Editorial Open Access
Copyright ©2009 The WJG Press and Baishideng. All rights reserved.
World J Gastroenterol. Dec 21, 2009; 15(47): 5907-5915
Published online Dec 21, 2009. doi: 10.3748/wjg.15.5907
Colorectal cancer screening in Europe
Miroslav Zavoral, Stepan Suchanek, Filip Zavada, Premysl Fric, Clinic of Medicine, Central Military Hospital, 1st Faculty of Medicine, Charles University, Prague, CZ16902, Czech Republic
Ladislav Dusek, Jan Muzik, Institute of Biostatistics and Analyses, Masaryk University, Brno, CZ60200, Czech Republic
Bohumil Seifert, Institute of General Medicine, 1st Faculty of Medicine, Charles University, Prague, CZ12800, Czech Republic
Author contributions: Zavoral M, Suchanek S and Zavada F carried out the data collection and wrote the initial draft of the manuscript; Dusek L and Muzik J wrote the epidemiology section of the manuscript; Fric P and Seifert B performed the overall scientific direction and revision.
Supported by International Agency for Research on Cancer (Lawrence von Karsa, MD); International Digestive Cancer Alliance (Professor Meinhard Classen, MD, Professor Sidney J Winawer, MD)
Correspondence to: Miroslav Zavoral, MD, PhD, Professor of Medicine, Chief, Clinic of Medicine, Central Military Hospital, 1st Faculty of Medicine, Charles University, U vojenske nemocnice 1200, Prague 6, CZ16902, Czech Republic. miroslav.zavoral@uvn.cz
Telephone: +420-973203061 Fax: +420-973203068
Received: October 15, 2009
Revised: November 12, 2009
Accepted: November 21, 2009
Published online: December 21, 2009

Abstract

Colorectal cancer (CRC) is the second most frequent malignant disease in Europe. Every year, 412 000 people are diagnosed with this condition, and 207 000 patients die of it. In 2003, recommendations for screening programs were issued by the Council of the European Union (EU), and these currently serve as the basis for the preparation of European guidelines for CRC screening. The manner in which CRC screening is carried out varies significantly from country to country within the EU, both in terms of organization and the screening test chosen. A screening program of one sort or another has been implemented in 19 of 27 EU countries. The most frequently applied method is testing stool for occult bleeding (fecal occult blood test, FOBT). In recent years, a screening colonoscopy has been introduced, either as the only method (Poland) or the method of choice (Germany, Czech Republic).

Key Words: Colorectal cancer, Europe, Fecal occult blood test, Screening colonoscopy, Screening programs



INTRODUCTION

Colorectal cancer (CRC) poses a serious health problem in countries with a Westernized lifestyle. Over the last decade, a whole range of new technologies have been introduced in clinical practice to diagnose and treat the disease, with therapeutic modalities extending to advanced stages of the disease. Nevertheless, prevention undoubtedly remains the key to reducing morbidity and mortality. The introduction of national or transnational population-wide screening programs is a priority for the healthcare policy of individual states, and this is also being addressed at the highest level by European Union (EU) administrators. The approach of individual countries to screening programs varies significantly because of differences in health insurance systems and budgets. This summary article focuses on a brief description and comparison of these programs.

EPIDEMIOLOGY

CRC is the second most frequent malignant disease in developed countries. The incidence of CRC is generally higher for men, and the risk of the disease increases with age, as the majority of cases are diagnosed in patients more than 50 years of age[1]. European countries rank highest in the global statistics, both in terms of incidence and mortality. In 1998 to 2002, the incidence of CRC in the USA for men and women was 38.6 and 28.3, respectively; in Europe, it was 38.5 and 24.6 [world age standardization (ASR-W)], as calculated per 100 000 inhabitants[2]. However, mortality over the same period of time was much higher in Europe than in the US, both for men and women: in the USA, the figures were 13.5 and 9.2, respectively, while in Europe, they were 18.5 and 10.7 (ASR-W), as calculated per 100 000 inhabitants[3]. A detailed comparison of data for European countries is made difficult because of the absence of a unified data source. Not all countries maintain sophisticated population and cancer registers, and it is sometimes necessary to obtain input data by projecting aggregated data. In this outline, figures available from international studies summarizing global and European epidemiologic data have been used[4,5]. A detailed comparison of countries within Europe using the ASR-W of incidence and mortality is presented in Figure 1. Most recent epidemiologic data on CRC for 2006 recalculated to the European age standard are given in Tables 1 and 2.

