Research Article | Open Access
Ashis Kumar Saha, Somnath Maitra, Subhas Chandra Hazra, "Epidemiology of Gastric Cancer in the Gangetic Areas of West Bengal", International Scholarly Research Notices, vol. 2013, Article ID 823483, 6 pages, 2013. https://doi.org/10.1155/2013/823483
Epidemiology of Gastric Cancer in the Gangetic Areas of West Bengal
There is marked geographical variation in the distribution and incidence of stomach cancer. We tried here to describe the pattern of relationships of age, sex, religion distribution, symptom profile, histological subtypes and Helicobacter pylori (H. pylori) infection with gastric cancer in Gangetic West Bengal. This study was done over a period of five years (2006–2010). The patients residing in the Gangetic areas of West Bengal presenting with upper gastrointestinal symptoms underwent UGI endoscopy. Among gastric cancer patients, demographic characteristics, symptomatology, macroscopic and histologic lesions and H. pylori status were analyzed. At confidence level 95%, “” and “” value were calculated to find significance. Among 23851 patients underwent UGI endoscopy, 14106 were males, 9745 females, 17889 Hindus and 5962 Muslims. Among 462 gastric cancer patients, Male : Female 2.7 : 1, Hindus : Muslim 3 : 1, abdominal pain, indigestion, and weight-loss were commonest presentations. Antrum was the commonest site whereas ulceroproliferative type was commonest type. H. pylori positivity was 80.89% in adenocarcinoma with statistically significant relation with intestinal type. In future, our target will be to modify risk factors; it will need further demographic studies and analysis, so that we can detect it earliest.
The incidence of gastric carcinoma has fallen dramatically in the last 50 years, but according to IARC-Globocan 2008, it is the third commonest cause of cancer death after lung and liver cancer in male and after breast and lung cancer in female in the world. It is still the 2nd and 4th most common cancer in males and females, respectively [1, 2]. Interestingly there is a marked geographical variation in stomach cancer. Highest incidence rates were reported in Japan, China, Eastern Europe and a few areas of Latin America and low rise in North America, India, Philippines, most countries in Africa, some Western European countries, and Australia previously. Globally, smoking, tobacco chewing, and alcohol are the risk factors for gastric cancer . In India, there are strong associations between them. Histologically, there are three subtypes of gastric adenocarcinoma-intestinal, diffuse, and indeterminate or mixed type. Of those, intestinal subtype influences the changes in the epidemiological incidence . Case fatality ratio of gastric cancer is higher than other common malignancies, like, colon, breast, and prostate cancer . Worldwide, the well known epidemiological observation in gastric cancer includes the following. (a) If migrants from high risk areas move to low risk areas (China to North America); the incidence rate shows remarkable reduction reaching to almost equal rates as in low risk countries . (b) Preventable by lifestyle modification such as reduced salt intake and increased vegetable and fruits consumption, together with avoidance of smoking and countermeasures against H. pylori infection, reduce the risk of gastric cancer . This cancer is usually diagnosed late when the disease has already invaded the lamina propria and musculature, because in early stages, the patient usually complains of trivial and nonspecific symptoms. Hence a new look to epidemiological studies in gastric cancer is necessary to establish new strategies for its early treatment and prevention of recurrence. In this study, we tried to explore the epidemiological characteristics of gastric cancer in Gangetic West Bengal, India, by searching relationships with age, sex, religion distribution, symptom profile, histological subtypes, and association with H. pylori infection.
2. Materials and Method
We started performing our original and honest study only after getting permission from the ethical committee. This work has been approved by the appropriate ethical committee of our Institution. This study was performed over a period of five years. The study population was from different districts on both sides of Ganges in West Bengal, India (Malda, Nadia, Howrah, Hoogly, North and South twenty-four parganas, and Kolkata). The patients were first screened by the doctors in rural urban health centers, public and district hospitals, nursing homes, and chambers, and then they were sent to hospitals or diagnostic centers of respective districts having facility for upper gastrointestinal endoscopy for evaluation of symptoms related to upper gastrointestinal tract. After getting informed consent from the subjects, demographic data was collected in a proforma containing structured questionnaire from patients and/or patients’ party. Then esophagogastroduodenoscopy was performed using 15% xylocaine spray as local anesthesia.
