Abstract

INTRODUCTION

Stomach cancer is the second-most common cancer among men and third-most among females in Asia and worldwide.[1] The symptoms and sign of the stomach cancer are often reported late when the disease is already in advanced stages and 5-year survival is less than 30% in developed countries and around 20% in developing countries.[2]

About 8.6% of all cancers that occurred in 2002 were gastric cancer. The gastric cancer rates shows marked geographical variation, with high-risk areas in Japan, China, Eastern Europe and certain countries in Latin America. Low-risk population is seen among whites in North America, India, Philippines, most countries in Africa, some Western European countries and Australia.[2] In India, the number of new stomach cancer cases in 2001 was estimated to be approximately 35,675 (n=23,785 in men; 11,890 in women).[3] These differences in incidence rates can be attributed to many factors but refer particularly to differences in dietary habits, and infection to Helicobacter pylori.

This review includes an update of distribution of gastric cancer in India, as well as systematic review of published findings on association between various risk factors related to gastric cancer.

MATERIALS AND METHODS

A search was undertaken in MEDLINE (www.pubmed.com) using Pubmed database, using key words such as “stomach cancer, treatment, clinical characteristics, stomach cancer outcome, epidemiology, etiological factor and their corresponding Mesh terms were used in combination like OR, AND.” The search was limited to only English literature including those studies which were published from 2000 to 2009 by Indian institutes only. This search yielded a total of 256 articles of which the following studies were excluded: Animal model (48), studies which were not conducted in India (13), studies other than gastric cancer (25), case reports (42) and other studies unrelated to the topic concerned (80) as these studies did not satisfy the review purpose. Total 48 studies fulfilled the inclusion criterion. The descriptive health statistical data for gastric cancer was mainly obtained from publications of National Cancer Registry, UICC, IARC and WHO (GLOBOCON-2008). In most of the case-control studies definition of gastric cancer used was not specified.

DESCRIPTIVE EPIDEMIOLOGY

The data obtained from the National Cancer Registries indicates that gastric cancer is a leading problem in North-eastern and Southern states of Indian subcontinent [Tables ​[Tables11 and ​and2].2]. The rates for gastric cancer in North-eastern registries are higher than rest of the countries. However, this should be interpreted with caution as these registries are in initial years of registry operation, and it has been demonstrated that registries might include prevalent cases in their initial years. The age-adjusted incidence rate of stomach cancer in males varies widely among registries, highest being 11.1 per 100,000 in Chennai compared to 1.6 per 100,000 in Bhopal.[4] Similar to trends of stomach cancer globally, Indian registries have also observed statistically significant decreasing trend over the last 20-year period [Table 3].

Table 1

Salt intake is a risk factor for gastric carcinoma as it damages the gastric mucosa, which results in gastritis and increased cell proliferation.[26] Salted tea, a peculiar beverage, is commonly consumed by a majority of population in Kashmir valley was observed to be a risk factor.[27] Indian studies have not observed salt intake as a separate factor but salted and processed products were taken into consideration. Soda, which is an additive commonly added in the foods, was found to be associated with increased risk (OR=2.9). A protective effect of leafy vegetables and fruits was observed in these studies. Tea consumption was shown to have protective effects in one study. Reheated foods, reheated oils and refrigeration were not observed to be associated with risk of gastric cancer.[24]

The studies on diet and stomach cancer could provide breakthrough in understanding role of diet because of heterogeneous food consumption throughout India. Although the inter-individual variation might be high, the intra-individual variation is usually low. Unlike western countries where animal foods are the major part of diet and being a vegetarian is voluntary, in India the effect of lifelong vegetarianism on risk of gastric cancer could be explored.

TOBACCO AND ALCOHOL

Globally tobacco smoking has been indicated as the risk factor for gastric cancer in case-control and cohort studies.[28,29] The association between gastric cancer and tobacco smoking has been observed in various epidemiological studies [Table 7]. In India, not only tobacco smoking but also tobacco chewing is highly prevalent. Tobacco is used in various forms like, hukka, snuff, bidis, cigarettes, taibur, Meiziol, etc. About 229,392,725 adult males and 11,908,517 adult females are estimated to use tobacco in India.[28]

Table 7

Smoking tobacco has been found to be an independent risk factor for stomach cancer.[29] Current smokers were found to be at a higher risk as compared to non-smokers and ex-smokers.[30] A significantly increased risk was observed with increased smoking in South Indian study.[24]

Increased risk was also observed among the tobacco chewers.[30] The risk showed an increasing trend with the increase in frequency and amount of tobacco use and decreasing trend with the number of years since the practice of consuming tobacco was discontinued.

Tobacco use in any form (chewing, smoking and drinking) was observed to increase the risk of stomach cancer in Mizoram, a North-eastern state of India.[30]

Literature suggest that alcohol may be carcinogenic to the esophagus and cardia cancers but not to distal gastric cancer. In a study conducted in Mumbai, alcohol intake did not emerge as a risk factor[25] for gastric cancer. In Indian context, due to social stigma attached, it is difficult to measure the alcohol intake of an individual.

