Brief Articles
Copyright ©2009 The WJG Press and Baishideng. All rights reserved.
World J Gastroenterol. Apr 21, 2009; 15(15): 1854-1862
Published online Apr 21, 2009. doi: 10.3748/wjg.15.1854
Incidence and survival of stomach cancer in a high-risk population of Chile
Katy Heise, Enriqueta Bertran, Marcelo E Andia, Catterina Ferreccio
Katy Heise, Enriqueta Bertran, Regional Office of the Chilean Ministry of Health, Region de Los Ríos, Valdivia, 5110422, Chile
Marcelo E Andia, Radiology Department, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, 8330024, Chile
Catterina Ferreccio, Public Health Department, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, 8330073, Chile
Author contributions: Heise K designed the study, directed and conducted the data collection, processing and analysis, and wrote the first draft of the article; Bertran E collaborated in data collection and analysis; Andia ME collaborated in data analysis and review of the drafts of the manuscript; Ferreccio C participated in the study design, data analysis, and reviewed, edited and translated the final manuscript.
Correspondence to: Catterina Ferreccio, Public Health Department, School of Medicine, Pontificia Universidad Católica de Chile, Marcoleta 434, Santiago, 8330073, Chile.
Telephone: +56-2-3543038
Fax: +56-2-6331840
Received: January 8, 2009
Revised: March 13, 2009
Accepted: March 20, 2009
Published online: April 21, 2009


AIM: To study the incidence and survival rate of stomach cancer (SC) and its associated factors in a high risk population in Chile.

METHODS: The population-based cancer registry of Valdivia, included in the International Agency for Research on Cancer system, covers 356 396 residents of Valdivia Province, Southern Chile. We studied all SC cases entered in this Registry during 1998-2002 (529 cases). Population data came from the Chilean census (2002). Standardized incidence rates per 100 000 inhabitants (SIR) using the world population, cumulative risk of developing cancer before age 75, and rate ratios by sex, age, ethnicity and social factors were estimated. Relative survival (Ederer II method) and age-standardized estimates (Brenner method) were calculated. Specific survival rates (Kaplan-Meier) were measured at 3 and 5 years and survival curves were analyzed with the Logrank and Breslow tests. Survival was studied in relation to demographics, clinical presentation, laboratory results and medical management of the cases. Those variables significantly associated with survival were later included in a Cox multivariate model.

RESULTS: Between 1998 and 2002, 529 primary gastric cancers occurred in Valdivia (crude incidence rate 29.2 per 100 000 inhabitants). Most cases were male (69.0%), residents of urban areas (57.5%) and Hispanic (83.2%), with a low education level (84.5% < 8 school years). SC SIR was higher in men than women (40.8 and 14.8 respectively, P < 0.001), risk factors were low education RR 4.4 (95% CI: 2.9-6.8) and 1.6, (95% CI: 1.1-2.1) for women and men respectively and Mapuche ethnicity only significant for women (RR 2.2, 95% CI: 1.2-3.7). Of all cases, 76.4% were histologically confirmed, 11.5% had a death certificate only (DCO), 56.1% were TNM stage IV; 445 cases (84.1%) were eligible for survival analysis, all completed five years follow-up; 42 remained alive, 392 died of SC and 11 died from other causes. Specific 5-year survival, excluding cases with DCO, was 10.6% (95% CI: 7.7-13.5); 5-year relative survival rate was 12.3% (95% CI: 9.1-16.1), men 10.9% (95% CI: 7.4-15.2) and women 16.1% (95% CI: 9.5-24.5). Five-year specific survival was higher for patients aged < 55 years (17.3%), with intestinal type of cancer (14.6%), without metastasis (22.2%), tumor size < 4 cm (60.0%), without lymphatic invasion (77.1%), only involvement of the mucous membrane (100%). Statistically significant independent prognostic factors were: TNM staging, diffuse type, metastasis, supraclavicular adenopathy, palpable tumor, and hepatitis or ascites.

CONCLUSION: Social determinants are the main risk factors for SC, but not for survival. An advanced clinical stage at consultation is the main cause of poor SC survival.

Key Words: Survival analysis, Stomach neoplasms, Survival rate, Incidence, Risk factors, Gastrectomy


In 2002, stomach cancer (SC) was the fourth most common cancer in the world, with 900 937 cases and 700 349 deaths. Two-thirds of these occurred in developing countries[1]. The high risk zones encompass Asia, Eastern Europe, and the Andean region of South America, all of diverse geographical characteristics[2]. Chile, a representative of the Andean Region, presents an SC average mortality rate per 100 000 in 1990-2005 of 25.1 for men and 13.2 for women[1]. This high SC mortality has not changed in the last 20 years[3]. The existence of a population-based Cancer Registry in Valdivia[4] gave us the opportunity to measure SC incidence and survival in a middle developing country. The Cancer Registry of Valdivia was initiated in 1982 and encompasses the inhabitants of an area of 18 429 square kilometres in Southern Chile; the data are included in the International Agency for Research on Cancer (IARC) cancer reports in 5 continents[4]. The aims of this study were to measure SC incidence and risk factors and to assess SC survival.