After detecting the lesion, at least eight biopsies were taken from the suspected areas in each patient. Biopsy materials were fixed in ten percent formalin at room temperature and later on processed for histopathology.
Multiple biopsies were also taken from normal looking mucosa adjacent to the growth for determining Helicobacter pylori status. For Helicobacter pylori testing, rapid urease testing was performed by using HP kit-TM manufactured by Allied Marketing Corporation, Kolkata, with sensitivity of 90% and specificity of 90%. Colour change from yellow to red within the time period of 15–20 minutes confirmed H. pylori.
After getting histologically confirmed gastric cancer patients, their demographic characteristics (age, sex, and religion), symptomatology, types of lesions (macroscopic and histologic), and Helicobacter pylori status were analyzed.
Statistical methods used as follows.(1)For significance of percentages, values (normal deviates) have been calculated. value indicates the maximum probability for a given level of significance.(2)95% CI for difference of percentage: (3)Chi-square test has been used with two degrees of freedom for Table 5 to show significance of association of affected cases according to types of lesions.
A total of 23851 patients underwent upper GI endoscopy of which 14106 were males and 9745 were females; 17889 were Hindus and 5962 were Muslims. A total of 462 cases were detected to have gastric malignancy. Demographic data for age, sex, and religion were tabulated in (Tables 1 and 2). Amongst the affected cases (), 340 were males and 122 were females (ratio 2.7 : 1). Religion distribution showed 310 Hindus and 152 Muslims (ratio 3 : 1). Table 1 also revealed that in more than 40 years, males were predominantly involved in comparison to females. Table 2 showed that incidence of Muslims was more common in 1st age group. Comparison of presenting symptoms was shown in Table 3. Abdominal pain was most common (66.23%) followed by indigestion (45.88%) and weight loss (43.29%), and the least common was melena (9.52%). Table 4 showed antrum as a commonest site of involvement (51.9%) followed by body (18.6%) and fundus (16.5%), the least common being incisura (12.9%). It was also revealed that body mucosa was significantly involved in males as compared to females (). Table 5 revealed that ulcerative lesion (57.8%) was significantly common as compared to ulceroproliferative (24.9%) and polypoidal lesion (17.3%). Table 6 revealed intestinal subtype as commonest (53.6%) and indeterminate subtype being the least common (15.1%) histological findings. Again, incidences of intestinal and indeterminate subtypes were more common in antral (61.3%, 57.1%, resp.) while diffuse subtype in fundal (37.5%) mucosa. Helicobacter pylori was positive in 80.09% of gastric carcinoma with the commonest incidence in intestinal subtype (89.1%) followed by diffuse type (85.2%).
| Figures within parenthesis indicate percentages.|
|Figures within the parenthesis indicate percentages.|
There was a spectrum of median age incidence reported in different parts of the world. In the western world, it was 71 years in the USA. In Asian countries, median ages in different countries were low. For example, in Japan it was 61 years , in Pakistan years, and in Saudi Arabia 47 years. In our study, the median age was years, which was near similar to the study done in South India ( years) and in Mizoram (male 58 and female 57 years), and male : female ratio was 2.7 : 1, where as in Mizoram, it was 2.3 : 1, , in Kashmir 3.3 : 1, in Saudi Arabia 2.2 : 1 , and in Pakistan 1.5 : 1 .
Our cohort showed males over age of forty years were significantly affected, which was not shown in any Indian study. In the age group of 20–39 years, Muslims were significantly affected than Hindus. It may be due to dietary indiscretion in the form of pickled food, high protein diet, and high tobacco consumption, in the form of bidi smoking and chewing [6, 7].
In astudy done by Kabir et al., abdominal pain (100%), vomiting (78%), dysphagia (24%), and weight loss (62%) were predominant symptoms pertaining gastric carcinoma . In a review of 18365 patients by the American College of Surgeons, common presentations were weight loss (66.6%), abdominal pain (51.6%), nausea/vomiting (34%), anorexia (32%), and melena (20.2%). Again Qurieshi et al. showed common presenting symptoms as weight loss (35%), dyspepsia (76%), anorexia (35%), and vomiting (35.8%) . Our study showed that abdominal pain (66.2%) was the commonest symptom followed by weight loss (43.3%), indigestion (45.9%), anorexia (39.9%), nausea/vomiting (34.2%), postprandial pain (29%), and melena (9.5%). Our findings were similar to the findings of the study done by Qurieshi et al. . Our cohort study showed that the obstructive symptoms like postprandial abdominal pain, nausea/vomiting, and weight loss were common in fundal and obstructive variety of antral carcinoma, which was not shown in any study after thorough Medline search.
