Topic Highlight Open Access
Copyright ©2014 Baishideng Publishing Group Co., Limited. All rights reserved.
World J Gastroenterol. Apr 28, 2014; 20(16): 4483-4490
Published online Apr 28, 2014. doi: 10.3748/wjg.v20.i16.4483
Characteristics of gastric cancer in Asia
Rubayat Rahman, Akwi W Asombang, Jamal A Ibdah, Division of Gastroenterology and Hepatology, University of Missouri School of Medicine, One Hospital Drive, Columbia, MO 65212, United States
Author contributions: Rahman R wrote the manuscript; Asombang AW was involved in reviewing the literature and manuscript; Ibdah JA provided overall intellectual input into the design and edited the manuscript.
Correspondence to: Jamal A Ibdah, MD, PhD, Professor, Director, Division of Gastroenterology and Hepatology, University of Missouri School of Medicine, One Hospital Drive, CE 405, Columbia, MO 65212, United States. ibdahj@health.missouri.edu
Telephone: +1-573-8827349 Fax: +1-573-8844595
Received: October 28, 2013
Revised: January 26, 2014
Accepted: February 17, 2014
Published online: April 28, 2014
Processing time: 183 Days and 7.2 Hours

Abstract

Gastric cancer (GC) is the fourth most common cancer in the world with more than 70% of cases occur in the developing world. More than 50% of cases occur in Eastern Asia. GC is the second leading cause of cancer death in both sexes worldwide. In Asia, GC is the third most common cancer after breast and lung and is the second most common cause of cancer death after lung cancer. Although the incidence and mortality rates are slowly declining in many countries of Asia, GC still remains a significant public health problem. The incidence and mortality varies according to the geographic area in Asia. These variations are closely related to the prevalence of GC risk factors; especially Helicobacter pylori (H. pylori) and its molecular virulent characteristics. The gradual and consistent improvements in socioeconomic conditions in Asia have lowered the H. pylori seroprevalence rates leading to a reduction in the GC incidence. However, GC remains a significant public health and an economic burden in Asia. There has been no recent systemic review of GC incidence, mortality, and H. pylori molecular epidemiology in Asia. The aim of this report is to review the GC incidence, mortality, and linkage to H. pylori in Asia.

Key Words: Gastric cancer; Asia; Epidemiology; Gastric cancer incidence; Gastric cancer mortality

Core tip: Gastric cancer (GC) is the third most common cancer and the second most common cause of cancer death in Asia. Highest incidence rates are observed in Eastern Asia and varies in other parts of Asia. Mortality rates are slowly declining but remain a significant public health problem. The seroprevalence of Helicobacter pylori is very closely related to the incidence of GC in Asia. In contrast to Western world, management of GC is focused on prevention and early detection in Eastern Asia.



INTRODUCTION

Gastric cancer (GC) is a heterogeneous, multi factorial disease. It endangers human physical and psycho-social wellbeing, causing a significant public health and economic burden both in the developed and developing countries[1,2]. According to International Agency for Research on Cancer, the global and regional burden of GC is enormous[3]. The incidence and mortality vary widely according to geographic areas, socio-cultural and economic entities. GLOBOCAN 2008 data revealed that about one million new cases of GC were estimated to have diagnosed in 2008, making it the fourth most common malignancy in the world, after lung, breast, and colorectal cancers. More than 70% of GC cases occur in developing countries with half the world’s total cases occurring in Eastern Asia[1,2]. Overall, GC incidence and mortality have fallen dramatically over the past 70 years. Despite its recent decline, GC is the second leading cause of cancer death in both sexes worldwide. The highest mortality rates occur in Eastern Asia while the lowest occur in Northern America. In Asia, GC is the third most common cancer after breast and lung. But is the second most cause of cancer death in Asia after lung cancer[2,3]. Although the incidence and mortality rates of GC are slowly declining in Asia, it still remains a significant health problem. Asia is the world’s largest and most populous continent. With approximately 4.3 billion people, it accounts for 60% of the world’s current human population. Asia’s growth rate is very high for the modern era and has quadrupled during the last 100 years. It is estimated that Asia’s growth rate will remain high[3,4]. There has been no recent systemic review of GC incidence, mortality and Helicobacter pylori (H. pylori) molecular epidemiology in Asia.

CURRENT EPIDEMIOLOGY OF GC

More than 727000 cases of GC were diagnosed in Asia in 2008, accounting for 11.9% of all the cancers diagnosed. It is the third most common cancer in Asia after breast and lung cancer[3]. Table 1 shows that the age-standardized rate (ASR) of incidence is highest in Asia (18.5%) compared to other continents. The ASR of mortality is also highest (13.4%) and it is second only to lung cancer (19.15) in Asia. It is the third most prevalent cancer in Asia after breast and colorectal cancers[3]. The incidence and mortality rates of GC are also the highest in both males and females in Asia compared to other continents (Tables 2 and 3)[3,5].

Table 1 Gastric cancer incidence, mortality and prevalence in the world as reported in GLOBOCAN 2008[3].
Total incidenceIncidence rateTotal mortalityMortality rate5-yr prevalencePrevalence
(in 1000s)per 100000(in 1000s)per 100000(in 1000s)
World98814.073710.315985.5%
Asia72718.553013.4121610.4%
Europe14510.31167.92012.4%
Northern America244.2122.1370.8%
Africa224.0213.8302.1%
Table 2 Male gastric cancer incidence, mortality and prevalence in the world as reported in GLOBOCAN 2008[3].
Total incidenceIncidence rateTotal mortalityMortality rate5-yr prevalencePrevalence
(in 1000s)per 100000(in 1000s)per 100000(in 1000s)
World64019.746314.210507.8%
Asia48425.934218.381915.7%
Europe8614.56811.31212.9%
Northern America155.872.8231.0%
Africa124.7114.5163.0%
Table 3 Female gastric cancer incidence, mortality and prevalence in the world as reported in GLOBOCAN 2008[3].
Total incidenceIncidence rateTotal mortalityMortality rate5-yr prevalencePrevalence
(in 1000s)per 100000(in 1000s)per 100000(in 1000s)
World3489.12736.95483.6%
Asia24311.71888.93966.2%
Europe597.0475.3791.9%
Northern America92.851.5130.6%
Africa103.393.2131.5%