Cancer registry of Valdivia

The cancer registry of Valdivia covers a population of 356 396 people, and encompasses a systematic review of records in private and public clinical centers, hospitals and laboratories, and death certificates to identify every cancer case or cancer death occurring among residents of the Valdivia area. To guarantee complete case-ascertainment, it includes various national databases of particular cancers, death certificates and hospital records to identify residents of Valdivia who may have been diagnosed in other regions. This allows near 100% case ascertainment verification in the catchment area.


The subjects in the study were the 535 SC cases residents of Valdivia, identified in the Cancer Registry of Valdivia between the years 1998 and 2002. Of these, 6 cases were deemed non-eligible due to lack of information, leaving 529 subjects eligible for the study (98.9% of the total cases). In calculating the survival rate, 18 cases were excluded because they had a history of a previous cancer, apart from non-melanoma skin cancer; and 66 were excluded because the only information came from a death certificate or autopsy, leaving 445 cases (84.1%) to estimate SC survival. Deaths occurring within 30 d of a surgery with curative intention (3 cases) were considered deaths from other causes[5]. Deaths from other causes were included, but censored.

Incidence and risk factors of stomach cancer

Standardized incidence rates, using the world population, cumulative risk of developing cancer before the age of 75 and rate ratios were estimated according to the methodology proposed by the IARC[6]. Population data were obtained from the National Institute of Statistics and the Chilean census of 2002[79]. The risk of developing SC was estimated by sex, age, ethnicity (considering anyone with at least one Mapuche surname to be Mapuche, and the rest of the population to be Hispanic/European), education level (0-8 years and more than 8 years of education), urban or rural residency.

Survival analysis

Relative survival was calculated following the Ederer II method[10] and age-standardized estimates were calculated using the approach proposed by Brenner et al[11]. Specific survival rates were measured at 3 and 5 years using the Kaplan-Maier method and survival curves for selected characteristics were compared using the Logrank and Breslow tests[12]. Those variables significantly associated with survival were later included in a Cox multivariate model[12]. Survival was studied in relation to demographics, clinical presentation, laboratory results and medical management of the cases. The characteristics of the tumor registered were: morphology according to the Lauren classification[13], size measured at its largest diameter, location in the stomach (fundus, body or antrum or all the stomach) and invasion of the gastric wall. Stage of the tumor was based on TNM classification system[14]. The intervals between the onset of symptoms, the diagnosis and definitive treatment were determined.

Incidence of gastric cancer

Between 1998 and 2002, 529 primary gastric cancers were detected amongst the residents of Valdivia (crude incidence rate 29.2 per 100 000 inhabitants). The majority of cases were men (69.0%), residents of urban areas (57.5%), had a low education level (84.5% had 8 or less years of schooling) and were predominantly of Hispanic origin (83.2%) (Table 1). Age of cases ranged from 27 to 94 years, being significantly lower in men than women with mean age of 66.8 years [95% confidence intervals (CI): 65.5-68.1] and 70.4 years (95% CI: 68.2-72.6), respectively. Relative risk (RR) of SC was higher among men, particularly at age 55-64 years. Mapuche ethnicity was a significant risk factor only for women (RR 2.2, 95% CI: 1.2-3.7), and low education status was a stronger risk factor for women than for men: RR 4.4, (95% CI: 2.9-6.8) and 1.6, (95% CI: 1.1-2.1), respectively; the highest differential of risk between men and women was found among cases with more than 8 years of education (RR = 7.5, P < 0.001) (Table 1).

Table 1 SIR of stomach cancer by selected characteristics, Valdivia, Chile, 1998-2002.
CharacteristicCasesMales: 365
Females: 164
Male vs female
%SIR95% CI%SIR95% CIRRP-value
All5296940.836.7-45.23114.812.1-16.72.8< 0.001
Age (yr)
< 3580.80.50.0-
45-545511.244.630.9-58.28.415.47.3-23.42.9< 0.001
55-649421.4125.797.8-153.69.623.912.2-35.65.3< 0.001
65-7416432.1291.3238.6-344.028.7100.572.1-128.92.9< 0.001
≥ 8510015.3501.4370.4-632.426.9292.2206.9-377.41.70.006
Ethnicity Mapuche891547.234.5-59.921.028.1a18.5-
Hispanic/European4408540.035.5-44.579.012.7a10.5-15.03.1< 0.001
School years
≤ 84208143.3a38.1-48.592.016.2a13.3-19.12.7< 0.001
> 8771927.6a20.5-< 0.001
Residence rural2204848.0a40.7-55.330.014.510.4-18.73.3< 0.001
Urban2975234.5a29.5-39.670.013.911.2-16.62.5< 0.001
Clinical characteristics of the cases

Weight loss and epigastric pain were the most common symptoms in patients at diagnosis, and both symptoms were significantly more common in males than females (Table 2). Signs considered to indicate poor prognosis: palpable epigastric mass, ascites or supraclavicular adenopathy, each were present in less than 15% of cases; only a palpable epigastric mass was significantly more common among females (Table 2). The main detection source was histology; only 11.5% of cases were identified by their death certificate only. The latter cases were significantly older: in those over 80, 45.5% and 15.1% were confirmed by death certificate only and histology, respectively (P < 0.001); there was also a higher proportion of women (22.6% versus 6.6%, P < 0.001) in this group.

