The information on this website is not intended for diagnosis or treatment. Please consult your physician for health concerns.

Skip to main content

Early Gastric Adenocarcinoma

Gastric cancer confined to mucosa or submucosa with excellent prognosis

Written by: Saygı Hospital Health Guide Editorial Board
Last updated:

This content has been compiled by the Saygı Hospital Health Guide Editorial Board and is periodically reviewed by a specialist physician.

References (5)

This content is for informational purposes only and does not constitute medical advice. You can book an appointment at our Onkoloji department. Book Appointment →

What is Early Gastric Adenocarcinoma?

Early gastric adenocarcinoma (EGC) is defined as gastric carcinoma confined to mucosa (T1a, intramucosal) or submucosa (T1b) regardless of lymph node involvement, distinct from advanced gastric cancer which extends beyond muscularis propria. Histologically classified using Lauren classification (intestinal type — well-differentiated, glandular, often associated with H. pylori atrophic gastritis; diffuse type — poorly cohesive, signet ring cells, more aggressive, hereditary in CDH1 mutation) or WHO classification (tubular, papillary, mucinous, poorly cohesive). Endoscopic appearance classified by Paris classification: type 0-I protruding (0-Is sessile, 0-Ip pedunculated), 0-IIa elevated (<2.5 mm), 0-IIb flat (entirely flat), 0-IIc depressed (<2.5 mm depression), 0-III excavated.

Epidemiology shows substantial geographic variation: highest incidence in East Asia (Japan, Korea, China — 30-40% of all gastric cancers detected as EGC due to mass screening), intermediate in Eastern Europe, Latin America, lower in Western countries (5-10% of all gastric cancers as EGC due to lack of screening). Risk factors include H. pylori infection (most important — atrophic gastritis, intestinal metaplasia, dysplasia, cancer sequence), pernicious anemia, partial gastrectomy, hereditary diffuse gastric cancer (CDH1, CTNNA1), Lynch syndrome, familial adenomatous polyposis, smoking, dietary factors (high salt, smoked foods, low fruit/vegetables), Epstein-Barr virus association in 10%. Pathogenesis follows Correa cascade for intestinal type (chronic gastritis → atrophy → intestinal metaplasia → dysplasia → carcinoma) over decades.

Diagnosis is by upper endoscopy with high-definition white light, narrow-band imaging, magnification endoscopy, chromoendoscopy with indigo carmine or acetic acid, careful evaluation of lesion characteristics (size, depth, margins, ulceration), targeted biopsies. Endoscopic ultrasound assesses depth of invasion (mucosa, submucosa, muscularis propria) and regional lymph nodes. CT chest/abdomen/pelvis for distant staging. Treatment: endoscopic submucosal dissection (ESD) for absolute indications (mucosal differentiated adenocarcinoma ≤2 cm without ulceration), expanded indications (larger differentiated mucosal lesions, undifferentiated mucosal ≤2 cm, slight submucosal invasion <500 μm) — curative if R0, no lymphovascular invasion, no ulceration in undifferentiated. Surgical gastrectomy (subtotal or total) with D1+ or D2 lymphadenectomy for unsuitable for ESD or non-curative ESD. Adjuvant therapy generally not required for EGC. Surveillance endoscopy every 6-12 months for 5 years post-resection. H. pylori eradication mandatory. Five-year survival: 90%+ overall, near 100% for T1a NO, 85-95% for T1b N0.

Symptoms

Often asymptomatic (especially screening-detected)
Vague epigastric discomfort
Mild dyspepsia
Postprandial fullness
Mild nausea
Occasional vomiting
Loss of appetite
Mild weight loss
Iron deficiency anemia (chronic blood loss)
Occult positive stool tests
Hematemesis (rare with EGC)
Melena (rare with EGC)
Early satiety
Symptoms of H. pylori infection
Dysphagia (rare, suggests cardia involvement)
Reflux symptoms
Mild anemia symptoms (fatigue, pallor)
Abdominal pain (uncommon)
Bloating
Symptoms of underlying gastritis

Risk Factors

Helicobacter pylori infection (most important)
Atrophic gastritis with intestinal metaplasia
Pernicious anemia
Partial gastrectomy (15-20 years prior)
Hereditary diffuse gastric cancer (CDH1 mutation)
Lynch syndrome (MLH1, MSH2, MSH6, PMS2)
Familial adenomatous polyposis (APC)
Li-Fraumeni syndrome (TP53)
Peutz-Jeghers syndrome (STK11)
Juvenile polyposis (SMAD4, BMPR1A)
First-degree relative with gastric cancer
East Asian, Eastern European, Latin American ethnicity
Older age (>50 years, peak 60-70)
Male sex (2:1 ratio)
Smoking
High salt and salt-preserved foods
Smoked, cured, processed meats
Low fruit and vegetable consumption
Obesity (cardia adenocarcinoma)
Epstein-Barr virus association

When to See a Doctor?

