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CA STOMACH
Incidence
• Fifth most common malignancy worldwide*
• Twice more common in males than females
• Mean Age: 63 years ( above 40 years)
• Site:
*source: eClinicalMedicine
Risk Factors
DIETARY AND
ENVIRIONENTAL
FACTORS
PRE-CANCEROUS
CONDITIONS
FAMILIAL AND GENETIC
FACTORS
Risk Factors
• Red Meat
• Spices
• Salt-fish
• Smoked Salmon
• Smoking
• Polycyclic hydrocarbons
• Alcohol
• Low carb High fat Diet
DIETARY AND
ENVIRIONENTAL FACTORS
Risk Factors
• Atrophic Gastritis
• Pernicious Anaemia
(4-6X more risk)
• Hypogammaglobulinemia
• H pylori infection
• Adenomatous polyps
(20% malignant transformation)
• Menetrier’s Disease
• Gastric Ulcer
• Previous Gastric Resection
PRE-CANCEROUS
CONDITIONS
Risk Factors
• E-Cadherin Mutation: 60-90% RISK
• 10% patients = Family history
• Blood Group Association: A+
( due to different mucopolysaccharide secretion and increased susceptibility to
ingested carcinogens)
• Diagnosed <40 years of age
FAMILIAL AND GENETIC
FACTORS
Risk Factors
Proximal Cancer
• Obesity
• High Socioeconomic group
• Group A Gastritis
• More Aggressive
• More Advanced stage
Distal Cancer
• Assn with H pylori Infection
• Low Socioeconomic group
• Group B Gastritis
• Less Aggressive
Pathogenesis
Normal
Gastric
Mucosa
Superficial
Gastritis
Chronic
Inflammation
Atrophic
Gastritis
Metaplasia Dysplasia Cancer
• H. Pylori
• Smoking
• High salt
• Low Vitamin C
• High Nitrates
• High pH
• Bacterial
Overgrowth
• Chronic inflammation
• Carcinogens
• Reactive oxygen
species
Reversible Irreversible
Classification
• Lauren’s Classification {Pathological Classification}
• Japanese Classification {Early Gastric Cancer}
• Bormann’s Classification {Advanced Gastric Cancer}
• WHO classification
• Molecular Classification
Lauren’s Classification
INTESTINAL DIFFUSE
Environmental Familial
Gastric Atrophy, Intestinal Metaplasia Blood type A
Male> Female Female> Male
Increase incidence with Age Younger Age group
Gland formation Poorly differentiated signet ring cells
hematogenous spread Lymphatic spread
APC gene mutation Decrease E Cadherin, CDH gene
Japanese Classification
For Early cancers
Type I Exophytic lesion extending into the gastric
lumen
Type II
(superficial
variant)
II A Elevated lesions with a height no more
than the thickness of the adjacent mucosa
II B Flat lesions
II C Depressed lesions with an eroded but not
deeply ulcerated appearance
Type III Excavated lesions that may extend into the
muscularis propria without invasion of this layer
by actual cancer cells
Bormann’s Classification
For Advanced Cancer
type I polypoid or fungating lesions
type II ulcerating lesions surrounded by elevated borders
type III ulcerating lesions with infiltration into the gastric
wall
type IV diffusely infiltrating lesions
(LINITIS PLASTICA)
type V lesions that do not fit into any of the other
categories.
WHO Classification
1. Adenocarcinoma (95%): Papillary, tubular
Mucinous
Signet ring
2. Adenosquamous cell carcinoma
3. Squamous cell carcinoma
4. Undifferentiated carcinoma
5. Unclassified carcinoma
Molecular Classification
1. Micro-Satellite Instability type (MSI)- BEST prognosis
2. Epstein-Barr Virus type (EBV)
3. Chromosomal Instability type(CIN)
4. Genomically Stable type (GS)- WORST prognosis
Clinical Presentation
L. O. A. D. S.
L.= Lump: Hard and irregular lump
O.= Outlet Obstruction: cancer is most common cause of gastric outlet obstruction.