Various reports revealed progressive increase in proximal stomach cancer and concomitant decline in distal stomach cancer in the western world [14, 15]. Reports from Asian countries were conflicting. Japanese and Korean population had predominant incidence of noncardia cancer, whereas an Iranian study showed the predominance of cardia cancer. In our study antrum was mostly involved (51.9%) followed by body (18.6%) and fundus (16.4%). Gastric body was significantly involved in males (). Recent study from Kerala in India showed that though predominant site of cancer was antral mucosa, there was a trend towards proximal shift. Cherian et al. showed no change in site specificity of carcinoma of stomach in South Indian population . Again Qurieshi et al. showed that in the Kashmiri population, incidences of cancer in proximal, mid, and distal stomach were 42%, 6.2%, and 45.7%, respectively . Afridi et al. reported growth at cardiac end in 33%, pylorus and antrum in 40%, linitis plastica in 13.3%, and only body and body and pylorus in 6.7% of patients .
Macroscopically, gastric cancer has been classified into 4 types: type one: polypoidal lesion, type two: fungating lesion, type three: ulcerated lesion, and type four: infiltrating lesion on the gastric wall or linitis plastica lesion. But there is considerable overlap between the above different types. Qurieshi et al. showed 35.5% ulceroproliferative, 26% proliferative, 31% ulcerative, and 7.4% infiltrative lesions during endoscopic procedure performed in Kashmiri patients . Another study done by Kabir et al. showed that ulcerative lesion was 56%, ulceroproliferative lesion 10%, and polypoidal lesion 34% . In our study ulcerative lesion was 57.8% followed by ulceroproliferative lesion 24.9% and polypoidal lesion 17.3% with significant incidence of ulcerative lesion ().
Over the past half century, the histological classification of gastric carcinoma has been largely based on Lauren’s criteria, which describes that gastric carcinoma is of two major subtypes: (1) intestinal subtype, an expansive epidemic type, corpus-dominant, more common in males, black, and elder age group most commonly associated with Helicobacter pylori infection and intestinal metaplasia, associated with chronic atrophic gastritis [17, 18]. Here, glandular structures are retained. This type is little invasive and has a sharp margin. It carries better prognosis. (2) Diffuse endemic cancer is more common in females and young individuals, but male to female ratio is equal . It originates in the areas of pangastritis without atrophy, consisting of scattered clusters of cells with poor differentiation and deceptive margins, and much virulent . Third common type, mixed type (indeterminate type), is also a common variant . Relative frequencies are approximately 54% for intestinal type, 32% for diffuse type, and 15% for indeterminate type . Regarding histopathological diagnosis, Afridi et al. showed that two-thirds of (66.6%) patients had diffuse subtype, 20% had intestinal subtype, and 13.3% gastric lymphoma . On the other hand, Qurieshi et al. showed 38.2% poorly differentiated adenocarcinoma and 60% moderately differentiated adenocarcinoma . In contrary to the Saudi study , our study showed that intestinal, diffuse, and indeterminate subtypes were 53.6%, 31.1%, and 15.1%, respectively, which was near identical to the study done by Kabir et al, in which intestinal, diffuse, and indeterminate type were 52%, 28%, and 20%, respectively . In our study, intestinal type and indeterminate type were significantly predominant in antral mucosa (61.3% and 57.1%, resp.) whereas diffuse type was more significant in fundal mucosa (37.5%) followed by antral mucosa (33.3%).
Helicobacter pylori, a gm negative bacillus, colonizes in stomach mucosa and triggers the progressive sequences of gastric lesions from chronic gastritis, gastric atrophy, intestinal metaplasia, dysplasia, and finally gastric carcinogenesis . Studies from different parts of the world showed linear relationship between gastric cancer and H. pylori infection [23, 24]. H. pylori infection is mainly acquired in childhood through oral ingestion, and infection may persist throughout the life . Its prevalence is closely linked to socioeconomic factors such as low income and poor education and living conditions during childhood such as poor sanitation and overcrowding [26, 27]. The study in US and Japan showed increased prevalence of Helicobacter pylori with age; it was mainly due to birth cohort rather than late acquisition of infection .
