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GASTRIC CANCER
DONE BY : MUSTAFA KHALIL IBRAHIM
TBILISI STATE MEDICAL UNIVERSITY
4th year, 1st semester, 2nd group
ANATOMY & PHYSIOLOGY
ANATOMY
 The stomach J-shaped. It has two surfaces (the anterior &
posterior), two curvatures (the greater & lesser), two orifices (the
cardia & pylorus). It has fundus, body and pyloric antrum.
 Blood supply
The left gastric artery
Right gastric artery
Right gastro-epiploic artery
Left gastro-epiploic artery
Short gastric arteries
GASTRIC CANCER
 Stomach cancer begins when cancer cells form in the
inner lining of your stomach. These cells can grow into a
tumor. Also called gastric cancer, the disease usually
grows slowly over many years.
 It could be:
 malignant or benign
 primary or secondary
TYPES
Tumor Type Percent
Malignant tumors 93.0
Carcinoma 87.9
Lymphoma 3.0
Leiomyosarcoma 1.7
Carcinoid 0.3
Others 0.1
Benign tumors 7.0
Polyp 3.1
Leiomyoma 2.0
Inflammatory lesions 0.7
Heterotopic pancreas 0.4
Others 0.8
Adenocarcinoma (95%) : Cancer that begins in the
glandular cells.
Lymphoma (4%) : Cancer that begins in immune
system cells .
Carcinoid cancer(3%) : Cancer that begins in
hormone-producing cell.
Gastrointestinal stromal tumor (GIST) (1%) :
Cancer that begins in nervous system tissues of
stomach .
The four most common primary
malignant gastric neoplasms are:
EARLY GASTRIC CANCER
 Defined as a tumor confined to the mucosal or sub-mucosal
layer, with or without lymph node metastasis
ADVANCED GASTRIC CANCER
invasion depth beyond sub-mucosal layer
BORMANN CLASSIFICATIONS
Gross classification
• phymatoid type
• ulcerative type
• infiltrative ulcerative
• diffuse infiltrative type
TNM
T: Primary tumor
Tis Carcinoma in situ; intraepithelial tumor without invasion of
lamina propria
T1 Tumor invades lamina propria or submucosa
T2 Tumor invades muscularis propria or subserosa
T3 Tumor penetrates serosa (visceral peritoneum) without
invasion of adjacent structures
T4 Clinical Manifestations Tumor invades adjacent structures
N: Regional lymph node
N0 No regional lymph node metastasis
N1 Metastasis in 1 to 6 regional lymph nodes
N2 Metastasis in 7 to 15 lymph nodes
N3 Metastasis in more than 15 regional lymph nodes
M: Distant metastasis
M0 No distant metastasis
M1 Distant metastasis
SPREAD PATTERNS
Direct invasion
Lymph node
dissemination
Blood spread
Intraperitoneal
colonization
ETIOLOGY
 Gastric cancer is more common
in patients with
 pernicious anemia.
 blood group A.
 Gastric ulcer .
 A family history of gastric
cancer.