A.= Anemia: Achlorhydria causes poor conversion of Ferrous to ferric, resulting in anemia
D.= Dyspepsia
S.= Silent Presentation. Pt have vague symptoms: early satiety, flatulence, discomfort,
pain abdomen, weight loss
Atypical Presentations
1. Sister Mary Joseph Nodules: Peri-umblical metastasis
2. Krukenberg Tumor: Bilateral ovarian metastasis
3. Irish Nodule: left axillary node
4. Blumer Shelf: Metastasis to pelvis/ Pouch of Douglas
5. Virchow’s Node: Left Supraclavicular node
6. Trosseau syndrome: Migratory thrombophlebitis
7. Lesser Trelat sign: Multiple seborrheic keratosis
8. Tripe Palms: Hyperkeratotic palms
Investigations
1. CBC: may indicate Anemia (microcytic hypochromic anemia)-20% cases
2. Endoscopy (Oesophagogastroduodenoscopy)
1. To know the extent of lesion
2. To confirm diagnosis
3. To take biopsy
3. USG and CT Scan: to rule out secondaries in liver
4. Endoscopic USG: to differentiate between early and advanced cancer
5. CEA (Carcinoembryonic Antigen): elevated in 60-70% cases
6. Barium Meal: used as screening tool in Japan
not done nowadays due to availability of endoscopy
TNM Staging
Primary Tumor (T)
Tx Primary Tumor cannot be assessed
T0 No evidence of primary tumor
Tis CA in situ
TI
A Tumor invades the lamina propria/ muscularis mucosae
B Tumor invades the submucosa
T2 Tumor invades the muscularis
T3 Tumor penetrates the subserosal C.t without invasion of visceral
peritoneum/ adjacent structures
T4
A Tumor invades visceral peritoneum (serosa)
B Tumor invades adjoining structures
TNM Staging
Regional Lymph Nodes (N)
Nx Regional Lymph Nodes cannot be assessed
N0 No Regional lymph node metastasis
N1 Metastasis in 1-2 regional lymph nodes
N2 Metastasis in 3-6 regional lymph nodes
N3
A Metastasis in 7-15 regional lymph nodes
B Metastasis in >16 regional lymph nodes
Distant Metastasis (M)
M0 No distant metastasis
M1 Positive peritoneal cytology/ Distant metastasis +
Treatment
SURGICAL MGMT
• Primary tumor
resection
• Lymph node
resection
CHEMOTHERAPY
1. 5-fluorouracil & Cisplatin
• Node+ cases
• Advned cancer
2. Neoadjuvant chemo
• to stage down tumor in
T3&T4 disease
RADIOTHERAPY
Given at gastric bed, to
prevent local recurrence
after surgery
MULTIMODAL
TREATMENT
Primary Resection of Tumor
• Distal Gastrectomy
• Partial/Subtotal Gastrectomy
• Total Gastrectomy
Distal Gastrectomy
• Proximal margin: 5cm
• Distal margin: Pylorus
(irrespective of site of cancer)
Stomach removed: 30%
Tumor Site: Pylorus/ Antrum of stomach
Reconstruction: Bilroth II
Partial/Subtotal Gastrectomy
• Proximal margin: 5cm
• Distal margin: Pylorus
(irrespective of site of cancer)
Reconstruction: Roux en Y
Gastrojejunostomy
Tumor Site: Body of stomach
Stomach removed: 60-70%
Total Gastrectomy
Reconstruction: esophago-jejunal
anastomosis
Tumor Site: Fundus/ distal to gastro-
esophageal junction (Siewart type 3)
Stomach removed: 100%
R- Resections
R Resection
Ro describes a microscopically margin-negative resection,
in which no gross or microscopic tumour remains in the
tumour bed.
R1 indicates removal of all macroscopic disease but
microscopic margins are positive for tumour.
R2 indicates gross residual disease.
