Next Article in Journal
Decreased Blood Asprosin in Hyperglycemic Menopausal Women as a Result of Whole-Body Cryotherapy Regardless of Metabolic Syndrome
Next Article in Special Issue
Strategies in Developing Immunotherapy for Pancreatic Cancer: Recognizing and Correcting Multiple Immune “Defects” in the Tumor Microenvironment
Previous Article in Journal
The Effect of Perioperative Pregabalin on Pain after Arthroscopic Anterior Cruciate Ligament Reconstruction: A Randomized Controlled Trial
Previous Article in Special Issue
Lung Metastases in Patients with Stage IV Pancreatic Cancer: Prevalence, Risk Factors, and Survival Impact
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
JCM
Volume 8
Issue 9
10.3390/jcm8091427
jcm-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Environmental Risk Factors of Pancreatic Cancer

by
Hui-Jen Tsai
1,2,3 and
Jeffrey S. Chang
1,*
1
National Institute of Cancer Research, National Health Research Institutes, Tainan 70456, Taiwan
2
Department of Internal Medicine, National Cheng Kung University Hospital, Tainan 70403, Taiwan
3
Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung 80756, Taiwan
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2019, 8(9), 1427; https://doi.org/10.3390/jcm8091427
Submission received: 19 August 2019 / Revised: 6 September 2019 / Accepted: 7 September 2019 / Published: 10 September 2019
(This article belongs to the Special Issue Current Standards and New Innovative Approaches for Treatment of Pancreatic Cancer)
Browse Figures
Versions Notes

Abstract

:
Despite the advancement in medical knowledge that has improved the survival rate of many cancers, the survival rate of pancreatic cancer has remained dismal with a five-year survival rate of only 9%. The poor survival of pancreatic cancer emphasizes the urgent need to identify the causes or the risk factors of pancreatic cancer in order to establish effective preventive strategies. This review summarizes the current evidence regarding the environmental (non-genetic, including lifestyle, and clinical factors) risk factors of pancreatic cancer. Based on the current evidence, the established risk factors of pancreatic cancer are cigarette smoking, chronic diabetes, and obesity. Other strong risk factors include low consumption of fruits and vegetables, excess consumption of alcohol, poor oral hygiene, and the lack of allergy history. In the future, more studies are needed to identify additional risk factors of pancreatic cancer, especially the modifiable risk factors that could be included in a public health campaign to educate the public in order to reduce the incidence of pancreatic cancer.

1. Introduction

Every year, approximately 460,000 cases (incidence rate = 4.8 per 100,000) of pancreatic cancer are diagnosed worldwide, making it the twelfth most common cancer in the world [1]. Despite advancement in medical knowledge that has improved the survival rate of many cancers, the survival rate of pancreatic cancer has remained dismal with a five-year survival rate of only 9% [2]. As a consequence, the annual number of pancreatic deaths (approximately 430,000 deaths per year with a mortality rate = 4.4 per 100,000) is almost equal to the number of incident cases, making it the cancer with the seventh highest mortality rate in the world [1]. The majority of pancreatic cancers are diagnosed at a late stage. Only 15–20% of pancreatic cancers are resectable with a five-year survival rate of approximately 20% [3,4]. In the era of gemcitabine monotherapy as the standard of systemic primary or adjuvant chemotherapy, the median overall survival (OS) of patients with metastatic, unresectable locally advanced, and resectable pancreatic ductal adenocarcinoma was 5.5–6.5, 13–15, and 22–24 months, respectively, in the randomized phase III trials [5,6,7,8,9,10]. The introduction of a more effective combination of chemotherapy regimens, the FOLFIRINOX (combination chemotherapy that includes folinic acid, fluorouracil (also known as 5FU), irinotecan, and oxaliplatin) and nab–paclitaxel plus gemcitabine combination, improves the median OS of patients with metastatic diseases to 8.5–11.0 months [11,12]. FOLFIRINOX may increase the surgical resection conversion rates and is thus associated with an overall survival of 15.1–18.5 and 21.7–37.7 months in patients with initially borderline resectable and un-resectable locally advanced diseases, respectively [13,14,15,16]. While given as an adjuvant therapy, modified FOLFIRINOX had a 54.4 months overall survival rate in patients with R0/R1 resection in the PRODIGE 24/CCTG PA.6 trial (a multicenter randomized phase III trial comparing FOLFIRINOX vs. gemcitabine as adjuvant therapy for pancreatic cancer) [17]. However, both FOLFIRINOX and nab–paclitaxel plus gemcitabine combination are associated with significant adverse neutropenia events, especially in the Asian population, as compared to gemcitabine monotherapy. The other agents for gemcitabine refractory disease, such as MM398 combined with 5FU/folinic acid or weekly 5FU/folinic acid plus oxaliplatin, are shown to prolong the OS of 1.9 or 2.6 months when compared with the patients who received weekly 5FU/folinic acid. While many other novel agents are under investigation, the overall prognosis of the advanced pancreatic cancer is poor [6,18]. The poor survival of pancreatic cancer emphasizes the urgent need to identify the causes or the risk factors associated with the development of pancreatic cancer in order to establish effective preventive strategies. Furthermore, knowing the risk factors may help identify high-risk individuals for pancreatic cancer screening in order to increase the rate of early diagnosis. The main reason for the abysmal prognosis of pancreatic cancer, in most cases, is due to late stage diagnosis, with approximately 53% showing distant metastasis and 29% having spread to the regional lymph nodes [19]. While the survival of pancreatic cancer overall is very poor, the five-year survival rate can be improved to more than 75% when the tumor is detected and removed at a size less than 10 mm [20].
Many studies have investigated the risk factors of pancreatic cancer. This review summarizes the current evidence regarding the environmental (non-genetic, including lifestyle, and clinical factors) risk factors of pancreatic cancer (Table 1). Many of the environmental risk factors, particularly the lifestyle factors, are modifiable; therefore, knowing the environmental factors influencing the risk of pancreatic cancer may provide opportunities to prevent the occurrence of pancreatic cancer.

2. Lifestyle Risk Factors of Pancreatic Cancer

2.1. Cigarette Smoking and Other Tobacco Products

Cigarette smoking is a well-recognized risk factor of pancreatic cancer. Approximately 20–25% of pancreatic cancers can be attributed to cigarette smoking [21]. A pooled analysis combined data from 12 case-control studies and reported a positive association between cigarette smoking and pancreatic cancer (former smokers: Odd ratio (OR) = 1.2, 95% confidence interval (CI): 1.0–1.3; current smokers: OR = 2.2, 95% CI: 1.7–2.8) [22]. In addition, the pooled analysis also showed that pancreatic cancer risk could be reduced to the level of never smokers after 20-years of cigarette smoking cessation [22]. Another pooled analysis combining data from eight nested case-control studies reported an increased risk of pancreatic cancer among current cigarette smokers (OR = 1.8, 95% CI: 1.4–2.3) and 15-years of smoking cessation could reduce the risk of pancreatic cancer to the level of never smokers [23]. A dose-response analysis combining data from 78 studies showed that pancreatic risk increased sharply with only a low number of cigarettes per day or just a few years of smoking [24]. The analysis also showed that pancreatic risk decreased rapidly after a few years of smoking cessation, although it may take up to 20-years for the risk to reach the level of never smokers [24]. In addition to cigarette smoking, studies with other tobacco products reported an elevated pancreatic cancer risk associated with cigar smoking, but not with pipe smoking or smokeless tobacco [25].
In contrast to the established association between active smoking and pancreatic cancer, studies on the association between environmental tobacco smoke and pancreatic cancer have been inconclusive. A meta-analysis of data from eight studies reported no significant association between environmental tobacco smoke and pancreatic cancer risk (summary relative risk (RR) = 1.23, 95% CI: 0.86–1.77) [26].

2.2. Alcohol Drinking

Studies on the association between alcohol drinking and pancreatic cancer have generated inconsistent results. A positive association was only observed at a high level of alcohol consumption. In a pooled analysis of 14 cohort studies, pancreatic cancer risk increased by approximately 20% for daily consumption of 30 or more grams of alcohol (approximately three cans of beer) (RR = 1.22, 95% CI: 1.03–1.45) [27]. A pooled analysis of 10 case-control studies reported that heavy drinking with nine or more drinks per day was associated with a significantly increased risk of pancreatic cancer (OR = 1.6, 95% CI: 1.2–2.2), while no significant association was found with light to moderate drinking (≤4 drinks/day) [28]. A meta-analysis of 19 cohort studies also found that only high alcohol intake was associated with an increased pancreatic cancer risk [29]. In many East Asian countries, 30–50% of the population carry the ALDH2*2 allele, which is associated with reduced enzyme activity, resulting in the inefficient metabolism of the carcinogenic acetaldehyde generated from ethanol metabolism. Individuals carrying the ALDH2*2 allele have a higher risk of developing alcohol-related cancers [30]. Kanda et al. found that even light to moderate alcohol drinking (<30 g day) may be associated with an increased pancreatic cancer risk among those carrying the ALDH2*2 allele [31]. This suggests that, because of the high percentage of East Asians with inefficient acetaldehyde metabolism, alcohol drinking may play a more significant role in the development of pancreatic cancer among East Asians. Due to the very limited number of studies on the effect modification of the ALDH2 polymorphism on the association between alcohol drinking and pancreatic cancer, more investigations are needed.