The incidence and mortality rates are also higher in Eastern Asia compared to other regions in Asia. This region includes China, Japan and South Korea, the three countries with the highest GC incidence and mortality rates, while the lowest rates occur in South-Central Asia[1,3,5,6]. The age adjusted GC incidence, mortality, and prevalence rates in the various regions in Asia are summarized in Table 4. In all the four parts of Asia, the rates are lower in females than males as shown in Tables 5 and 6[1-5].

Table 4 Gastric cancer incidence, mortality and prevalence in Asia as reported in GLOBOCAN 2008[3].
Total incidenceIncidence rateTotal mortalityMortality rate5-yr prevalencePrevalence
(in 1000s)per 100000(in 1000s)per 100000(in 1000s)
Eastern Asia60130.241820.3107115.2%
South-Eastern Asia438.6357.1563.9%
South-Central Asia684.8636.5682.6%
Western Asia149.4138.3194.2%
Table 5 Male gastric cancer incidence, mortality and prevalence in Asia as reported in GLOBOCAN 2008[3].
Total incidenceIncidence rateTotal mortalityMortality rate5-yr prevalencePrevalence
(in 1000s)per 100000(in 1000s)per 100000(in 1000s)
Eastern Asia40842.427428.173221.0%
South-Eastern Asia2410.9208.9326.2%
South-Central Asia426.7396.3424.3%
Western Asia912.6811.2125.8%
Table 6 Female gastric cancer incidence, mortality and prevalence in Asia as reported in GLOBOCAN 2008[3].
Total incidenceIncidence rateTotal mortalityMortality rate5-yr prevalencePrevalence
(in 1000s)per 100000(in 1000s)per 100000(in 1000s)
Eastern Asia19318.314413.03389.5%
South-Eastern Asia186.7155.6232.6%
South-Central Asia263.9233.6261.6%
Western Asia56.745.973.0%
CURRENT INCIDENCE TREND OF GC IN ASIA

More than half of the world’s population live in Asia[2] China, Japan and South Korea have reported the highest GC incidence rate both in males and females in the world. More than half of the total cases of GC are diagnosed in East Asia each year[1,2,5,6]. Overall, the incidence rate trend of GC in Asia is declining in the last two decades. Although the incidence rate of GC remains somewhat unchanged in some countries of Asia, the overall incidence rate of GC in East Asia is declining[7]. In China, the incidence rate of GC in males declined from 41.9 per 100000 in 2000 to 37.1 per 100000 in 2005[8,9]. While from 2000 to 2005, GC incidence rate decreased from 19.5 to 17.4 per 100000, respectively in females[1,8,9]. In Japan, the incidence rate of GC declined from about 80 to 60 per 100000 from 1980 to 2000. In 2008, the incidence rate of GC in Japan was 31.1 per 100000 both in males and females[5,10,11]. In South Korea, the incidence rate of GC also declined to 65.6 per 100000 in males and 25.8 per 100000 in females[2,6,12]. Many countries of South-East Asia (Singapore, Thailand, and Malaysia) have also observed a slow decline of GC incidence rate over the last few decades[2,3].

The overall incidence rate of GC in South-Central Asia is low in comparison to the other parts of Asia. The incidence of GC in India (3.8 per 100000) is overall less than the worldwide incidence. The age-adjusted rate of GC among urban registries in India is 3.0-13.2 per 100000[2,3]. Overall, the incidence rate of GC in India is decreasing. However, this declining trend has not been seen in certain parts of India. Among the major population-based cancer registries in India, only Mumbai and Chennai have reported a decline in incidence. The incidence rate of GC in other parts of South-Central Asia like Pakistan, Bangladesh and Sri Lanka is also decreasing slowly[2-4,13,14].

Western Asia is the land of multiple ethnic groups, principally from three main backgrounds: Semitic (Arabs and Jews), Indo-European (Persians and Kurdish) and Turkic (Turkish and Turkmens). Its geographic location, which has been under continuous influences from Asia, Europe and Africa, has variable incidence rates of GC. The GC rate differs in this region from very high in Iran (26.1 per 100000) to low in Israel (12.5 per 100000)[3,15,16]. GC occurs nearly 7 times more frequently in Iran than in Iraq[17]. In Jordan, the overall incidence rate is 4.8 per 100000 (males 5.6 and females 4.1)[3,15,16]. The incidence rate of GC and its trend remains stable or improving slowly in most of the countries in Western Asia[3,15-17].

GC MORTALITY IN ASIA

The overall GC mortality rate and its variations according to geographic areas closely follow the distribution of the GC incidence rate in the world as well as in Asia. In Asia, the mortality rate is higher in males than females[3]. Similar to the incidence rate, GC mortality rate is the highest in Eastern Asia (Table 4)[3]. Mortality rates also vary in different countries in Asia (Table 7). China has the highest mortality rate from GC (30.1 per 100000) followed by Japan (20.5 per 100000) and South Korea (13.8 per 100000). The mortality rate is moderate to low in South-Eastern Asia (Malaysia 8.5 per 100000), while relatively low in South-Central Asia (India 4.6 and Bangladesh 5.7 per 100000). The mortality rates vary in Western Asia (Iran 19.9, Israel 6.7, Jordan 5.2 and Iraq 3.7 per 100000)[1,3,5,6,8,15].