 Smoking
 Being overweight or obese
 Stomach surgery for an ulcer
 Epstein-Barr virus infection
 Working in coal, metal,
timber, or rubber industries
 Exposure to asbestos
 Infection with Helicobacter
pylori
 Long-term stomach
inflammation
 Had a polyp larger than 2
centimeters in your stomach
 A diet high in smoked,
pickled, or salty foods
SIGNS AND SYMOTOMS
Early Gastric Cancer
 Asymptomatic or silent 80%
 Peptic ulcer symptoms 10%
 Nausea or vomiting 8%
 Anorexia 8%
 Early satiety 5%
 Abdominal pain 2%
 Gastrointestinal blood loss <2%
 Weight loss <2%
 Dysphagia <1%
Advanced Gastric Cancer
 Weight loss 60%
 Abdominal pain 50%
 Nausea or vomiting 30%
 Anorexia 30%
 Dysphagia 25%
 Gastrointestinal blood loss 20%
 Early satiety 20%
 Peptic ulcer symptoms 20%
 Abdominal mass or fullness 5%
 Asymptomatic or silent <5%
SPECIAL SIGNS
 Linitis plastica:
--- diffusely infiltrating with a rigid stomach
 Virchow’s node:
--- left supraclavicular lymph node
 Sister Mary Joseph’s node:
--- umbilical lymph node
 prerectal pouch mass (Blumer shelf)
--- seeding metastasis
SISTER MARY JOSEPH’S NODE
COMPLICATIONS
Peritoneal and pleural effusion
Obstruction of gastric outlet or small bowel
Bleeding
Intrahepatc jaundice by hepatomegaly
STAGES OF GASTRIC CANCER
 Stage I. At this stage, the tumor is limited to the layer of tissue
that lines the inside of the stomach. Cancer cells may also have
spread to a limited number of nearby lymph nodes.
 Stage II. The cancer at this stage has spread deeper, growing
into the muscle layer of the stomach wall. Cancer may also have
spread to more of the lymph nodes.
 Stage III. At this stage, the cancer may have grown through all
the layers of the stomach and spread to nearby structures. Or it
may be a smaller cancer that has spread more extensively to the
lymph nodes.
 Stage IV. This stage indicates that the cancer has spread to
distant areas of the body.
. PHNS Staging System (Japanese)
 P-factor(Peritonealdissemination)
 H-factor (Thepresenceof hepaticmetastases)
 N-factor(Lymphnodesinvolvement)
 S-factor(Serosal invasion)
LABORATORY TESTS
 blood test
• check for anemia(may be caused by bleeding, liver dysfunction, or
poor nutrition.
• test for the presence of H. pylori bacteria.
 Fecal occult blood test (FOBT)
 Tumor markers
• CEA:carcino-embryonic antigen
• CA19-9:carbohydrate antigen
• CA724:carbohydrate antigen
Physical examination
 The best way to stage the tumor locally is via endoscopic
ultrasound , it gives (80%) information about the depth of
tumor penetration into the gastric wall, and can usually show
enlarged (>5 mm) perigastric and celiac lymph nodes.
ENDOSCOPIC MUCOSAL RESECTION
Gastric cancer
lesion confined
to mucosa layer
Endoscopic
ultrasound (EUS)
is helpful in
staging GC
ENDOSCOPIC FEATURES OF GASTRIC
CANCER
Esophagogastro
duodenoscopy
(EGD)
endoscopy has
become the
gold standard
for the
diagnosis of
gastric
malignancy.
 Biopsy . taking a small piece of tissue from the stomach to look
at under a microscope for signs of cancer cells. It might done
during an endoscopy.
RADIOLOGIC DIAGNOSIS
Distal GC Proximal GC Linitis plastica
X-ray test. with barium. The fluid coats the stomach and
makes it show up more clearly on X-rays.
CT SCAN TEST
MRI : benign regional lymph nodes
Positron Emission Tomography Scanning
Whole-body PET scanning uses the principle that tumor
cells preferentially accumulate positron-emitting 18F-
fluorodeoxyglucose.
This modality is most useful in the evaluation of distant
metastasis in gastric cancer but can also be useful in
locoregional staging.
PET scan is most useful when combined with spiral CT
(PET-CT)95 and should be considered before major surgery
in patients with particularly high-risk tumors or multiple
medical comorbidities
POSITRON EMISSION TOMOGRAPHY (PET).
PET  CT SCAN
DETECTION OF EARLY GASTRIC
CANCER
• Endoscopic screening
general population or high risk persons
• Careful observation
• Japan is the only country that had conducted large
nationwide mass population screening of
asymptomatic
individuals for gastric malignancy
DIFFERENTIAL DIAGNOSIS
Gastric
Cancer
Gastric
Ulcer
X-ray showing Gastric ulcer
With symmetrical radiating
Mucosal folds.