2.3. Diet

Numerous studies have investigated the association between diet and pancreatic cancer risk and the results have been inconsistent. Generally, diets that are rich in fruits and vegetables and other plant-based foods have been associated with a reduced pancreatic cancer risk, while dietary patterns rich in meat and animal products have been be associated with an increased pancreatic cancer risk [32,33,34,35,36]. Studies have shown that phytochemicals and dietary fibers contained in plant-based foods, including fruits, vegetables, whole grains, and nuts are beneficial in reducing the risk of cancer [37,38]. Phytochemicals, including carotenoids, phenolics, alkaloids, nitrogen-containing compounds, and organosulfur compounds, have been shown to possess anti-cancer activities [37]. These anti-cancer activities encompass a wide range of mechanisms, including antioxidant properties, anti-inflammatory action, inhibition of the growth, progression, and invasion of cancer cells, and DNA damage repair, etc. Another important component of the plant-based foods is dietary fiber [37]. A meta-analysis combining data from 13 case-control studies and one cohort study reported an inverse association between a higher intake of dietary fiber and pancreatic cancer risk (OR = 0.52, 95% CI: 0.44–0.61), and every 10 grams of daily intake of dietary fiber was associated with a 12% reduction in pancreatic cancer risk (OR = 0.88, 95% CI: 0.84–0.92) [39].

2.4. Physical Activities

Studies investigating the association between physical activities and pancreatic cancer have generated inconsistent results. A meta-analysis using data from 28 studies found that increasing the level of total and occupational activities were associated with a reduced pancreatic cancer risk [40]. However, the association did not show a dose-response relationship. The largest reduction of pancreatic cancer risk was observed for moderate activity [40]. Another meta-analysis analyzed data from 26 studies and reported that leisure time physical activity was inversely associated with pancreatic cancer risk (RR = 0.89, 95% CI: 0.82–0.96), although the inverse association only occurred in case-control studies (RR = 0.69, 95% CI: 0.59–0.81) and not in cohort studies (RR = 0.96, 95% CI: 0.91–1.02) [41]. Three subsequent studies also produced inconsistent results. A cohort study from USA found no association between physical activity and pancreatic cancer [42]. Another cohort study from Europe reported that physical activity was associated with a reduced pancreatic cancer risk among individuals younger than 60-years (hazard ratio (HR) = 0.27, 95% CI: 0.07–0.99), but not among those older than 60-years (HR = 1.23, 95% CI: 0.96–1.57) [43]. A study analyzed data from two cohort studies in China and reported a reduced pancreatic cancer risk associated with physical activities among men (HR = 0.71, 95% CI: 0.50–1.00) but not among women (HR = 1.06, 95% CI: 0.81–1.38) [44]. Overall, the role of physical activities in preventing the occurrence of pancreatic cancer is inconclusive. However, physical activity, in addition to a healthy diet, is important to prevent obesity, which is a known risk factor of pancreatic cancer. Future studies should consider investigating the interaction between physical activities and diet on the risk of pancreatic cancer. In addition, mediation analysis could be performed to determine the extent to which body weight mediates the effect physical activity has on the risk of pancreatic cancer.

2.5. Obesity

Studies have consistently found a positive association between obesity and an increased risk of pancreatic cancer. A pooled analysis of 2,170 pancreatic cancer cases and 2,209 controls reported an increased pancreatic cancer risk among individuals in the highest quartile BMI group compared to those in the lowest quartile (OR = 1.33, 95% CI: 1.12–1.58) [45]. A meta-analysis with data from 23 cohort studies showed an increased pancreatic cancer risk associated with higher BMI (RR for every five-unit increment = 1.10, 95% CI: 1.07–1.14) [46]. A pooled analysis of 20 prospective cohort studies showed that central obesity was associated with increased pancreatic cancer mortality independent of the baseline BMI [47]. Furthermore, BMI during early adulthood was associated with increased pancreatic cancer mortality later in life [47]. A pooled analysis combining data from nine Japanese cohort studies found a significantly increased pancreatic cancer risk among men, but not among women [48]. A nationwide study of 1.79 million Israeli adolescents reported that adolescent obesity (≥95th percentile) was associated with an increased pancreatic cancer risk later in life compared to normal weight (5th to <85th percentile) for both men (HR = 3.67, 95% CI: 2.52–5.34) and women (HR = 4.07, 95% CI: 1.78–9.29) [49]. The biological mechanisms underlying the association between obesity and pancreatic cancer are not well understood, but inflammation and hormonal misbalance are two possible mediators [50]. More studies are needed to decipher the biological mechanisms that could explain the association between obesity and pancreatic cancer.

2.6. Oral Health/Hygiene

Previous studies have consistently reported a significant positive association between poor oral health, including periodontal diseases and tooth loss, and an increased pancreatic cancer risk. In a meta-analysis combining data from eight studies, having periodontitis was significantly associated with an elevated pancreatic cancer risk (RR = 1.74, 95% CI: 1.41–2.15) [51]. A cohort study with 29,104 male smokers reported that tooth loss was associated with an increased pancreatic cancer risk (HR = 1.63, 95% CI: 1.09–2.46) [52]. A study with approximately 40,000 African American women also reported that tooth loss, periodontal disease, or both was associated with an increased pancreatic cancer risk [53]. Overall, studies have concurred on the positive association between poor oral health/hygiene and the risk of pancreatic cancer, although the underlying biological mechanism is yet to be elucidated.

2.7. Oral Microbiome

Poor oral health such as periodontal diseases and tooth loss may be due to an infection from oral pathogenic bacteria. Recent studies have begun to study the role of oral microbiome in the development of pancreatic cancer. Michaud et al. indirectly assessed the association between oral bacteria and pancreatic risk by analyzing the blood antibody levels for oral bacteria in a nested case-control study of 405 pancreatic cancer cases and 416 controls [54]. Their results showed that higher levels of serum antibody for P. gingivalis ATTC53978, a periodontopathogenic bacterium, were associated with an elevated pancreatic cancer risk [54]. In addition, they showed that higher levels of antibodies for commensal oral bacteria, which may inhibit the growth of the oral pathogenic bacteria, were associated with a decreased pancreatic cancer risk [54]. Fan et al. collected oral wash samples from 361 pancreatic cancer cases and 371 controls and examined the association between oral bacteria and pancreatic cancer risk by sequencing the bacterial 16S rRNA gene [55]. They reported that individuals with a carriage of oral pathogens, including P. gingivalis and A. actinomycetemcomitans, had an increased risk of pancreatic cancer [55]. A study by Olson et al. compared the oral bacteria profiles of 40 pancreatic cancer patients, 39 patients with intraductal papillary mucinous neoplasm (IPMN) (a precursor condition with an increased risk of developing into pancreatic cancer), and 58 controls [56]. They found that pancreatic cancer cases had a higher proportion of Firmicutes, whereas controls had a higher proportion of Probacteria; however, these bacteria profiles showed no correlation with measures of oral health [56]. What are the possible explanations for the positive association between oral pathogenic bacteria and pancreatic cancer?
It is possible that infection in the oral cavity may promote systemic inflammation, which may include inflammation at a distant site, such as the pancreas (Figure 1). Chronic inflammation, in turn, may promote carcinogenesis [57,58]. Alternatively, oral pathogenic bacteria may be transported to distant sites through circulation and induce local inflammation at the pancreas, leading to an increased risk of developing pancreatic cancer (Figure 1). Overall, the limited numbers of published studies have demonstrated an association between oral bacteria and pancreatic cancer risk. However, the biological role of oral bacteria in the development of pancreatic cancer is inconclusive and more investigations are needed.