Table 7 Incidence, mortality and prevalence of gastric cancer in selected countries in Asia as reported in GLOBOCAN 2008[3].
CountryIncidence rate per 100000Mortality rate per 100000Prevalence
China29.922.35.6%
Japan31.113.518.1%
South Korea12.19.87.0%
Indonesia9.48.84.8%
Malaysia8.47.43.3%
Thailand3.52.51.5%
India3.83.61.5%
Bangladesh5.25.02.8%
Pakistan6.35.93.0%
Iran15.614.18.8%
Iraq3.63.51.9%
Jordan4.84.52.2%
Saudi Arabia3.33.02.0%
Israel8.64.72.4%
CURRENT MORTALITY TREND OF GC IN ASIA

In the new millennium, there have been some distinct and progressive changes in the pattern of gastrointestinal cancer - especially in GC in Asia. Despite all the recent changes in screening, diagnosis, treatment and surveillance, GC still remains the second most common cause of cancer mortality in Asia[3]. The mortality rate of GC remains statistically unchanged in some countries of Asia, however, a significant decline in the mortality rate of GC in Eastern Asia led to an overall decline in the mortality rate in Asia[7]. In China, the highest mortality rate was observed in rural areas, especially in Gansu, Henan, Hebei, Shanxi and Shaanxi Provinces in the middle-western part of China[8,9]. Although there was a slight increase from the 1970s to early 1990s, a significant decline in GC mortality was noticed in almost the entire population during the last decade in China. Between 2000 and 2005, Mortality from GC declined in males, while the number slightly increased in females, despite the significant declining trend in mortality rates among all age groups in China. In 2008, the mortality rates of GC in China were 30.1 in males and 14.6 in females per 100000[1,7,8].

There has been a significant change in the mortality trend of GC in Japan. This country has had a significant decline in the mortality rate of GC from 1980 to 2010. In 2008, the overall mortality rate was 14.7 per 100000 (20.5 and 12.6 per 100000 in males and females, respectively)[2,3,11]. Similar decline was also observed in South Korea[2,3,12]. The mortality rate also declined in most of the countries in Eastern and South-Eastern Asia[2,3,7,18].

There was a decline in the mortality rates of GC in urban areas of India (overall 3.6, male 4.6, and female 2.7 per 100000 in 2008). But in many rural areas, the mortality rate still remains high and unchanged. The mortality rates in other countries in South-Central Asia remain low and unchanged. Iran has the highest mortality rate of GC in South-Central and Western Asia. The overall mortality rate is 14.1 per 100000 (male 19.9 and female 8.2) and is slowly declining. The mortality rate remains low and improving slowly in Jordan (overall 4.5, male 5.2 and female 3.8 per 100000) and Israel (overall 4.7, male 6.7 and female 3.0 per 100000)[3,13-15].

EPIDEMIOLOGY OF HELICOBACTER PYLORI INFECTION IN ASIA

It is well postulated that the seroprevalence of H. pylori is very closely related to the incidence of GC. There is a difference in the seroprevalence of H. pylori infection between countries and within specific regions and communities of individual countries, not only in Asia but also in other countries of the world. In tandem with the socioeconomic development in many countries, a temporal decrease in the seroprevalence rate has been reported[2].

The seroprevalence rates of H. pylori infection in under-developed or developing countries are higher than in developed countries. The highest seroprevalence rate is reported in Bangladesh (92%) followed by Kuwait (84%) and India (79%)[2,19,20]. On the other hand, the seroprevalence rates in developed countries are reported to be lower. Among East Asian countries, the overall seroprevalence rate is 58.07% in China, 39.3% in Japan, 59.6% in South Korea and 54.5% in Taiwan[21-24]. Among Southeast Asian countries, the reported seroprevalence rate was 35.9% in Malaysia, 31% in Singapore, 75% in Vietnam and 57% in Thailand[2,7,18,25-27]. The seroprevalence rates are also high in many countries of the South-Central and Western Asia - 78% in Jordan, 77% in Iran, 78% in Iraq, 75% in Saudi Arabia and 72% in Israel[15,28]. In addition, a temporal effect was also evident with the younger population having low prevalence rates similar to developed Western countries[2].

A temporal effect in H. pylori seroprevalence rate has also been noted in Asia[29,30]. In a study from Guangzhou province in China, it was found that the overall H. pylori seroprevalence rate had decreased from 62.5% in 1993 to 47% in 2003. Among children aged 1-5 years, the seroprevalence rate was 19.4% and this rose to 63.2% among subjects aged 40-50 years. In Japan, the overall seroprevalence rate was 72.7% in 1974, decreased to 54.6% in 1984 and was 39.3% in 1994. In South Korea, the seroprevalence rate decreased from 66.9% in 1998 to 59.6% in 2005[31]. In addition to a temporal decline in the overall seroprevalence rate over time, the younger population generally has a lower seroprevalence rate. Current evidence suggests that most H. pylori infection is acquired in childhood. The data from Asia also indicates that the rate of H. pylori infection has been decreasing over the last 40-50 years, with an overall decline in H. pylori seroprevalence, similar to that of Western developed countries[2,32-34]. Evidence related to the survival of H. pylori outside the gastric niche is limited. Principal route of transmission yet to be confirmed. There is strong evidence that indicates the prevalence of H. pylori infection has a strong correlation with access to clean water, suggesting a transmission route to the host[35,36].

The Indian enigma is a subset of the Asian enigma, which refers to the observations that there are regions where H. pylori infection is high yet the GC incidence is relatively low. The term was coined based on the epidemiological observation. The regions where these observations are made are India, Bangladesh, Pakistan and Thailand[2,4,5]. It is to be acknowledged that there are still gaps in our appreciation of the process of gastric carcinogenesis. There is also a lack of data documenting the precise gastric histology in these populations with low GC but high H. pylori seroprevalence rates[37,38].