Several case control studies have shown significant association between Helicobacter pylori and risk of gastric adenocarcinoma. The risk is 2.1 to 16.7 fold greater than that in seronegative individual [29, 30]. Effect of H. pylori on gastric cancer development may vary with anatomic sites. Meta-analysis of prospective cohort studies showed that H. pylori infection was associated with rise of noncardia gastric adenocarcinoma . Most of the H. pylori infections are asymptomatic. Virulent strain of H. pylori carrying cytotoxin associated gene A (cagA) is responsible for gastric cancer in distal sites following atrophic gastritis [32, 33]. In Bangladesh, Talukdar et al. showed that the prevalence of H. pylori detected by CLO test and histology was 66% out of 50 cases of gastric cancer . Kabir et al. showed prevalence of H. pylori in 71.8% of gastric cancer patients and 20% among control group, showing significant () difference. Among the patients with intestinal type gastric cancer, H. pylori was present in 86.96% of cases, 50% of diffuse type and poorly differentiated type harbored H. pylori infection . In study by Qurieshi et al., 39% of gastric cancers were H. pylori positive . A study done by Satti et al. showed that among the patients with intestinal type gastric carcinoma, 37% were H. pylori positive, whereas among the patients with diffuse signet ring type gastric carcinoma, 29% were H. pylori positive . Other Indian studies did not found any association between H. pylori and gastric cancer [34–37]. Seroprevalence of H. pylori infection in adult population in India is 55%–92%, as compared to 44% and 55% in Chinese and Japanese population, respectively. In our study, 80.09% of gastric carcinoma was H. pylori positive, which was contradictory to the observation in developing countries by Miwa et al. and other Indian studies . 89.1% of intestinal type, 85.2% of diffuse type and 37.1% of indeterminate type of gastric cancer were H. pylori positive. Our observation of H. pylori positivity in case of intestinal type was similar to observation by Kabir et al. In comparison to other Indian studies, H. pylori positivity in case of gastric cancer in West Bengal was much higher.
In summary, in this study the male and female ratio was 2.7 : 1, religion trend Hindus : Muslim 3 : 1. Median age of Stomach cancer in Gangetic West Bengal, India, was mainly around 55 years of age. Abdominal pain indigestion and weight loss were the commonest symptoms of presentation. Anatomically antral mucosa was mostly commonly involved. Surprisingly Fundus was significantly involved in females. Histologically interstitial type was the most common subtype of adenocarcinoma and more commonly associated with H. pylori infection. Macroscopically ulcerative type was detected as the commonest lesion. Future target for gastric cancer prevention is to modify the risk factors, and further demographic studies and analysis for future screening will be needed.
Conflict of Interests
The authors have no financial interests in any company or institution that might benefit from their publication. They have no personal financial interests. They have no research support from organizations that might gain or lose financially through publication of the paper. They have no conflict of interests or any source of funding.
- G. Danaei, S. Vander Hoorn, A. D. Lopez, C. J. L. Murray, and M. Ezzati, “Causes of cancer in the world: comparative risk assessment of nine behavioural and environmental risk factors,” The Lancet, vol. 366, no. 9499, pp. 1784–1793, 2005.
- V. Catalano, R. Labianca, G. D. Beretta, G. Gatta, F. de Braud, and E. Van Cutsem, “Gastric cancer,” Critical Reviews in Oncology/Hematology, vol. 71, no. 2, pp. 127–164, 2009.
- IARC, “Tobacco smoke and involuntary smoking,” IARC Monographs on the Evaluation of Carcinogenic Risks To Humans, vol. 83, pp. 1–1438, 2004.
- P. Lauren, “The histological main types of gastric carcinoma: diffuse and so-called intestinal type carcinoma. An attempt at a histo-clinical classification,” Acta Pathologica et Microbiologica Scandinavica, vol. 64, pp. 31–49, 1965.