Table 2 Clinical characteristics of the stomach cancer cases entered in the population-based cancer registry of Valdivia 1998-2002 (n = 529).
CharacteristicCasesTotal (%)Males (%)Females (%)P-value sex diff.
Sign and symptoms at diagnosis
Weight loss29455.661.143.3< 0.001
Epigastric pain28553.957.047.00.03
Gastrointestinal bleeding10820.421.418.30.42
Abdominal distension8315.714.817.70.40
Palpable epigastric mass5614.712.919.20.016
Supraclavicular adenopathy318.
Main detection source
Histological studies140476.481.365.2< 0.001
Radiological diagnosis254.
Clinical or autopsy397.
Only death certificate6111.56.622.6< 0.001
Duration of symptoms2
< 3 mo12632.935.924.20.033
3 to 6 mo9825.625.426.30.86
> 6 mo15941.538.749.50.06
Main diagnostic workout
Gastric endoscopy41279.484.667.7< 0.001
Gastric biopsy40175.880.864.6< 0.001
Computed tomography11421.622.718.9< 0.001
Staging TNM
Stage I91.
Stage II203.
Stage III5310.
Stage IV29756.158.650.60.09
Not determined15028.426.332.90.12
Histological type
Tubular adenocarcinoma14836.
Tubulopapillary adenocarcinoma358.57.611.20.25
Papillary adenocarcinoma112.
Mucinous adenocarcinoma112.
Undefined adenocarcinoma8320.222.414.00.06
Signet ring cell carcinoma7718.718.120.60.57
Non Hodgkin lymphoma61.
Neuroendocrine carcinoma41.
Other carcinoma368.
Tumor location
All stomach336.
Tobacco use34644.851.429.1< 0.001
Alcohol use33861.273.631.3< 0.001

In the majority of cases, the time interval between the beginning of symptoms and diagnosis was more than 3 mo. Early diagnoses were more frequent among men (Table 2). The main diagnostic procedures were gastric endoscopy and gastric biopsy (Table 2). At diagnosis only 5.5% of cases were in Stage I or II of the TNM classification; these earlier stages were more frequent among women (7.3%) than men (4.7%) (Table 2). The three most common histological types of SC both in men and women were: tubular adenocarcinoma (36%), undefined adenocarcinoma (20.2%) and signet ring cell carcinoma (18.7%) (Table 2). The fundus was the most frequent localization of the SC (29.9%) and the tumor location was not determined in a third of the cases. Information about tobacco or alcohol consumption was available for 65.4% and 63.9% of cases, respectively; tobacco use was declared by 51.4% of men and 29.1% of women (P < 0.001), and alcohol consumption was declared by 73.6% of men and 31.3% of women (P < 0.001) (Table 2).

Five years survival

Follow-up of the 445 cases included in the survival analysis was concluded on December 31st 2007, with 100% of the cases included in the 5-year analysis; only 42 cases remained alive, 392 cases had died of SC and 11 died from other causes. Specific survival at 5 years, including cases with a death certificate only, was 9.6% (95% CI: 6.9-12.3), excluding cases with a death certificate only, the survival was 10.6% (95% CI: 7.7-13.5); lower in men 9.8%, (95% CI: 6.5-13.1) than in women 12.9% (95% CI: 6.7-19.1). The 5-year relative survival rate, adjusted for the life expectancy of the population, was 12.3% (95% CI: 9.1-16.1), increasing the difference in survival of men 10.9% (95% CI: 7.4-15.2) and women 16.1% (95% CI: 9.5-24.5).

In univariate analysis, the significant factors for greater than 5 years survival were: younger age; Hispanic/European ethnicity; urban residency; lack of some clinical markers (supraclavicular adenopathy, palpable mass, ascites, or vomiting); gastrectomy; intestinal histological type; localized tumor (Figure 1A); size less than 4 cm, limited to the mucosa, without lymphatic invasion or metastasis; TNM stage 1 (Table 3). Tumors with proximal and distal localization had the same TNM distribution. However, tumors localized in the body had better 5-year survival than those localized to the fundus or in all the stomach, 23.0% vs 11.4% (P = 0.049) and 0% (P < 0.001), respectively; there was no statistical difference in survival between tumor location in the body and antrum (23.0% and 14.8%, P = 0.16, respectively).