2.8. Gut Microbiome

Besides oral microbiome, some researchers have also investigated the roles of gut microbiome in the development of pancreatic cancer. Ren et al. compared the gut microbial profiles of 85 pancreatic cancer patients with 57 healthy controls. They observed that some specific pathogens and lipopolysaccharides-producing bacteria were increased in the gut microbial profiles of the pancreatic cancer patients, while probiotics and butyrate-producing bacteria decreased in comparison to the healthy controls [59]. Pushalkar et al. showed the capacity of gut bacteria to migrate to the pancreas, suggesting the possibility of a direct interaction between gut bacteria and the microenvironment of the pancreas [60]. In addition, they showed that pancreatic cancer harbors more bacteria than a normal pancreas [60]. Mendez et al. observed microbial dysbiosis in the early stage of pancreatic cancer oncogenesis in the pancreatic cancer mouse model, suggesting the possibility of measuring gut microbes as biomarkers for the early detection of pancreatic cancer [61]. The current information regarding the association between gut microbiome and pancreatic cancer is very limited and more investigations are required. In addition, several of the pancreatic cancer-associated factors, including cigarette smoking, obesity, heavy alcohol drinking, diabetes, chronic pancreatitis, and allergies, have been associated with alterations in gut microbiome [62]. It would be important to determine whether gut microbiome is a mediator for these other environmental factors in the oncogenesis of pancreatic cancer or has an independent influence on the development of pancreatic cancer.

2.9. Coffee

Many studies have investigated the association between coffee and pancreatic cancer and the results have been inconsistent. Most of these studies were case-control studies that may suffer from biases of recall and control selection. Recent larger cohort studies have reported a null association between coffee consumption and pancreatic cancer. Zhou et al. analyzed the data of 309,797 never-smoking women with a median follow-up time of 13.7-years from the UK prospective Million Women Study and found no significant association between coffee drinking and pancreatic cancer risk (RR for 1–2 daily cups: 1.02, 95% CI: 0.83–1.26; RR for 3–4 daily cups: 0.96, 95% CI: 0.76–1.22; and RR for 5 or more daily cups: 0.87, 95% CI: 0.64–1.18) [63]. They further combined their data with data from three other cohort studies in a meta-analysis and reported a null association between daily drinking of two or more cups of coffee and pancreatic cancer risk (RR = 1.00, 95% CI: 0.86–1.17) [63]. Guertin analyzed data of 457,366 US adults from the US NIH-AARP Diet and Health Study with a total follow-up time of more than 4,155,256 person-years and observed no significant association between coffee consumption and pancreatic cancer risk (RR for <1 daily cup: 1.05, 95% CI: 0.85–1.30; RR for 1 daily cup: 1.06, 95% CI: 0.86–1.31; RR for 2–3 daily cups: 1.03, 95% CI: 0.85-1.25; RR for 4–5 daily cups: 1.00, 95% CI: 0.79–1.25; and RR for 6 or more daily cups: 1.24, 95% CI: 0.93–1.65) [64].

3. Clinical Risk Factors of Pancreatic Cancer

3.1. Diabetes

Diabetes is a well-established risk factor of pancreatic cancer (Figure 2). A pooled analysis combining data from 15 case-control studies showed that having diabetes for >2-years was associated with an elevated pancreatic cancer risk (OR = 1.90, 95% CI: 1.72–2.09), and the increased risk even persisted for diabetes with a duration of >20-years (OR = 1.30, 95% CI: 1.03–1.63) [65]. A meta-analysis of 23 cohort studies showed that previously diagnosed diabetes was associated with a 52% increase in pancreatic cancer risk (HR = 1.52, 95% CI: 1.43–1.63) [66]. Overall, studies have concurred that long-term diabetes is a risk factor of pancreatic cancer.
Besides being a risk factor, diabetes may also be a consequence of pancreatic cancer. Chari et al. showed that new-onset diabetes might occur as early as two-years before the diagnosis of pancreatic cancer [67] (Figure 2). A cohort study of 48,995 African Americans and Latinos showed that although both recent onset (<3-years) diabetes and long-term diabetes were associated with an increased pancreatic cancer risk, recent onset diabetes was associated with a 2.3 times greater increase in pancreatic cancer risk than long-term diabetes, thus supporting that recent onset diabetes may be an indicator for the occurrence of pancreatic cancer [68].

3.2. Chronic Pancreatitis

Studies have indicated a strong positive association between chronic pancreatitis and pancreatic cancer. A meta-analysis combining data from 13 studies showed that chronic pancreatitis was strongly associated with an increased risk of pancreatic cancer diagnosed within two-years of chronic pancreatitis (RR = 16.16, 95% CI: 12.59–20.73); however, the association diminished in strength when the lag-time between chronic pancreatitis and pancreatic cancer was set at five-years (RR = 7.90, 95% CI: 4.26–14.66) and nine-years (RR = 3.53, 95% CI: 1.69–7.38) [69], suggesting that part of the association could be due to reverse causality and the role of chronic pancreatitis in the occurrence of pancreatic cancer might be weaker than expected. It has been estimated that patients with chronic pancreatitis have only a 5% lifetime risk of developing pancreatic cancer [70]. This suggests that, although chronic pancreatitis is associated with an elevated pancreatic cancer risk, it likely only accounts for a small percentage of pancreatic cancer cases.

3.3. Allergies

Studies have often reported an inverse association between allergy and pancreatic cancer risk. In 2005, a meta-analysis combining data from 14 studies showed that having any allergic symptoms was associated with a decreased pancreatic cancer risk (RR = 0.82, 95% CI: 0.68–0.99) [71]. A pooled analysis of 10 case-control studies reported that having any allergy (OR = 0.79, 95% CI: 0.62–1.00), hay fever (OR = 0.74, 95% CI: 0.56–0.96), or allergy to animals (OR = 0.62, 95% CI: 0.41–0.94) were all associated with a lower pancreatic cancer risk [72]. A cohort study of 187,226 subjects with an average follow-up time of 16-years observed a null association between allergy and pancreatic cancer incidence (RR = 1.00, 95% CI: 0.88–1.12), although among individuals aged 70-year or older, an inverse association between allergy and pancreatic cancer incidence was reported (RR = 0.74, 95% CI: 0.56–0.98) [73]. More cohort studies are needed to confirm the association observed by the majority of case-control studies between allergy and a reduced pancreatic cancer risk. In addition, the biological mechanism underlying this inverse association needs to be deciphered in order to determine whether this can be translated into a strategy to prevent the occurrence of pancreatic cancer. Two hypotheses, the “immunosurveillance hypothesis” and the “prophylaxis hypothesis”, have been proposed to explain the inverse association between allergy and various cancers [74]. The “immunosurveillance hypothesis” states that allergy does not play a direct role in preventing the occurrence of cancer, but is merely a manifestation of an overactive immune function that has a high efficiency of surveying and eradicating cancer cells [74] (Figure 3A). In contrast, the “prophylaxis hypothesis” states that allergy is directly involved in cancer prevention because allergic reactions are the body’s method of expelling the carcinogens [74,75] (Figure 3B). How the inverse association between allergy and pancreatic cancer fits into these two hypotheses requires further investigations.

3.4. Infections

Several infections, including hepatitis B and C and Helicobacter pylori (H. pylori), have been examined in regards to their association with pancreatic cancer. A meta-analysis of eight studies reported that both hepatitis B and C infections were associated with an elevated risk of pancreatic cancer [76]. However, one subsequent cohort study from Japan reported no association between either hepatitis B or C and pancreatic cancer [77]. A retrospective cohort study from Taiwan reported a significantly increased pancreatic cancer risk associated with hepatitis B, while the association with hepatitis C was not statistically significant [78]. A case-control study from Taiwan measured the blood markers for hepatitis B and C infections among 585 pancreatic cancer cases and 1,716 controls and found no association between hepatitis B or C and the risk of pancreatic cancer after adjusting for age, sex, diabetes, and smoking [79]. In a cohort study of 12,126 patients with chronic hepatitis, hepatitis C infection was associated with a significantly higher incidence of pancreatic cancer [80]. Overall, the majority of studies suggested that hepatitis B or C infection may be associated with an increased pancreatic cancer risk.
In a meta-analysis combining data from 10 studies, H. pylori seropositivity showed no overall association with pancreatic risk; however, seropositivity for CagA-positive H. pylori was associated with a reduced pancreatic cancer risk (OR = 0.78, 95% CI: 0.67–0.91), while seropositivity for CagA-negative H. pylori was associated with an increased pancreatic cancer risk (OR = 1.30, 95% CI: 1.02–1.65) [81]. The differential risk of pancreatic cancer according to the strain of H. Pylori has yet to be confirmed by additional studies. A nested case-control study published after the meta-analysis reported seropositivities for H. pylori overall, for CagA-positive H. pylori, and for CagA-negative H. Pylori were all not associated with pancreatic cancer risk [82]. More studies on the association between the different strains of H. pylori and pancreatic cancer are needed to confirm the strain-specific association between H. pylori and pancreatic cancer.