Table 1 Colorectal cancer incidence in European countries in 2006.
ParameterIncidence
Countries with the highest incidence> 70/100 000 men (ASR-E): Hungary (106), Czech Republic (94.4), Slovakia (87.1), Switzerland (79.1), Germany (70.2)
> 45/100 000 women (ASR-E): Switzerland (55.6), Norway (51.2), Hungary (50.6), Denmark (48), Czech Republic (46), Germany (45.1)
Countries with the lowest incidence< 40/100 000 men (ASR-E): Albania (13.6), Greece (31), Bosnia Herzegovina (34.6), Republic of Moldova (38.7), Finland (39.2)
< 26/100 000 women (ASR-E): Greece (21.3), Albania (21.4), Romania (25.1), Spain (25.4)
Figure 1
Figure 1 Epidemiology of colorectal cancer in European countries. A: Incidence in international comparison-European countries; B: Mortality in international comparison-European countries. Adapted from: Ferlay J, Bray F, Pisani P, Parkin DM. GLOBOCAN 2002: Cancer incidence, mortality and prevalence worldwide. IARC Cancer Base No. 5 version 2.0. Lyon: IARC press, 2004. Available from: URL: http://www-dep.iarc.fr/, section CI5 I-VIII (Detailed). Last accessed on August 8, 2009.
Table 2 Colorectal cancer mortality in European countries in 2006.
ParameterMortality
Countries with the highest mortality> 40/100 000 men (ASR-E): Hungary (54.4), Czech Republic (51), Slovakia (43.3), Croatia (40.7)
> 20/100 000 women (ASR-E): Hungary (26.7), Slovakia (24.4), Czech Republic (24.1), Denmark (24.1), Norway (21.4)
Countries with the lowest mortality< 20/100 000 men (ASR-E): Albania (7.3), Greece (15.5), Finland (17.9), Switzerland (19.1), Cyprus (19.3), Bosnia Herzegovina (19.5)
< 12/100 000 women (ASR-E): Albania (9.9), Greece (10.8), Finland (11.3), Switzerland (11.6)

CRC comprises 12.9% of all newly-diagnosed carcinomas in the European population (men 12.8%, women 13.1%) and account for 12.2% of deaths caused by malignancy. CRC is the second most frequent malignancy, after breast carcinoma (13.5% of all malignancies) and bronchogenic carcinoma (12.1% of all malignancies). It has been estimated that in 2006, 412 000 people were diagnosed with CRC in Europe, and 207 400 of them die of the disease[6]. The average incidence has shown a tendency to increase in recent years (2001-2005), with a year-on-year growth of 0.5%. Available data on time trends of CRC incidence and mortality are shown in Figures 2 and 3. A detailed analysis of individual diagnoses confirms that malignant disease of the colon is the most frequent, accounting for 57% of all cases (> 35 cases/105 inhabitants), followed by malignant diseases of the rectum and rectosigmoid (> 22 cases/105 inhabitants) and tumors of the anus and anal channel (> 1.0 cases/105 inhabitants) (Table 3). According to recently published data, CRC-related mortality has stabilized or shown a slight decrease over recent years.

Figure 2
Figure 2 Incidence trends of colorectal cancer in Europe. Thirty nine cancer registries in 1990-1996, 37 cancer registries in 1997, 96 cancer registries in 1998-2002. Adapted from: Parkin DM, Whelan SL, Ferlay J, Storm H. Cancer Incidence in Five Continents, Vol. I to VIII. IARC CancerBase No. 7, Lyon, 2005. Available from: URL: http://www-dep.iarc.fr/, section CI5 I-VIII (Detailed). Last accessed on August 8, 2009; Curado MP, Edwards B, Shin HR, Storm H, Ferlay J, Heanue M, Boyle P, editors. Cancer Incidence in Five Continents, Vol. IX. IARC Scientific Publications No. 160, Lyon: IARC, 2007. Available from: URL: http://www-dep.iarc.fr/ section CI5 IX. Last accessed on August 8, 2009.
Table 3 Epidemiology of colorectal cancer in the Europe (96 individual cancer registries, 1998-2002).
Parameter incidenceSexC18-C21Individual diagnoses
C18C19-C20C21
Crude incidence (cases/100.000 inhabitants)Men63.937.126.00.8
Women53.734.817.61.3
All58.635.921.71.1
ASR-EMen58.033.523.70.8
Women36.823.412.41.0
All45.827.617.30.9
ASR-WMen38.522.015.90.5
Women24.615.58.40.7
All30.618.311.70.6
Mean age (yr)Men69.169.768.265.4
Women71.371.970.467.7
All70.170.869.166.8
Ratio (males: females) (based on No. of cases)1.1:11.0:11.4:10.6:1
Figure 3
Figure 3 Mortality trends of colorectal cancer in Europe. As available in WHO database, countries with cancer registry (Cancer Incidence in Five Continents, Vol. IX). Adapted from: CancerMondial - WHO, International Agency for Research on Cancer, 2008. Available from: URL: http://www-dep.iarc.fr/; World Health Organization (2006), mortality database http://www.who.int/whosis/whosis/, United Nations, World Population Prospects, the 2006 revision. Available from: URL: http://www-dep.iarc.fr/. Last accessed on August 8, 2009.

The most extensive population study monitoring the relative survival rate (RSR) is the EUROCARE program[7], which takes registers of patients suffering from malignant diseases as a basis. Data have been gathered and evaluated since 1978. The most recent version, EUROCARE-4, uses comparative analyses of data from the year 1995 to 1999, while data are also available for the years 2000 to 2002[8]. Data from the European population carcinoma register are also used in the CONCORD study[9], which focuses on a systematic comparison of statistical data between Europe and Northern America. Apart from these two studies, data from population registers of carcinoma have been published for some European countries. Data available regarding the 5-year RSR show high variability across European countries, with borderline values in the Czech Republic (50%) on the one hand and Germany (60%) on the other hand[7-16] (Table 4). Several studies have confirmed a favorable time trend in the 5-year RSR; however, these results have to be interpreted carefully with respect to the hidden reasons leading to such positive conclusions. Evaluation of survival rate based on clinical studies of CRC is, unfortunately, rather rare, and therefore, it is impossible to make a representative evaluation of this indicator. This fact should be seen as a challenge when improving population registers of malignant diseases.