Figure 1
Figure 1 Stomach cancer-specific survival in Valdivia 1998-2005. A: Tumor location; B: TNM stage classification; C: Men by TNM; D: Women by TNM.
Table 3 Factors associated with SC survival. Valdivia 1998-2002. Kaplan-Meier (n = 445 cases). Univariate analyses.
Variablen(%)3-yr survival
5-yr survival
P-value 5-yr survival
%95% CI%95% CI
Female120 (27.0)20.313.0-27.612.96.7-19.1-
Male325 (73.0)13.49.7-
Age (yr)
< 5581 (18.2)21.012.1-29.917.39.1-25.50.037
55-79300 (67.4)15.511.3-
> 8064 (14.4)6.30-12.84.20-9.7-
Ethnic group
Mapuche176 (17.1)7.31.2-13.44.40-9.2-
Hispanic369 (82.9)16.913.0-20.811.98.5-15.30.02
School years
0 to 8348 (83.6)9.16.0-
> 868 (16.4)19.710.2-
Urban248 (57.1)18.713.8-23.612.98.6-17.20.006
Rural186 (42.9)10.66.1-
Sign and symptoms at diagnosis
Supraclavicular adenopathy
Yes28 (8.0)0-0--
No321 (92.0)18.614.3-22.913.89.9-17.70.00018
Palpable mass
Yes52 (14.4)8.71.0-16.46.20-13.1-
No310 (85.6)17.813.5-
Yes47 (13.0)0-0--
No315 (87.0)18.914.5-23.313.89.9-17.00.000002
GI bleeding
Yes101 (22.7)20.112.2-
No344 (77.3)13.810.1-
Yes100 (22.5)10.34.3-
No345 (77.5)16.812.8-20.811.98.4-15.40.046
Weight loss
Yes277 (62.2)13.69.5-17.710.06.4-13.60.45
No168 (37.8)18.112.2-
Abdominal distension
Yes78 (17.5)11.54.4-
No367 (82.5)16.112.3-19.911.27.9-14.5
Yes271 (60.9)19.014.2-23.814.510.2-18.80.14
No174 (39.1)9.65.2-
Months with symptoms
< 3117 (32.3)14.98.3-
3 to 695 (26.2)17.69.9-25.314.27.1-21.30.32
> 6150 (41.4)16.610.5-22.713.78.1-19.40.30
Yes128 (28.8)44.836.0-53.633.625.1-42.10.0000001
No317 (71.2)3.51.4-5.61.30-2.6-
Surgical intention
Curative89 (42.4)50.439.9-60.938.628.3-48.90. 0000001
Palliative121 (57.6)14.45.8-
Lauren class
Intestinal220 (59.1)21.015.5-26.514.69.8-19.40.0000003
Diffuse152 (40.9)11.26.1-
Localized325 (91.0)20.015.6-24.414.610.6-18.60.004
All stomach32 (9.0)0-0--
< 4 cm16 (12.8)67.043.3-90.760.035.1-84.9-
4 to 9.9 cm71 (56.8)48.336.3-60.335.523.9-47.10.161
> 10 cm38 (30.4)29.015.6-43.421.18.1-34.10.006
Mucosa9 (7.1)100-100--
Muscle/subserosa7 (5.6)85.759.8-10071.437.9-1000.14
Serosa110 (87.3)38.229.0-47.527.218.6-35.80.003
Lymphatic invasion stage
021 (17.8)94.985.1-10077.157.3-96.9-
I36 (30.5)55.439.1-71.740.223.8-56.60.008
II33 (28.0)38.321.5-55.125.310.1-40.50.0005
III28 (23.7)10.70-22.210.70-22.20.00001
0185 (47.0)30.623.5-37.422.216.0-28.4-
1209 (53.0)2.50.3-4.71.50-3.20.0000001
I9 (2.1)100-85.759.8-100-
II18 (4.1)77.357.7-96.965.442.9-87.90.24
III53 (12.1)49.235.5-62.932.219.1-45.30.011
IV281 (64.0)3.01.0-
Unknown78 (17.8)12.34.9-19.73.80-8.30.00007

The cumulative survival curve of Stage I SC was significantly higher than Stage III, Stage IV or unknown stage (Figure 1B), and was similar in men and women (Figure 1C and D).

Multivariate survival analysis

The multivariate models only included cases with sufficient clinical data (271 cases, 69%). All cases (445) had “unknown staging” more frequently than the cases included in the multivariate models (17.8% and 8.9% respectively, P = 0.001) while their 5-year survival was lower (10.6% vs 14.1% P = 0.002). Nevertheless, all cases were similar to those included in the multivariate analysis with regard to socio-demographics and to the variables associated with survival in the univariate analysis (listed in Table 3).