By histology, no evidence of
Malignancies was observed.
X-ray showing Extensive
carcinoma involving
the cardia & Fundus
Pyloric stenosis
IF YOU SEE ULCER ASK UR SELF…BENIGN OR
MALIGNANT?
MALIGNANTBENIGN
Irregular outline with
necrotic or hemorrhagic
base
Round to oval punched out
lesion with straight walls & flat
smooth base
Irregular & raised marginsSmooth margins with normal
surrounding mucosa
AnywhereMostly on lesser curvature
Any sizeMajority<2cm
Prominent & edematous
rugal folds that usually do
not extend to the margins
Normal adjoining rugal folds
that extend to the margins of
the base
Treatment
Surgical resection is the only curative treatment for gastric cancer.
Obvious exceptions include patients who cannot tolerate an abdominal
operation, and patients with overwhelming metastatic disease.
The goal of curative surgical treatment is resection of all tumor. Thus, all
margins (proximal, distal, and radial) should be negative and an adequate
lymphadenectomy performed.
Treatment
Generally, the surgeon strives for a grossly negative margin of at least 5 cm.
Some gastric tumors, particularly the diffuse variety, are quite infiltrative and
tumor cells can extend well beyond the tumor mass; thus, gross margins
beyond 5 cm may be desirable.
More than 15 resected lymph nodes are required for adequate staging.
The primary tumor may be resected en bloc with adjacent involved organs
(e.g., distal pancreas, transverse colon, or spleen) during the course of curative
gastrectomy.
Palliative gastrectomy may be indicated in some patients with obviously
incurable disease, but most patients presenting with stage IV gastric cancer
can be managed without major operation.
Extent of Gastrectomy
The standard operation for gastric cancer is radical subtotal gastrectomy.
Subtotal gastric resection typically entails ligation of the left and right gastric
and gastroepiploic arteries at the origin, as well as the en bloc removal of the
distal 75% of the stomach, including the pylorus and 2 cm of duodenum, the
greater and lesser omentum, and all associated lymphatic tissue.
Reconstruction is usually by Billroth II gastrojejunostomy, but if a small
gastric remnant is left (<20%), a Roux-en-Y reconstruction is considered.
The operative mortality is around 2 to 5%. Radical subtotal gastrectomy is
generally deemed to be an adequate cancer operation in most Western
countries, provided that the contingencies stated result in tumor-free
margins, >15 lymph nodes, and the resection of all gross tumor.
In the absence of involvement by direct extension, the spleen and pancreatic
tail are not removed.
Extent of Lymphadenectomy
The Japanese Research Society for Gastric Cancer has numbered the lymph node
stations that potentially drain the stomach.
Generally these are grouped into level D1 (i.e., stations 3 to 6), level D2 (i.e.,
stations 1, 2, 7, 8, and 11), and level D3 (i.e., stations 9, 10, and 12) nodes.
Generally, D1 nodes are perigastric, D2 nodes are along the hepatic and splenic
arteries, and D3 nodes are the most distant.
The operation described above (radical subtotal gastrectomy in the Extent of
Gastrectomy section), which is by far the most commonly performed procedure in
the United States for gastric cancer, is called a D1 resection because it removes the
tumor and the perigastric D1 nodes.
Extent of Lymphadenectomy
The standard operation for gastric cancer in Asia and specialized U.S. centers is
the D2 gastrectomy, which involves a more extensive lymphadenectomy (removal
of the D1 and D2 nodes).
In addition to the tissue removed in a D1 resection, the standard D2 gastrectomy
removes the peritoneal layer over the anterior mesocolon and selectively over the
pancreas, along with nodes along the hepatic and splenic arteries, and the crural
nodes.