- A. Jemal, F. Bray, M. M. Center, J. Ferlay, E. Ward, and D. Forman, “Global cancer statistics,” CA Cancer Journal for Clinicians, vol. 61, no. 2, pp. 69–90, 2011.
- W. Haenszel, M. Kurihara, M. Segi, and R. K. Lee, “Stomach cancer among Japanese in Hawaii,” Journal of the National Cancer Institute, vol. 49, no. 4, pp. 969–988, 1972.
- T. P. Nyren and J. Yuen, “Protective effect of fruits and vegetables on stomach cancer in a cohort of Swedish twins,” International Journal of Cancer, vol. 76, pp. 35–37, 1998.
- A. A. Julian and C. W. Timothy, “Adenocarcinoma and other tumors of the stomach,” in Sleisenger and Fordtrean’s Gastrointestinal and Liver Disease, M. Feldman, L. S. Friedman, and L. J. Brandt, Eds., Elsevier Saunders, Philadelphia, Pa, USA, 9th edition, 2010.
- R. K. Phukan, E. Zomawia, N. C. Hazarlka, D. Baruah, and J. Mahanta, “High prevalence of stomach cancer among the people of Mizoram, India,” Current Science, vol. 87, no. 3, pp. 285–286, 2004.
- B. Satti, A. A. Al-Quorain, Y. M. Al-Gindan, A. A. Al Hamdam, and H. Y. Al-Idrissi, “Gastric malignancy: clinicopathologic spectrum and relationship to Helicobacter pylori infection,” Saudi Journal of Gastroenterology, vol. 11, pp. 149–156, 2005.
- S. P. Afridi, F. Bano, and S.-U. Shafiq-ur-Rahman, “Pattern and presentation of carcinoma stomach,” Journal of the College of Physicians and Surgeons Pakistan, vol. 21, no. 3, pp. 161–163, 2011.
- M. A. Kabir, R. Barua, H. Masud et al., “Clinical presentation, histological findings and prevalence of Helicobacter pylori in patients of gastric carcinoma,” Faridpur Medical College Journal, vol. 6, pp. 78–81, 2011.
- M. A. Qurieshi, M. A. Masoodi, S. A. Kadla, S. Z. Ahmad, and P. Gangadharan, “Gastric cancer in Kashmir,” Asian Pacific Journal of Cancer Prevention, vol. 12, no. 1, pp. 303–307, 2011.
- W. J. Blot, S. S. Devesa, R. W. Kneller, and J. F. Fraumeni Jr., “Rising incidence of adenocarcinoma of the esophagus and gastric cardia,” The Journal of the American Medical Association, vol. 265, no. 10, pp. 1287–1289, 1991.
- J. R. Kelley and J. M. Duggan, “Gastric cancer epidemiology and risk factors,” Journal of Clinical Epidemiology, vol. 56, no. 1, pp. 1–9, 2003.
- J. V. Cherian, R. Sivaraman, A. K. Muthusamy, and J. Venkataraman, “Stomach carcinoma in the Indian subcontinent: a 16-year trend,” Saudi Journal of Gastroenterology, vol. 13, no. 3, pp. 114–117, 2007.
- S. Kaneko and T. Yoshimura, “Time trend analysis of gastric cancer incidence in Japan by histological types, 1975–1989,” British Journal of Cancer, vol. 84, no. 3, pp. 400–405, 2001.
- J. Parsonnet, D. Vandersteen, J. Goates, R. K. Sibley, J. Pritikin, and Y. Chang, “Helicobacter pylori infection in intestinal- and diffuse-type gastric adenocarcinomas,” Journal of the National Cancer Institute, vol. 83, no. 9, pp. 640–643, 1991.
- K. D. Crew and A. I. Neugut, “Epidemiology of gastric cancer,” World Journal of Gastroenterology, vol. 12, no. 3, pp. 354–362, 2006.
- S. W. Hwang, D. H. Lee, S. H. Lee et al., “Preoperative staging of gastric cancer by endoscopic ultrasonography and multidetector-row computed tomography,” Journal of Gastroenterology and Hepatology, vol. 25, no. 3, pp. 512–518, 2010.
- W. Polkowski, J. W. van Sandick, G. J. A. Offerhaus et al., “Prognostic value of Lauren classification and c-erbB-2 oncogene overexpression in adenocarcinoma of the esophagus and gastroesophageal junction,” Annals of Surgical Oncology, vol. 6, no. 3, pp. 290–297, 1999.