In the multivariate analysis, only 6 variables maintained their statistical significance as independent prognostic factors (Table 4). TNM staging was the strongest prognostic variable, the risk of dying in the following year was 23 times higher with stage IV compared with stage I . Other factors of poor prognosis were: diffuse type, presence of metastasis, supraclavicular adenopathy, a palpable tumor and hepatitis or ascites (Table 4).

Table 4 Multivariate analysis of prognostic factors of stomach cancer survival population-based registry of Valdivia (Kaplan-Meier).
OR95% CIP-value
Staging TNM
Stage I1.0
Stage II2.770.3-23.80.35
Stage III6.870.9-50.60.06
Stage IV22.533.1-165.20.002
Lauren classification
Diffuse1.681.3-2.2< 0.001
Supraclavicular adenopathy
Palpable tumor
Hepatitis or ascites
Yes2.511.6-3.9< 0.001

We confirmed that Chile, in particular southern Chile, where Valdivia is located, has one of the highest risks of stomach cancer reported, particularly among men (SIR 40.8 per 100 000 inhabitants). This population has many factors that have been associated with SC such as poverty, a high rural population (32%), poor sanitary conditions in 43% of houses[15], high prevalence of smokers (37.4%), high alcohol consumption (alcohol dependence in the Chilean population varies from 7.2% to 14.1% among low and high socioeconomic groups and from 5.0% to 17.6% among females and males respectively)[16]; low daily consumption of fruits and vegetables (32.1%)[17]; and high prevalence of Helicobacter pylori (H pylori) infection, especially among young people[18].

We could not demonstrate an independent effect of race in the incidence of SC among men; but, for women, Mapuche ancestry was a significant risk factor (RR: 2.2, 95% CI: 1.2-3.7). Similarly low schooling was a stronger risk factor among women (RR: 4.4 and 1.6 for women and men, respectively) and the highest male/female ratio of 7.5 occurred among people with greater schooling, suggesting that behavioral or environmental factors preferentially protect women of Hispanic origin and with more years of education. In the 2003 National Health Survey of Chile, more educated women had significantly better nutritional indicators than men of high or low educational level and women of low educational level, with body mass index of 25.0 vs 27.8, 26.1 and 28.0, respectively[19]. This better nutritional status is associated with a higher intake of fruits and vegetables among these women, a protective factor for gastric cancer[20]. Also, the 2006 Quality of Life National Survey showed that women added salt to the meals before eating less frequently than men (8.5% and 10.9%, respectively)[17]. In the population, as well as in our series, smoking and alcohol consumption we less frequent in women than men. Interaction of smoking and drinking has been demonstrated to play a role in SC[21]. Plus, in Chile, H pylori infection was also 10% lower among women than men[18]. These environmental factors may interact with susceptibility factors, such as alcohol dehydrogenase polymorphisms[2224], to explain the predominance among men and also the higher frequency of this cancer in the Mapuche areas of southern Chile[18].

In this population-based study only 10.6% of SC survived the 5-year period following the detection of SC. When cases detected by death certificate only were included, the 5-year survival dropped to 9.6% (95% CI: 6.9-12.3). Previous studies based on cases detected at the hospital, reported higher survival rates of 12% to 48.9%[2527], probably due to a selection bias created at hospital admission, when cases in the advanced stages of the disease who will not benefit from medical care are referred to palliative care units. The mean age of SC in our series was similar to that reported by European population-based cancer registries[2829], and was 10 years greater than the mean age reported in hospital-based survival studies. The 5-year relative survival rate, adjusted for the life expectancy of the population, was 12.3%, half that reported in population registries in North America[30] and Europe[31], where the survival rates are between 20.1% and 25.6%. Main risk factors of this poor survival were either clinical (palpable tumor, ascites, hepatitis) or related to the tumor characteristics (stage, histological type, metastasis, nodes); there were no significant social determinants of survival. This underlines the relevance of the advanced stage at consultation of most cases. When a gastrectomy with the intention to cure was undertaken the 5-year specific survival was 38.6%, which is comparable to reports from Europe and North America in either population-based or hospital-based registries: 45% in Spain[32], 46.1% in Japan[33], 29.7% in Florence[29] and 32.6% in Côte d’Or[34]. We found that the stage of the disease was the main prognostic factor for survival as has been reported by others[26273233]. Thus, in our population the high incidence of SC was aggravated by a very late diagnosis of the disease. 11.5% of cases were never recognized by the medical system and were discovered based on death certificates, while another 20% of cases were inoperable at their first medical consultation. Only 5.5% of cases were found in stages I or II at the moment of diagnosis, lower than what has been reported in other population-based cancer registries in places with no screening programs such as Florence (36.7% of cases in stages I or II)[29] and Changle, China (30.9% in stages I or II)[35]; in Florence, where methods are the same as those in our study, a higher 5-year relative survival was reported than in our series (22.7%, 95% CI: 20.5%-24.9% and 12.3%, 95% CI: 9.1-16.1, respectively). Most cases presenting at earlier stages, stage I or II, were under age 54 in men and under age 68 in women, suggesting that in men the disease is initiated earlier or evolves faster (data not presented in the tables). Time elapsed between the onset of symptoms and medical attention, 8.4 mo, was twice as high as that reported in La Coruña, Spain[32]. Most cases (55%), exceeded the current Chilean standard of less than 45 d between first consultation and diagnosis, and 44% of operated cases exceeded the 30 d interval between diagnosis and treatment. Thus late consultation and slow medical management contributed to the high mortality of SC in this series.