Extent of Lymphadenectomy
Splenectomy and distal pancreatectomy are not routinely performed, because this
clearly has been shown to increase the morbidity of the operation. The purported
survival advantage of D2 gastrectomy in gastric cancer is shown in Table 26-20,
which shows the 5-year survival rates for gastric cancer stratified by pathologic
stage for the United States and Japan. Unfortunately, the randomized prospective
trials that have been performed have not confirmed this survival advantage, but
the morbidity and mortality in the D2 group was higher This was mostly
attributable to the splenectomy and distal pancreatectomy, which are no longer
routinely done as part of the D2 gastrectomy.
Maruyama (Japan),
1971–1985
American College of
Surgeons, 1982–1987
No. patients 3176 18,365
Stage I 91% 50%
Stage II 72% 29%
Stage III 44% 13%
Stage IV 9% 3%
Operative mortality 1% 7%
Gastric Cancer 5-Year Survival and
Operative Mortality in the USA and Japan
Randomized Trials Comparing D1 and D2
Gastrectomy for Gastric Cancer
Authors Numbe
r of
Patients
Type of
Surgery
Postoperative
Complications
(%)
Postoperative
Mortality (%)
5-Year
Survival (%)
Bonenkamp et al. 711 D1 25 4 45
D2 43 10 47
Cuschieri et al. 400 D1 28 6.5 35
D2 46 13 33
Chemotherapy and Radiation for Gastric
Cancer
In general, the actuarial 5-year survival for resected gastric adenocarcinoma
stages 1, 2, and 3 is about 75%, 50%, and 25%, respectively.
Because most surgical patients have stage 2 disease or greater, it is common to
refer gastric cancer patients postoperatively to a medical and/or radiation
oncologist.
Adjuvant treatment with chemotherapy (5-fluorouracil and leucovorin) and
radiation (4500 cGy) has demonstrated a survival benefit in resected patients with
stage II and III adenocarcinoma of the stomach.
Chemotherapy and Radiation for Gastric Cancer
• Adequacy of lymphadenectomy has clearly been shown to impact survival,
particularly in patients with stage III gastric cancer it has been suggested that
the benefits of adjuvant chemoradiation shown in this study would be vitiated
by an adequate operation.
• A recently published study from the Japan Clinical Oncology Group showed a
69% overall 5-year survival rate in patients with clinically curable T2b, T3, and
T4 gastric cancer, treated with D2 gastrectomy alone (no chemotherapy)
• There was no incremental benefit from para-aortic lymph node dissection.
There is no indication for the routine use of radiation alone in the adjuvant
setting, but in certain patients, it can be effective palliation for bleeding or pain.
In patients with gross unresectable, metastatic, or recurrent disease, palliative
chemotherapy has not been demonstrated to conclusively prolong survival, but
occasionally, a patient has a dramatic response. These patients should be
considered for clinical trials. Agents that have shown activity against gastric
cancer include 5-fluorouracil, cisplatin, doxorubicin, and methotrexate.
Neoadjuvant treatment of gastric adenocarcinoma is being evaluated,
particularly in patients with clinical T3 or N1 disease.
Endoscopic Resection
• It has been demonstrated initially at numerous East Asian centers that
some patients with early gastric cancer can be adequately treated by an
EMR.
• Small tumors (<3 cm) confined to the mucosa have an extremely low
chance of lymph node metastasis (3%), which approaches the operative
mortality rate for gastrectomy.
• If the resected specimen demonstrates no ulceration, no penetration of
the muscularis mucosae, no lymphatic invasion, and size <3 cm, then
the risk of lymph node metastases is less than 1%.
• Thus, some patients with early gastric cancer might be better treated
with the endoscopic technique.
• Currently, this should be limited to patients with tumors <2 cm in size
that are node negative and confined to the mucosa on EUS, in the
absence of other gastric lesions.
