene; selenium; and fiber
9) Blood type A
10)Alcohol
SCREENING
PATHOPHYSIOLOGY
Most gastric cancers are adenocarcinomas (more than 90%) of two distinct
histologic types: intestinal and diffuse. In general, the term “gastric cancer” is
commonly used to refer to adenocarcinoma of the stomach. Other cancers of the
stomach include non-Hodgkin’s lymphomas (NHL), leiomyosarcomas, carcinoids
and gastrointestinal stromal tumors (GIST).
Differentiating between adenocarcinoma and lymphoma is critical because the
prognosis and treatment for these two entities differ considerably. Although less
common, metastases to the stomach include melanoma, breast, and ovarian
cancers.
intestinal type :
The epidemic form of cancer is further differentiated by gland formation and is
associated with precancerous lesions, gastric atrophy, and intestinal metaplasia.
The intestinal form accounts for most distal cancers with a stable or declining
incidence. These cancers in particular are associated with H. pylori infection.
Diffuse Type :
The endemic form of carcinoma is more common in younger patients and exhibits
undifferentiated signet-ring histology. There is a predilection for diffuse submucosal
spread because of lack of cell cohesion, leading to linitis plastica. Contiguous
spread of the carcinoma to the peritoneum is common. Precancerous lesions have
not been identified
STAGING
The American Joint Committee on Cancer (AJCC) has designated staging by TNM
classification. In the 2010 AJCC 7th edition, tumors arising at the GEJ or in the
cardia of the stomach within 5 cm of the GEJ that extend into the GEJ or esophagus
are termed esophageal rather than gastric cancers. Gastric tumors involving
muscolaris propria (T2), subserosa (T3), and serosa (T4a) are considered resectable,
whereas invasion of adjacent structures (T4b) is not involved.
PROGNOSIS
Pathologic staging remains the most important determinant of prognosis Other
prognostic variables that have been proposed to be associated with an unfavorable
outcome include the following:
■■ Older age
■■ Male gender
■■ Weight loss greater than 10%
■■ Location of tumor
■■ Tumor histology: diffuse versus intestinal high-grade or undifferentiated tumors
■■ Four or more lymph nodes involved.
Paraneoplastic Syndromes
■■ Skin syndromes: acanthosis nigricans, dermatomyositis, circinate erythemas,
pemphigoid, and acute onset of seborrheic keratoses (Leser- Trélat sign)
■■ Central nervous system syndromes: dementia and cerebellar ataxia
■■ Miscellaneous: thrombophlebitis, microangiopathic hemolytic
anemia,membranous nephropathy Tumor Markers Carcinoembryonic antigen (CEA)
is elevated in 40% to 50% of cases. It is useful in follow-up and monitoring response
to therapy, but not for screening. α-Fetoprotein and CA 19-9 are elevated in 30% of
patients with gastric cancer, but are of limited clinical use.
FOLLOW-UP
Follow-up in patients after complete surgical resection should include routine history
and physical examination, with liver function tests and CEA measurements being
performed .Evaluation intervals of every 3 to 6 months for the first 3 years and then
annually thereafter have been suggested.