In our series, there were 0.7 proximal tumors for each distal tumor, half of that described in industrialized countries such as the USA 1.46[36] or Canada 1.5[37]. Distal cancers, the majority in our series, are mostly associated with H pylori and poverty, and have a somewhat better prognosis than proximal cancers, so that the biological characteristics of the tumor did not provide a plausible explanation for our poor survival rates.

Screening of SC based on endoscopy and radiography has been shown to reduce the mortality rate in Japan[38] but not in Chile[3940]. In mid 2006, a nationwide screening program was initiated in Chile, offering endoscopic examination to patients over 40 years with dyspeptic symptoms. The usefulness of symptoms as selection criteria for endoscopy has recently been discussed by Maconi[41] because symptoms of early stage SC are highly nonspecific while warning symptoms, such as a palpable abdominal mass, represent an advanced stage of the disease. Others are proposing a combination of serological tests to screen for gastric atrophy, Helicobacter[42] plus alcohol dehydrogenase[24], followed by gastroscopy of cases that screen positive. Such a strategy would allow screening of a broad population in a short time to be followed by more invasive techniques in a much smaller group, estimated as 12% in Chile[42].

SC has a high incidence rate and a poor prognosis in the province of Valdivia. Main factors associated with poor survival were delays in obtaining medical care: time taken to seek medical care, time to be diagnosed and time to receive medical treatment; once medical care was obtained survival was comparable to other series. Current efforts to shorten these times with greater use of gastric endoscopy may improve this situation.


Stomach cancer (SC) has been the main cancer killer in the Chilean population since the 1950s. Despite important socioeconomic development of the country and improvements in health indicators, SC mortality has not decreased. To date, there are no population-based studies of SC incidence and survival in Chile which would illuminate the causes behind the high SC mortality, particularly among men. The cancer registry of Valdivia is currently the only population-based cancer registry in Chile included in the International Agency for Research on Cancer reports and is one of 10 cancer registries in Latin America. This is the first report of SC survival in the Chilean population.

Research frontiers

There have been few studies of the real magnitude of the SC problem and the characteristics of the patients who survive or die from this cancer.

Innovations and breakthroughs

The most innovative product is the exact measurement of the incidence and survival of SC using the most up-to-date statistical methods which provide data which is easily comparable among populations.


This report represents a baseline of the SC situation in Valdivia and will permit evaluation of future interventions aimed to control SC. The methods presented here can be used to analyze any other cancer covered by a cancer registry.


Incidence rate: calculated from the new occurrences of primary SC in the whole area divided by its population in the study period. Standardized incidence rate: the incidence rate adjusted by the age structure of a theoretical population, the world population, to permit direct comparisons between populations of diverse age structure. Specific survival rate: the number of cancer cases that are alive at the end of the study period divided by the person-time of cases over the period at risk of dying of SC. Relative survival rate: the specific survival rate adjusted by the life expectancy of the baseline population.

Peer review

This report presents invaluable data on SC incidence and SC survival in an area at high risk of SC in a middle developing country of Latin America. It provides information about the clinical presentation of SC cases, their socio-demographic characteristics and risk factors and prognostic factors of survival. The results indicate that a late stage at diagnoses is by far the principal explanatory factor of poor survival of SC in the area.


Peer reviewer: Dr. Mark S Pearce, Paediatric and Lifecourse Epidemiology Research Group, School of Clinical Medical Sciences, University of Newcastle, Sir James Spence Institute, Royal Victoria Infirmary, Newcastle upon Tyne, NE1 4LP, United Kingdom