REFERENCES
 http://www.healthline.com/health/gastric-cancer#Diagnosis5
 http://www.webmd.com/cancer/stomach-gastric-cancer?page=2
 http://www.mayoclinic.org/diseases-conditions/stomach-
cancer/diagnosis-treatment/diagnosis/dxc-20202339
 https://www.nlm.nih.gov/medlineplus/ency/article/000223.htm
Gastric Cancer ( stomach tumor )
Gastric Cancer ( stomach tumor )

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Gastric Cancer ( stomach tumor )

  • 1. GASTRIC CANCER DONE BY : MUSTAFA KHALIL IBRAHIM TBILISI STATE MEDICAL UNIVERSITY 4th year, 1st semester, 2nd group
  • 3. ANATOMY  The stomach J-shaped. It has two surfaces (the anterior & posterior), two curvatures (the greater & lesser), two orifices (the cardia & pylorus). It has fundus, body and pyloric antrum.  Blood supply The left gastric artery Right gastric artery Right gastro-epiploic artery Left gastro-epiploic artery Short gastric arteries
  • 4. GASTRIC CANCER  Stomach cancer begins when cancer cells form in the inner lining of your stomach. These cells can grow into a tumor. Also called gastric cancer, the disease usually grows slowly over many years.  It could be:  malignant or benign  primary or secondary
  • 5. TYPES Tumor Type Percent Malignant tumors 93.0 Carcinoma 87.9 Lymphoma 3.0 Leiomyosarcoma 1.7 Carcinoid 0.3 Others 0.1 Benign tumors 7.0 Polyp 3.1 Leiomyoma 2.0 Inflammatory lesions 0.7 Heterotopic pancreas 0.4 Others 0.8
  • 6. Adenocarcinoma (95%) : Cancer that begins in the glandular cells. Lymphoma (4%) : Cancer that begins in immune system cells . Carcinoid cancer(3%) : Cancer that begins in hormone-producing cell. Gastrointestinal stromal tumor (GIST) (1%) : Cancer that begins in nervous system tissues of stomach . The four most common primary malignant gastric neoplasms are:
  • 7. EARLY GASTRIC CANCER  Defined as a tumor confined to the mucosal or sub-mucosal layer, with or without lymph node metastasis
  • 8. ADVANCED GASTRIC CANCER invasion depth beyond sub-mucosal layer
  • 9. BORMANN CLASSIFICATIONS Gross classification • phymatoid type • ulcerative type • infiltrative ulcerative • diffuse infiltrative type
  • 10. TNM T: Primary tumor Tis Carcinoma in situ; intraepithelial tumor without invasion of lamina propria T1 Tumor invades lamina propria or submucosa T2 Tumor invades muscularis propria or subserosa T3 Tumor penetrates serosa (visceral peritoneum) without invasion of adjacent structures T4 Clinical Manifestations Tumor invades adjacent structures N: Regional lymph node N0 No regional lymph node metastasis N1 Metastasis in 1 to 6 regional lymph nodes N2 Metastasis in 7 to 15 lymph nodes N3 Metastasis in more than 15 regional lymph nodes M: Distant metastasis M0 No distant metastasis M1 Distant metastasis
  • 11. SPREAD PATTERNS Direct invasion Lymph node dissemination Blood spread Intraperitoneal colonization
  • 12. ETIOLOGY  Gastric cancer is more common in patients with  pernicious anemia.  blood group A.  Gastric ulcer .  A family history of gastric cancer.  Smoking  Being overweight or obese  Stomach surgery for an ulcer  Epstein-Barr virus infection  Working in coal, metal, timber, or rubber industries  Exposure to asbestos  Infection with Helicobacter pylori  Long-term stomach inflammation  Had a polyp larger than 2 centimeters in your stomach  A diet high in smoked, pickled, or salty foods
  • 13. SIGNS AND SYMOTOMS Early Gastric Cancer  Asymptomatic or silent 80%  Peptic ulcer symptoms 10%  Nausea or vomiting 8%  Anorexia 8%  Early satiety 5%  Abdominal pain 2%  Gastrointestinal blood loss <2%  Weight loss <2%  Dysphagia <1%
  • 14. Advanced Gastric Cancer  Weight loss 60%  Abdominal pain 50%  Nausea or vomiting 30%  Anorexia 30%  Dysphagia 25%  Gastrointestinal blood loss 20%  Early satiety 20%  Peptic ulcer symptoms 20%  Abdominal mass or fullness 5%  Asymptomatic or silent <5%
  • 15. SPECIAL SIGNS  Linitis plastica: --- diffusely infiltrating with a rigid stomach  Virchow’s node: --- left supraclavicular lymph node  Sister Mary Joseph’s node: --- umbilical lymph node  prerectal pouch mass (Blumer shelf) --- seeding metastasis
  • 16.