If you experience any of the following symptoms, seek medical attention promptly:

  • Persistent dyspepsia >4 weeks especially over age 45
  • New-onset upper GI symptoms over age 50
  • Iron deficiency anemia of unknown cause
  • Unintentional weight loss with GI symptoms
  • Occult positive fecal blood
  • Family history of gastric cancer
  • Pernicious anemia diagnosis
  • Post-partial gastrectomy 15+ years
  • Atrophic gastritis or intestinal metaplasia found on biopsy
  • Confirmed H. pylori infection
  • CDH1 or other hereditary syndrome carrier
  • Persistent epigastric pain
  • Dysphagia
  • Recurrent vomiting
  • Hematemesis or melena (urgent)

Treatment Methods

01
Comprehensive evaluation by gastroenterologist and surgical/medical oncologist
02
Detailed history and physical examination
03
High-definition upper endoscopy with white light
04
Narrow-band imaging (NBI) for vascular and mucosal pattern
05
Magnification endoscopy for surface architecture
06
Chromoendoscopy with indigo carmine or acetic acid
07
Multiple targeted biopsies including transitional zones
08
Mapping biopsies for extent assessment
09
Endoscopic ultrasound (EUS) for depth assessment
10
CT chest/abdomen/pelvis for staging
11
PET-CT for selected cases
12
H. pylori testing and eradication
13
Pathology with Lauren and WHO classification
14
Lymphovascular invasion and depth assessment
15
HER2 status if advanced
16
Endoscopic submucosal dissection (ESD) for selected lesions
17
Endoscopic mucosal resection (EMR) for small lesions
18
Subtotal gastrectomy for distal lesions
19
Total gastrectomy for proximal or diffuse lesions
20
D1+ lymphadenectomy for low-risk EGC
21
D2 lymphadenectomy for higher-risk lesions
22
Laparoscopic or robotic minimally invasive surgery
23
Sentinel lymph node biopsy in selected cases
24
Frozen section for margins during surgery
25
Roux-en-Y reconstruction
26
Adjuvant chemotherapy not routinely needed for EGC
27
Adjuvant chemotherapy for high-risk pathology (LVI, undifferentiated, deep submucosal)
28
H. pylori eradication therapy
29
Surveillance endoscopy every 6-12 months
30
CT surveillance for 5 years
31
Tumor markers (CEA, CA 19-9, CA 72-4)
32
Nutritional support and B12 supplementation post-gastrectomy
33
Genetic counseling for hereditary syndromes
34
Family screening if hereditary syndrome
35
Multidisciplinary tumor board approach

Which Department to Visit?

You can visit our Onkoloji department for these complaints. Our specialist physicians will create the most suitable treatment plan for you.

Learn About Onkoloji Department

Let us help you

You can make an appointment with our specialists or contact us for your concerns.

Related Health Topics

Other articles from the same department you may want to explore.

Anaemia

Dahiliye (İç Hastalıkları)

Anaemia is a low haemoglobin level that reduces oxygen delivery, causing fatigue, pallor, and shortness of breath. It is not a disease itself but a sign of many underlying conditions. Most cases are correctable with appropriate diagnosis and treatment.

Iron Deficiency Anaemia

Dahiliye (İç Hastalıkları)

Iron deficiency anaemia develops when dietary intake, absorption, or losses create an iron shortfall, most often affecting women and children. Identifying the underlying cause is the core of management, alongside iron replacement.

Vitamin B12 Deficiency

Dahiliye (İç Hastalıkları)

Vitamin B12 deficiency can cause megaloblastic anaemia, neurological symptoms, and cognitive impairment. Early treatment with intramuscular or oral B12 largely prevents irreversible complications.

Hypertension (High Blood Pressure) Management

Dahiliye (İç Hastalıkları)

Hypertension is often called the silent killer because it progresses symptom-free for years and can damage the heart, brain, kidneys, and eyes. Regular monitoring, lifestyle change, and evidence-based drug therapy dramatically reduce cardiovascular risk.

Chronic Kidney Disease

Dahiliye (İç Hastalıkları)

Chronic kidney disease is one of the most common complications of chronic conditions such as diabetes and hypertension, and can be silent in its early stages.

Hepatitis B (HBV)

Dahiliye (İç Hastalıkları)

Hepatitis B is a DNA virus infection causing acute and chronic hepatitis with risk of cirrhosis and hepatocellular carcinoma; diagnosis integrates HBsAg, HBeAg, anti-HBc, and HBV DNA with management based on disease phase using nucleos(t)ide analogues (entecavir, tenofovir) and universal infant vaccination.

Hepatitis C (HCV)

Dahiliye (İç Hastalıkları)

Hepatitis C is an RNA virus causing chronic hepatitis that may progress to cirrhosis and hepatocellular carcinoma; modern direct-acting antiviral (DAA) pangenotypic regimens (sofosbuvir/velpatasvir, glecaprevir/pibrentasvir) achieve sustained virologic response over 95% in 8–12 weeks with universal adult screening and cure for nearly all patients.

Fatty Liver Disease

Dahiliye (İç Hastalıkları)

Non-alcoholic fatty liver disease (NAFLD) is closely related to obesity and metabolic syndrome and is largely reversible with early treatment.

Health Disclaimer: The information on this page is prepared for general informational purposes only. It does not replace medical diagnosis and treatment. Please consult your physician for your complaints. Saygı Hospital does not accept responsibility for actions taken based on the information on this page.