Table 4 Five-year relative survival rate (RSR) for colorectal cancer for selected European countries.
CountryDiagnosesAssessment periodFive-year RSR (%)Change in time (%)Stage-specific estimates
EUROCARE pool[7]C18-C211995-199953.54.2NA
EUROCARE pool[8]C18-C212000-200256.2NANA
England & Wales[10,11]C181996-199947.6 M; 47.4 F5.6 M; 5.6 FNA
C19-C201996-199948.7 M; 51.3 F7.4 M; 8.1 FNA
Germany[12]C18-C212000-200260.8NA85.4 L; 58.1 R; 10.7 M
Finland[13]C18-C202000-200457.92.4NA
Norway[14]C18-C212000-200459.23.6NA
Slovenia[15]C18-C212000-200446.98.0NA
Sweden[16]C182000-200258.1 M; 59.7 F1.8 M; 2.6 FNA
C19-C212000-200257.5 M; 59.1 F2.5 M; -1.7 FNA
SCREENING METHODS

CRC screening focuses on asymptomatic individuals more than 50 years of age. Age is a low (average) risk factor for sporadic CRC, that is, carcinoma in patients with negative family or case history of CRC or chronic inflammatory bowel disease; this type of carcinoma accounts for 70 to 95% of all CRC cases. Three groups of screening methods are currently used as indicated in Table 5.

Table 5 Screening methods.
Type of methodMethod
Stool testsFor presence of occult blood (FOBT)
Guaiac-based (gFOBT)
Immunochemical (iFOBT)
For presence of abnormal DNA
Endoscopic examinationsFlexible sigmoidoscopy (FS) colonoscopy
Radiologic examinationsComputed tomographic colonography (CTC)
Double contrast barium enema (DCBE)

Guaiac-based fecal occult bleeding test (gFOBT) is at present the most frequently used method in screening programs. It detects the peroxidase reaction of hemoglobin, which causes the detection paper impregnated with guaiac resin to turn blue. Dietetic provisions are necessary to exclude false-positive results. A recent study showed limited sensitivity of this test for both, advanced adenomas (11%) and carcinomas (13%)[17]. With the use of gFOBT, a decrease in mortality for CRC by 15 to 33% has been proved[18].

Immunochemical fecal occult bleeding test (iFOBT) reacts exclusively to human hemoglobin, so no dietetic restrictions are necessary. Taking and assessing the stool samples are easier than is the case with gFOBTs, which may explain a higher participation rate in the target group. A wide range of qualitative and quantitative tests is presently available, with varying levels of sensitivity and specificity. The advantage of quantitative tests is the possibility to set cut-off limits; the most frequently used values are 75 or 100 ng/mL. The disadvantage of iFOBT is its cost; however, the price is now approaching that of gFOBT, particularly for qualitative tests[19].

New screening methods include tests which examine the stool for the presence of abnormal DNA. Studies published to date focused on the characteristics of the test rather than the reduction in CRC incidence or mortality. Generally, these tests have higher sensitivity but lower specificity than gFOBT. The major obstacle to their implementation in screening programs is price[20].

Flexible sigmoidoscopy (FS) is an endoscopic examination with maximum reach to the splenic flexure. On the basis of the information available, this is a promising screening test, although the studies published to date do not show sufficient statistical significance to determine reduction in CRC mortality. The recommended interval varies from 3 to 5 years. The risk of serious complications is 0% to 0.03%[21].

Unlike FS, colonoscopy also detects lesions in the proximal colon. Its biggest advantage is the possibility of removing pathological lesions within a single examination. It is more sensitive in detecting both adenomas and carcinomas, although limited information is available on reducing CRC incidence and mortality, and on the recommended interval between examinations. The risk of serious adverse events is higher than for FS, at 3 to 5 events per 1000 colonoscopies[22]. To date, no prospective, randomized, multicenter study has been published supporting a reduction in CRC incidence and mortality with the use of screening colonoscopy. Nevertheless, its implementation in screening programs is one of the most widely discussed topics and the American College of Gastroenterology recommends screening colonoscopy as a preferred screening test[23]. On the other hand, no study addressing reductions in the incidence and mortality rates through stool analyses would have been completed without the “gold standard” of colonoscopy.

Computed tomographic colonography (CTC) shows lesions in the colorectum by reconstructing two- and three-dimensional images. To date, no studies have been published assessing reduction in CRC incidence or mortality. The majority of studies have focused on comparing the characteristics of this method with colonoscopy. For larger polyps (over 10 mm), the sensitivity of the methods is comparable; for smaller polyps (less than 5 mm), flat and depressed adenomas, the sensitivity is much higher for optical colonoscopy. Results of studies assessing the effect in terms of reduction in incidence and mortality, cost-effectiveness, and the potential risk of radiation are awaited[24].