  • 18. COMPLICATIONS Peritoneal and pleural effusion Obstruction of gastric outlet or small bowel Bleeding Intrahepatc jaundice by hepatomegaly
  • 19. STAGES OF GASTRIC CANCER  Stage I. At this stage, the tumor is limited to the layer of tissue that lines the inside of the stomach. Cancer cells may also have spread to a limited number of nearby lymph nodes.  Stage II. The cancer at this stage has spread deeper, growing into the muscle layer of the stomach wall. Cancer may also have spread to more of the lymph nodes.  Stage III. At this stage, the cancer may have grown through all the layers of the stomach and spread to nearby structures. Or it may be a smaller cancer that has spread more extensively to the lymph nodes.  Stage IV. This stage indicates that the cancer has spread to distant areas of the body.
  • 20. . PHNS Staging System (Japanese)  P-factor(Peritonealdissemination)  H-factor (Thepresenceof hepaticmetastases)  N-factor(Lymphnodesinvolvement)  S-factor(Serosal invasion)
  • 21. LABORATORY TESTS  blood test • check for anemia(may be caused by bleeding, liver dysfunction, or poor nutrition. • test for the presence of H. pylori bacteria.  Fecal occult blood test (FOBT)  Tumor markers • CEA:carcino-embryonic antigen • CA19-9:carbohydrate antigen • CA724:carbohydrate antigen Physical examination
  • 22.  The best way to stage the tumor locally is via endoscopic ultrasound , it gives (80%) information about the depth of tumor penetration into the gastric wall, and can usually show enlarged (>5 mm) perigastric and celiac lymph nodes.
  • 23. ENDOSCOPIC MUCOSAL RESECTION Gastric cancer lesion confined to mucosa layer Endoscopic ultrasound (EUS) is helpful in staging GC
  • 24. ENDOSCOPIC FEATURES OF GASTRIC CANCER Esophagogastro duodenoscopy (EGD) endoscopy has become the gold standard for the diagnosis of gastric malignancy.
  • 25.  Biopsy . taking a small piece of tissue from the stomach to look at under a microscope for signs of cancer cells. It might done during an endoscopy.
  • 26. RADIOLOGIC DIAGNOSIS Distal GC Proximal GC Linitis plastica
  • 27. X-ray test. with barium. The fluid coats the stomach and makes it show up more clearly on X-rays.
  • 29. MRI : benign regional lymph nodes
  • 30. Positron Emission Tomography Scanning Whole-body PET scanning uses the principle that tumor cells preferentially accumulate positron-emitting 18F- fluorodeoxyglucose. This modality is most useful in the evaluation of distant metastasis in gastric cancer but can also be useful in locoregional staging. PET scan is most useful when combined with spiral CT (PET-CT)95 and should be considered before major surgery in patients with particularly high-risk tumors or multiple medical comorbidities
  • 32. PET CT SCAN
  • 33. DETECTION OF EARLY GASTRIC CANCER • Endoscopic screening general population or high risk persons • Careful observation • Japan is the only country that had conducted large nationwide mass population screening of asymptomatic individuals for gastric malignancy
  • 35. X-ray showing Gastric ulcer With symmetrical radiating Mucosal folds. By histology, no evidence of Malignancies was observed. X-ray showing Extensive carcinoma involving the cardia & Fundus Pyloric stenosis
  • 36. IF YOU SEE ULCER ASK UR SELF…BENIGN OR MALIGNANT? MALIGNANTBENIGN Irregular outline with necrotic or hemorrhagic base Round to oval punched out lesion with straight walls & flat smooth base Irregular & raised marginsSmooth margins with normal surrounding mucosa AnywhereMostly on lesser curvature Any sizeMajority<2cm Prominent & edematous rugal folds that usually do not extend to the margins Normal adjoining rugal folds that extend to the margins of the base
  • 37.