MOLECULAR EPIDEMIOLOGY OF H. PYLORI IN ASIA

Different H. pylori strains transpire across diverse geographic regions, and the differences in these strains have been correlated with the variation in GC epidemiology. Six main geographic strains were identified, the hpEastAsia is the strain from East Asian countries[39]. It has been perceived that populations with high GC rates correspond almost exactly to populations with the hpEastAsia strain. In South Asian countries where H. pylori seroprevalence rates are high but GC prevalence rates are low, the strains were predominantly hpAsia[29,39-41].

In the milieu of GC carcinogenesis, bacterial virulence factors that have been implicated include the cytotoxin-associated gene A antigen (CagA), vacuolating cytotoxin (VacA), and outer membrane proteins (OMP)[41]. Huang et al[42] performed a meta-analysis of 16 studies with 2284 cases and 2770 controls to scrutinize the relationship between CagA seropositivity and the risk of GC and indicated that infection with cagA-positive strains of H. pylori amplified the risk for GC over the risk associated with H. pylori infection alone. CagA protein has been classified into Western and Eastern types. The East Asian strain has been documented to be more virulent than the Western CagA with respect to clinical outcomes[42,43]. Azuma et al[44] validated that in the grades of inflammation and mucosal atrophy were significantly higher in patients infected with Eastern CagA-positive strains than in those infected with Western CagA-positive strains. Satomi et al[45] revealed that in Okinawa, Japan, where both Western and East Asian CagA were present, the prevalence of East Asian CagA-positive strains was significantly higher in patients with GC (84.6%) than in patients with duodenal ulcer (27.3%). There are increased frequencies of GC in individuals with type O blood and in secretors [expressing Le (b) antigen], but other studies have not found any relationship between blood groups and this infection[46,47]. The prevalence of H. pylori infection in intestinal-type GC is higher than in the diffuse type and in the control group. An association was found between H. pylori infection and GC located distally (antrum/pylorus)[48].

MANAGEMENT AND OUTCOME OF GC IN ASIA

GC management has been principally focused on the management of advanced GC in western populations, where the risk of GC tends to fall into the low-risk category. But this statement does not hold true for the highest-risk continent - Asia, where resources have focused on preventive strategies as well as management of early stage GC[49]. It is widely accepted that GC, like many other malignancies, progresses through a cancer cascade[50]. However, why certain individuals and families have a greater propensity to move along the cascade towards GC, is most certainly a multi-factorial process, and arises from complex and multifaceted interactions between host factors, H. pylori and environmental factors. Diets high in salt and nitrates carry the highest risks, with salt in particular demonstrating an ability to augment the effects of carcinogens. Fresh fruits and vegetables are associated with a reduced risk of GC. But fortification of the diet with ascorbic acid or use of multivitamins does not appear to confer the same protection. Studies focusing on sustained measurable alterations in diet sufficient to affect GC incidence and prevalence are underway[51-53].

However, H. pylori infection has proven to be an interesting target and multiple studies have indicated that H. pylori infection is a necessary, but not a sufficient causal factor in the development of GC[51]. Unfortunately, four randomized placebo-controlled trials evaluating the impact of H. pylori screening and eradication on GC prevalence did not show a significant reduction in GC development; however, there was a non-significant trend towards risk reduction for GC with H. pylori eradication. The strategy of population screening and treatment of H. pylori infection appears to be the strategy of choice in high GC risk populations in Eastern Asia[54-57].

China, Japan and South Korea are the in champions in the management of early GC, and this has primarily been driven by need. Given that these countries have some of the highest GC, screening is done through barium meal (Japan), gastroscopy (Japan and South Korea) and serum pepsinogen/gastroscopy (China)[55-57]. Studies from the eastern Asia examining the techniques of endoscopic mucosal resection and endoscopic submucosal dissection for early stage GC have proven that with improving technical expertise and careful surveillance, the outcome is excellent with high 5-year survival[58]. However, the detection of early GC is difficult and only systematic population screening has been shown to increase early detection and confer a survival advantage[59,60]. Health economics modeling indicates that population endoscopic screening for early GC is cost effective in moderate- to high-risk populations and may not be economically prudent for other part of Asia[59,61].

In the management and outcome of advanced GC, the majority of the studies have been carried out in the Western world, as most of the cases of GC are diagnosed at advanced stages[62]. The backbone of the management of advanced GC is chemotherapy, which is comparable between Western world and Asia[63]. The S1-cisplatin doublet remains the standard chemotherapy regimen for advanced GC in Japan, replacing 5FU-cisplatin. S1-cisplatin is also available in South Korea, Singapore, Taiwan, Philippines and China for this indication, but is not approved in North America[64,65]. Fluoro-pyrimidines show less toxicity in Asian populations, possibly secondary to polymorphisms in genes encoding drug-metabolizing enzymes, translating into more options for advanced GC treatments in Asian populations. Better survival differences after gastrectomy for GC favoring Asians patients may be explained by different disease patterns, the related need for fewer extensive procedures, and fewer patient risk factors in Eastern Asia. In other parts of Asia, the outcomes after surgery are variable[9,58,66]. The overall 1 and 5-year survivals are comparable between Asia, Europe, and North America according to gender and stage. there are slight variations of outcomes among different regions of Asia, depending on socioeconomic condition and access to medical care[9,65,67].

CONCLUSION

GC is exerting a significant health and economic burden in many countries of Asia[3]. The gradual and consistent improvement in socioeconomic condition in Asia has brought about an overall decrease in H. pylori seroprevalence rates and thus improvement of GC incidence[2,7]. Nonetheless, differences in still exist between developed and less developed countries of Asia[7,68]. There is now better understanding of the process of gastric carcinogenesis, and the role of bacterial virulence factors interrelating with host immune factors. In order to address the high clinical burden of GC, a recent Asia-Pacific Gastric Cancer Consensus meeting has strongly recommended a strategy for H. pylori screening and eradication in high-risk populations to reduce GC incidence. On the other hand, there have been continuous efforts to improve the screening, early diagnosis, surgical and medical management and surveillance of GC[7].