4. Incorporation of Environmental Risk Factors for Constructing Pancreatic Cancer Risk Prediction Models

One of the important purposes of identifying the risk factors of pancreatic cancer is to construct pancreatic cancer risk prediction models to identify high-risk individuals for screening in order to increase early diagnosis and improve survival rates. Several study groups have constructed pancreatic cancer risk prediction models with environmental risk factors alone or in combination with laboratory biomarkers or genetic polymorphisms. Klein et al. constructed a pancreatic cancer prediction model based on data from 3,349 pancreatic cancer patients and 3,654 controls [83]. The variables included in their risk model were current smoking, heavy alcohol use (more than 3 drinks per day), BMI > 30 kg/m2, history of diabetes >3-years, family history of pancreatic cancer, non-O ABO genotype, and three single nucleotide polymorphisms (SNPs) (1q32 rs3790844, 5p15 rs401681, 13q22 rs9543325) [83]. The area under the curve (AUC) for their prediction model was 0.61 [83]. Risch et al. constructed a pancreatic cancer prediction model by combining data from 362 pancreatic cancer cases and 690 controls with the 2008–2010 incidence data from US surveillance epidemiology and end results [84]. Their model included current cigarette smoking, current use of proton pump-inhibitor anti-heartburn medications, recent diagnosis of diabetes, recent diagnosis of pancreatitis, Jewish ancestry, and the non-O ABO blood group [84]. They were able to calculate the five-year absolute risk of pancreatic cancer based on the different combinations of risk factors with some of the five-year risks reaching 5–10%, which may warrant pancreatic cancer screening [84]. Yu et al. constructed sex-specific pancreatic cancer prediction models using data from a cohort of 1,289,933 Korean men and 557,701 Korean women with a validation cohort of 500,046 Korean men and 627,629 Korean women [85]. The prediction model for men included age, height, BMI, fasting glucose, urine glucose, smoking, and age of smoking initiation [85]. The prediction model for women included height, BMI, fasting glucose, urine glucose, smoking, and alcohol drinking. The models showed good discrimination ability with an AUC of 0.813 for men and 0.804 for women [85]. Using data from 664 Japanese pancreatic cancer cases and 664 age and sex-matched Japanese controls, Nakatochi et al. constructed two pancreatic cancer risk prediction models with cigarette smoking, family history of pancreatic cancer, and five SNPs [86]. The full model with all seven factors had an AUC of 0.63, while the model with only the five SNPs had an AUC of 0.61, suggesting an advantage of including both environmental and genetic factors in the risk prediction model [86]. As new-onset diabetes may be a consequence of the development of pancreatic cancer, individuals with new-onset diabetes have been considered as candidates for pancreatic cancer screening. Chari et al. compared the prevalence of diabetes between 736 pancreatic cancer cases and 1,875 controls and found that the prevalence of diabetes became significantly different at three-years prior to the cases’ pancreatic cancer diagnosis [67]. This suggests that pancreatic cancer-associated diabetes may occur as early as three-years prior to the diagnosis of pancreatic cancer and screening patients with new-onset diabetes may therefore provide a sufficient window of opportunity for the early diagnosis of pancreatic cancer at an operable stage. However, because the majority of new-onset diabetes cases are type-2 diabetes, screening every new-onset diabetes case for pancreatic cancer is not cost-effective. In addition to new-onset diabetes, other risk factors or clinical parameters are needed to improve the accuracy of the pancreatic cancer prediction model. Boursi et al. constructed a pancreatic cancer prediction model using data from 109,385 new-onset diabetes patients [87]. The model, which has an AUC of 0.82, included age, BMI, change in BMI, smoking, use of proton pump inhibitors, anti-diabetic medications, and several biomarkers, including haemoglobin A1C, cholesterol, haemoglobin, creatinine, and alkaline phosphatise [87]. If the risk of developing pancreatic cancer were set at 1% over three-years of follow-up, only 6.2% of the new-onset diabetes would need to be screened for pancreatic cancer, achieving a sensitivity of 44.7%, a specificity of 94%, and a positive predictive value of 2.6% [87]. While several pancreatic cancer prediction models have been proposed, validation studies and cost-effective analysis for these models need to be performed. In the future, more investigations are needed to search for risk factors and biomarkers that may improve the accuracy of the pancreatic cancer prediction model.

5. Conclusions

Based on the current evidence, the current recommendations to reduce the risk of pancreatic cancer include cessation of cigarette smoking, diabetes control, and maintenance of an ideal body weight (Table 2 summarizes the key points for each of the environmental factors discussed in this paper). Other actions that may be beneficial for pancreatic cancer prevention include a diet rich in vegetables and fruits, good oral hygiene practice, and avoidance of excess alcohol consumption. While many studies have investigated the association between various environmental risk factors and pancreatic cancer, only a few environmental risk factors have shown strong and consistent evidence. In the future, more studies are needed to identify additional risk factors of pancreatic cancer, especially the modifiable risk factors that can be included in a public health campaign to educate the public in order to reduce the incidence of pancreatic cancer. Furthermore, the identification of additional risk factors may improve the accuracy of the pancreatic cancer risk prediction model to identify high-risk individuals for pancreatic cancer screening in order to increase the probability of early diagnosis and to improve patient outcomes.

Author Contributions

Conceptualization: H.-J.T. and J.S.C; Writing—Original Draft Preparation, H.-J.T. and J.S.C.; Writing—Review & Editing: H.-J.T. and J.S.C.; Approval of the final manuscript: H.-J.T. and J.S.C.

Funding

This work was supported by a grant from the Ministry of Science and Technology, Taiwan (105-2628-B-400 -006 -MY3).

Conflicts of Interest

The authors declare no conflicts of interest.

Abbreviations

AUCArea under the curve
CIconfidence interval;
IPMNintraductal papillary mucinous neoplasm;
HRhazard ratio;
OSoverall survival;
ORodds ratio;
RRrelative risk;
SNPSingle nucleotide polymorphism