  • 38. Treatment Surgical resection is the only curative treatment for gastric cancer. Obvious exceptions include patients who cannot tolerate an abdominal operation, and patients with overwhelming metastatic disease. The goal of curative surgical treatment is resection of all tumor. Thus, all margins (proximal, distal, and radial) should be negative and an adequate lymphadenectomy performed.
  • 39. Treatment Generally, the surgeon strives for a grossly negative margin of at least 5 cm. Some gastric tumors, particularly the diffuse variety, are quite infiltrative and tumor cells can extend well beyond the tumor mass; thus, gross margins beyond 5 cm may be desirable. More than 15 resected lymph nodes are required for adequate staging. The primary tumor may be resected en bloc with adjacent involved organs (e.g., distal pancreas, transverse colon, or spleen) during the course of curative gastrectomy. Palliative gastrectomy may be indicated in some patients with obviously incurable disease, but most patients presenting with stage IV gastric cancer can be managed without major operation.
  • 40. Extent of Gastrectomy The standard operation for gastric cancer is radical subtotal gastrectomy. Subtotal gastric resection typically entails ligation of the left and right gastric and gastroepiploic arteries at the origin, as well as the en bloc removal of the distal 75% of the stomach, including the pylorus and 2 cm of duodenum, the greater and lesser omentum, and all associated lymphatic tissue. Reconstruction is usually by Billroth II gastrojejunostomy, but if a small gastric remnant is left (<20%), a Roux-en-Y reconstruction is considered. The operative mortality is around 2 to 5%. Radical subtotal gastrectomy is generally deemed to be an adequate cancer operation in most Western countries, provided that the contingencies stated result in tumor-free margins, >15 lymph nodes, and the resection of all gross tumor. In the absence of involvement by direct extension, the spleen and pancreatic tail are not removed.
  • 41. Extent of Lymphadenectomy The Japanese Research Society for Gastric Cancer has numbered the lymph node stations that potentially drain the stomach. Generally these are grouped into level D1 (i.e., stations 3 to 6), level D2 (i.e., stations 1, 2, 7, 8, and 11), and level D3 (i.e., stations 9, 10, and 12) nodes. Generally, D1 nodes are perigastric, D2 nodes are along the hepatic and splenic arteries, and D3 nodes are the most distant. The operation described above (radical subtotal gastrectomy in the Extent of Gastrectomy section), which is by far the most commonly performed procedure in the United States for gastric cancer, is called a D1 resection because it removes the tumor and the perigastric D1 nodes.
  • 42. Extent of Lymphadenectomy The standard operation for gastric cancer in Asia and specialized U.S. centers is the D2 gastrectomy, which involves a more extensive lymphadenectomy (removal of the D1 and D2 nodes). In addition to the tissue removed in a D1 resection, the standard D2 gastrectomy removes the peritoneal layer over the anterior mesocolon and selectively over the pancreas, along with nodes along the hepatic and splenic arteries, and the crural nodes.