Double contrast barium enema shows the entire colorectum, although with significantly lower sensitivity and specificity than colonoscopy or CTC. The percentage of undetected carcinomas is up to 22%. The test is no longer widespread and available, but still has a purpose in countries lacking sufficient resources for other examinations[25].

CRC screening is a complex process which, to function properly, requires the coexistence of a number of factors, such as a functioning invitation-reminder system, media campaigns targeted at the general public, the development of recommendations for general practitioners, patient compliance, sufficient funding, stratification of risks, and last but not least the selection of the most suitable screening test. Of the above described tests, only the fecal occult blood tests meet the WHO criteria for screening. As published recently, most CRC screening strategies lead not only to a reduction in CRC incidence and mortality, but also to better control of the costs of CRC treatment, especially with increased chemotherapy costs for advanced CRC[26].

GENERAL ONCOLOGY PREVENTATIVE PROGRAMS IN EUROPE

In 1985, the Europe Against Cancer program was initiated, which aimed at a reduction of 15% in the number of deaths caused by tumors (from 1 000 000 to 850 000) by 2000. The program was implemented, thanks to the cooperation of professional and lay public, charities and anti-smoking groups, healthcare media, and healthcare workers. The project focused on three major areas: prevention, screening, and education. Results published show that although the planned goal was not achieved, the mortality due to tumors was reduced by 10% in the EU. In some countries (Austria and Finland), the desired reduction of 15% was achieved, while in others (Portugal and Greece), the mortality reduction was much lower[27]. The experience gained in this program served as a basis for the Recommendations of the Council of the EU for screening programs following comprehensive European quality assurance guidelines. In December 2003, these recommendations were unanimously approved by the health ministers of the individual EU states. European guidelines for quality assurance of breast and cervical cancer screening have been developed by experts and published by the European Commission; quality assurance guidelines for CRC screening are currently under preparation[28].

CRC SCREENING IN EUROPE

In 2008, the Report on the Implementation of the Council Recommendation on Cancer Screening[29], which provides the most comprehensive available data, was published; giving the definitions of program screening as requiring public responsibility by law or official regulation and supervision in contrast to “wild” screening outside of any program. In program screening, the screening test, the examination interval and the eligible group of persons should be specified. Organized screening should generally include a regional or national team responsible for the implementation, quality assurance and reporting of results. Comprehensive guidelines, rules and a quality assurance structure should be available. Population-based screening requires the identification and personal invitation of each person in the eligible target population (by an office or special agency). According to this report CRC screening is running or being established in 19 of 27 EU countries. The target group contains approximately 136 million individuals suitable for CRC screening (aged 50 to 74 years). Of this number, 43% individuals come from 12 countries where CRC population screening is performed or being prepared on either national or regional levels; 34% come from 5 countries where national population screening has been implemented (Finland, France, Italy, Poland, and United Kingdom). In 7 EU countries, national non-population based screening is carried out, which covers 27% of the target population. In 2007, gFOBT (which in 2003 was the only test recommended by the Council of the European Union) was used as the only screening method in twelve countries (Bulgaria, Czech Republic, Finland, France, Hungary, Latvia, Portugal, Romania, Slovenia, Spain, Sweden, and United Kingdom). Colonoscopy was the only screening method used in Poland. In six countries, two types of tests were used: iFOBT and FS in Italy, and gFOBT and colonoscopy in Austria, Cyprus, Germany, Greece, and Slovak Republic. In the remaining eight states (Belgium, Denmark, Estonia, Ireland, Lithuania, Luxembourg, Malta, and the Netherlands), CRC screening has not been implemented yet. The age limit for the target population varies across EU countries (Table 6). In 2007, it was estimated that a total of 12 million individuals participated in CRC screening.

Table 6 Colorectal cancer screening programs in 2007.
Program
Test typeScreening interval years or times in LTAge eligible national population
TypeStatusAge (yr)Persons (× 1000)
AustriaNonPBNatwFOBT1 or 2> 502210
NonPBNatwCS10> 502210
BelgiumNo Prog2880
BulgariaNonPBNatwFOBT1> 312340
CyprusPBNatw-planFOBT1 in LT5010
PBNatw-planCS1 in LT5510
Czech RepublicNonPBNatwFOBT2> 503010
DenmarkNo Prog1540
EstoniaNo Prog370
FinlandPBNatw-roll ongFOBT260-69570
FrancePBNatw-roll ongFOBT250-7416 600
GermanyNonPBNatwFOBT1 and 2> 5024 500
NonPBNatwCS10 (2 in LT)55-7418 800
GreeceNonPBNatwFOBT5> 503180
NonPBNatwCS5> 503180
HungaryPBNatw-pilotFOBT250-702630
IrelandNo Prog940
ItalyPBNatw-roll ongFOBT250-69 (70-75)13 800
PBReg-roll ongFS1 in LT58 or 6080
LatviaNonPBNatwFOBT1> 50630
LithuaniaNo Prog870
LuxembourgNo Prog120
MaltaNo Prog120
NetherlandsNo Prog4460
PolandPBNatw-roll ongCS1050-657500
PortugalPBNatw-planFOBT250-702520
RomaniaPBNatw-planFOBT250-745800
Slovak RepublicNonPBNatwFOBT> 501360
NonPBNatw-planCS10> 501360
SloveniaPBNatw-planFOBT250-69490
SpainPBReg-pilotFOBT250-69210
SwedenPBReg-planFOBT260-69220
UKPBNatw-roll ongFOBT2(50) 60-69 (74)7600
Dual prog/test-25 630
Subtotal106 490
Excluded pop.29 500
Total135 990

In the United Kingdom, a screening program was announced in 2004 and initiated in 2006, with the prospect of national coverage in 2009. It has been designed in two stages, with gFOBT examinations at 2-year intervals and colonoscopy for positive tests. In 2007, compliance was 52%. The program is carried out through regional centers falling under one of five national hubs. The role of general practitioners is less significant here[30].