References

  1. Cancer Today: Data visualization tool for exploring the global cancer burden in 2018. International Agency for Research on Cancer, Lyon France. 2018. Available online: http://gco.iarc.fr/today/home (accessed on 7 November 2018.).
  2. Siegel, R.L.; Miller, K.D.; Jemal, A. Cancer statistics, 2019. CA Cancer J. Clin. 2019, 69, 7–34. [Google Scholar] [CrossRef] [PubMed]
  3. Yeo, C.J.; Cameron, J.L.; Lillemoe, K.D.; Sitzmann, J.V.; Hruban, R.H.; Goodman, S.N.; Dooley, W.C.; Coleman, J.; Pitt, H.A. Pancreaticoduodenectomy for cancer of the head of the pancreas. 201 patients. Annals. Surg. 1995, 221, 721–731. [Google Scholar] [CrossRef] [PubMed]
  4. Li, D.; Xie, K.; Wolff, R.; Abbruzzese, J.L. Pancreatic cancer. Lancet (London, England) 2004, 363, 1049–1057. [Google Scholar] [CrossRef]
  5. Ueno, H.; Ioka, T.; Ikeda, M.; Ohkawa, S.; Yanagimoto, H.; Boku, N.; Fukutomi, A.; Sugimori, K.; Baba, H.; Yamao, K.; et al. Randomized phase III study of gemcitabine plus S-1, S-1 alone, or gemcitabine alone in patients with locally advanced and metastatic pancreatic cancer in Japan and Taiwan: GEST study. J. clin. Oncol. : j. American Soc. Clin. Oncol. 2013, 31, 1640–1648. [Google Scholar] [CrossRef] [PubMed]
  6. Garrido-Laguna, I.; Hidalgo, M. Pancreatic cancer: From state-of-the-art treatments to promising novel therapies. Nature reviews. Clin. Oncol. 2015, 12, 319–334. [Google Scholar] [CrossRef] [PubMed]
  7. Kalser, M.H.; Ellenberg, S.S. Pancreatic cancer. Adjuvant combined radiation and chemotherapy following curative resection. Arch. surg. (Chicago, Ill. : 1960) 1985, 120, 899–903. [Google Scholar] [CrossRef]
  8. Oettle, H.; Neuhaus, P.; Hochhaus, A.; Hartmann, J.T.; Gellert, K.; Ridwelski, K.; Niedergethmann, M.; Zulke, C.; Fahlke, J.; Arning, M.B.; et al. Adjuvant chemotherapy with gemcitabine and long-term outcomes among patients with resected pancreatic cancer: The CONKO-001 randomized trial. Jama 2013, 310, 1473–1481. [Google Scholar] [CrossRef] [PubMed]
  9. Neoptolemos, J.P.; Stocken, D.D.; Tudur Smith, C.; Bassi, C.; Ghaneh, P.; Owen, E.; Moore, M.; Padbury, R.; Doi, R.; Smith, D.; et al. Adjuvant 5-fluorouracil and folinic acid vs observation for pancreatic cancer: Composite data from the ESPAC-1 and -3(v1) trials. Br. J. Cancer 2009, 100, 246–250. [Google Scholar] [CrossRef] [PubMed]
  10. Mukherjee, S.; Hurt, C.N.; Bridgewater, J.; Falk, S.; Cummins, S.; Wasan, H.; Crosby, T.; Jephcott, C.; Roy, R.; Radhakrishna, G.; et al. Gemcitabine-based or capecitabine-based chemoradiotherapy for locally advanced pancreatic cancer (SCALOP): A multicentre, randomised, phase 2 trial. Lancet 2013, 14, 317–326. [Google Scholar] [CrossRef]
  11. Conroy, T.; Desseigne, F.; Ychou, M.; Bouche, O.; Guimbaud, R.; Becouarn, Y.; Adenis, A.; Raoul, J.L.; Gourgou-Bourgade, S.; de la Fouchardiere, C.; et al. FOLFIRINOX versus gemcitabine for metastatic pancreatic cancer. N. Engl. J. Med. 2011, 364, 1817–1825. [Google Scholar] [CrossRef] [PubMed]
  12. Von Hoff, D.D.; Ervin, T.; Arena, F.P.; Chiorean, E.G.; Infante, J.; Moore, M.; Seay, T.; Tjulandin, S.A.; Ma, W.W.; Saleh, M.N.; et al. Increased survival in pancreatic cancer with nab-paclitaxel plus gemcitabine. N. Engl. J. Med. 2013, 369, 1691–1703. [Google Scholar] [CrossRef] [PubMed]
  13. Maggino, L.; Malleo, G.; Marchegiani, G.; Viviani, E.; Nessi, C.; Ciprani, D.; Esposito, A.; Landoni, L.; Casetti, L.; Tuveri, M.; et al. Outcomes of Primary Chemotherapy for Borderline Resectable and Locally Advanced Pancreatic Ductal Adenocarcinoma. JAMA surg. 2019, 10.1001/jamasurg.2019.2277. [Google Scholar] [CrossRef] [PubMed]
  14. Matsumoto, I.; Kamei, K.; Omae, K.; Suzuki, S.; Matsuoka, H.; Mizuno, N.; Ozaka, M.; Ueno, H.; Kobayashi, S.; Uesugi, K.; et al. FOLFIRINOX for locally advanced pancreatic cancer: Results and prognostic factors of subset analysis from a nation-wide multicenter observational study in Japan. Pancreatology 2019, 19, 296–301. [Google Scholar] [CrossRef] [PubMed]
  15. Katz, M.H.; Shi, Q.; Ahmad, S.A.; Herman, J.M.; Marsh Rde, W.; Collisson, E.; Schwartz, L.; Frankel, W.; Martin, R.; Conway, W.; et al. Preoperative Modified FOLFIRINOX Treatment Followed by Capecitabine-Based Chemoradiation for Borderline Resectable Pancreatic Cancer: Alliance for Clinical Trials in Oncology Trial A021101. JAMA surg. 2016, 151, e161137. [Google Scholar] [CrossRef] [PubMed]
  16. Murphy, J.E.; Wo, J.Y.; Ryan, D.P.; Jiang, W.; Yeap, B.Y.; Drapek, L.C.; Blaszkowsky, L.S.; Kwak, E.L.; Allen, J.N.; Clark, J.W.; et al. Total Neoadjuvant Therapy With FOLFIRINOX Followed by Individualized Chemoradiotherapy for Borderline Resectable Pancreatic Adenocarcinoma: A Phase 2 Clinical Trial. JAMA oncol. 2018, 4, 963–969. [Google Scholar] [CrossRef] [PubMed]
  17. Conroy, T.; Hammel, P.; Hebbar, M.; Ben Abdelghani, M.; Wei, A.C.; Raoul, J.L.; Chone, L.; Francois, E.; Artru, P.; Biagi, J.J.; et al. FOLFIRINOX or Gemcitabine as Adjuvant Therapy for Pancreatic Cancer. N. Engl. J. Med. 2018, 379, 2395–2406. [Google Scholar] [CrossRef] [PubMed]
  18. Wang-Gillam, A.; Li, C.P.; Bodoky, G.; Dean, A.; Shan, Y.S.; Jameson, G.; Macarulla, T.; Lee, K.H.; Cunningham, D.; Blanc, J.F.; et al. Nanoliposomal irinotecan with fluorouracil and folinic acid in metastatic pancreatic cancer after previous gemcitabine-based therapy (NAPOLI-1): A global, randomised, open-label, phase 3 trial. Lancet 2016, 387, 545–557. [Google Scholar] [CrossRef]
  19. National Cancer Institute. SEER Stat Fact Sheets: Pancreas Cancer. Available online: https://seer.cancer.gov/statfacts/html/pancreas.html (accessed on 6 September 2019).
  20. Pannala, R.; Basu, A.; Petersen, G.M.; Chari, S.T. New-onset diabetes: A potential clue to the early diagnosis of pancreatic cancer. Lancet. Oncol. 2009, 10, 88–95. [Google Scholar] [CrossRef]
  21. Raimondi, S.; Maisonneuve, P.; Lowenfels, A.B. Epidemiology of pancreatic cancer: An overview. Nat. Rev. Gastroenterol. Hepatol. 2009, 6, 699–708. [Google Scholar] [CrossRef]
  22. Bosetti, C.; Lucenteforte, E.; Silverman, D.T.; Petersen, G.; Bracci, P.M.; Ji, B.T.; Negri, E.; Li, D.; Risch, H.A.; Olson, S.H.; et al. Cigarette smoking and pancreatic cancer: An analysis from the International Pancreatic Cancer Case-Control Consortium (Panc4). Ann. Oncol. 2012, 23, 1880–1888. [Google Scholar] [CrossRef]
  23. Lynch, S.M.; Vrieling, A.; Lubin, J.H.; Kraft, P.; Mendelsohn, J.B.; Hartge, P.; Canzian, F.; Steplowski, E.; Arslan, A.A.; Gross, M.; et al. Cigarette smoking and pancreatic cancer: A pooled analysis from the pancreatic cancer cohort consortium. Am. J. Epidemiol. 2009, 170, 403–413. [Google Scholar] [CrossRef] [PubMed]
  24. Lugo, A.; Peveri, G.; Bosetti, C.; Bagnardi, V.; Crippa, A.; Orsini, N.; Rota, M.; Gallus, S. Strong excess risk of pancreatic cancer for low frequency and duration of cigarette smoking: A comprehensive review and meta-analysis. Eur. J. Cancer 2018, 104, 117–126. [Google Scholar] [CrossRef] [PubMed]
  25. Bertuccio, P.; La Vecchia, C.; Silverman, D.T.; Petersen, G.M.; Bracci, P.M.; Negri, E.; Li, D.; Risch, H.A.; Olson, S.H.; Gallinger, S.; et al. Cigar and pipe smoking, smokeless tobacco use and pancreatic cancer: An analysis from the International Pancreatic Cancer Case-Control Consortium (PanC4). Ann. Oncol. 2011, 22, 1420–1426. [Google Scholar] [CrossRef] [PubMed]