Lymph node Clearance
Lymph node clearance
D1 Resection removal of primary group of nodes
such as nodes along the lesser and
greater curvature, and
juxtapyloric nodes (stations 1-6)
D2 Resection removal of lymph nodes such as
left gastric, common hepatic,
splenic, retropancreatic nodes
(stations 7-12a)
D3 Resection removal of lymph nodes such as
para-aortic, porta hepatis nodes
(>12 stations)

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Stomach cancer

  • 2. Incidence • Fifth most common malignancy worldwide* • Twice more common in males than females • Mean Age: 63 years ( above 40 years) • Site: *source: eClinicalMedicine
  • 4. Risk Factors • Red Meat • Spices • Salt-fish • Smoked Salmon • Smoking • Polycyclic hydrocarbons • Alcohol • Low carb High fat Diet DIETARY AND ENVIRIONENTAL FACTORS
  • 5. Risk Factors • Atrophic Gastritis • Pernicious Anaemia (4-6X more risk) • Hypogammaglobulinemia • H pylori infection • Adenomatous polyps (20% malignant transformation) • Menetrier’s Disease • Gastric Ulcer • Previous Gastric Resection PRE-CANCEROUS CONDITIONS
  • 6. Risk Factors • E-Cadherin Mutation: 60-90% RISK • 10% patients = Family history • Blood Group Association: A+ ( due to different mucopolysaccharide secretion and increased susceptibility to ingested carcinogens) • Diagnosed <40 years of age FAMILIAL AND GENETIC FACTORS
  • 7. Risk Factors Proximal Cancer • Obesity • High Socioeconomic group • Group A Gastritis • More Aggressive • More Advanced stage Distal Cancer • Assn with H pylori Infection • Low Socioeconomic group • Group B Gastritis • Less Aggressive
  • 8. Pathogenesis Normal Gastric Mucosa Superficial Gastritis Chronic Inflammation Atrophic Gastritis Metaplasia Dysplasia Cancer • H. Pylori • Smoking • High salt • Low Vitamin C • High Nitrates • High pH • Bacterial Overgrowth • Chronic inflammation • Carcinogens • Reactive oxygen species Reversible Irreversible
  • 9. Classification • Lauren’s Classification {Pathological Classification} • Japanese Classification {Early Gastric Cancer} • Bormann’s Classification {Advanced Gastric Cancer} • WHO classification • Molecular Classification
  • 10. Lauren’s Classification INTESTINAL DIFFUSE Environmental Familial Gastric Atrophy, Intestinal Metaplasia Blood type A Male> Female Female> Male Increase incidence with Age Younger Age group Gland formation Poorly differentiated signet ring cells hematogenous spread Lymphatic spread APC gene mutation Decrease E Cadherin, CDH gene
  • 11. Japanese Classification For Early cancers Type I Exophytic lesion extending into the gastric lumen Type II (superficial variant) II A Elevated lesions with a height no more than the thickness of the adjacent mucosa II B Flat lesions II C Depressed lesions with an eroded but not deeply ulcerated appearance Type III Excavated lesions that may extend into the muscularis propria without invasion of this layer by actual cancer cells
  • 12. Bormann’s Classification For Advanced Cancer type I polypoid or fungating lesions type II ulcerating lesions surrounded by elevated borders type III ulcerating lesions with infiltration into the gastric wall type IV diffusely infiltrating lesions (LINITIS PLASTICA) type V lesions that do not fit into any of the other categories.
  • 13. WHO Classification 1. Adenocarcinoma (95%): Papillary, tubular Mucinous Signet ring 2. Adenosquamous cell carcinoma 3. Squamous cell carcinoma 4. Undifferentiated carcinoma 5. Unclassified carcinoma
  • 14. Molecular Classification 1. Micro-Satellite Instability type (MSI)- BEST prognosis 2. Epstein-Barr Virus type (EBV) 3. Chromosomal Instability type(CIN) 4. Genomically Stable type (GS)- WORST prognosis
  • 15. Clinical Presentation L. O. A. D. S. L.= Lump: Hard and irregular lump O.= Outlet Obstruction: cancer is most common cause of gastric outlet obstruction. A.= Anemia: Achlorhydria causes poor conversion of Ferrous to ferric, resulting in anemia D.= Dyspepsia S.= Silent Presentation. Pt have vague symptoms: early satiety, flatulence, discomfort, pain abdomen, weight loss
  • 16. Atypical Presentations 1. Sister Mary Joseph Nodules: Peri-umblical metastasis 2. Krukenberg Tumor: Bilateral ovarian metastasis 3. Irish Nodule: left axillary node 4. Blumer Shelf: Metastasis to pelvis/ Pouch of Douglas 5. Virchow’s Node: Left Supraclavicular node 6. Trosseau syndrome: Migratory thrombophlebitis 7. Lesser Trelat sign: Multiple seborrheic keratosis 8. Tripe Palms: Hyperkeratotic palms
  • 17.