In France, a screening program was initiated in 2003, based on gFOBT tests at 2-year intervals with colonoscopy for positive results. The role of general practitioners as coordinators is of crucial importance. The major advantage of the French program is its good organization, with a call-recall system comprising central management at national level and individual steps taken by centers in individual departments. Asymptomatic individuals aged from 50 to 74 are mailed gFOBT tests, with a reminder at three-monthly intervals for nonparticipants. Compliance in referred districts achieved 42%, and the overall positive test rate was 2.7%[31].

In Italy, a nation-wide campaign was initiated in 2005; the implementation was entrusted entirely to 21 regional centers, including choice of the testing method. With state financial support, screening has been initiated in 11 regions to date, mostly in the industrial areas of northern Italy. In the Piedmont region, FS is the method of choice, in other regions immunochemical FOBT, with colonoscopy for positive tests. Compliance in iFOBT and FS programs was 44.6% and 51.4%, respectively. Positivity rate of iFOBT was 5.3% at first and 3.9% at repeat screening[32].

In Spain, no screening program has taken place as yet. The main obstacle to its implementation is the highly heterogeneous healthcare system, in terms of organization and insurance coverage in individual self-governing units. Catalonia, for instance, considers implementation of country-wide screening in 2010, while in other regions only limited pilot studies have been held so far.

In Finland, a structured screening program was initiated in 2004. The target population, aged from 60 to 69 years (106 000 individuals), was randomized into two groups. Individuals in the screening group were mailed a gFOBT test at intervals of 2 years. The Finnish program shows a high level of compliance of the target population (70.8%), particularly for females[33].

In the Netherlands, the optimum screening strategy is still being developed. It will be based on the results of studies currently taking place at major academic workplaces, comparing the effect of endoscopic procedures, various types of FOBTs, and fecal DNA analysis.

Poland is the only state at the moment using colonoscopy as the only screening method, without the alternative of FOBT. An opportunistic screening program was initiated in 2000, and by 2005, this had grown to 57 centers across Poland. The program is financed by the Ministry of Health, independent of the overall healthcare system. The target population (asymptomatic individuals aged 55-66 years) is recruited through general practitioners. High emphasis is placed on the quality control of colonoscopies, with complications reported for 0.1% of procedures, and no patient mortality. The advantage of the program is thorough monitoring and evaluation, including monitoring of interval cancers[34].

Germany was the first country to introduce a population screening program (in 1976) based on annual gFOBT for individuals more than 44 years of age. Starting from 2002, it has been offering participants a choice between colonoscopy at 55 years of age and FOBT at annual intervals between 50 and 55 years of age. After 55 years of age, examinations are carried out at 2-year intervals. If the test results are positive, colonoscopy is indicated. Those who undergo a screening colonoscopy with no neoplasia detected at the initial examination are recommended reexamination in 10 years time if the first colonoscopy was carried out before they were 65 years. The positive feature of the screening and data gathering in Germany is the emphasis on staging the disease at the time of its diagnosis. Recent cost analyses have proven that this type of screening is cost-efficient[35].

In the Czech Republic, CRC screening has many years of tradition[36,37]. The country was the second in the world to start screening nation-wide, in 2000. In the initial years, gFOBT was the first method offered to asymptomatic individuals more than 50 years of age by their general practitioners at preventative medical checks, followed by colonoscopy if tests were positive. From 2000 to 2008, 1 685 289 gFOBTs were carried out, of which 63 296 were positive (3.76%). In 2006, a central database for online data input was established. Between 2006 and 2008, 17 813 colonoscopies were carried out, indicated as a result of a positive FOBT; carcinoma was diagnosed in 1047 (5.9%) individuals, and 5362 (30.1%) adenomas were removed by endoscopic polypectomy. The participation of the target group, however, was only 20%[38]. In order to achieve a higher compliance rate, screening colonoscopy was added to current FOBT screening as an alternative method, in the same intervals as in the German program. Both, gFOBT and iFOBT are offered as well. The implementation of the newly designed program is supported by an intensive media campaign (http://www.kolorektum.cz/index-en.php).

The first study which focused on monitoring the effect of colonoscopy screening on reducing CRC incidence and mortality is NordICC (The Nordic-European Initiative on Colorectal Cancer), which is currently underway in northern states of Europe (Norway, Sweden, and Iceland), Poland, and the Netherlands. It will involve a minimum of 66 000 individuals aged 55 to 64 years. Individuals in the screening group will undergo a screening colonoscopy once in a lifetime. The primary objective is to compare incidence and mortality against the control group (with no screening) after 10 years[39].