  26. Zhou, J.; Wellenius, G.A.; Michaud, D.S. Environmental tobacco smoke and the risk of pancreatic cancer among non-smokers: A meta-analysis. Occup. Environ. Med. 2012, 69, 853–857. [Google Scholar] [CrossRef] [PubMed]
  27. Genkinger, J.M.; Spiegelman, D.; Anderson, K.E.; Bergkvist, L.; Bernstein, L.; van den Brandt, P.A.; English, D.R.; Freudenheim, J.L.; Fuchs, C.S.; Giles, G.G.; et al. Alcohol intake and pancreatic cancer risk: A pooled analysis of fourteen cohort studies. Cancer Epidemiol. Biomarkers Prev. 2009, 18, 765–776. [Google Scholar] [CrossRef] [PubMed]
  28. Lucenteforte, E.; La Vecchia, C.; Silverman, D.; Petersen, G.M.; Bracci, P.M.; Ji, B.T.; Bosetti, C.; Li, D.; Gallinger, S.; Miller, A.B.; et al. Alcohol consumption and pancreatic cancer: A pooled analysis in the International Pancreatic Cancer Case-Control Consortium (PanC4). Ann. Oncol. 2012, 23, 374–382. [Google Scholar] [CrossRef] [PubMed]
  29. Wang, Y.T.; Gou, Y.W.; Jin, W.W.; Xiao, M.; Fang, H.Y. Association between alcohol intake and the risk of pancreatic cancer: A dose-response meta-analysis of cohort studies. BMC Cancer 2016. [Google Scholar] [CrossRef] [PubMed]
  30. Chang, J.S.; Hsiao, J.R.; Chen, C.H. ALDH2 polymorphism and alcohol-related cancers in Asians: A public health perspective. J. Biomed. Sci. 2017, 24, 19. [Google Scholar] [CrossRef] [PubMed]
  31. Kanda, J.; Matsuo, K.; Suzuki, T.; Kawase, T.; Hiraki, A.; Watanabe, M.; Mizuno, N.; Sawaki, A.; Yamao, K.; Tajima, K.; et al. Impact of alcohol consumption with polymorphisms in alcohol-metabolizing enzymes on pancreatic cancer risk in Japanese. Cancer Sci. 2009, 100, 296–302. [Google Scholar] [CrossRef]
  32. Chan, J.M.; Gong, Z.; Holly, E.A.; Bracci, P.M. Dietary patterns and risk of pancreatic cancer in a large population-based case-control study in the San Francisco Bay Area. Nutr. Cancer 2013, 65, 157–164. [Google Scholar] [CrossRef]
  33. Bosetti, C.; Bravi, F.; Turati, F.; Edefonti, V.; Polesel, J.; Decarli, A.; Negri, E.; Talamini, R.; Franceschi, S.; La Vecchia, C.; et al. Nutrient-based dietary patterns and pancreatic cancer risk. Ann. Epidemiol. 2013, 23, 124–128. [Google Scholar] [CrossRef] [PubMed]
  34. Jansen, R.J.; Robinson, D.P.; Stolzenberg-Solomon, R.Z.; Bamlet, W.R.; de Andrade, M.; Oberg, A.L.; Rabe, K.G.; Anderson, K.E.; Olson, J.E.; Sinha, R.; et al. Nutrients from fruit and vegetable consumption reduce the risk of pancreatic cancer. J. Gastrointest. Cancer 2013, 44, 152–161. [Google Scholar] [CrossRef] [PubMed]
  35. Wu, Q.J.; Wu, L.; Zheng, L.Q.; Xu, X.; Ji, C.; Gong, T.T. Consumption of fruit and vegetables reduces risk of pancreatic cancer: Evidence from epidemiological studies. Eur. J. Cancer Prev. 2016, 25, 196–205. [Google Scholar] [CrossRef] [PubMed]
  36. Taunk, P.; Hecht, E.; Stolzenberg-Solomon, R. Are meat and heme iron intake associated with pancreatic cancer? Results from the NIH-AARP diet and health cohort. Int. J. Cancer 2016, 138, 2172–2189. [Google Scholar] [CrossRef] [PubMed]
  37. Casari, I.; Falasca, M. Diet and Pancreatic Cancer Prevention. Cancers 2015, 7, 2309–2317. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  38. Falasca, M.; Casari, I.; Maffucci, T. Cancer chemoprevention with nuts. J. Natl. Cancer Inst. 2014, 106. [Google Scholar] [CrossRef] [PubMed]
  39. Mao, Q.Q.; Lin, Y.W.; Chen, H.; Qin, J.; Zheng, X.Y.; Xu, X.; Xie, L.P. Dietary fiber intake is inversely associated with risk of pancreatic cancer: A meta-analysis. Asia Pac. J. Clin. Nutr. 2017, 26, 89–96. [Google Scholar] [CrossRef] [PubMed]
  40. O'Rorke, M.A.; Cantwell, M.M.; Cardwell, C.R.; Mulholland, H.G.; Murray, L.J. Can physical activity modulate pancreatic cancer risk? a systematic review and meta-analysis. Int. J. Cancer 2010, 126, 2957–2968. [Google Scholar] [CrossRef] [PubMed]
  41. Farris, M.S.; Mosli, M.H.; McFadden, A.A.; Friedenreich, C.M.; Brenner, D.R. The Association between Leisure Time Physical Activity and Pancreatic Cancer Risk in Adults: A Systematic Review and Meta-analysis. Cancer Epidemiol. Biomarkers Prev. 2015, 24, 1462–1473. [Google Scholar] [CrossRef] [Green Version]
  42. Keum, N.; Bao, Y.; Smith-Warner, S.A.; Orav, J.; Wu, K.; Fuchs, C.S.; Giovannucci, E.L. Association of Physical Activity by Type and Intensity With Digestive System Cancer Risk. JAMA oncology 2016, 2, 1146–1153. [Google Scholar] [CrossRef] [Green Version]
  43. Noor, N.M.; Banim, P.J.; Luben, R.N.; Khaw, K.T.; Hart, A.R. Investigating Physical Activity in the Etiology of Pancreatic Cancer: The Age at Which This Is Measured Is Important and Is Independent of Body Mass Index. Pancreas 2016, 45, 388–393. [Google Scholar] [CrossRef] [PubMed]
  44. Wu, L.; Zheng, W.; Xiang, Y.B.; Gao, Y.T.; Li, H.L.; Cai, H.; Shu, X.O. Physical Activity and Pancreatic Cancer Risk among Urban Chinese: Results from Two Prospective Cohort Studies. Cancer Epidemiol. Biomarkers Prev. 2018, 27, 479–487. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Arslan, A.A.; Helzlsouer, K.J.; Kooperberg, C.; Shu, X.O.; Steplowski, E.; Bueno-de-Mesquita, H.B.; Fuchs, C.S.; Gross, M.D.; Jacobs, E.J.; Lacroix, A.Z.; et al. Anthropometric measures, body mass index, and pancreatic cancer: A pooled analysis from the Pancreatic Cancer Cohort Consortium (PanScan). Arch. Intern. Med. 2010, 170, 791–802. [Google Scholar] [CrossRef] [PubMed]
  46. Aune, D.; Greenwood, D.C.; Chan, D.S.; Vieira, R.; Vieira, A.R.; Navarro Rosenblatt, D.A.; Cade, J.E.; Burley, V.J.; Norat, T. Body mass index, abdominal fatness and pancreatic cancer risk: A systematic review and non-linear dose-response meta-analysis of prospective studies. Ann. Oncol. 2012, 23, 843–852. [Google Scholar] [CrossRef] [PubMed]
  47. Genkinger, J.M.; Kitahara, C.M.; Bernstein, L.; Berrington de Gonzalez, A.; Brotzman, M.; Elena, J.W.; Giles, G.G.; Hartge, P.; Singh, P.N.; Stolzenberg-Solomon, R.Z.; et al. Central adiposity, obesity during early adulthood, and pancreatic cancer mortality in a pooled analysis of cohort studies. Ann. Oncol. 2015, 26, 2257–2266. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  48. Koyanagi, Y.N.; Matsuo, K.; Ito, H.; Tamakoshi, A.; Sugawara, Y.; Hidaka, A.; Wada, K.; Oze, I.; Kitamura, Y.; Liu, R.; et al. Body-Mass Index and Pancreatic Cancer Incidence: A Pooled Analysis of Nine Population-Based Cohort Studies With More Than 340,000 Japanese Subjects. J. Epidemiol. 2018, 28, 245–252. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  49. Zohar, L.; Rottenberg, Y.; Twig, G.; Katz, L.; Leiba, A.; Derazne, E.; Tzur, D.; Eizenstein, S.; Keinan-Boker, L.; Afek, A.; et al. Adolescent overweight and obesity and the risk for pancreatic cancer among men and women: A nationwide study of 1.79 million Israeli adolescents. Cancer 2019, 125, 118–126. [Google Scholar] [CrossRef] [PubMed]
  50. Rawla, P.; Thandra, K.C.; Sunkara, T. Pancreatic cancer and obesity: Epidemiology, mechanism, and preventive strategies. Clin. J. Gastroenterol. 2019. [Google Scholar] [CrossRef]
  51. Maisonneuve, P.; Amar, S.; Lowenfels, A.B. Periodontal disease, edentulism, and pancreatic cancer: A meta-analysis. Ann. Oncol. 2017, 28, 985–995. [Google Scholar] [CrossRef]
  52. Stolzenberg-Solomon, R.Z.; Dodd, K.W.; Blaser, M.J.; Virtamo, J.; Taylor, P.R.; Albanes, D. Tooth loss, pancreatic cancer, and Helicobacter pylori. Am. J. Clin. Nutr. 2003, 78, 176–181. [Google Scholar] [CrossRef]