Other risk factors observed by studies conducted in India are education and occupation. Case-control study conducted in Mumbai, observed that male agricultural workers had 50% excess risk (OR-1.5; 95%CI-1.1-2.6) as compared to unskilled laborers or mill workers.[25]

GENETIC SUSCEPTIBILITY

Globally literature suggest that polymorphism in genes involved in inflammation viz interleukin,[31] toll-like receptor 4,[32] hyuman leukocyte antigen,[33] metabolic phase I enzyme viz CYP1A1,[34] metabolic phase II enzyme viz GSTM1, GSTT1 (Glutathione-S-transferase)[35] and NAT1, NAT2 (N-acetyltransferase), DNA repair Viz XRCC1,[36] are involved in development of gastric cancer. Indian studies on this topic are limited because of inadequate sample size, improper study designs and inability to controls for confounders. Only small numbers of polymorphism were investigated in all these studies. Most of the Indian studies have used RFLP method for genotyping while studies conducted outside India have used Taqman and Illumina assays for genotyping.

Only six studies are reported from India on genetic polymorphism and development of gastric cancer [Table 8]. Malik et al. have found GSTM1null and CYP2E1c1c2 genotypes imparted risk for gastric cancer [OR=1.98 (95% CI=1.22-3.21) and OR=2.26 (95% CI=1.25-5.25)] in population from Kashmir valley.[37] Another study has stated that GSTT1 null genotype increases the risk of gastric cancer.[38] Prasad et al. have stated that combination of G carrier and H. pylori infection increased the risk of gastric adenocarcinoma [OR=3.504, (95% CI=1.195-7.0807)].[39] Another study from Northern India has indicated the risk of gastric adenocarcinoma was significantly higher in patients having C carrier and H. pylori infection [OR=7.06, (95% CI=2.61-19.09)].[40]

Table 8

Single nucleotide polymorphism (SNP) in genes NAT2 (N-acetyltransferase),[41] interlukin-1B,[42] GSTM1 and GSTT1 (Glutathione S-transferase),[37,38] Pro12Ala peroxisome proliferator-activated receptor γ,[39] COX (cyclooxygenase)[40] have reported significant association in the development of gastric cancer.

Multiplicative interaction was observed between H. pylori infection and COX-2 polymorphism.[40] However, other studies failed to observe interaction between SNPs studied and infection with H. pylori and/or with other lifestyle factors.

PRIMARY PREVENTION

SECONDARY PREVENTION

No screening trials to observe reduction in gastric cancer mortality have been conducted in India to date. In Japan endoscopy has been tested as a screening test for gastric cancer (77.4-84% sensitivity).[44] Owing to the complications involved with endoscopy procedure and lack of large number of trained and experienced personnel who can conduct the test in field endoscopy is not considered to be an ideal tool for a population-based screening program. There is evidence from Japan about early detection and treatment of gastric cancer and finally the reduction of mortality due to the use of double contrast barium X-ray photoflurography.[45]

Serum pepsinogen is a non-invasive serological test which is being advocated for gastric cancer screening.[46] Although it makes the detection of gastric cancer easier, it can, however, detect the presence of only intestinal type of gastric cancers.

Occult Blood bead test has a specificity of 55% and a sensitivity of 65%.[47] This might also be explored for screening as it is easier to administer than endoscopy.

Mass eradication of H. pylori has been proposed as an alternative to mass screening in reducing incidence of gastric cancer. Screening young adults for H. pylori followed by treatment in those who test positive has a potential to prevent one in every 4–6 GC cases in China.[48] However, the timing of H. pylori eradication may be critical i.e., H. pylori eradication after initiation of cancer may prove unsuccessful, so medication should be administered prior to carcinogenesis (APOCP, Cancer report 2010). The data indicating the prevention of GC by H. pylori eradication needs to be critically evaluated as many conflicting results have been reported.[43] No appropriately designed RCT regarding screening has been reported in the past 10 years in India.

CONCLUSION

India has a high prevalence of H. pylori infection and comparatively low gastric cancer incidence rates. Stomach cancer is decreasing but its burden is high in India. There are limited studies from India to explain the etiology of gastric cancer. Given the high prevalence of H. pylori, trials are required to judge the potential benefit for its eradication to reduce gastric cancer. Providing medication for H. pylori eradication has to be further evaluated. More research is required not only to develop suitable screening test, but also to demarcate high-risk population and the effect of primary prevention programs. There is a need to clearly understand the risk associated with diet for any kind of prevention. Properly designed genetic susceptibility studies considering interaction with H. pylori, diet and tobacco use are required to understand etiology of gastric cancer.

As stomach cancer is one of the common cancers in India, studies are required to understand the etiology and prevention of gastric cancer.

Footnotes