  • 18. Investigations 1. CBC: may indicate Anemia (microcytic hypochromic anemia)-20% cases 2. Endoscopy (Oesophagogastroduodenoscopy) 1. To know the extent of lesion 2. To confirm diagnosis 3. To take biopsy 3. USG and CT Scan: to rule out secondaries in liver 4. Endoscopic USG: to differentiate between early and advanced cancer 5. CEA (Carcinoembryonic Antigen): elevated in 60-70% cases 6. Barium Meal: used as screening tool in Japan not done nowadays due to availability of endoscopy
  • 19. TNM Staging Primary Tumor (T) Tx Primary Tumor cannot be assessed T0 No evidence of primary tumor Tis CA in situ TI A Tumor invades the lamina propria/ muscularis mucosae B Tumor invades the submucosa T2 Tumor invades the muscularis T3 Tumor penetrates the subserosal C.t without invasion of visceral peritoneum/ adjacent structures T4 A Tumor invades visceral peritoneum (serosa) B Tumor invades adjoining structures
  • 20. TNM Staging Regional Lymph Nodes (N) Nx Regional Lymph Nodes cannot be assessed N0 No Regional lymph node metastasis N1 Metastasis in 1-2 regional lymph nodes N2 Metastasis in 3-6 regional lymph nodes N3 A Metastasis in 7-15 regional lymph nodes B Metastasis in >16 regional lymph nodes Distant Metastasis (M) M0 No distant metastasis M1 Positive peritoneal cytology/ Distant metastasis +
  • 21. Treatment SURGICAL MGMT • Primary tumor resection • Lymph node resection CHEMOTHERAPY 1. 5-fluorouracil & Cisplatin • Node+ cases • Advned cancer 2. Neoadjuvant chemo • to stage down tumor in T3&T4 disease RADIOTHERAPY Given at gastric bed, to prevent local recurrence after surgery MULTIMODAL TREATMENT
  • 22. Primary Resection of Tumor • Distal Gastrectomy • Partial/Subtotal Gastrectomy • Total Gastrectomy
  • 23. Distal Gastrectomy • Proximal margin: 5cm • Distal margin: Pylorus (irrespective of site of cancer) Stomach removed: 30% Tumor Site: Pylorus/ Antrum of stomach Reconstruction: Bilroth II
  • 24. Partial/Subtotal Gastrectomy • Proximal margin: 5cm • Distal margin: Pylorus (irrespective of site of cancer) Reconstruction: Roux en Y Gastrojejunostomy Tumor Site: Body of stomach Stomach removed: 60-70%
  • 25. Total Gastrectomy Reconstruction: esophago-jejunal anastomosis Tumor Site: Fundus/ distal to gastro- esophageal junction (Siewart type 3) Stomach removed: 100%
  • 26. R- Resections R Resection Ro describes a microscopically margin-negative resection, in which no gross or microscopic tumour remains in the tumour bed. R1 indicates removal of all macroscopic disease but microscopic margins are positive for tumour. R2 indicates gross residual disease.
  • 27. Lymph node Clearance Lymph node clearance D1 Resection removal of primary group of nodes such as nodes along the lesser and greater curvature, and juxtapyloric nodes (stations 1-6) D2 Resection removal of lymph nodes such as left gastric, common hepatic, splenic, retropancreatic nodes (stations 7-12a) D3 Resection removal of lymph nodes such as para-aortic, porta hepatis nodes (>12 stations)