  • 43. Extent of Lymphadenectomy Splenectomy and distal pancreatectomy are not routinely performed, because this clearly has been shown to increase the morbidity of the operation. The purported survival advantage of D2 gastrectomy in gastric cancer is shown in Table 26-20, which shows the 5-year survival rates for gastric cancer stratified by pathologic stage for the United States and Japan. Unfortunately, the randomized prospective trials that have been performed have not confirmed this survival advantage, but the morbidity and mortality in the D2 group was higher This was mostly attributable to the splenectomy and distal pancreatectomy, which are no longer routinely done as part of the D2 gastrectomy.
  • 44. Maruyama (Japan), 1971–1985 American College of Surgeons, 1982–1987 No. patients 3176 18,365 Stage I 91% 50% Stage II 72% 29% Stage III 44% 13% Stage IV 9% 3% Operative mortality 1% 7% Gastric Cancer 5-Year Survival and Operative Mortality in the USA and Japan
  • 45. Randomized Trials Comparing D1 and D2 Gastrectomy for Gastric Cancer Authors Numbe r of Patients Type of Surgery Postoperative Complications (%) Postoperative Mortality (%) 5-Year Survival (%) Bonenkamp et al. 711 D1 25 4 45 D2 43 10 47 Cuschieri et al. 400 D1 28 6.5 35 D2 46 13 33
  • 46. Chemotherapy and Radiation for Gastric Cancer In general, the actuarial 5-year survival for resected gastric adenocarcinoma stages 1, 2, and 3 is about 75%, 50%, and 25%, respectively. Because most surgical patients have stage 2 disease or greater, it is common to refer gastric cancer patients postoperatively to a medical and/or radiation oncologist. Adjuvant treatment with chemotherapy (5-fluorouracil and leucovorin) and radiation (4500 cGy) has demonstrated a survival benefit in resected patients with stage II and III adenocarcinoma of the stomach.
  • 47. Chemotherapy and Radiation for Gastric Cancer • Adequacy of lymphadenectomy has clearly been shown to impact survival, particularly in patients with stage III gastric cancer it has been suggested that the benefits of adjuvant chemoradiation shown in this study would be vitiated by an adequate operation. • A recently published study from the Japan Clinical Oncology Group showed a 69% overall 5-year survival rate in patients with clinically curable T2b, T3, and T4 gastric cancer, treated with D2 gastrectomy alone (no chemotherapy) • There was no incremental benefit from para-aortic lymph node dissection. There is no indication for the routine use of radiation alone in the adjuvant setting, but in certain patients, it can be effective palliation for bleeding or pain. In patients with gross unresectable, metastatic, or recurrent disease, palliative chemotherapy has not been demonstrated to conclusively prolong survival, but occasionally, a patient has a dramatic response. These patients should be considered for clinical trials. Agents that have shown activity against gastric cancer include 5-fluorouracil, cisplatin, doxorubicin, and methotrexate. Neoadjuvant treatment of gastric adenocarcinoma is being evaluated, particularly in patients with clinical T3 or N1 disease.
  • 48. Endoscopic Resection • It has been demonstrated initially at numerous East Asian centers that some patients with early gastric cancer can be adequately treated by an EMR. • Small tumors (<3 cm) confined to the mucosa have an extremely low chance of lymph node metastasis (3%), which approaches the operative mortality rate for gastrectomy. • If the resected specimen demonstrates no ulceration, no penetration of the muscularis mucosae, no lymphatic invasion, and size <3 cm, then the risk of lymph node metastases is less than 1%. • Thus, some patients with early gastric cancer might be better treated with the endoscopic technique. • Currently, this should be limited to patients with tumors <2 cm in size that are node negative and confined to the mucosa on EUS, in the absence of other gastric lesions.
  • 49. REFERENCES  http://www.healthline.com/health/gastric-cancer#Diagnosis5  http://www.webmd.com/cancer/stomach-gastric-cancer?page=2  http://www.mayoclinic.org/diseases-conditions/stomach- cancer/diagnosis-treatment/diagnosis/dxc-20202339  https://www.nlm.nih.gov/medlineplus/ency/article/000223.htm