- Research article
- Open Access
- Open Peer Review
Esophageal cancer risk by type of alcohol drinking and smoking: a case-control study in Spain
© Vioque et al; licensee BioMed Central Ltd. 2008
- Received: 25 February 2008
- Accepted: 01 August 2008
- Published: 01 August 2008
The effect of tobacco smoking and alcohol drinking on esophageal cancer (EC) has never been explored in Spain where black tobacco and wine consumptions are quite prevalent. We estimated the independent effect of different alcoholic beverages and type of tobacco smoking on the risk of EC and its main histological cell type (squamous cell carcinoma) in a hospital-based case-control study in a Mediterranean area of Spain.
We only included incident cases with histologically confirmed EC (n = 202). Controls were frequency-matched to cases by age, sex and province (n = 455). Information on risk factors was elicited by trained interviewers using structured questionnaires. Multiple logistic regression was used to estimate adjusted odds ratios and 95% confidence intervals (CI).
Alcohol drinking and tobacco smoking were strong and independent risk factors for esophageal cancer. Alcohol was a potent risk factor with a clear dose-response relationship, particularly for esophageal squamous-cell cancer. Compared to never-drinkers, the risk for heaviest drinkers (≥ 75 g/day of pure ethanol) was 7.65 (95%CI, 3.16–18.49); and compared with never-smokers, the risk for heaviest smokers (≥ 30 cigarettes/day) was 5.07 (95%CI, 2.06–12.47). A low consumption of only wine and/or beer (1–24 g/d) did not increase the risk whereas a strong positive trend was observed for all types of alcoholic beverages that included any combination of hard liquors with beer and/or wine (p-trend<0.00001). A significant increase in EC risk was only observed for black-tobacco smoking (2.5-fold increase), not for blond tobacco. The effects for alcohol drinking were much stronger when the analysis was limited to the esophageal squamous cell carcinoma (n = 160), whereas a lack of effect for adenocarcinoma was evidenced. Smoking cessation showed a beneficial effect within ten years whereas drinking cessation did not.
Our study shows that the risk of EC, and particularly the squamous cell type, is strongly associated with alcohol drinking. The consumption of any combination of hard liquors seems to be harmful whereas a low consumption of only wine may not. This may relates to the presence of certain antioxidant compounds found in wine but practically lacking in liquors. Tobacco smoking is also a clear risk factor, black more than blond.
- Smoking Cessation
- Esophageal Cancer
- Tobacco Smoking
- Alcohol Drinking
- Heavy Drinker
Most epidemiological studies have identified tobacco smoking and alcohol drinking as the main risk factors for esophageal squamous-cell carcinoma or unspecified esophageal cancer [1–3], usually with a monotonic and strong dose-response relationship . The evidence that high alcohol consumption increases the risk of cancer of the esophagus is quite convincing at present; most of it suggests that it is the amount of alcohol consumed, rather than the particular drink that determines the risk. However, a prospective cohort study in Denmark observed that low wine consumption, compared to beer and hard liquor, did not increase risk . Two population-based case-control studies also presented data supporting this observation [6, 7]. In an ecological study in Spain, trends of per capita consumption of beer, spirits, and total alcohol consumption were positively correlated with oesophageal cancer mortality in men whereas wine consumption showed no relationship with oesophageal cancer mortality either in men or women. As the consumption of all types of alcoholic drinks is quite prevalent in Spain, it is relevant to assess the risk of esophageal cancer in relation to them.
Tobacco smoking has also a clear role in the aetiology of esophageal cancer [1, 2]. Despite the high prevalence of consumption, particularly of black tobacco, an association between the type of tobacco smoking and esophageal cancer has never been explored by epidemiological studies in Spain, only in South America or France[4, 9].
In addition to smoking and alcohol, other factors such as a low socioeconomic status, an infrequent consumption of fruits and vegetables and, in some areas of Asia, the betel nut chewing, have also been related to esophageal cancer [10–13]; these factors account for a high proportion of cases, particularly for the esophageal squamous cell type, the most frequent histological type [11, 12, 14].
We conducted a case-control study in Valencia and Alicante, Spain, to estimate the independent effects of different alcoholic beverages (beer, wine and spirits) and type of tobacco smoking (black and blond) on the risk of esophageal cancer and its main histological cell type (squamous cell carcinoma).
This research was part of the PANESOES project, a prospective hospital-based case-control study designed to explore the influence of major lifestyles and diet on the risk of three gastrointestinal cancers, pancreas, oesophagus and stomach. The PANESOES Study aimed to recruit approximately 200 cases for oesophagus, 200 for pancreas cancer, 400 cases for stomach cancer, and 400–450 controls. This sample size was planned to estimate as statistically significant (p < 0.05) a RR over 1.5 for stomach cancer and high prevalent exposures such as tobacco smoking and alcohol drinking, and a RR over 1.8 for oesophagus and pancreas cancer.
Eligible subjects were Spanish-speaking men and women 30–80 years old, and hospitalized between January 1995 and March 1999 in any of nine participant hospitals in the provinces of Alicante and Valencia. These nine hospitals are among the ten main hospitals from the Health Care Service in Valencia and Alicante that were invited to participate (only one hospital in Valencia declined participation). The access to the Health Care System in Spain is free and universal; thus, our case series may be considered representative as the participant hospitals accounted for approximately 90% of cases in both provinces.
All subjects were informed of the study objectives and gave their informed consent before the interview. Research protocols were approved by the local ethics and/or research committees of the participating Hospitals and the University.
Cases were patients newly diagnosed with a primary invasive cancer of the oesophagus. Pathology reports were obtained for all case patients initially diagnosed as esophageal cancer, and final inclusion in the case series was based on histological confirmation. A total of 211 cases were initially identified as eligible for participation; two cases refused interview (0.9%), and seven cases were not finally confirmed (3.3%). The final analysis was thus based on 202 cases. The pathological diagnosis was confirmed as squamous cell carcinoma in 160 cases (79.2%) and adenocarcinoma in 42 cases (20.8%).
Control subjects were selected from the same hospitals from which cases were identified and during the same period. Controls were frequency matched to the expected distribution of case subjects of the whole PANESOES study (i.e. cases of oesophagus, stomach and pancreas, and controls) by three age groups (<60 years, 60–69 and 70–80 years), sex, and province (Alicante and Valencia). A wide inclusion criterion was used to select controls from diseases not related a priori to the main exposures of interest (tobacco, alcohol and diet). The overall participation rate of the 457 eligible controls was 99.6%, leaving 455 controls subjects with completed interviews. The distribution of the main diagnoses for the control group was, in decreasing order: hernia (34.0%), degenerative osteoarthritis/arthritis (21.3%), fractures/injuries/orthopaedic processes (18.9%), appendicitis (6.4%) and other, less prevalent, conditions (19.3%).
Face-to-face interviews were conducted in-hospital for all participants by trained interviewers, using a structured questionnaire. Interviews were administered directly to the study subjects, rather than to the next of kin, for 89.2% of the target case subjects and for 96% of the target control subjects. The average time required to complete the questionnaire was 40 minutes. While interviewers could not be blinded to the case/control status, they were unaware of the main study hypothesis and were trained to administer strictly the structured questionnaires in an equal manner to case and controls.
Information was collected on demographic characteristics, tobacco and alcohol use, medical history and other lifestyle factors. The interview elicited details on usual tobacco use, including the product/tobacco type (black or blond cigarettes, cigars, pipes) as well as intensity of use, the age at which the habit started and stopped, the total duration of use excluding the years stopped, the years since last use for each type of product, and the level of inhalation when smoking (partially or totally). A never smoker was defined as someone having smoked fewer than 100 cigarettes ever or less than one cigarette per day for one year. A former smoker was defined as someone having stopped smoking 1 or more years before the interview. We computed the average number of cigarettes smoked per day including type of tobacco smoked, lifetime number of cigarettes smoked and pack-years of smoking (number of 20-cigarette packs per day multiplied by number of years smoking). Only 2 cases and 8 controls simultaneously smoked both blond and black tobacco, and they were considered as mainly blond tobacco smokers.
Alcohol consumption patterns were assessed through inquiries into the usual intake for each type of beverage separately, i.e. beer, wine, or liquor. Since the intake of only wine and/or beer intake was uncommon among cases, these two alcoholic beverages were combined in the analysis. Since only 8 participants consumed liquors but not beer or wine, we estimated a category for the combined consumption of liquors with any combination of beer and/or wine (All types of beverages). The average relative contributions of beer, wine and liquor consumption in this category were 30%, 50% and 20% respectively. The three types of alcohol were also combined to give an overall estimate of the alcohol consumption. A never drinker was defined as having consumed less than one drink per month. One drink was defined as 200 cc of beer, 125 cc of wine, or 50 cc of hard liquor. The content of pure alcohol was calculated according to the following concentrations specific for Spain: 5% for beer; 12 percent for wine; and 40 percent for hard liquors. The resulting values were converted to grams multiplying 1 ml of pure ethanol per 789 mg . The average in grams of pure ethanol consumed per day, type of alcoholic beverage, and life time duration of the habit, the age at starting and stopping the habit, and then the years since quitting drinking were also estimated. A former drinker was defined as having stopped drinking 1 or more years before the interview.
The fruit and vegetable intake was assessed by a food frequency questionnaire (FFQ). For this study, we adapted and validated a FFQ of 93 food items similar to the Harvard questionnaire in order to assess the diet five years before the interview in the hospital [16–18]. Participants were asked to report their average consumption of 12 vegetables and 10 fruit items. The average daily intakes for each fruit and vegetable were summed to compute the total fruit and vegetable intake in grams, and they were adjusted for energy intake using the residual method . We further computed tertiles of energy-adjusted intake of fruit and vegetable using the distribution of cases and controls in the whole PANESOES study (cases of oesophagus, stomach and pancreas, and controls).
We used unconditional logistic regression to estimate odds ratios (OR), as an estimate of relative risk, and corresponding 95% confidence intervals (CIs) . All regression models included as covariates the three frequency-matched factors, sex (men/women), age (<60 years, 60–69 years, 70–80 years) and hospital origin (Valencia/Alicante) entered as indicator variables; the educational level (<primary, primary completed, and ≥ secondary school entered as indicator variable); and the different variables of alcohol intake and tobacco smoking also using indicator variables. In addition, we adjusted for a potential confounding effect of fruit and vegetable intake (in tertiles and entered as indicator variables), and energy intake.
Tests for trend in the ORs across exposure strata were calculated for ordinal variables by using logistic models that included categorical terms as continuous variables in a model with all the potential confounders and, where appropriate, omitting the never or former users/exposed. For trend-tests, we used the likelihood ratio test statistic with one degree of freedom. Although the study sample size did not allow us to estimate tests of interactions, we performed exploratory analyses for the effects of alcohol and tobacco by strata of never-ever smoking status and never-ever drinking status, respectively. All analyses were performed with STATA-8 . Statistical significance was set at 0.05. All reported P values are from two-sided tests.
Distribution of socio-demographic characteristics and other exposure variables among case and control subjects
<60 years old
60–69 years old
≥ 70 years old
Fruit and Vegetable daily intake (in tertile)
< 166 g/d
Adjusteda odds ratios (OR) for esophageal cancer, and esophageal squamous-cell carcinoma, according to alcohol consumption
No. of controls
All esophageal cancer cases
Esophageal squamous-cell carcinoma cases
Alcohol Drinking Status
(1.24 – 4.71)
(2.05 – 13.91)
(1.92 – 9.56)
(3.73 – 32.62)
(1.04 – 4.08)
(1.69 – 11.83)
Average of pure ethanol (g/day)
(2.43 – 12.00)
(5.34 – 48.07)
(0.54 – 2.49)
(0.56 – 5.20)
(1.29 – 6.48)
(2.64 – 24.40)
≥ 75 g/d
(3.16 – 18.49)
(7.19 – 74.90)
p-value for linear trend
Type of drink (g/day)
(0.49 – 2.91)
(0.56 – 6.64)
(1.06 – 8.90)
(2.13 – 29.92)
Only wine and/or beer
(0.59 – 3.47)
(0.73 – 88.46)
All types of beverages
(2.08 – 9.22)
(4.17 – 34.56)
(2.47 – 12.27)
(5.53 – 50.67)
Wine and/or Beer 1–24 g/d
(0.45 – 2.41)
(0.43 – 5.05)
Wine and/or Beer ≥ 25 g/d
(0.76 – 5.46)
(1.52 – 19.71)
All types 1–24 g/d
(0.58 – 4.01)
(0.62 – 9.86)
All types ≥ 25 g/d
(2.59 – 12.83)
(5.68 – 52.21)
All types 25–74 g/d
(1.64 – 9.15)
(3.26 – 33.64)
All types ≥ 75 g/d
(4.14 – 27.24)
(10.28 – 119.31)
p-value for linear trend
Years of alcohol drinking
(1.37 – 12.00)
(2.08 – 32.32)
(1.42 – 6.14)
(2.27 – 17.35)
(0.80 – 3.61)
(1.41 – 11.24)
p-value for linear trend
Age at starting
(0.88 – 4.27)
(0.29 – 1.37)
(0.53 – 2.02)
(0.34 – 2.02)
≥ 30 yr
(0.86 – 3.40)
(0.36 – 2.29)
Years since quitting
(1.34 – 9.69)
(2.01 – 17.25)
≥ 5 yr
(0.86 – 3.41)
(0.79 – 3.66)
Regarding duration of drinking, statistically significant increased risks were observed for up to 40 years of drinking, after which no significant increase was observed (Table 2). Age at start drinking was not significantly associated to a higher risk of esophageal cancer. Drinking cessation in the last 5 years was associated with a strong risk excess compared with persistent drinkers (OR = 3.60, 95% CI 1.34–9.69); the risk decreased thereafter although still remained higher than in current drinkers.
Table 2 also shows the estimated ORs according to various patterns of alcohol intake specifically for the esophageal squamous-cell carcinoma histological type (n = 160 cases). Most effects were approximately 3 times higher than risk estimates for the whole case series (n = 202 cases). The effects of all types of alcoholic beverages, were in general 2 to 4-fold higher than those observed for drinkers of only wine and/or beer. The highest risk of esophageal cancer was observed among cases with an average daily intake of pure ethanol ≥ 75 g/d (OR = 23.20, 95% CI: 7.19–74.90), and particularly for those consuming ≥ 75 g/d of all types of alcoholic beverages (OR = 35.03, 95% CI: 10.28–119.31). No significant effects were observed for only wine or beer drinkers 1–24 g/d.
Adjusteda odds ratios (OR) for esophageal cancer, and esophageal squamous-cell carcinoma, according to tobacco smoking
No. of controls
All esophageal cancer cases
Esophageal squamous-cell carcinoma cases
(1.06 – 4.23)
(0.72 – 4.03)
(0.76 – 3.40)
(0.43 – 2.73)
(1.26 – 5.28)
(0.95 – 5.51)
Average No. of cigarettes/day
(0.79 – 3.57)
(0.45 – 2.99)
(0.63 – 4.58)
(0.41 – 4.48)
(1.11 – 5.44)
(0.78 – 5.42)
(2.06 – 12.47)
(1.96 – 17.23)
(0.41 – 6.21)
(0.30 – 7.46)
p-value for linear trend
Years of cigarette smoking
(0.69 – 4.59)
(0.12 – 2.11)
(0.81 – 4.63)
(0.57 – 4.65)
(1.10 – 4.58)
(0.84 – 4.92)
p-value for linear trend
Never smoker (0 p-y)
(0.79 – 3.55)
(0.45 – 2.95)
(0.49 – 3.47)
(0.19 – 2.51)
(1.27 – 6.19)
(0.96 – 6.51)
(1.60 – 8.95)
(1.40 – 10.99)
p-value for linear trend
Age at starting
(0.56 – 2.21)
(0.65 – 3.23)
(0.47 – 1.74)
(0.57 – 2.58)
Years since quitting
(0.29 – 1.06)
(0.20 – 0.96)
(0.35 – 1.21)
(0.23 – 1.06)
Type of tobacco
(0.50 – 2.82)
(0.28 – 2.30)
(1.23 – 5.09)
(0.85 – 4.97)
Inhalation of smoke
(0.74 – 3.07)
(0.54 – 3.25)
(1.37 – 6.06)
(1.00 – 6.46)
Our results confirm that alcohol drinking and tobacco smoking are both strong and independent risk factors for esophageal cancer in Spain. We found that heavy drinkers had higher increased risk than heavy smokers, particularly for the esophageal squamous-cell carcinoma. These results are consistent with most of the epidemiological studies carried out in Western countries and some areas of Asia [4, 11, 12, 22–25]. Other studies have found however, chewing or tobacco smoking to be a similar or even a stronger risk factor than alcohol drinking [13, 26–28] although some of these studies did not include subjects with a high consumption of alcohol [13, 26].
Regarding alcohol drinking, we found that the intensity (i.e. the average daily alcohol intake in grams of pure ethanol) was a more relevant predictor of risk than the duration of the habit. The age at which subjects started drinking was not associated with risk and the cessation of drinking was not associated with any beneficial effect even ≥ 5y after cessation. The consequences of drinking cessation has been studied less frequently than smoking cessation and results are more controversial, probably because the number of people who quit drinking is lower than those who quit smoking. A beneficial effect has been found in some studies particularly 10 years after giving up drinking [25, 29] although some studies have shown a rapid decline in risk after cessation of drinking [4, 30, 31]. On the contrary, other studies have shown either a non beneficial effect  or a higher risk among former drinkers [31, 32]. In our study we observed a statistically significant increased risk among former drinkers who stopped drinking <5y. Unfortunately, we had an insufficient number of former drinkers to explore the drinking cessation after 10 years in more detail. Although we considered as former drinkers those who reported quitting at least one year before the interview, it is possible that some of the patients were in fact heavy drinkers quitting the habit because of their disease; alternatively, it may also be possible that some heavy drinker cases misreported their habit, declaring no consumption when in fact they were still drinking and consequently exhibited a higher risk than never drinkers.
We were also interested in exploring the effect of the alcohol type since the consumption of wine, beer and spirits is quite common in Spain  and thus, it may have a great interest for public health. Most of the studies have supported the hypothesis that the amount of alcohol consumed is the determinant of the risk rather than the particular drink, however, a prospective cohort study in Denmark showed that a moderate intake of wine, compared to beer and hard liquor, did not increase the risk . Previously, two population-based case-control studies in the United States did not find an association between wine drinking and the risk of esophageal cancer [34, 35], and later, two other studies showed data supporting a lack of effect for wine drinking as well [6, 7]. Conversely, in other studies where wine was by far the most common alcoholic beverage, wine drinkers showed higher risk than those of other beverages [23, 36]. In our study, the consumption of all types of beverages that include hard liquors was a much stronger risk factor than wine and/or beer. We observed a statistically significant increased risk of EC among only beer drinkers but not among only wine or wine/beer drinkers. When the daily amount by type of beverage was considered, no increased risks were observed for a low-moderate wine-beer consumption (1–24 d/day), and a 2-fold increase risk among drinkers of ≥ 25g/d although it was not statistically significant. However, we observed a 5.76-fold increase risk among drinkers of ≥ 25 g/d of all types of beverages (risk for the combined categories of 25–74 g/d and ≥ 75 g/d of all types of beverages, table 2). A low-moderate wine-beer consumption of 1–24 g/d did not increase significantly the risk of esophageal squamous-cell carcinoma either. If the lack of effect of wine and/or beer is real, there may be some protective ingredients in wine such as resveratrol  and other antioxidants that may cause such a protective effect .
It is not clear the exact mechanisms by which alcoholic beverages induce esophageal cancer risk. An ingredient common to all beverages is ethanol although it is possible that other components or contaminants such as N-nitrosamines and urethane with carcinogenic properties may increase cancer risk. It has been shown in practically all the studies that the risks are greatest for drinkers of hard liquors which is consistent with evidence that the concentration of ethanol plays an important role in alcohol-related tumours of the upper aero-digestive tract [13, 39, 40]. Although ethanol has not been shown as carcinogenic in laboratory animals, it may act through its major metabolite, acetaldehyde, a carcinogen in animal models [41, 42]. Thus, it has been suggested that in addition to a systemic effect, ethanol can be converted to acetaldehyde in saliva and exert a promoting effect by either solubilising tobacco-specific carcinogens or enhancing their penetration into the esophageal mucosa, by nutritional deficiencies associated with heavy drinking or by other mechanisms (e.g., direct toxic or oxidative effect on the epithelial mucosa) [41, 43]. In order to explain the differential effect of alcoholic beverages it should be considered that certain compounds such as N-nitrosamines are found in liquors and to lesser extent in beer, and urethane, a potential carcinogen in experimental studies, may be found in liquor but not in beer and wine. In addition, while most of the antioxidant compounds found in wine and to some extent in beer, are almost completely lacking in spirits .
It has been also suggested that part of the effect observed for alcohol and/or tobacco smoking could be due to other factors or different lifestyles, such as a low fruit and vegetable intake . However, our data were adjusted for the intake of fruit and vegetables showing that alcohol and tobacco were strong risk factors although the risk estimates were much higher when we did not adjust for fruits and vegetables intake (data not shown). We also observed that alcohol drinking was a much stronger risk factor for squamous-cell carcinoma than for the whole control series. This finding would indirectly support the hypothesis that the effect of alcohol for adenocarcinoma may be much weaker, if any. In fact, when we estimated the risk of adenocarcinoma for wine-beer drinkers and all types of alcohol beverages with respect to never drinkers, we did not find any increase of risk (OR = 0.83 and OR = 0.97, respectively); and for former and current drinker vs never drinkers, we did not find any significant risk either (OR = 1.83 and OR 0.74, respectively). Although some studies have found slight excesses of adenocarcinoma among drinkers [34, 35, 44], most of the previous case-control studies between alcohol drinking and the risk of oesophageal adenocarcinoma have generally found no association [6, 7, 45–47]. Unfortunately, the number of adenocarcinoma cases in our study was too small (n = 42) to allow us a separate analysis in great detail. The reasons for the differential effect of alcohol drinking on oesophageal squamous cell-carcinoma and adenocarcinoma should be further examined.
Concerning tobacco smoking, the effect estimates were lower than the observed for alcohol intake although dose-response trends were still evident for the amount and the duration of smoking. Although the effect of tobacco smoking has been considered by practically all studies on esophageal cancer only a few have explored the effects by type of tobacco black/blond. The increased risk of black tobacco compared to blond tobacco is consistent with ecological studies showing a relatively high incidence of cancers of upper aero-digestive tract in southern Europe and Latin America, where this kind of tobacco is mainly consumed . Our results are consistent with other studies carried out in high-risk areas of South America [4, 49]. We observed a statistically significant effect for black tobacco but not for blond tobacco although the lack of effect for low-to-moderate blond tobacco smoking was based on a small number of cases (n = 31). It has been suggested that the higher concentrations of some carcinogenic compounds such as N-nitrosamines found in smoke of black tobacco could be a mechanism involved .
Unlike our findings for alcohol cessation, we observed a beneficial effect of cessation of smoking. Similarly to others [4, 6], we found that the risk of esophageal cancer declined within a decade of smoking cessation which may suggest that smoking could act during later stages as a promoter in the development of esophageal cancer, predominantly for the esophageal squamous-cell carcinoma.
In order to explore the joint effects of alcohol and tobacco, unfortunately we could not perform interaction tests because of the small numbers. There was evidence that the effect of both exposures were nearly multiplicative. If we accept a multiplicative effect, we could assume that the risk of being simultaneously a heavy drinker (≥ 75 g/d) and heavy smoker (>50 p/y) could be as high as 40 times that of abstainers, or even 100 times when referring to esophageal squamous-cell carcinoma.
As in other case-control studies, this study may present limitations. The sample size was small, and we could not explore interaction between tobacco and alcohol in more detail but the effects of each exposure became evident even among those non-exposed to the other. Another limitation may relate to the use of hospital controls. It is known that controls in hospital-based studies may be heavier smokers and heavier drinkers compared with general population; but we used a wide criterion to select controls from diagnosis a priori not related to the main risk factors of our study. In fact, the prevalence of drinking or smoking among control subjects was similar to that observed in the adult general population of the same sex and age composition of Alicante and Valencia, and thus it could be considered as representative of that population. The presence of other types of bias were minimized by selecting controls from the same hospital as the cases, using the same interviews and procedures in both cases and controls to avoid any differential misclassification. The strength of the associations, the existence of a dose-response, the reduction of effect after cessation, the control for other potential confounder such as education and the intake of fruits and vegetables, and the consistency with other studies would support that the study results are real, and that alcohol drinking and tobacco smoking are likely to be causally related to esophageal cancer.
In conclusion, this case-control study shows that the risk of esophagus cancer, and particularly the squamous cell type, is strongly associated with alcohol drinking. The consumption of any combination of hard liquors seems to be harmful whereas a low consumption of only wine may not. Tobacco smoking is also a strong risk factor, black more than blond. Smoking cessation was shown a beneficial effect within ten years whereas drinking cessation was not. A possible differential effect of alcohol drinking on oesophageal squamous cell-carcinoma (harmful) and adenocarcinoma (no effect) should be further examined.
Funded by the Spanish Ministry of Health (Instituto Salud Carlos III FIS 91/0435, CIBERESP), and the Generalitat Valenciana (CTGCA/2002/06; G03/136). We would like to appreciate the writing assistance provided by Mr. Jonathan Whitehead.
We would like to acknowledge all members of PANESOES Study Group for their contribution to the selection of the study participants and the provision of information for them: Jesus Vioque (principal investigator and coordinator of the study), Esperanza Ponce, María Guillén, Miguel Santibáñez, Xavier Barber Departamento de Salud Pública, Universidad Miguel Hernández, Elche-Alicante, Spain; Miguel Bixquert, Jorge Alonso, Vicente Cervera, Remedios Giner, Juan Ruiz, Carlos Sanchos-Aldás, Javier Arenas, Hospital Arnau Vilanova de Valencia; Joaquin Berenguer, Teresa Sala, Sonia Pascual, Liria Argüello, Marco Bustamante, Salvador Sancho, Constantino Herranz, Jorge Aparicio, Dr. Baixauli, Jorge Mir, Pedro Sendrá, Hospital La Fe de Valencia; Enrique Medina, Alicia Tomé, Luis Ferrer, Ramón Truyenque, Luis Olabarrieta, Ricardo Fabra, Carlos Camps, Jose Maria Vicent, Hospital General de Valencia; Eduardo Moreno-Osset, Ramón Añón, José Ballester, Vicente Alfonso, Dr. Martínez-Abad, Francisco Blanes, Carmen Molins, Daniel Almenar, Santiago Olmos, Dr. Fenollosa, Hospital Doctor Peset de Valencia; Adolfo Benages-Martinez, Andrés Peña-Aldea, Dra. I. Pascual, Dr. García-Conde, Andrés Cervantes, Pilar Azagra, Dr. Lledó, Blas Flor, Vicente Martí, Hospital Clínico de Valencia; Miguel Pérez-Mateos, Juan Antonio Casellas, Eva Girona, Jose Ramón Aparicio, Mar López, Antonio Arroyo, Fernando Camuñas, Jesus de Anta, Hospital General de Alicante; Juan Custardoy, Concepción Martínez, Enrique Gaspar, Eduardo Muñoz, Hospital Comarcal de la Vega Baja; Alfredo Carrato, Maria Luisa Gozálvez, Rafael Calpena, Dr. Gassent, Dr. Pérez, Carlos Sillero C, Hospital General de Elche; Justo Medrano, Francisco Mauri, Marta Corona, Jorge Minguel, Hospital Universitario Sant Joan de Alicante.
- Day NE, Muñoz N: Esophagus. Cancer epidemiology and prevention. Edited by: Schottenfeld D, Fraumeni J. 1996, New York: Oxford University, 681-706.Google Scholar
- Nyrén O, Adami H: Esophageal cancer. Textbook of Cancer Epidemiology. Edited by: Adami HO, Hunter D. 2002, Oxford: Oxford University, 137-161.Google Scholar
- Enzinger P, Mayer R: Esophageal cancer. N Engl J Med. 2003, 349 (23): 2241-2252. 10.1056/NEJMra035010.View ArticlePubMedGoogle Scholar
- Castellsagué X, Muñoz N, De Stefani E, Victora C, Castelletto R, Rolón P, Quintana M: Independent and joint effects of tobacco smoking and alcohol drinking on the risk of esophageal cancer in men and women. Int J Cancer. 1999, 82 (5): 657-664. 10.1002/(SICI)1097-0215(19990827)82:5<657::AID-IJC7>3.0.CO;2-C.View ArticlePubMedGoogle Scholar
- Grønbaek M, Becker U, Johansen D, Tønnesen H, Jensen G, Sørensen T: Population based cohort study of the association between alcohol intake and cancer of the upper digestive tract. BMJ. 1998, 317 (7162): 844-847.View ArticlePubMedPubMed CentralGoogle Scholar
- Gammon M, Schoenberg J, Ahsan H, Risch H, Vaughan T, Chow W, Rotterdam H, West A, Dubrow R, Stanford J, Mayne ST, Farrow DC, Niwa S, Blot WJ, Fraumeni JF: Tobacco, alcohol, and socioeconomic status and adenocarcinomas of the esophagus and gastric cardia. J Natl Cancer Inst. 1997, 89 (17): 1277-1284. 10.1093/jnci/89.17.1277.View ArticlePubMedGoogle Scholar
- Lagergren J, Bergström R, Lindgren A, Nyrén O: The role of tobacco, snuff and alcohol use in the aetiology of cancer of the oesophagus and gastric cardia. Int J Cancer. 2000, 85 (3): 340-346. 10.1002/(SICI)1097-0215(20000201)85:3<340::AID-IJC8>3.0.CO;2-N.View ArticlePubMedGoogle Scholar
- Cayuela A, Vioque J, Bolumar F: Oesophageal cancer mortality: relationship with alcohol intake and cigarette smoking in Spain. J Epidemiol Community Health. 1991, 45 (4): 273-276.View ArticlePubMedPubMed CentralGoogle Scholar
- Launoy G, Milan C, Faivre J, Pienkowski P, Gignoux M: Tobacco type and risk of squamous cell cancer of the oesophagus in males: a French multicentre case-control study. Int J Epidemiol. 2000, 29 (1): 36-42. 10.1093/ije/29.1.36.View ArticlePubMedGoogle Scholar
- Vainio H, Weiderpass E: Fruit and vegetables in cancer prevention. Nutr Cancer. 2006, 54 (1): 111-142. 10.1207/s15327914nc5401_13.View ArticlePubMedGoogle Scholar
- Brown L, Hoover R, Silverman D, Baris D, Hayes R, Swanson G, Schoenberg J, Greenberg R, Liff J, Schwartz A, Dosemeci M, Pottern L, Fraumeni JF: Excess incidence of squamous cell esophageal cancer among US Black men: role of social class and other risk factors. Am J Epidemiol. 2001, 153 (2): 114-122. 10.1093/aje/153.2.114.View ArticlePubMedGoogle Scholar
- Wu I, Lu C, Kuo F, Tsai S, Lee K, Kuo W, Cheng Y, Kao E, Yang M, Ko Y: Interaction between cigarette, alcohol and betel nut use on esophageal cancer risk in Taiwan. Eur J Clin Invest. 2006, 36 (4): 236-241. 10.1111/j.1365-2362.2006.01621.x.View ArticlePubMedGoogle Scholar
- Znaor A, Brennan P, Gajalakshmi V, Mathew A, Shanta V, Varghese C, Boffetta P: Independent and combined effects of tobacco smoking, chewing and alcohol drinking on the risk of oral, pharyngeal and esophageal cancers in Indian men. Int J Cancer. 2003, 105 (5): 681-686. 10.1002/ijc.11114.View ArticlePubMedGoogle Scholar
- Engel L, Chow W, Vaughan T, Gammon M, Risch H, Stanford J, Schoenberg J, Mayne S, Dubrow R, Rotterdam H, West AB, Blaser M, Blot WJ, Gail MH, Fraumeni JF: Population attributable risks of esophageal and gastric cancers. J Natl Cancer Inst. 2003, 95 (18): 1404-1413.View ArticlePubMedGoogle Scholar
- IARC working group on the evaluation of carcinogenic risks to humans: IARC monographs on the evaluation of carcinogenic risks to humans. Alcohol drinking. 1988, Lyon, france: International Agency for Research on Cancer, 44:Google Scholar
- Willett W, Sampson L, Stampfer M, Rosner B, Bain C, Witschi J, Hennekens C, Speizer F: Reproducibility and validity of a semiquantitative food frequency questionnaire. Am J Epidemiol. 1985, 122 (1): 51-65.PubMedGoogle Scholar
- Vioque J, Gonzalez L: Validity of a food frequency questionnaire (preliminary results). Eur J Cancer Prev. 1991, 1: 19-20. 10.1097/00008469-199110001-00029.View ArticleGoogle Scholar
- Vioque J: Validez de la evaluación de la ingesta dietética. Nutrición y Salud Pública Métodos, bases científicas y aplicaciones. Edited by: Serra-Majem L Aranceta J. 2006, Barcelona: Masson-Elservier, 199-210.Google Scholar
- Willett W: Reproducibility and validity of food-frecuency questionnaires. Nutritional Epidemiology. Edited by: Willett W. 1998, New York: Oxford University, 101-147.View ArticleGoogle Scholar
- Breslow N, Day N: Statistical methods in cancer research. The analysis of case-control studies. IARC Sci Publ. 1980, I: 5-338.Google Scholar
- Stata Statistical Sofware: STATA 8.2. 2005, College Station, TX: Stata CorporationGoogle Scholar
- Garidou A, Tzonou A, Lipworth L, Signorello L, Kalapothaki V, Trichopoulos D: Life-style factors and medical conditions in relation to esophageal cancer by histologic type in a low-risk population. Int J Cancer. 1996, 68 (3): 295-299. 10.1002/(SICI)1097-0215(19961104)68:3<295::AID-IJC5>3.0.CO;2-X.View ArticlePubMedGoogle Scholar
- Zambon P, Talamini R, La Vecchia C, Dal Maso L, Negri E, Tognazzo S, Simonato L, Franceschi S: Smoking, type of alcoholic beverage and squamous-cell oesophageal cancer in northern Italy. Int J Cancer. 2000, 86 (1): 144-149. 10.1002/(SICI)1097-0215(20000401)86:1<144::AID-IJC23>3.0.CO;2-B.View ArticlePubMedGoogle Scholar
- Takezaki T, Shinoda M, Hatooka S, Hasegawa Y, Nakamura S, Hirose K, Inoue M, Hamajima N, Kuroishi T, Matsuura H, Tajima K: Subsite-specific risk factors for hypopharyngeal and esophageal cancer (Japan). Cancer Causes Control. 2000, 11 (7): 597-608. 10.1023/A:1008909129756.View ArticlePubMedGoogle Scholar
- Lee C, Lee J, Wu D, Hsu H, Kao E, Huang H, Wang T, Huang M, Wu M: Independent and combined effects of alcohol intake, tobacco smoking and betel quid chewing on the risk of esophageal cancer in Taiwan. Int J Cancer. 2005, 113 (3): 475-482. 10.1002/ijc.20619.View ArticlePubMedGoogle Scholar
- Kjaerheim K, Gaard M, Andersen A: The role of alcohol, tobacco, and dietary factors in upper aerogastric tract cancers: a prospective study of 10,900 Norwegian men. Cancer Causes Control. 1998, 9 (1): 99-108. 10.1023/A:1008809706062.View ArticlePubMedGoogle Scholar
- Ishikawa A, Kuriyama S, Tsubono Y, Fukao A, Takahashi H, Tachiya H, Tsuji I: Smoking, alcohol drinking, green tea consumption and the risk of esophageal cancer in Japanese men. J Epidemiol. 2006, 16 (5): 185-192. 10.2188/jea.16.185.View ArticlePubMedGoogle Scholar
- Wu M, Zhao J, Hu X, Wang P, Qin Y, Lu Y, Yang J, Liu A, Wu D, Zhang Z, Frans KJ, van 't Veer P: Association of smoking, alcohol drinking and dietary factors with esophageal cancer in high- and low-risk areas of Jiangsu Province, China. World J Gastroenterol. 2006, 12 (11): 1686-1693.View ArticlePubMedPubMed CentralGoogle Scholar
- Launoy G, Milan C, Faivre J, Pienkowski P, Milan C, Gignoux M: Alcohol, tobacco and oesophageal cancer: effects of the duration of consumption, mean intake and current and former consumption. Br J Cancer. 1997, 75 (9): 1389-1396.View ArticlePubMedPubMed CentralGoogle Scholar