CONCLUSION

CRC presents a serious public healthcare issue for the population of Europe. Understandably, the number of countries introducing population screening has been growing constantly. Although epidemiologic data differ in various European countries, implementation of screening programs in accordance with the principles spelled out in the Council Recommendation on Cancer Screening of 2 December 2003 may be expected to have a favorable effect on the burden of this disease in the population. Countries in the EU may benefit from unified policy, knowhow and central oncology registers, while economically less developed countries may draw on special funding for the development of preventative programs. At the same time, varying epidemiologic situations, economic conditions, and different systems of health insurance and organization of healthcare are factors that may limit the implementation of a unified screening program. Therefore, to respond to the needs of the member countries, the EU should consider adopting the recommendation of the World Gastroenterology Organization for CRC screening, possibly even in a modified form[40]. This is a cascade concept in which recommendations for individual countries are graded into six levels, depending on the resources available (financial and professional) (Table 7). In the case of lack of funds, FOBT at intervals of 1 or 2 years for individuals with average risk is a realistic possibility. This open concept best fulfils the simple recommendation by Sydney Winawer, Co-Chair of IDCA (International Digestive Cancer Alliance): “The best screening test is the one that gets done...and gets done well. Do what you can with what you have”.

Table 7 Cascade concept.
LevelAverage riskHigh risk
1Colonoscopy in 10 years interval, from 50 years of ageSpecial procedure, for individual groups
2Colonoscopy once in a lifetime, at 50 years of ageSpecial procedure, for individual groups
3Flexible sigmoidoscopy in 5 years interval, from 50 years of age; colonoscopy to follow if positiveSpecial procedure, for individual groups
4Flexible sigmoidoscopy once in a lifetime, at 50 years of age; colonoscopy to follow if positiveSpecial procedure, for individual groups
5Flexible sigmoidoscopy once in a lifetime, at 50 years of age; colonoscopy to follow only if advanced adenoma is detectedSame as individuals with average risk, if resources are not available for colonoscopy
6FOBT in annual interval after 50 years of age; if positively tested, colonoscopy or double contrast barium enemaSame as individuals with average risk, if resources are not available for colonoscopy

In most European countries, fortunately, the majority of the population is covered by some form of health insurance, meaning that economic aspects need not critically affect the availability of screening programs. Although at the end of 2007, CRC screening was still not running or being established in 8 of 27 EU member states, some of which rank among the most developed economies of the world, additional programs are currently under development. Given the substantial burden of the disease, implementation and continuous improvement in CRC screening programs should remain high on the healthcare agenda in Europe.

Footnotes

Peer reviewer: Dr. James Hardwick, Department of Gastroenterology, Leiden University Medical Center, Albinusdreef 2, 2300RC, Leiden, The Netherlands

S- Editor Tian L L- Editor Webster JR E- Editor Ma WH

References
1.  Spann SJ, Rozen P, Young GP, Levin B. Colorectal cancer: how big is the problem, why prevent it, and how might it present? Colorectal Cancer in Clinical Practice. London: Martin Dunitz Ltd 2002; 1-18.  [PubMed]  [DOI]  [Cited in This Article: ]
2.  Curado MP, Edwards B, Shin HR, Storm H, Ferlay J, Heanue M, Boyle P, editors .  Cancer Incidence in Five Continents, Vol. IX. IARC Scientific Publications No. 160, Lyon: IARC 2007;  Available from: http://www-dep.iarc.fr/ section CI5 IX. Last accessed on August 8, 2009.  [PubMed]  [DOI]  [Cited in This Article: ]
3.  World Health Organization (2006), mortality database http://www.who.int/whosis/whosis/ United Nations, World Population Prospects, the. 160, Lyon: IARC 2006; revision Available from: http://www-dep.iarc.fr/. Last accessed on August 8, 2009.  [PubMed]  [DOI]  [Cited in This Article: ]
4.  Ferlay J, Bray F, Pisani P, Parkin DM.  GLOBOCAN 2002: Cancer incidence, mortality and prevalence worldwide. IARC Cancer Base No. 5 version 2.0. Lyon: IARC press 2004;  Available from: http://www-dep.iarc.fr/, section CI5 I-VIII (Detailed). Last accessed on August 8, 2009.  [PubMed]  [DOI]  [Cited in This Article: ]
5.  Parkin DM, Whelan SL, Ferlay J, Storm H.  Cancer Incidence in Five Continents, Vol. I to VIII. IARC CancerBase No. 7, Lyon. Lyon: IARC press 2005;  Available from: http://www-dep.iarc.fr/, section CI5 I-VIII (Detailed). Last accessed on August 8, 2009.  [PubMed]  [DOI]  [Cited in This Article: ]
6.  Ferlay J, Autier P, Boniol M, Heanue M, Colombet M, Boyle P. Estimates of the cancer incidence and mortality in Europe in 2006. Ann Oncol. 2007;18:581-592.  [PubMed]  [DOI]  [Cited in This Article: ]
7.  Berrino F, De Angelis R, Sant M, Rosso S, Bielska-Lasota M, Coebergh JW, Santaquilani M. Survival for eight major cancers and all cancers combined for European adults diagnosed in 1995-99: results of the EUROCARE-4 study. Lancet Oncol. 2007;8:773-783.  [PubMed]  [DOI]  [Cited in This Article: ]
8.  Verdecchia A, Francisci S, Brenner H, Gatta G, Micheli A, Mangone L, Kunkler I. Recent cancer survival in Europe: a 2000-02 period analysis of EUROCARE-4 data. Lancet Oncol. 2007;8:784-796.  [PubMed]  [DOI]  [Cited in This Article: ]
9.  Coleman MP, Quaresma M, Berrino F, Lutz JM, De Angelis R, Capocaccia R, Baili P, Rachet B, Gatta G, Hakulinen T. Cancer survival in five continents: a worldwide population-based study (CONCORD). Lancet Oncol. 2008;9:730-756.  [PubMed]  [DOI]  [Cited in This Article: ]
10.  Mitry E, Rachet B, Quinn MJ, Cooper N, Coleman MP. Survival from cancer of the colon in England and Wales up to 2001. Br J Cancer. 2008;99 Suppl 1:S26-S29.  [PubMed]  [DOI]  [Cited in This Article: ]
11.  Mitry E, Rachet B, Quinn MJ, Cooper N, Coleman MP. Survival from cancer of the rectum in England and Wales up to 2001. Br J Cancer. 2008;99 Suppl 1:S30-S32.  [PubMed]  [DOI]  [Cited in This Article: ]
12.  Gondos A, Arndt V, Holleczek B, Stegmaier C, Ziegler H, Brenner H. Cancer survival in Germany and the United States at the beginning of the 21st century: an up-to-date comparison by period analysis. Int J Cancer. 2007;121:395-400.  [PubMed]  [DOI]  [Cited in This Article: ]
13.  Gondos A, Bray F, Brewster DH, Coebergh JW, Hakulinen T, Janssen-Heijnen ML, Kurtinaitis J, Brenner H. Recent trends in cancer survival across Europe between 2000 and 2004: a model-based period analysis from 12 cancer registries. Eur J Cancer. 2008;44:1463-1475.  [PubMed]  [DOI]  [Cited in This Article: ]
14.  Gondos A, Bray F, Hakulinen T, Brenner H. Trends in cancer survival in 11 European populations from 1990 to 2009: a model-based analysis. Ann Oncol. 2009;20:564-573.  [PubMed]  [DOI]  [Cited in This Article: ]
15.  Janssen-Heijnen ML, Houterman S, Lemmens VE, Brenner H, Steyerberg EW, Coebergh JW. Prognosis for long-term survivors of cancer. Ann Oncol. 2007;18:1408-1413.  [PubMed]  [DOI]  [Cited in This Article: ]
16.  Talback M, Rosen M, Stenbeck M, Dickman PW. Cancer patient survival in Sweden at the beginning of the third millennium--predictions using period analysis. Cancer Causes Control. 2004;15:967-976.  [PubMed]  [DOI]  [Cited in This Article: ]
17.  Imperiale TF, Ransohoff DF, Itzkowitz SH, Turnbull BA, Ross ME. Fecal DNA versus fecal occult blood for colorectal-cancer screening in an average-risk population. N Engl J Med. 2004;351:2704-2714.  [PubMed]  [DOI]  [Cited in This Article: ]
18.  Mandel JS, Bond JH, Church TR, Snover DC, Bradley GM, Schuman LM, Ederer F. Reducing mortality from colorectal cancer by screening for fecal occult blood. Minnesota Colon Cancer Control Study. N Engl J Med. 1993;328:1365-1371.  [PubMed]  [DOI]  [Cited in This Article: ]
19.  van Rossum LG, van Rijn AF, Laheij RJ, van Oijen MG, Fockens P, van Krieken HH, Verbeek AL, Jansen JB, Dekker E. Random comparison of guaiac and immunochemical fecal occult blood tests for colorectal cancer in a screening population. Gastroenterology. 2008;135:82-90.  [PubMed]  [DOI]  [Cited in This Article: ]
20.  Ahlquist DA, Sargent DJ, Loprinzi CL, Levin TR, Rex DK, Ahnen DJ, Knigge K, Lance MP, Burgart LJ, Hamilton SR. Stool DNA and occult blood testing for screen detection of colorectal neoplasia. Ann Intern Med. 2008;149:441-450, W81.  [PubMed]  [DOI]  [Cited in This Article: ]
21.  Single flexible sigmoidoscopy screening to prevent colorectal cancer: baseline findings of a UK multicentre randomised trial Lancet. 2002;359:1291-1300.  [PubMed]  [DOI]  [Cited in This Article: ]
22.  Lieberman DA. Clinical practice. Screening for colorectal cancer. N Engl J Med. 2009;361:1179-1187.  [PubMed]  [DOI]  [Cited in This Article: ]
23.  Rex DK, Johnson DA, Lieberman DA, Burt RW, Sonnenberg A. Colorectal cancer prevention 2000: screening recommendations of the American College of Gastroenterology. American College of Gastroenterology. Am J Gastroenterol. 2000;95:868-877.  [PubMed]  [DOI]  [Cited in This Article: ]
24.  Johnson CD, Chen MH, Toledano AY, Heiken JP, Dachman A, Kuo MD, Menias CO, Siewert B, Cheema JI, Obregon RG. Accuracy of CT colonography for detection of large adenomas and cancers. N Engl J Med. 2008;359:1207-1217.  [PubMed]  [DOI]  [Cited in This Article: ]
25.  Toma J, Paszat LF, Gunraj N, Rabeneck L. Rates of new or missed colorectal cancer after barium enema and their risk factors: a population-based study. Am J Gastroenterol. 2008;103:3142-3148.  [PubMed]  [DOI]  [Cited in This Article: ]
26.  Lansdorp-Vogelaar I, van Ballegooijen M, Zauber AG, Habbema JD, Kuipers EJ. Effect of rising chemotherapy costs on the cost savings of colorectal cancer screening. J Natl Cancer Inst. 2009;101:1412-1422.  [PubMed]  [DOI]  [Cited in This Article: ]
27.  Boyle P, d‘Onofrio A, Maisonneuve P, Severi G, Robertson C, Tubiana M, Veronesi U. Measuring progress against cancer in Europe: has the 15% decline targeted for 2000 come about? Ann Oncol. 2003;14:1312-1325.  [PubMed]  [DOI]  [Cited in This Article: ]
28.  European Council. Council Recommendation of 2 December 2003 on cancer Screening (2003/878/EC). OJ L 327 (16 December 2003), 3, 14-15.  Available from: http://eurlex.europa.eu/LexUriServ/LexUriServ.do?uri=OJ:L:2003:327:0034:0038:EN:PDF. Last accessed on August 4, 2009.  [PubMed]  [DOI]  [Cited in This Article: ]
29.  von Karsa L, Anttila A, Ronco G, Ponti A, Malila N, Arbyn M, Segnan N, Castillo-Beltran M, Boniol M, Ferlay J.  Cancer screening in the European Union. Report on the implementation of the Council Recommendation on cancer screening - First Report. ISBN 978-92-79-08934-3. European Communities (publ.) Printed in Luxembourg by the services of the European Commission. Lyon: IARC press 2008;  Available from: http://ec.europa.eu/health/ph_determinants/genetics/documents/cancer_screening.pdf. Last accessed on August 4, 2009.  [PubMed]  [DOI]  [Cited in This Article: ]
30.  West NJ, Boustiere C, Fischbach W, Parente F, Leicester RJ. Colorectal cancer screening in Europe: differences in approach; similar barriers to overcome. Int J Colorectal Dis. 2009;24:731-740.  [PubMed]  [DOI]  [Cited in This Article: ]
31.  Goulard H, Boussac-Zarebska M, Ancelle-Park R, Bloch J. French colorectal cancer screening pilot programme: results of the first round. J Med Screen. 2008;15:143-148.  [PubMed]  [DOI]  [Cited in This Article: ]
32.  Zorzi M, Falcini F, Fedato C, Grazzini G, de’ Bianchi PS, Senore C, Vettorazzi M, Visioli C, Zappa M. Screening for colorectal cancer in Italy: 2006 survey. Epidemiol Prev. 2008;32:55-68.  [PubMed]  [DOI]  [Cited in This Article: ]
33.  Malila N, Oivanen T, Malminiemi O, Hakama M. Test, episode, and programme sensitivities of screening for colorectal cancer as a public health policy in Finland: experimental design. BMJ. 2008;337:a2261.  [PubMed]  [DOI]  [Cited in This Article: ]
34.  Regula J, Rupinski M, Kraszewska E, Polkowski M, Pachlewski J, Orlowska J, Nowacki MP, Butruk E. Colonoscopy in colorectal-cancer screening for detection of advanced neoplasia. N Engl J Med. 2006;355:1863-1872.  [PubMed]  [DOI]  [Cited in This Article: ]
35.  Pox C, Schmiegel W, Classen M. Current status of screening colonoscopy in Europe and in the United States. Endoscopy. 2007;39:168-173.  [PubMed]  [DOI]  [Cited in This Article: ]
36.  Fric P, Zavoral M, Dvorakova H, Zoubek V, Roth Z. An adapted program of colorectal cancer screening--7 years experience and cost-benefit analysis. Hepatogastroenterology. 1994;41:413-416.  [PubMed]  [DOI]  [Cited in This Article: ]
37.  Zavoral M, Zavada Filip, Salek C. Czech Society of Gastroenterology: Colorectal Cancer Screening in the Czech Republic. Endoscopy. 2006;38:550-551.  [PubMed]  [DOI]  [Cited in This Article: ]
38.  Seifert B, Zavoral M, Fric P, Bencko V. The role of primary care in colorectal cancer screening: experience from Czech Republic. Neoplasma. 2008;55:74-80.  [PubMed]  [DOI]  [Cited in This Article: ]
39.  NordiCC Study Protocol. Version MB 260409.  Available from: http://www.kreftregisteret.no/en/Research/Projects/NordICC. Last accessed on August 4, 2009.  [PubMed]  [DOI]  [Cited in This Article: ]
40.  World Gastroenterology Organization/International Digestive Cancer Alliance. Practice Guidelines: Colorectal cancer screening.  Available from: http://www.worldgastroenterology.org/colorectal-cancer-screening.html. Last accessed on August 4, 2009.  [PubMed]  [DOI]  [Cited in This Article: ]