  53. Gerlovin, H.; Michaud, D.S.; Cozier, Y.C.; Palmer, J.R. Oral Health in Relation to Pancreatic Cancer Risk in African American Women. Cancer Epidemiol. Biomarkers Prev. 2019, 28, 675–679. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  54. Michaud, D.S.; Izard, J.; Wilhelm-Benartzi, C.S.; You, D.H.; Grote, V.A.; Tjonneland, A.; Dahm, C.C.; Overvad, K.; Jenab, M.; Fedirko, V.; et al. Plasma antibodies to oral bacteria and risk of pancreatic cancer in a large European prospective cohort study. Gut 2013, 62, 1764–1770. [Google Scholar] [CrossRef] [PubMed]
  55. Fan, X.; Alekseyenko, A.V.; Wu, J.; Peters, B.A.; Jacobs, E.J.; Gapstur, S.M.; Purdue, M.P.; Abnet, C.C.; Stolzenberg-Solomon, R.; Miller, G.; et al. Human oral microbiome and prospective risk for pancreatic cancer: A population-based nested case-control study. Gut 2016. [Google Scholar]
  56. Olson, S.H.; Satagopan, J.; Xu, Y.; Ling, L.; Leong, S.; Orlow, I.; Saldia, A.; Li, P.; Nunes, P.; Madonia, V.; et al. The oral microbiota in patients with pancreatic cancer, patients with IPMNs, and controls: A pilot study. Cancer Causes Control. 2017, 28, 959–969. [Google Scholar] [CrossRef] [PubMed]
  57. Hayashi, C.; Gudino, C.V.; Gibson, F.C., 3rd; Genco, C.A. Review: Pathogen-induced inflammation at sites distant from oral infection: Bacterial persistence and induction of cell-specific innate immune inflammatory pathways. Mol. Oral. Microbiol. 2010, 25, 305–316. [Google Scholar] [CrossRef] [PubMed]
  58. Coussens, L.M.; Werb, Z. Inflammation and cancer. Nature 2002, 420, 860–867. [Google Scholar] [CrossRef] [PubMed]
  59. Ren, Z.; Jiang, J.; Xie, H.; Li, A.; Lu, H.; Xu, S.; Zhou, L.; Zhang, H.; Cui, G.; Chen, X.; et al. Gut microbial profile analysis by MiSeq sequencing of pancreatic carcinoma patients in China. Oncotarget 2017, 8, 95176–95191. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  60. Pushalkar, S.; Hundeyin, M.; Daley, D.; Zambirinis, C.P.; Kurz, E.; Mishra, A.; Mohan, N.; Aykut, B.; Usyk, M.; Torres, L.E.; et al. The Pancreatic Cancer Microbiome Promotes Oncogenesis by Induction of Innate and Adaptive Immune Suppression. Cancer discov. 2018, 8, 403–416. [Google Scholar] [CrossRef] [Green Version]
  61. Mendez, R.; Kesh, K.; Arora, N.; Di Martino, L.; McAllister, F.; Merchant, N.; Banerjee, S.; Banerjee, S. Microbial dysbiosis and polyamine metabolism as predictive markers for early detection of pancreatic cancer. Carcinogenesis 2019, 10.1093/carcin/bgz116. [Google Scholar] [CrossRef]
  62. Archibugi, L.; Signoretti, M.; Capurso, G. The Microbiome and Pancreatic Cancer: An Evidence-based Association? J. Clin. Gastroenterol. 2018. [Google Scholar] [CrossRef]
  63. Zhou, C.D.; Kuan, A.S.; Reeves, G.K.; Green, J.; Floud, S.; Beral, V.; Yang, T.O. Coffee and pancreatic cancer risk among never-smokers in the UK prospective Million Women Study. Int. J. Cancer 2019, 145, 1484–1492. [Google Scholar] [CrossRef] [PubMed]
  64. Guertin, K.A.; Freedman, N.D.; Loftfield, E.; Stolzenberg-Solomon, R.Z.; Graubard, B.I.; Sinha, R. A prospective study of coffee intake and pancreatic cancer: Results from the NIH-AARP Diet and Health Study. Br. J. Cancer 2015, 113, 1081–1085. [Google Scholar] [CrossRef] [PubMed]
  65. Bosetti, C.; Rosato, V.; Li, D.; Silverman, D.; Petersen, G.M.; Bracci, P.M.; Neale, R.E.; Muscat, J.; Anderson, K.; Gallinger, S.; et al. Diabetes, antidiabetic medications, and pancreatic cancer risk: An analysis from the International Pancreatic Cancer Case-Control Consortium. Ann. Oncol. 2015, 25, 2065–2072. [Google Scholar] [CrossRef] [PubMed]
  66. Pang, Y.; Kartsonaki, C.; Guo, Y.; Bragg, F.; Yang, L.; Bian, Z.; Chen, Y.; Iona, A.; Millwood, I.Y.; Lv, J.; et al. Diabetes, plasma glucose and incidence of pancreatic cancer: A prospective study of 0.5 million Chinese adults and a meta-analysis of 22 cohort studies. Int. J. Cancer 2017, 140, 1781–1788. [Google Scholar] [CrossRef] [PubMed]
  67. Chari, S.T.; Leibson, C.L.; Rabe, K.G.; Timmons, L.J.; Ransom, J.; de Andrade, M.; Petersen, G.M. Pancreatic cancer-associated diabetes mellitus: Prevalence and temporal association with diagnosis of cancer. Gastroenterology 2008, 134, 95–101. [Google Scholar] [CrossRef]
  68. Setiawan, V.W.; Stram, D.O.; Porcel, J.; Chari, S.T.; Maskarinec, G.; Le Marchand, L.; Wilkens, L.R.; Haiman, C.A.; Pandol, S.J.; Monroe, K.R. Pancreatic Cancer Following Incident Diabetes in African Americans and Latinos: The Multiethnic Cohort. J. Natl. Cancer Inst. 2019, 111, 27–33. [Google Scholar] [CrossRef]
  69. Kirkegard, J.; Mortensen, F.V.; Cronin-Fenton, D. Chronic Pancreatitis and Pancreatic Cancer Risk: A Systematic Review and Meta-analysis. Am. J. Gastroenterol. 2017, 112, 1366–1372. [Google Scholar] [CrossRef] [Green Version]
  70. Raimondi, S.; Lowenfels, A.B.; Morselli-Labate, A.M.; Maisonneuve, P.; Pezzilli, R. Pancreatic cancer in chronic pancreatitis; aetiology, incidence, and early detection. Best Pract. Res. Clin. Gastroenterol. 2010, 24, 349–358. [Google Scholar] [CrossRef]
  71. Gandini, S.; Lowenfels, A.B.; Jaffee, E.M.; Armstrong, T.D.; Maisonneuve, P. Allergies and the risk of pancreatic cancer: A meta-analysis with review of epidemiology and biological mechanisms. Cancer Epidemiol. Biomarkers Prev. 2005, 14, 1908–1916. [Google Scholar] [CrossRef]
  72. Olson, S.H.; Hsu, M.; Satagopan, J.M.; Maisonneuve, P.; Silverman, D.T.; Lucenteforte, E.; Anderson, K.E.; Borgida, A.; Bracci, P.M.; Bueno-de-Mesquita, H.B.; et al. Allergies and risk of pancreatic cancer: A pooled analysis from the Pancreatic Cancer Case-Control Consortium. Am. J. Epidemiol. 2013, 178, 691–700. [Google Scholar] [CrossRef]
  73. Huang, B.Z.; Le Marchand, L.; Haiman, C.A.; Monroe, K.R.; Wilkens, L.R.; Zhang, Z.F.; Setiawan, V.W. Atopic allergic conditions and pancreatic cancer risk: Results from the Multiethnic Cohort Study. Int. J. Cancer 2018, 142, 2019–2027. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  74. Sherman, P.W.; Holland, E.; Sherman, J.S. Allergies: Their role in cancer prevention. Q. Rev. Biol. 2008, 83, 339–362. [Google Scholar] [CrossRef] [PubMed]
  75. Profet, M. The function of allergy: Immunological defense against toxins. Q. Rev. Biol. 1991, 66, 23–62. [Google Scholar] [CrossRef] [PubMed]
  76. Xu, J.H.; Fu, J.J.; Wang, X.L.; Zhu, J.Y.; Ye, X.H.; Chen, S.D. Hepatitis B or C viral infection and risk of pancreatic cancer: A meta-analysis of observational studies. World J. Gastroenterol. 2013, 19, 4234–4241. [Google Scholar] [CrossRef] [PubMed]
  77. Krull Abe, S.; Inoue, M.; Sawada, N.; Iwasaki, M.; Shimazu, T.; Yamaji, T.; Sasazuki, S.; Saito, E.; Tanaka, Y.; Mizokami, M.; et al. Hepatitis B and C Virus Infection and Risk of Pancreatic Cancer: A Population-Based Cohort Study (JPHC Study Cohort II). Cancer Epidemiol. Biomarkers Prev. 2016, 25, 555–557. [Google Scholar] [CrossRef] [PubMed]
  78. Kamiza, A.B.; Su, F.H.; Wang, W.C.; Sung, F.C.; Chang, S.N.; Yeh, C.C. Chronic hepatitis infection is associated with extrahepatic cancer development: A nationwide population-based study in Taiwan. BMC Cancer 2016, 16, 861. [Google Scholar] [CrossRef] [PubMed]
  79. Chang, M.C.; Chen, C.H.; Liang, J.D.; Tien, Y.W.; Hsu, C.; Wong, J.M.; Chang, Y.T. Hepatitis B and C viruses are not risks for pancreatic adenocarcinoma. World J. Gastroenterol. 2014, 20, 5060–5065. [Google Scholar] [CrossRef] [PubMed]