- La Vecchia C, Negri E: The role of alcohol in oesophageal cancer in non-smokers, and of tobacco in non-drinkers. Int J Cancer. 1989, 43 (5): 784-785. 10.1002/ijc.2910430507.View ArticlePubMedGoogle Scholar
- Cheng K, Duffy S, Day N, Lam T, Chung S, Badrinath P: Stopping drinking and risk of oesophageal cancer. BMJ. 1995, 310 (6987): 1094-1097.View ArticlePubMedPubMed CentralGoogle Scholar
- Rolón P, Castellsagué X, Benz M, Muñoz N: Hot and cold mate drinking and esophageal cancer in Paraguay. Cancer Epidemiol Biomarkers Prev. 1995, 4 (6): 595-605.PubMedGoogle Scholar
- Vioque J, Quiles J: Encuesta de Nutrición y salud de la Comunidad Valenciana. 2003, Alicante; Universidad Miguel HernandezGoogle Scholar
- Brown L, Silverman D, Pottern L, Schoenberg J, Greenberg R, Swanson G, Liff J, Schwartz A, Hayes R, Blot W: Adenocarcinoma of the esophagus and esophagogastric junction in white men in the United States: alcohol, tobacco, and socioeconomic factors. Cancer Causes Control. 1994, 5 (4): 333-340. 10.1007/BF01804984.View ArticlePubMedGoogle Scholar
- Vaughan T, Davis S, Kristal A, Thomas D: Obesity, alcohol, and tobacco as risk factors for cancers of the esophagus and gastric cardia: adenocarcinoma versus squamous cell carcinoma. Cancer Epidemiol Biomarkers Prev. 1995, 4 (2): 85-92.PubMedGoogle Scholar
- La Vecchia C, Franceschi S, Favero A, Talamini R, Negri E: Alcohol intake and cancer of the upper digestive tract. Pattern of risk in Italy is different from that in Denmark. BMJ. 1999, 318 (7193): 1289-1290. author reply 1291View ArticlePubMedGoogle Scholar
- Jang M, Cai L, Udeani G, Slowing K, Thomas C, Beecher C, Fong H, Farnsworth N, Kinghorn A, Mehta R, Moon RC, Pezzuto JM: Cancer chemopreventive activity of resveratrol, a natural product derived from grapes. Science. 1997, 275 (5297): 218-220. 10.1126/science.275.5297.218.View ArticlePubMedGoogle Scholar
- German J, Walzem R: The health benefits of wine. Annu Rev Nutr. 2000, 20: 561-593. 10.1146/annurev.nutr.20.1.561.View ArticlePubMedGoogle Scholar
- Blot W: Alcohol and cancer. Cancer Res. 1992, 52 (7 Suppl): 2119s-2123s.PubMedGoogle Scholar
- Huang W, Winn D, Brown L, Gridley G, Bravo-Otero E, Diehl S, Fraumeni JJ, Hayes R: Alcohol concentration and risk of oral cancer in Puerto Rico. Am J Epidemiol. 2003, 157 (10): 881-887. 10.1093/aje/kwg055.View ArticlePubMedGoogle Scholar
- Blot W, McLaughlin J, Fraumeni JF: Esophageal Cancer. Cancer Epidemiology and Prevention. Edited by: Schottenfeld D, Fraumeni J. 2006, New York: Oxford University Press, 697-706.View ArticleGoogle Scholar
- Harris E: Association of oral cancers with alcohol consumption: exploring mechanisms. J Natl Cancer Inst. 1997, 89 (22): 1656-1657. 10.1093/jnci/89.22.1656.View ArticlePubMedGoogle Scholar
- Castellsagué X, Quintana M, Martínez M, Nieto A, Sánchez M, Juan A, Monner A, Carrera M, Agudo A, Quer M, Muñoz N, Herrero R, Franceschi S, Bosch FX: The role of type of tobacco and type of alcoholic beverage in oral carcinogenesis. Int J Cancer. 2004, 108 (5): 741-749. 10.1002/ijc.11627.View ArticlePubMedGoogle Scholar
- Kabat G, Ng S, Wynder E: Tobacco, alcohol intake, and diet in relation to adenocarcinoma of the esophagus and gastric cardia. Cancer Causes Control. 1993, 4 (2): 123-132. 10.1007/BF00053153.View ArticlePubMedGoogle Scholar
- Levi F, Ollyo J, La Vecchia C, Boyle P, Monnier P, Savary M: The consumption of tobacco, alcohol and the risk of adenocarcinoma in Barrett's oesophagus. Int J Cancer. 1990, 45 (5): 852-854. 10.1002/ijc.2910450511.View ArticlePubMedGoogle Scholar
- Gao Y, McLaughlin J, Blot W, Ji B, Benichou J, Dai Q, Fraumeni JJ: Risk factors for esophageal cancer in Shanghai, China. I. Role of cigarette smoking and alcohol drinking. Int J Cancer. 1994, 58 (2): 192-196. 10.1002/ijc.2910580208.View ArticlePubMedGoogle Scholar
- Wu A, Wan P, Bernstein L: A multiethnic population-based study of smoking, alcohol and body size and risk of adenocarcinomas of the stomach and esophagus (United States). Cancer Causes Control. 2001, 12 (8): 721-732. 10.1023/A:1011290704728.View ArticlePubMedGoogle Scholar
- Bosch F, Cardis E: Black tobacco and cancer: introducing an epidemiological review. Eur J Cancer. 1991, 27 (11): 1345-1348.View ArticlePubMedGoogle Scholar
- De Stefani E, Barrios E, Fierro L: Black (air-cured) and blond (flue-cured) tobacco and cancer risk. III: Oesophageal cancer. Eur J Cancer. 1993, 29A (5): 763-766. 10.1016/S0959-8049(05)80363-6.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2407/8/221/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.