SSAT Patient Care Guidelines
Surgical Treatment of Gastric Cancer
Gastric cancer is the fourth most frequent gastrointestinal cancer in the U.S. In 2003, it is estimated that there will be 22,400 new cases and 12,100 deaths from gastric cancer. Using national data from 1992 to 1998, gastric cancer presented as localized disease in 22%, with an associated 5-year relative survival rate of 59%. About 30% presented with regional disease, with an associated 22% 5-year relative survival rate. As the absolute incidence of gastric cancer has decreased, the relative incidence of proximal gastric cancer has increased. In addition, the absolute incidence of gastroesophageal (GE) junction cancer has increased. The guidelines discussed below will not include GE junction cancer; this cancer will be dealt with separately.
Surgical resection is necessary to cure local or regional disease, but recently postoperative chemoradiotherapy was shown to improve survival rates.
Patients with gastric cancer typically present with upper gastrointestinal complaints such as pain, heartburn, dysphagia, and bloating. Unfortunately, by the time these symptoms are evaluated about one third of gastric cancer patients will have metastatic disease with an associated 2 % 5-year relative survival rate. In the vast majority of cases, diagnosis is made by flexible esophagogastroduodenoscopy (EGD) with biopsy. Heartburn is a very frequent complaint that generally is managed by a trial of an H2 blocker or a proton-pump inhibitor. However, if a patient presents with both heartburn and anemia, EGD should be performed to exclude cancer. Some patients with gastric cancer present with bleeding from a gastric ulcer. The initial bleed may be sufficiently severe to preclude endoscopic biopsy at the time of the initial bleed, but follow-up EGD in several days with biopsy is mandatory as 10-15% of malignant ulcers can heal with H2 blocker or proton pump inhibitor treatment. Proximal gastric cancers can present with heartburn and/or dysphagia. A complaint of dysphagia mandates EGD to exclude malignancy. Some patients present with nausea, vomiting, or weight loss. Usually they are evaluated with CT scans or upper gastrointestinal barium studies. Unless these studies unequivocally diagnose a non-malignant etiology for the symptoms, an EGD should be performed.
The recent TNM staging system for gastric cancer changed to incorporate the fact that the prognosis of gastric cancer is dependent upon the number of nodes that are positive3. Further, the T2 stage has been divided into T2a (invasion into the muscularis propria) and T2b (invasion into the subserosa) to reflect the impression that node negative tumors should have postoperative chemoradiotherapy if the T stage is greater than or equal to T2b.
Patients with a diagnosis of gastric cancer should be evaluated with a history and physical examination; basic laboratory tests including liver function tests and a complete blood count; a chest radiograph; and a CT scan of the abdomen and pelvis. If a patient without evidence of metastatic disease does not require a palliative gastrectomy for persistent bleeding, then staging laparoscopy should be considered to exclude incurable disease on the basis of peritoneal carcinomatosis. In this setting, staging laparoscopy typically is done at the time of a planned curative resection. If laparoscopy documents metastatic disease, then the planned resection is abandoned and the patient is referred for possible palliative chemotherapy. If a particular treatment protocol depends upon specific knowledge of the T and N stages, then endoscopic ultrasound should be considered although the accuracy of this test is far from ideal.
Treatment depends upon the clinical stage at presentation and the comorbid disease of the patient. For patients who are medically fit and who have potentially resectable disease, surgery should be performed with an effort to achieve an R0 resection that is defined as a curative en bloc resection with negative proximal, distal, and radial margins (i.e. no obvious residual tumor). The surgeon should attempt to achieve > 5 cm proximal and distal margins. For distal tumors, this usually requires a distal gastrectomy. For proximal tumors, a total gastrectomy or proximal gastrectomy is acceptable. For gastric cancers that approach the gastroesophageal junction, the proximal margin should be at least 6 cm; this requirement usually mandates a formal esophagogastric resection with thoracotomy. An extended (D2) lymph node dissection (removing an average of 25-30 lymph nodes) can provide more complete staging than a limited (D1) lymph node dissection (removing an average of 15 lymph nodes), but there are no randomized Western trials that demonstrate a survival advantage associated with a D2 dissection yet. A large multi-center, randomized Dutch trial demonstrated that a D2 dissection was associated with increased morbidity and mortality but not with increased survival. A smaller, controlled British trial confirmed the findings of the Dutch study. Splenectomy should be avoided unless the spleen is involved by tumor and at least 15 lymph nodes should be assessed to properly stage the lymph nodes. To ensure that 15 lymph nodes are removed usually requires removal of the lesser omentum, greater omentum, common hepatic arterial lymph nodes, and the left gastric lymph nodes to the celiac axis. In most cases, this lymph node dissection approximates a D2 dissection with the important exception that the splenic hilar lymph nodes are not removed (which is an important component of most D2 dissections) to avoid removal of the spleen.
After curative resection, adjuvant combination chemotherapy and radiotherapy should be offered patients with node positive disease or tumors that penetrate the full thickness of the muscularis propria (T2b). This standard was set with the results from a randomized, controlled clinical trial published in 20017. This multi-center trial (INT-0116) treated patients with Stages Ib through IV M0 with one cycle of 5-FU and Leucovorin followed by 4.5 Gy external beam radiotherapy with 5-FU and Leucovorin, followed by two cycles of 5-FU and Leucovorin at monthly intervals. Between 1991 and 1998, 603 patients entered the study. Nodal metastases were noted in 85%. Improved survival was noted in the treatment arm, and will be discussed below.
For patients who are medically fit with locally advanced unresectable disease, combination chemotherapy and radiotherapy can be used. For patients who have comorbid disease that makes the risk of resection greater than the benefit, combination chemotherapy and radiation, chemotherapy alone, or no treatment (best supportive care) are options. For patients with metastatic disease, chemotherapy should be considered. For patients who present with bleeding and are not candidates for resection from the standpoint of either medical condition or metastases, radiation therapy can be helpful for palliation.
The risk of death from a gastrectomy should be < 5%. Complications include impaired transit of food ---either too slow or too fast, bleeding, and infection. The risk of death from adjuvant postoperative chemoradiotherapy was 1% in INT-0116.
Most Americans with gastric cancer present with tumor penetrating the full thickness of the stomach (T3) and positive lymph nodes. Unfortunately, surgery alone for this stage results in a 5-year survival rate of only 15-20%. As noted above, the randomized trial INT-0116 included predominantly patients with positive nodes (85%) and T3 tumors. INT-01Undefined subroutine &main::patientCareGuidelines called at C:\inetpub\wwwroot\WebsiteHosting\SSAT\website\cgi-bin\guidelines_SurgicalTreatmentGastricCancer_EN.cgi line 60.
16 showed that the 3-year overall survival time with surgery alone was only 41%; with adjuvant chemoradiotherapy, it rose to 52%. This study included T2bN0, Stage Ib, tumors and suggests that this subset will benefit by adjuvant postoperative chemoradiotherapy. However, only 36 patients had Stage Ib in INT-0116, and a recent study shows that T2a or T2b N0 gastric cancer resected with at least 15 lymph nodes in the specimen will be associated with a >85% 5-year survival rate without adjuvant postoperative chemoradiotherapy. Thus, it is not clear that Stage Ib gastric cancer benefits from adjuvant chemoradiotherapy.
For stage IV (M1) gastric cancer, combination chemotherapy is associated with about a 10 month median survival time, while “best supportive care” is associated with only a 3 to 4 month median survival time.
At a minimum, surgeons who are certified or eligible for certification by the American Board of Surgery, the Royal College of Physicians and Surgeons of Canada, or their equivalent should perform operations for gastric cancer. These surgeons have successfully completed at least 5 years of surgical training after medical school graduation and are qualified to perform operations for gastric cancer. The level of training in advanced laparoscopic techniques necessary to conduct minimally invasive surgery of the stomach is important to assess. The qualifications of a surgeon performing any operative procedure should be based on training (education), experience, and outcomes.
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Greene F, et al. AJCC Cancer Staging Manual, 6th edition. Springer-Verlag, New York, 2002.
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Cuschieri A, Weeden S, Fielding J, et al. Patient survival after D1 and D2 resection for gastric cancer: long-term results of the MRC randomized surgical trial. Surgical Co-operative Group. Br J Cancer 1999; 79:1522-1530.
Hundahl SA, Phillips JL, Menck HR. The National Cancer Data Base report on poor survival of U.S. gastric carcinoma patients treated with gastrectomy. Fifth edition American Joint Committee on Cancer staging, proximal disease, and the “different disease” hypothesis. Cancer 2000; 88:921-932.
MacDonald JS, Smalley SR, Benedetii J, et al. Chemoradiotherapy after surgery compared with surgery alone for adenocarcinoma of the stomach or gastroesophageal junction. New Engl J Med 2001; 345:725-730.
Sarela AI, Turnbull AD, Coit DG, et al. Accurate Lymph Node Staging is of Greater Prognostic Importance Than Subclassification of the T2 Category for Gastric Adenocarcinoma. Ann Surg Oncol 2003; 10:783-791.
Board Approved May 15, 2004