- P. Correa, “Helicobacter pylori and gastric cancer: state of the art,” Cancer Epidemiology Biomarkers and Prevention, vol. 5, no. 6, pp. 477–481, 1996.
- J. Parsonnet, “The incidence of Helicobacter pylori infection,” Alimentary Pharmacology and Therapeutics, vol. 9, supplement 2, pp. 45–51, 1995.
- C. P. Howson, T. Hiyama, and E. L. Wynder, “The decline in gastric cancer: epidemiology of an unplanned triumph,” Epidemiologic Reviews, vol. 8, no. 1, pp. 1–27, 1986.
- R. A. Feldman, “Epidemiologic observation and open questions about disease and infection caused by Helicobacter pylori,” in Helicobacter Pylori: Molecular and Cellular Biology, M. Achtman and S. Serbaum, Eds., pp. 29–51, Horizon Scientific, Wymondham, UK, 2001.
- P. M. Webb, T. Knight, S. Greaves et al., “Relation between infection with helicobacter pylori and living conditions in childhood: evidence for person to person transmission in early life,” British Medical Journal, vol. 308, no. 6931, pp. 750–753, 1994.
- M. Kurosawa, S. Kikuchi, Y. Inaba, T. Ishibashi, and F. Kobayashi, “Helicobacter pylori infection among Japanese children,” Journal of Gastroenterology and Hepatology, vol. 15, no. 12, pp. 1382–1385, 2000.
- M. Asaka, T. Kimura, M. Kudo et al., “Relationship of Helicobacter pylori to serum pepsinogens in an asymptomatic Japanese population,” Gastroenterology, vol. 102, no. 3, pp. 760–766, 1992.
- P. Sipponen, T. U. Kosunen, J. Valle, M. Riihela, and K. Seppala, “Helicobacter pylori infection and chronic gastritis in gastric cancer,” Journal of Clinical Pathology, vol. 45, no. 4, pp. 319–323, 1992.
- L.-E. Hansson, L. Engstrand, O. Nyren et al., “Helicobacter pylori infection: independent risk indicator of gastric adenocarcinoma,” Gastroenterology, vol. 105, no. 4, pp. 1098–1103, 1993.
- Helicobacter and Cancer Collaborative Group, “Gastric cancer and Helicobacter pylori: a combined analysis of 12 case control studies nested within prospective cohorts,” Gut, vol. 49, no. 3, pp. 347–353, 2001.
- J. F. Tomb, O. White, A. R. Kerlavage et al., “The complete genome sequence of the gastric pathogen Helicobacter pylori,” Nature, vol. 388, pp. 539–547, 1997.
- R. A. Alam, L. S. Ling, D. T. Moir et al., “Genomic sequence comparison of two unrelated isolates of the human gastric pathogen Helicobacter pylori,” Nature, vol. 397, pp. 176–180, 1999.
- K. Singh and U. C. Ghoshal, “Causal role of Helicobacter pylori infection in gastric cancer: an Asian enigma,” World Journal of Gastroenterology, vol. 12, no. 9, pp. 1346–1351, 2006.
- A. Venkateshwari, D. Krishnaveni, S. Venugopal, P. Shashikumar, A. Vidyasagar, and A. Jyothy, “Helicobacter pylori infection in relation to gastric cancer progression,” Indian Journal of Cancer, vol. 48, no. 1, pp. 94–98, 2011.
- V. Kate and N. Ananthakrishnan, “Helicobacter pylori and gastric carcinoma: evidence for the link,” The National Medical Journal of India, vol. 13, no. 6, p. 329, 2000.
- V. Kate, N. Ananthakrishnan, S. Badrinath, and C. Ratnakar, “Prevalence of Helicobacter pylori infection in disorders of the upper gastrointestinal tract in south India,” National Medical Journal of India, vol. 11, no. 1, pp. 5–8, 1998.
- H. Miwa, M. F. Go, and N. Sato, “H. pylori and Gastric cancer: the Asian enigma,” American Journal of Gastroenterology, vol. 97, no. 5, pp. 1106–1112, 2002.
Copyright © 2013 Ashis Kumar Saha et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.