Similar to the Western world, the incidence and prevalence of H. pylori infection and GC in Asia has decreased over the past few decades. Multiple factors have played interactive roles in this regard. With a better understanding of the molecular epidemiology of H. pylori infection, GC carcinogenesis and overall improved management of GC, the clinical outcome is slowly improving[69,70]. However, more elaborative and circumferential steps have to be taken for primary, secondary and tertiary prevention of GC in Asia which in turn will eventually decrease the global burden of GC.

Footnotes

P- Reviewers: Deans C, Dalamaga M, Goral V S- Editor: Song XX L- Editor: A E- Editor: Ma S

References
1.  Yang L. Incidence and mortality of gastric cancer in China. World J Gastroenterol. 2006;12:17-20.  [PubMed]  [DOI]  [Cited in This Article: ]
2.  Fock KM, Ang TL. Epidemiology of Helicobacter pylori infection and gastric cancer in Asia. J Gastroenterol Hepatol. 2010;25:479-486.  [PubMed]  [DOI]  [Cited in This Article: ]
3.   Available from: http://globocan.iarc.fr/. Accessed September 20, 2013.  [PubMed]  [DOI]  [Cited in This Article: ]
4.   Available from: http://www.who.int/en/. Accessed September 07, 2013.  [PubMed]  [DOI]  [Cited in This Article: ]
5.  Matsuda A, Matsuda T, Shibata A, Katanoda K, Sobue T, Nishimoto H. Cancer incidence and incidence rates in Japan in 2007: a study of 21 population-based cancer registries for the Monitoring of Cancer Incidence in Japan (MCIJ) project. Jpn J Clin Oncol. 2013;43:328-336.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 107]  [Cited by in F6Publishing: 107]  [Article Influence: 9.7]  [Reference Citation Analysis (0)]
6.  Kim JY, Lee HS, Kim N, Shin CM, Lee SH, Park YS, Hwang JH, Kim JW, Jeong SH, Lee DH. Prevalence and clinicopathologic characteristics of gastric cardia cancer in South Korea. Helicobacter. 2012;17:358-368.  [PubMed]  [DOI]  [Cited in This Article: ]
7.  Goh KL. Changing trends in gastrointestinal disease in the Asia-Pacific region. J Dig Dis. 2007;8:179-185.  [PubMed]  [DOI]  [Cited in This Article: ]
8.  Guo P, Huang ZL, Yu P, Li K. Trends in cancer mortality in China: an update. Ann Oncol. 2012;23:2755-2762.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 115]  [Cited by in F6Publishing: 134]  [Article Influence: 11.2]  [Reference Citation Analysis (0)]
9.  Zhou HJ, So JB, Yong WP, Luo N, Zhu F, Naidoo N, Li SC, Yeoh KG. Validation of the functional assessment of cancer therapy-gastric module for the Chinese population. Health Qual Life Outcomes. 2012;10:145.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 21]  [Cited by in F6Publishing: 25]  [Article Influence: 2.1]  [Reference Citation Analysis (0)]
10.  Matsuzaka M, Fukuda S, Takahashi I, Shimaya S, Oyama T, Yaegaki M, Shimoyama T, Sakamoto J, Nakaji S, Umeda T. The decreasing burden of gastric cancer in Japan. Tohoku J Exp Med. 2007;212:207-219.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 17]  [Cited by in F6Publishing: 22]  [Article Influence: 1.3]  [Reference Citation Analysis (0)]
11.  Asaka M. A new approach for elimination of gastric cancer deaths in Japan. Int J Cancer. 2013;132:1272-1276.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 100]  [Cited by in F6Publishing: 92]  [Article Influence: 8.4]  [Reference Citation Analysis (0)]
12.  Choi KS, Jun JK, Park EC, Park S, Jung KW, Han MA, Choi IJ, Lee HY. Performance of different gastric cancer screening methods in Korea: a population-based study. PLoS One. 2012;7:e50041.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 88]  [Cited by in F6Publishing: 105]  [Article Influence: 8.8]  [Reference Citation Analysis (0)]
13.  Matsuhisa T, Aftab H. Observation of gastric mucosa in Bangladesh, the country with the lowest incidence of gastric cancer, and Japan, the country with the highest incidence. Helicobacter. 2012;17:396-401.  [PubMed]  [DOI]  [Cited in This Article: ]
14.  Dikshit RP, Mathur G, Mhatre S, Yeole BB. Epidemiological review of gastric cancer in India. Indian J Med Paediatr Oncol. 2011;32:3-11.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 68]  [Cited by in F6Publishing: 67]  [Article Influence: 5.2]  [Reference Citation Analysis (1)]
15.  Hussein NR. Helicobacter pylori and gastric cancer in the Middle East: a new enigma? World J Gastroenterol. 2010;16:3226-3234.  [PubMed]  [DOI]  [Cited in This Article: ]
16.  Malekzadeh R, Derakhshan MH, Malekzadeh Z. Gastric cancer in Iran: epidemiology and risk factors. Arch Iran Med. 2009;12:576-583.  [PubMed]  [DOI]  [Cited in This Article: ]
17.  Haidari M, Nikbakht MR, Pasdar Y, Najaf F. Trend analysis of gastric cancer incidence in Iran and its six geographical areas during 2000-2005. Asian Pac J Cancer Prev. 2012;13:3335-3341.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 17]  [Cited by in F6Publishing: 24]  [Article Influence: 2.2]  [Reference Citation Analysis (0)]
18.  Goh KL, Parasakthi N. The racial cohort phenomenon: seroepidemiology of Helicobacter pylori infection in a multiracial South-East Asian country. Eur J Gastroenterol Hepatol. 2001;13:177-183.  [PubMed]  [DOI]  [Cited in This Article: ]
19.  Ahmad MM, Rahman M, Rumi AK, Islam S, Huq F, Chowdhury MF, Jinnah F, Morshed MG, Hassan MS, Khan AK. Prevalence of Helicobacter pylori in asymptomatic population--a pilot serological study in Bangladesh. J Epidemiol. 1997;7:251-254.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 36]  [Cited by in F6Publishing: 40]  [Article Influence: 1.5]  [Reference Citation Analysis (0)]
20.  Graham DY, Adam E, Reddy GT, Agarwal JP, Agarwal R, Evans DJ, Malaty HM, Evans DG. Seroepidemiology of Helicobacter pylori infection in India. Comparison of developing and developed countries. Dig Dis Sci. 1991;36:1084-1088.  [PubMed]  [DOI]  [Cited in This Article: ]
21.  Wang KJ, Wang RT. [Meta-analysis on the epidemiology of Helicobacter pylori infection in China]. Zhonghua Liu Xing Bing Xue Zazhi. 2003;24:443-446.  [PubMed]  [DOI]  [Cited in This Article: ]
22.  Fujisawa T, Kumagai T, Akamatsu T, Kiyosawa K, Matsunaga Y. Changes in seroepidemiological pattern of Helicobacter pylori and hepatitis A virus over the last 20 years in Japan. Am J Gastroenterol. 1999;94:2094-2099.  [PubMed]  [DOI]  [Cited in This Article: ]
23.  Yim JY, Kim N, Choi SH, Kim YS, Cho KR, Kim SS, Seo GS, Kim HU, Baik GH, Sin CS. Seroprevalence of Helicobacter pylori in South Korea. Helicobacter. 2007;12:333-340.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 207]  [Cited by in F6Publishing: 203]  [Article Influence: 11.9]  [Reference Citation Analysis (0)]
24.  Teh BH, Lin JT, Pan WH, Lin SH, Wang LY, Lee TK, Chen CJ. Seroprevalence and associated risk factors of Helicobacter pylori infection in Taiwan. Anticancer Res. 1994;14:1389-1392.  [PubMed]  [DOI]  [Cited in This Article: ]
25.  Fock KM. Helicobacter pylori infection--current status in Singapore. Ann Acad Med Singapore. 1997;26:637-641.  [PubMed]  [DOI]  [Cited in This Article: ]
26.  Deankanob W, Chomvarin C, Hahnvajanawong C, Intapan PM, Wongwajana S, Mairiang P, Kularbkaew C, Sangchan A. Enzyme-linked immunosorbent assay for serodiagnosis of Helicobacter pylori in dyspeptic patients and volunteer blood donors. Southeast Asian J Trop Med Public Health. 2006;37:958-965.  [PubMed]  [DOI]  [Cited in This Article: ]
27.  Hoang TT, Bengtsson C, Phung DC, Sörberg M, Granström M. Seroprevalence of Helicobacter pylori infection in urban and rural Vietnam. Clin Diagn Lab Immunol. 2005;12:81-85.  [PubMed]  [DOI]  [Cited in This Article: ]
28.  Novis BH, Gabay G, Naftali T. Helicobacter pylori: the Middle East scenario. Yale J Biol Med. 1998;71:135-141.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 34]  [Cited by in F6Publishing: 50]  [Article Influence: 2.0]  [Reference Citation Analysis (0)]
29.  Falush D, Wirth T, Linz B, Pritchard JK, Stephens M, Kidd M, Blaser MJ, Graham DY, Vacher S, Perez-Perez GI. Traces of human migrations in Helicobacter pylori populations. Science. 2003;299:1582-1585.  [PubMed]  [DOI]  [Cited in This Article: ]
30.  Moodley Y, Linz B, Yamaoka Y, Windsor HM, Breurec S, Wu JY, Maady A, Bernhöft S, Thiberge JM, Phuanukoonnon S. The peopling of the Pacific from a bacterial perspective. Science. 2009;323:527-530.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 233]  [Cited by in F6Publishing: 209]  [Article Influence: 13.9]  [Reference Citation Analysis (1)]
31.  Chen J, Bu XL, Wang QY, Hu PJ, Chen MH. Decreasing seroprevalence of Helicobacter pylori infection during 1993-2003 in Guangzhou, southern China. Helicobacter. 2007;12:164-169.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 63]  [Cited by in F6Publishing: 176]  [Article Influence: 10.4]  [Reference Citation Analysis (0)]
32.  Fock KM, Dhamodaran S TE. Is H. pylori genotypes significant in Asian patients with gastric cancer and GERD? Gut. 2006;55:A258.  [PubMed]  [DOI]  [Cited in This Article: ]
33.  Jais M, Barua S. Seroprevalence of anti Helicobacter pylori IgG/IgA in asymptomatic population from Delhi. J Commun Dis. 2004;36:132-135.  [PubMed]  [DOI]  [Cited in This Article: ]
34.  Perez-Perez GI, Taylor DN, Bodhidatta L, Wongsrichanalai J, Baze WB, Dunn BE, Echeverria PD, Blaser MJ. Seroprevalence of Helicobacter pylori infections in Thailand. J Infect Dis. 1990;161:1237-1241.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 139]  [Cited by in F6Publishing: 139]  [Article Influence: 4.1]  [Reference Citation Analysis (0)]
35.  Percival SL, Thomas JG. Transmission of Helicobacter pylori and the role of water and biofilms. J Water Health. 2009;7:469-477.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 45]  [Cited by in F6Publishing: 37]  [Article Influence: 2.5]  [Reference Citation Analysis (0)]
36.  Calvet X, Ramírez Lázaro MJ, Lehours P, Mégraud F. Diagnosis and epidemiology of Helicobacter pylori infection. Helicobacter. 2013;18 Suppl 1:5-11.  [PubMed]  [DOI]  [Cited in This Article: ]
37.  Graham DY, Lu H, Yamaoka Y. African, Asian or Indian enigma, the East Asian Helicobacter pylori: facts or medical myths. J Dig Dis. 2009;10:77-84.  [PubMed]  [DOI]  [Cited in This Article: ]
38.  Ang TL, Fock KM, Dhamodaran S, Teo EK, Tan J. Racial differences in Helicobacter pylori, serum pepsinogen and gastric cancer incidence in an urban Asian population. J Gastroenterol Hepatol. 2005;20:1603-1609.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 44]  [Cited by in F6Publishing: 48]  [Article Influence: 2.5]  [Reference Citation Analysis (0)]
39.  Yamaoka Y, Kato M, Asaka M. Geographic differences in gastric cancer incidence can be explained by differences between Helicobacter pylori strains. Intern Med. 2008;47:1077-1083.  [PubMed]  [DOI]  [Cited in This Article: ]
40.  Linz B, Balloux F, Moodley Y, Manica A, Liu H, Roumagnac P, Falush D, Stamer C, Prugnolle F, van der Merwe SW. An African origin for the intimate association between humans and Helicobacter pylori. Nature. 2007;445:915-918.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 682]  [Cited by in F6Publishing: 615]  [Article Influence: 36.2]  [Reference Citation Analysis (3)]
41.  McNamara D, El-Omar E. Helicobacter pylori infection and the pathogenesis of gastric cancer: a paradigm for host-bacterial interactions. Dig Liver Dis. 2008;40:504-509.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 56]  [Cited by in F6Publishing: 59]  [Article Influence: 3.7]  [Reference Citation Analysis (0)]
42.  Huang JQ, Zheng GF, Sumanac K, Irvine EJ, Hunt RH. Meta-analysis of the relationship between cagA seropositivity and gastric cancer. Gastroenterology. 2003;125:1636-1644.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 365]  [Cited by in F6Publishing: 364]  [Article Influence: 17.3]  [Reference Citation Analysis (0)]
43.  Nguyen LT, Uchida T, Murakami K, Fujioka T, Moriyama M. Helicobacter pylori virulence and the diversity of gastric cancer in Asia. J Med Microbiol. 2008;57:1445-1453.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 38]  [Cited by in F6Publishing: 45]  [Article Influence: 3.0]  [Reference Citation Analysis (1)]
44.  Azuma T, Yamakawa A, Yamazaki S, Ohtani M, Ito Y, Muramatsu A, Suto H, Yamazaki Y, Keida Y, Higashi H. Distinct diversity of the cag pathogenicity island among Helicobacter pylori strains in Japan. J Clin Microbiol. 2004;42:2508-2517.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 62]  [Cited by in F6Publishing: 68]  [Article Influence: 3.4]  [Reference Citation Analysis (0)]
45.  Satomi S, Yamakawa A, Matsunaga S, Masaki R, Inagaki T, Okuda T, Suto H, Ito Y, Yamazaki Y, Kuriyama M. Relationship between the diversity of the cagA gene of Helicobacter pylori and gastric cancer in Okinawa, Japan. J Gastroenterol. 2006;41:668-673.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 50]  [Cited by in F6Publishing: 56]  [Article Influence: 3.1]  [Reference Citation Analysis (0)]
46.  Keramati MR, Sadeghian MH, Ayatollahi H, Badiee Z, Shakibayi H, Moghimi-Roudi A. Role of the Lewis and ABO Blood Group Antigens in Helicobacter pylori Infection. Malays J Med Sci. 2012;19:17-21.  [PubMed]  [DOI]  [Cited in This Article: ]
47.  Aryana K, Keramati MR, Zakavi SR, Sadeghian MH, Akbari H. Association of Helicobacter pylori infection with the Lewis and ABO blood groups in dyspeptic patients. Niger Med J. 2013;54:196-199.  [PubMed]  [DOI]  [Cited in This Article: ]
48.  Martín-de-Argila C, Boixeda D, Redondo C, Alvarez I, Gisbert JP, García Plaza A, Cantón R. Relation between histologic subtypes and location of gastric cancer and Helicobacter pylori. Scand J Gastroenterol. 1997;32:303-307.  [PubMed]  [DOI]  [Cited in This Article: ]
49.  Parkin DM, Bray F, Ferlay J, Pisani P. Global cancer statistics, 2002. CA Cancer J Clin. 2005;55:74-108.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 13286]  [Cited by in F6Publishing: 13462]  [Article Influence: 708.5]  [Reference Citation Analysis (1)]
50.  Correa P, Piazuelo MB, Camargo MC. The future of gastric cancer prevention. Gastric Cancer. 2004;7:9-16.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 111]  [Cited by in F6Publishing: 106]  [Article Influence: 5.3]  [Reference Citation Analysis (0)]
51.  Fock KM, Katelaris P, Sugano K, Ang TL, Hunt R, Talley NJ, Lam SK, Xiao SD, Tan HJ, Wu CY. Second Asia-Pacific Consensus Guidelines for Helicobacter pylori infection. J Gastroenterol Hepatol. 2009;24:1587-1600.  [PubMed]  [DOI]  [Cited in This Article: ]
52.  Goh KL, Cheah PL, Md N, Quek KF, Parasakthi N. Ethnicity and H. pylori as risk factors for gastric cancer in Malaysia: A prospective case control study. Am J Gastroenterol. 2007;102:40-45.  [PubMed]  [DOI]  [Cited in This Article: ]
53.  Tatematsu M, Takahashi M, Fukushima S, Hananouchi M, Shirai T. Effects in rats of sodium chloride on experimental gastric cancers induced by N-methyl-N-nitro-N-nitrosoguanidine or 4-nitroquinoline-1-oxide. J Natl Cancer Inst. 1975;55:101-106.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 63]  [Cited by in F6Publishing: 69]  [Article Influence: 4.1]  [Reference Citation Analysis (0)]
54.  Wong BC, Lam SK, Wong WM, Chen JS, Zheng TT, Feng RE, Lai KC, Hu WH, Yuen ST, Leung SY. Helicobacter pylori eradication to prevent gastric cancer in a high-risk region of China: a randomized controlled trial. JAMA. 2004;291:187-194.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1015]  [Cited by in F6Publishing: 995]  [Article Influence: 49.8]  [Reference Citation Analysis (0)]
55.  Kim YS, Park HA, Kim BS, Yook JH, Lee MS. Efficacy of screening for gastric cancer in a Korean adult population: a case-control study. J Korean Med Sci. 2000;15:510-515.  [PubMed]  [DOI]  [Cited in This Article: ]
56.  Tsubono Y, Hisamichi S. Screening for gastric cancer in Japan. Gastric Cancer. 2000;3:9-18.  [PubMed]  [DOI]  [Cited in This Article: ]
57.  Liu CY, Wu CY, Lin JT, Lee YC, Yen AM, Chen TH. Multistate and multifactorial progression of gastric cancer: results from community-based mass screening for gastric cancer. J Med Screen. 2006;13 Suppl 1:S2-S5.  [PubMed]  [DOI]  [Cited in This Article: ]
58.  Yamaguchi N, Isomoto H, Fukuda E, Ikeda K, Nishiyama H, Akiyama M, Ozawa E, Ohnita K, Hayashi T, Nakao K. Clinical outcomes of endoscopic submucosal dissection for early gastric cancer by indication criteria. Digestion. 2009;80:173-181.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 75]  [Cited by in F6Publishing: 86]  [Article Influence: 6.1]  [Reference Citation Analysis (0)]
59.  Whiting JL, Sigurdsson A, Rowlands DC, Hallissey MT, Fielding JW. The long term results of endoscopic surveillance of premalignant gastric lesions. Gut. 2002;50:378-381.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 183]  [Cited by in F6Publishing: 181]  [Article Influence: 8.2]  [Reference Citation Analysis (0)]
60.  Kubota H, Kotoh T, Masunaga R, Dhar DK, Shibakita M, Tachibana M, Kohno H, Nagasue N. Impact of screening survey of gastric cancer on clinicopathological features and survival: retrospective study at a single institution. Surgery. 2000;128:41-47.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 60]  [Cited by in F6Publishing: 68]  [Article Influence: 2.8]  [Reference Citation Analysis (0)]
61.  Dan YY, So JB, Yeoh KG. Endoscopic screening for gastric cancer. Clin Gastroenterol Hepatol. 2006;4:709-716.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 114]  [Cited by in F6Publishing: 126]  [Article Influence: 7.0]  [Reference Citation Analysis (0)]
62.  Wagner AD, Unverzagt S, Grothe W, Kleber G, Grothey A, Haerting J, Fleig WE. Chemotherapy for advanced gastric cancer. Cochrane Database Syst Rev. 2010;CD004064.  [PubMed]  [DOI]  [Cited in This Article: ]
63.  Bang YJ, Van Cutsem E, Feyereislova A, Chung HC, Shen L, Sawaki A, Lordick F, Ohtsu A, Omuro Y, Satoh T. Trastuzumab in combination with chemotherapy versus chemotherapy alone for treatment of HER2-positive advanced gastric or gastro-oesophageal junction cancer (ToGA): a phase 3, open-label, randomised controlled trial. Lancet. 2010;376:687-697.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 4615]  [Cited by in F6Publishing: 5048]  [Article Influence: 360.6]  [Reference Citation Analysis (1)]
64.  Koizumi W, Narahara H, Hara T, Takagane A, Akiya T, Takagi M, Miyashita K, Nishizaki T, Kobayashi O, Takiyama W. S-1 plus cisplatin versus S-1 alone for first-line treatment of advanced gastric cancer (SPIRITS trial): a phase III trial. Lancet Oncol. 2008;9:215-221.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1320]  [Cited by in F6Publishing: 1387]  [Article Influence: 86.7]  [Reference Citation Analysis (0)]
65.  Kim R, Tan A, Choi M, El-Rayes BF. Geographic differences in approach to advanced gastric cancer: Is there a standard approach? Crit Rev Oncol Hematol. 2013;88:416-426.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 25]  [Cited by in F6Publishing: 33]  [Article Influence: 3.0]  [Reference Citation Analysis (0)]
66.  Schwarz RE, Zagala-Nevarez K. Ethnic survival differences after gastrectomy for gastric cancer are better explained by factors specific for disease location and individual patient comorbidity. Eur J Surg Oncol. 2002;28:214-219.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 36]  [Cited by in F6Publishing: 41]  [Article Influence: 1.9]  [Reference Citation Analysis (0)]
67.  Ma BB, Hui EP, Mok TS. Population-based differences in treatment outcome following anticancer drug therapies. Lancet Oncol. 2010;11:75-84.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 97]  [Cited by in F6Publishing: 109]  [Article Influence: 7.8]  [Reference Citation Analysis (0)]
68.  Hu Y, Fang JY, Xiao SD. Can the incidence of gastric cancer be reduced in the new century? J Dig Dis. 2013;14:11-15.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 16]  [Cited by in F6Publishing: 23]  [Article Influence: 2.1]  [Reference Citation Analysis (0)]
69.  Tural D, Selçukbiricik F, Serdengeçti S, Büyükünal E. A comparison of patient characteristics, prognosis, treatment modalities, and survival according to age group in gastric cancer patients. World J Surg Oncol. 2012;10:234.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 9]  [Cited by in F6Publishing: 12]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
70.  Kato M, Asaka M. Recent development of gastric cancer prevention. Jpn J Clin Oncol. 2012;42:987-994.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 31]  [Cited by in F6Publishing: 41]  [Article Influence: 3.4]  [Reference Citation Analysis (0)]