1.  Ferlay J, Bray F, Pisani P, Parkin DM.  GLOBOCAN 2002: Cancer Incidence, Mortality and Prevalence Worldwide. IARC Cancer Base No. 5 version 2.0. Lyon: IARC Press 2004; .  [PubMed]  [DOI]
2.  Hamilton SR, Aaltonen LA.  Pathology and Genetics of Tumours of the Digestive System. Lyon: IARC Press 2000; 37-69 Available from: URL:  [PubMed]  [DOI]
3.  Ministerio de Salud de Chile. Anuario de estadísticas de natalidad y mortalidad 1999-2004.  Available from: URL:  [PubMed]  [DOI]
4.  Bertran E, Heise K, Jofre A. Cancer Incidence in Chile (1998-2002). Cancer Incidence in Five Continents. Lyon: IARC Press 2007;  Available from: URL:  [PubMed]  [DOI]
5.  Welch HG, Black WC. Are deaths within 1 month of cancer-directed surgery attributed to cancer? J Natl Cancer Inst. 2002;94:1066-1070.  [PubMed]  [DOI]
6.  Dos Santos I Epidemiología del cáncer: Principios y Métodos. Lyon: IARC Press, Organización Mundial de la Salud 1999; 279-295.  [PubMed]  [DOI]
7.  Instituto Nacional de Estadísticas de Chile. Estadísticas demográficas y vitales. Programa de proyecciones de la población de Chile 1990-2020. [Access on April 25, 2008].  Available from: URL:  [PubMed]  [DOI]
8.  Instituto Nacional de Estadística de Chile. Resultados generales censo de población y vivienda 2002. [Access on April 25, 2008].  Available from: URL:  [PubMed]  [DOI]
9.  Instituto Nacional de Estadística de Chile. Chile, División Político-Administrativa y Censal, 2001. [Access on April 25, 2008].  Available from: URL:  [PubMed]  [DOI]
10.  Ederer F, Axtell LM, Cutler SJ. The Relative Survival Rate: A Statistical Methodology. National Cancer Institute Monograph. 1961;6:101-121.  [PubMed]  [DOI]
11.  Brenner H, Arndt V, Gefeller O, Hakulinen T. An alternative approach to age adjustment of cancer survival rates. Eur J Cancer. 2004;40:2317-2322.  [PubMed]  [DOI]
12.  Le CT Applied Survival Analysis (Wiley Series in Probability & Mathematical Statistics). NJ: Wiley-Interscience 1997; .  [PubMed]  [DOI]
13.  Japanese Gastric Cancer Association. Japanese Classification of Gastric Carcinoma 2nd English Edition. Gastric Cancer. 1998;1:10-24.  [PubMed]  [DOI]
14.  Greene FL, Page DL Fleming ID, Fritz A, Balch CM, Haller DG, Morrow M.  American Joint Committee on Cancer Staging Manual. 6th ed. New York: Springer 2002; .  [PubMed]  [DOI]
15.  Ministerio de Planificación de Chile. Encuesta de caracterización socioeconómica nacional 2003 (CASEN). [Access on October 17, 2008].  Available from: URL:  [PubMed]  [DOI]
16.  Consejo Nacional para el Control de Estupefacientes de Chile (CONACE). Informe sobre Uso, Abuso y Dependencia al Alcohol en la Población General de Chile. 2003 [Access on February 20, 2009].  Available from: URL:  [PubMed]  [DOI]
17.  Ministerio de Salud de Chile. II Encuesta de calidad de vida y salud Chile 2006. [Access on October 17, 2008].  Available from: URL:  [PubMed]  [DOI]
18.  Ferreccio C, Rollán A, Harris PR, Serrano C, Gederlini A, Margozzini P, Gonzalez C, Aguilera X, Venegas A, Jara A. Gastric cancer is related to early Helicobacter pylori infection in a high-prevalence country. Cancer Epidemiol Biomarkers Prev. 2007;16:662-667.  [PubMed]  [DOI]
19.  Ministerio de Salud de Chile. Encuesta Nacional de Salud 2003.  Available from: URL:  [PubMed]  [DOI]
20.  De Stefani E, Correa P, Boffetta P, Deneo-Pellegrini H, Ronco AL, Mendilaharsu M. Dietary patterns and risk of gastric cancer: a case-control study in Uruguay. Gastric Cancer. 2004;7:211-220.  [PubMed]  [DOI]
21.  Sjödahl K, Lu Y, Nilsen TI, Ye W, Hveem K, Vatten L, Lagergren J. Smoking and alcohol drinking in relation to risk of gastric cancer: a population-based, prospective cohort study. Int J Cancer. 2007;120:128-132.  [PubMed]  [DOI]
22.  Terry MB, Gammon MD, Zhang FF, Vaughan TL, Chow WH, Risch HA, Schoenberg JB, Mayne ST, Stanford JL, West AB. Alcohol dehydrogenase 3 and risk of esophageal and gastric adenocarcinomas. Cancer Causes Control. 2007;18:1039-1046.  [PubMed]  [DOI]
23.  Zhang FF, Hou L, Terry MB, Lissowska J, Morabia A, Chen J, Yeager M, Zatonski W, Chanock S, Chow WH. Genetic polymorphisms in alcohol metabolism, alcohol intake and the risk of stomach cancer in Warsaw, Poland. Int J Cancer. 2007;121:2060-2064.  [PubMed]  [DOI]
24.  Yokoyama A, Yokoyama T, Omori T, Matsushita S, Mizukami T, Takahashi H, Higuchi S, Maruyama K, Ishii H, Hibi T. Helicobacter pylori, chronic atrophic gastritis, inactive aldehyde dehydrogenase-2, macrocytosis and multiple upper aerodigestive tract cancers and the risk for gastric cancer in alcoholic Japanese men. J Gastroenterol Hepatol. 2007;22:210-217.  [PubMed]  [DOI]
25.  García CC, Benavides CC, Apablaza SP, Rubilar PO, Covacevich SR, Peñaloza PM, Guerra JC, Horwitz BZ, Domancic PH, Bustamante RM. [Surgical treatment of gastric cancer: results in 423 cases]. Rev Med Chil. 2007;135:687-695.  [PubMed]  [DOI]
26.  Stambuk J. Immediate results and late survival of radical gastrectomy in 108 patients with resectable gastric cancer. Rev Chil Cir. 2006;58:420-430.  [PubMed]  [DOI]
27.  Cenitagoya GF, Bergh CK, Klinger-Roitman J. A prospective study of gastric cancer. 'Real' 5-year survival rates and mortality rates in a country with high incidence. Dig Surg. 1998;15:317-322.  [PubMed]  [DOI]
28.  Verdecchia A, Mariotto A, Gatta G, Bustamante-Teixeira MT, Ajiki W. Comparison of stomach cancer incidence and survival in four continents. Eur J Cancer. 2003;39:1603-1609.  [PubMed]  [DOI]
29.  Barchielli A, Amorosi A, Balzi D, Crocetti E, Nesi G. Long-term prognosis of gastric cancer in a European country: a population-based study in Florence (Italy). 10-year survival of cases diagnosed in 1985-1987. Eur J Cancer. 2001;37:1674-1680.  [PubMed]  [DOI]
30.  Cancer Surveillance Research Program Surveillance Epidemiology and End Results (SEER) Cancer Statistics Review 1975-2002. MD: National Cancer Institute 2005; .  [PubMed]  [DOI]
31.  Sant M, Aareleid T, Berrino F, Bielska Lasota M, Carli PM, Faivre J, Grosclaude P, Hédelin G, Matsuda T, Møller H. EUROCARE-3: survival of cancer patients diagnosed 1990-94--results and commentary. Ann Oncol. 2003;14 Suppl 5:v61-v118.  [PubMed]  [DOI]
32.  Casariego E, Pita S, Rigueiro MT, Pértega S, Rabuñal R, García-Rodeja ME, Álvarez L. Supervivencia en 2334 pacientes con cáncer gástrico y factores que modifican el pronóstico. Med Clin (Barc). 2001;117:361-365.  [PubMed]  [DOI]
33.  Nakamura K, Ueyama T, Yao T, Xuan ZX, Ambe K, Adachi Y, Yakeishi Y, Matsukuma A, Enjoji M. Pathology and prognosis of gastric carcinoma. Findings in 10,000 patients who underwent primary gastrectomy. Cancer. 1992;70:1030-1037.  [PubMed]  [DOI]
34.  Msika S, Benhamiche AM, Jouve JL, Rat P, Faivre J. Prognostic factors after curative resection for gastric cancer. A population-based study. Eur J Cancer. 2000;36:390-396.  [PubMed]  [DOI]
35.  Tian J, Wang XD, Chen ZC. Survival of patients with stomach cancer in Changle city of China. World J Gastroenterol. 2004;10:1543-1546.  [PubMed]  [DOI]
36.  Wilkinson NW, Howe J, Gay G, Patel-Parekh L, Scott-Conner C, Donohue J. Differences in the pattern of presentation and treatment of proximal and distal gastric cancer: results of the 2001 gastric patient care evaluation. Ann Surg Oncol. 2008;15:1644-1650.  [PubMed]  [DOI]
37.  MacDonald WC, Owen DA, Le N. Chronic advanced gastric cancer: clinicopathologic analysis of survival data. Hum Pathol. 2008;39:641-649.  [PubMed]  [DOI]
38.  Ogura M, Hikiba Y, Maeda S, Matsumura M, Okano K, Sassa R, Yoshida H, Kawabe T, Omata M. Mortality from gastric cancer in patients followed with upper gastrointestinal endoscopy. Scand J Gastroenterol. 2008;43:574-580.  [PubMed]  [DOI]
39.  Roder DM. The epidemiology of gastric cancer. Gastric Cancer. 2002;5 Suppl 1:5-11.  [PubMed]  [DOI]
40.  Calvo Belmar A, Pruyas M, Nilsen E, Verdugo P. [Populational research of gastric cancer in digestive symptomatic patients, from 1996 to 2000]. Rev Med Chil. 2001;129:749-755.  [PubMed]  [DOI]
41.  Maconi G, Manes G, Porro GB. Role of symptoms in diagnosis and outcome of gastric cancer. World J Gastroenterol. 2008;14:1149-1155.  [PubMed]  [DOI]
42.  Rollan A, Ferreccio C, Gederlini A, Serrano C, Torres J, Harris P. Non-invasive diagnosis of gastric mucosal atrophy in an asymptomatic population with high prevalence of gastric cancer. World J Gastroenterol. 2006;12:7172-7178.  [PubMed]  [DOI]