  80. Allison, R.D.; Tong, X.; Moorman, A.C.; Ly, K.N.; Rupp, L.; Xu, F.; Gordon, S.C.; Holmberg, S.D. Increased incidence of cancer and cancer-related mortality among persons with chronic hepatitis C infection, 2006-2010. J. Hepatol. 2015, 63, 822–828. [Google Scholar] [CrossRef] [PubMed]
  81. Schulte, A.; Pandeya, N.; Fawcett, J.; Fritschi, L.; Risch, H.A.; Webb, P.M.; Whiteman, D.C.; Neale, R.E. Association between Helicobacter pylori and pancreatic cancer risk: A meta-analysis. Cancer Causes Control. 2015, 26, 1027–1035. [Google Scholar] [CrossRef] [PubMed]
  82. Huang, J.; Zagai, U.; Hallmans, G.; Nyren, O.; Engstrand, L.; Stolzenberg-Solomon, R.; Duell, E.J.; Overvad, K.; Katzke, V.A.; Kaaks, R.; et al. Helicobacter pylori infection, chronic corpus atrophic gastritis and pancreatic cancer risk in the European Prospective Investigation into Cancer and Nutrition (EPIC) cohort: A nested case-control study. Int. J. Cancer 2017, 140, 1727–1735. [Google Scholar] [CrossRef] [PubMed]
  83. Klein, A.P.; Lindstrom, S.; Mendelsohn, J.B.; Steplowski, E.; Arslan, A.A.; Bueno-de-Mesquita, H.B.; Fuchs, C.S.; Gallinger, S.; Gross, M.; Helzlsouer, K.; et al. An absolute risk model to identify individuals at elevated risk for pancreatic cancer in the general population. PLoS ONE 2013, 8, e72311. [Google Scholar] [CrossRef] [PubMed]
  84. Risch, H.A.; Yu, H.; Lu, L.; Kidd, M.S. Detectable Symptomatology Preceding the Diagnosis of Pancreatic Cancer and Absolute Risk of Pancreatic Cancer Diagnosis. Am. J. Epidemiol. 2015, 182, 26–34. [Google Scholar] [CrossRef] [PubMed]
  85. Yu, A.; Woo, S.M.; Joo, J.; Yang, H.R.; Lee, W.J.; Park, S.J.; Nam, B.H. Development and Validation of a Prediction Model to Estimate Individual Risk of Pancreatic Cancer. PLoS ONE 2016, 11, e0146473. [Google Scholar] [CrossRef] [PubMed]
  86. Nakatochi, M.; Lin, Y.; Ito, H.; Hara, K.; Kinoshita, F.; Kobayashi, Y.; Ishii, H.; Ozaka, M.; Sasaki, T.; Sasahira, N.; et al. Prediction model for pancreatic cancer risk in the general Japanese population. PLoS ONE 2018, 13, e0203386. [Google Scholar] [CrossRef] [PubMed]
  87. Boursi, B.; Finkelman, B.; Giantonio, B.J.; Haynes, K.; Rustgi, A.K.; Rhim, A.D.; Mamtani, R.; Yang, Y.X. A Clinical Prediction Model to Assess Risk for Pancreatic Cancer Among Patients With New-Onset Diabetes. Gastroenterology 2017, 152, 840–850 e843. [Google Scholar] [CrossRef] [PubMed]
Jcm 08 01427 g001 550
Figure 1. Possible biological mechanisms explaining the association between poor oral health/hygiene and microbiome and an increased pancreatic cancer risk.
Figure 1. Possible biological mechanisms explaining the association between poor oral health/hygiene and microbiome and an increased pancreatic cancer risk.
Jcm 08 01427 g001
Jcm 08 01427 g002 550
Figure 2. Diabetes can be both a cause and a consequence of pancreatic cancer.
Figure 2. Diabetes can be both a cause and a consequence of pancreatic cancer.
Jcm 08 01427 g002
Jcm 08 01427 g003 550
Figure 3. A. Immunosurveillance hypothesis: Allergy does not play a direct role in preventing the occurrence of cancer, but is merely a manifestation of an overactive immune function that has a high efficiency of surveying and eradicating cancer cells. B. Prophylaxis hypothesis: Allergic reactions are the body’s method of expelling the carcinogens.
Figure 3. A. Immunosurveillance hypothesis: Allergy does not play a direct role in preventing the occurrence of cancer, but is merely a manifestation of an overactive immune function that has a high efficiency of surveying and eradicating cancer cells. B. Prophylaxis hypothesis: Allergic reactions are the body’s method of expelling the carcinogens.
Jcm 08 01427 g003
Table
Table 1. Environmental (non-genetic, including lifestyle, and clinical factors) risk factors of pancreatic cancer by the level of evidence.
Table 1. Environmental (non-genetic, including lifestyle, and clinical factors) risk factors of pancreatic cancer by the level of evidence.
The Level of Evidence Risk Factors
Very strongCigarette smoking, chronic diabetes, obesity
StrongPoor oral health/oral hygiene, chronic pancreatitis, no history of allergies, heavy alcohol drinking, dietary patterns with low amount of vegetables and fruits
Moderate, although further investigations are requiredDietary patterns rich in meat and animal products, oral/gut microbiome, hepatitis B or C infection
The level of evidence is unclear, further investigations are requiredEnvironmental tobacco smoke, light to moderate alcohol drinking, physical inactivity, coffee, Helicobacer pylori infection
Table
Table 2. Summary of key points for each of the environmental factors discussed in this paper.
Table 2. Summary of key points for each of the environmental factors discussed in this paper.
Environmental FactorsKey Points
Cigarette smokingCigarette smoking is an established risk factor of pancreatic cancer. Smoking cessation can reverse the increased risk of pancreatic cancer associated with cigarette smoking
Alcohol drinkingHeavy alcohol use is associated with an increased pancreatic cancer risk. The association between low to moderate level of alcohol use and pancreatic cancer is unclear.
DietDiet rich in fruits and vegetables and other plant-based foods has been associated with a reduced pancreatic cancer risk
Physical activitiesThe role of physical activities in preventing the occurrence of pancreatic cancer is inconclusive, although they may possibly reduce the pancreatic cancer risk by preventing obesity.
ObesityObesity is an established risk factor of pancreatic cancer, although biological mechanisms are yet to be delineated
Oral health/hygiene and oral microbiomePoor oral health/hygiene has consistently been associated with an increased pancreatic cancer risk. Poor oral health/hygiene may affect oral microbiome by promoting the growth of pathogenic oral bacteria, which may increased the risk of pancreatic cancer by inducing inflammation and other mechanisms. More investigations are needed for the role of oral microbiome in the development of pancreatic cancer
Gut microbiomeThe current information regarding the association between gut microbiome and pancreatic cancer is very limited and more investigations are required
CoffeeThe association between coffee and pancreatic cancer is unclear
DiabetesDiabetes can be both a risk factor and a consequence of pancreatic cancer
Chronic pancreatitisChronic pancreatitis is a known risk factor of pancreatic cancer with a lifetime risk of 5%
AllergiesAllergies are associated with a reduced pancreatic cancer risk, although the biological mechanisms are unclear
InfectionsThe majority of studies suggested that hepatitis B or C infection may be associated with an increased pancreatic cancer risk. More studies on the association between the different strains of H. Pylori and pancreatic cancer are needed to confirm the strain-specific association between H. Pylori and pancreatic cancer.

Share and Cite

MDPI and ACS Style

Tsai, H.-J.; Chang, J.S. Environmental Risk Factors of Pancreatic Cancer. J. Clin. Med. 2019, 8, 1427. https://doi.org/10.3390/jcm8091427

AMA Style

Tsai H-J, Chang JS. Environmental Risk Factors of Pancreatic Cancer. Journal of Clinical Medicine. 2019; 8(9):1427. https://doi.org/10.3390/jcm8091427

Chicago/Turabian Style

Tsai, Hui-Jen, and Jeffrey S. Chang. 2019. "Environmental Risk Factors of Pancreatic Cancer" Journal of Clinical Medicine 8, no. 9: 1427. https://doi.org/10.3390/jcm8091427

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop