Cancer in numbers: Do preventive measures for colorectal cancer apply?

Authors

  • Pedro J. Tarraga López Departamento de Medicina. Universidad de Castilla-La Mancha
  • José A. Rodríguez Montes Catedrático Emérito de Cirugía Universidad Autónoma de Madrid.
  • Juan Solera Albero Coordinador Médico EAP zona 7 Albacete
  • Almudena Tárraga Marcos Departamento de Medicina. Universidad de Castilla-La Mancha

DOI:

https://doi.org/10.19230/jonnpr.1597

Keywords:

Cancer, Colorectal cancer, Primary Prevention, Secondary Prevention

Abstract

Introduction: Cancer is a global problem as it will affect one in three men and one in four women during their lifetime. Colorectal cancer (CRC) is the second most common cancer in men, after lung cancer, and is the second most common cancer in women after breast cancer. It is also the second leading cause of death in men and women separately, and is the second most common cause of cancer death if both genders are considered together. CRC accounts for approximately 10% of cancer deaths. Modifiable risk factors for CRC include smoking, physical inactivity, overweight and obesity, processed meat consumption, and excessive alcohol consumption. CRC screening programs are possible in economically developed countries. However, attention should be paid in the future to geographically populated areas and western lifestyles.

Objective: To evaluate the effect on the incidence and mortality of diet and lifestyle of CRC and to determine the effect of secondary prevention through the early diagnosis of CRC.

Methodology: An exhaustive search of Medline and Pubmed articles related to primary and secondary prevention of CRC is carried out and a meta-analysis of the same blocks is carried out.

Results: 301 items related to primary or secondary prevention of CRC were recovered. Of these, 177 were considered valid in the meta-analysis: 12 in epidemiology, 56 in diet and lifestyle, and over 77 different projections for the early detection of CRC. Cancer is a global problem as it will affect one in three men and one in four women during their lifetime. There is no question of which environmental factors, probably diet, may explain these cancer rates. Excessive consumption of alcohol and high cholesterol diet are associated with a high risk of colon cancer. A diet low in folic acid and vitamin B6 is also associated with an increased risk of developing colon cancer with overexpression of p53. Eating pulses at least three times a week reduces the risk of developing colon cancer by 33% after eating less meat, while eating brown rice at least once a week reduces the risk of CRC by 40%. These associations suggest a dose-response effect. Frequently eating cooked vegetables, nuts, nuts, legumes and brown rice has been associated with a lower risk of colorectal polyps. High calcium intake provides a protective effect against distal colon and rectum tumors compared to the proximal colon. Increased intake of dairy and calcium reduces the risk of colon cancer. Regularly taking aspirin (ASA) after being diagnosed with colon cancer is associated with less risk of dying from this cancer, especially among people who have COX-2 overexpressing tumors. However, these data do not contradict the data obtained on a possible genetic predisposition, even in sporadic or non-hereditary CRC. CRC is susceptible to detection because it is a serious health problem due to its high incidence and high associated morbidity / mortality.

Conclusions: (1) Cancer is a global problem. (2) A modification of diet and lifestyle could reduce morbidity and mortality. (3) Early detection through screening improves prognosis and reduces mortality.

 

Downloads

Download data is not yet available.

References

Siegel R, Ward E, Brawley O, Jemal A. Cancer statistics, 2011: the impact of eliminating socioeconomic and racial disparities on premature cancer deaths. CA Cancer J Clin. 2011;61:212–236.

Bray F, Jemal A, Grey N, Ferlay J, Forman D. Global cancer transition according to the human development index (2008–2030): a population- based study. Lancet Oncol. 2012;13:790–801.

American Cancer Society. Cancer Facts & Figures, 2013. Atlanta, GA: American Cancer Society; 2013.

Ferlay J, Steliarova-Foucher E, Lortet-Tieulent J, et al. Cancer incidence and mortality patterns in Europe: estimated for 40 countries in 2012. Eur J Cancer. 2013;49:1374–1403.

Jemal A, Bray F, Center MM, Ferlay J, Ward E, Forman D. Global cancer statistics. CA Cancer J Clin. 2011;61:69–90.

Center MM, Jemal A, Ward E. International trends in colorectal cancer incidence rates. Cancer Epidemiol Biomarkers Prev. 2009;18:1688–1694.

Center MM, Jemal A, Smith RA, Ward E. Worldwide variatios in colorectal cancer. CA Cancer J Clin. 2009;59:366–378.

Boffetta P, Hazelton WD, Chen Y, et al. Body mass, tobacco smoking, alcohol drinkings and risk of cancer of the small intestine—a pooled analysis of over 500,000 subjects in the Asia Cohort Consortium. Ann Oncol. 2012;23:1894–1898.

Edwards BK, Ward E, Kohler BA, et al. Annual report to the nation on the status of cancer, 1975–2006, featuring colorectal cancer trends and impact of interventions (risk factors, screening, and treatment) to reduce future rates.Cancer. 2010;116:544–573.

Vargas AJ, Thompson PA. Diet and nutrient factors in colorectal cancer risk. Nutr Clin Pract. 2012;27:613–623.

Su LJ, Arab L. Alcohol consumption and risk of colon cancer: evidence from the National Health and Nutrition Examination Survey I Epidemiologic Follow-up study. Nutr Cancer. 2004;50: 111–119.

Hu J, La Vecchia C, de Groh M, Negri E, Morrison H, Mery L. Dietary cholesterol intake and cancer. Ann Oncol. 2012;23:491–500.

Schernhamer ES, Ogino S, Fuch CS. Folate and vitamin B6 intake and risk of colon cancer in relation to p53 expression. Gastroenterology. 2008;135:770–780.

Tantamango YM, Knutsen SF, Beeson WL, Fraser G, Sabate J. Foods and food groups associated with the incidence of colorectal polyps: the Adventist Health Study. Nutr Cancer. 2011;63:565–572.

Huncharek M, Muscat J, Kupelnick B. Colorectal cancer risk and dietary intake of calcium, vitamin D, and dairy products: a meta-analysis of 26,335 cases from 60 observational studies. Nutr Cancer. 2009;61:47– 69.

Chan AT, Giovannucci EL, Meyerhardt JA, Schernhammer ES, Wu K, Fuchs CS. Aspirin dose and duration of use and risk of colorectal cancer in men. Gastroenterology. 2008;134:21–28.

Ferrari P, Jenab M, Novat T, et al. Lifetime and baseline alcohol intake and risk of colon and rectal cancer in the European prospective investigations into cancer and nutrition (EPIC). Int J Cancer. 2007;121:2065–2072.

Boyle P, Levin B, eds. World Cancer Report 2008. Lyon: International Agency for Research on Cancer; 2008.

Mandel JS, Bond JH, Church TR, et al. Reducing mortality from colorectal cancer by screening for fecal occult blood. Minnesota Colon Cancer Control Study. N Engl J Med. 1993;328:1365–1371.

Muller AD, Sonnenberg A. Prevention of colorectal cancer by flexible endoscopy and polypectomy. A case–control study of 32,702 veterans. Ann Intern Med. 1995;123:904–910.

Atkin WS, Edwards R, Kralj-Hans I, et al. Once-only flexible sigmoidoscopy screening in prevention of colorectal cancer: a multicentre randomized controlled trial. Lancet. 2010;375:1624–1633.

Weitz J, Koch M, Debus J, Hôhler T, Gall PR, Büchler MW. Colorectal cancer. Lancet. 2005;365:153–165.

Winawer SJ, Zauber AG, Verdes H, et al. Risk of colorectal cancer in the families of patients with adenomatous polyps. National Polyp Study Work group. N Engl J Med. 1996;334:82–87.

Johns LE, Houlston RS. A systematic review and meta-analysis of familial colorectal cancer risk. Am J Gastroenterol. 2001;96:2992–3003.

Lynch KL, Ahnen DJ, Byers T, Weiss DG, Lieberman DA. First-degree relatives of patients with advanced colorectal adenomas have an increased prevalence of colorectal cancer. Clin Gastroenterol Hepatol. 2003;1:96–102.

Wingo PA, Jamison PM, Hiatt RA, et al. Building the infrastructure for nationwide cancer surveillance and control—a comparison between the National Program of Cancer Registries (NPGR) and the Survelillance, Epidemiology, and End Results (SEER) Program (United States). Cancer Causes Control. 2003;14:175–193.

Feig B, Berger D, Furnham G. Oncología Quirúrgica. Madrid: Editorial Marbán Libros SL; 2005:212.

Piñol V, Andreu M, Castells A, Payá A, Bessa X, Jover R. Frequency of hereditary non-polyposis colorectal cancer and other colorectal cancer familial forms in Spain. A multicenter, prospective, nation-wide study. Gastrointestinal Oncology Group of the Spanish Gastroenterological Association. Eur J Gastroenterol Hepatol 2004; 16: 39-45.

Hampel H, Frankel WL, Martin E, Arnold M, Khanduja K, Kuebler P, et al. Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer). N Engl J Med 2005; 352: 1851-60.

Lindor NM, Burgart LJ, Leontovich O, Goldberg RM, Cunningham JM, Sargent DJ, et al. Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors. J Clin Oncol 2002; 20: 1043-8.

Percesepe A, Borghi F, Menigatti M, Losi L, Foroni M, Di Gregorio C, et al. Molecular screening for hereditary nonpolyposis colorectal cancer: A prospective, population-based study. J Clin Oncol 2001; 19: 3944-50.

Pares D, Pera M, González S, Pascual Cruz M, Blanco I. Poliposis adenomatosa familiar. Gastroenterol Hepatol 2006; 29: 625-35.

Lynch HT, De la Chapelle A. Hereditary colorectal cancer. N Engl J Med 2003; 348: 919-32.

Anwar S, White J, Hall C, Farrell WE, Deakin M, Elder JB. Sporadic colorectal polyps: Management options and guidelines. Scand J Gastroenterol 1999; 34: 4-11.

Atkin WS, Saunders BP. Surveillance guidelines after removal of colorectal adenomatous polyps. Gut 2002; 51: V6-V9.

Martinez ME. Primary prevention of colorectal cancer: Lifestyle, nutrition, exercise. Recent Results Cancer Res 2005; 166: 177-211.

Cho E, Smith-Warner SA, Ritz J, Van den Brandt PA, Colditz GA, Folsom AR, et al. Alcohol intake and colorectal cancer: A pooled analysis of 8 cohort studies. Ann Intern Med 2004; 140: 603-13.

Van den Brandt PA, Goldbohm RA. Nutrition in the prevention of gastrointestinal cancer. Best Pract Res Clin Gastroenterol 2006; 20: 589- 603.

Bergstrom A, Pisani P, Tenet V, Wolk A, Adami HO. Overweight as an avoidable cause of cancer in Europe. Int J Cancer 2001; 91: 421-30.

Gunter MJ, Leitzmann MF. Obesity and colorectal cancer: Epidemiology, mechanisms and candidate genes. J Nutr Biochem 2006; 17: 145-56.

McTiernan A. Obesity and cancer: The risks, science, and potential management strategies. Oncology 2005; 19:871-81.

Ma J, Giovannucci E, Pollak M, Leavitt A, Tao Y, Gaziano JM, et al. A prospective study of plasma C-peptide and colorectal cancer risk in men. J Natl Cancer Inst 2004; 96: 546-53.

Park Y, Hunter DJ, Spiegelman D, Bergkvist L, Berrino F, Van den Brandt PA, et al. Dietary fiber intake and risk of colorectal cancer: A pooled analysis of prospective cohort studies. JAMA 2005; 294: 2849-57.

Alberts DS, Martínez ME, Roe DJ, Guillén-Rodríguez JM, Marshall JR, Van Leeuwen JB, et al. Lack of effect of a high-fiber cereal supplement on the recurrence of colorectal adenomas. Phoenix Colon Cancer Prevention Physician´s Network. N Engl J Med 2000; 342: 1156-62.

Norat T, Bingham S, Ferrari P, Slimani N, Jenab M, Mazuir M, et al. Meat, fish and colorectal cancer risk: The European Prospective Investigation into Cancer and Nutrition. J Natl Cancer Inst 2005; 97: 906- 16.

Sandhu MS, White IR, McPherson K. Systematic review of the prospective cohort studies on meat consumption and colorectal cancer risk: A meta-analytical approach. Cancer Epidemiol Biomarkers Prev 2001; 10: 439-46.

Cho E, Smith-Warner SA, Spiegelman D, Beeson WL, Van den Brandt PA, Colditz GA, et al. Dairy foods, calcium and colorectal cancer: A pooled analysis of 10 cohort studies. J Natl Cancer Inst 2004; 96: 1015-22.

Baron JA, Beach M, Mandel JS, Van Stolk RU, Haile RW, Sandler RS, et al. Calcium supplements for the prevention of colorectal adenomas. Calcium Polyp Prevention Study Group. N Engl J Med 1999; 340: 101-7.

Solera Albero J, Tárraga López PJ, López Cara MA, Celada Rodríguez A, Cerdán Oliver M, Ocaña López JM. Influencia de la dieta y los estilos de vida en el cáncer colorrectal. Rev Esp Enferm Dig 2007; 99: 190-200.

Pedro J Tárraga López, Juan Solera Albero, and José Antonio Rodríguez-Montes. Primary and Secondary Prevention of Colorectal Cancer Clin Med Insights Gastroenterol. 2014; 7: 33–46.

Franco A, Sikalidis AK, Solís Herruzo JA. Colorectal cancer: influence of diet and lifestyle factors. Rev Esp Enferm Dig 2005; 97: 432-48.

Sandhu MS, White IR, McPherson K. Systematic review of the prospective cohort studies on meat consumption and colorectal cancer risk: a meta-analytical approach. Cancer Epidemiol Biomarkers Prev. 2001;10:439–446.

Norat T, Lukanova A, Ferrari P, Riboli E. Meat consumption and colorectal cancer risk: dose–response metaanalysis of epidemiological studies. Int J Cancer. 2002;98:241–256.

Norat T, Lukanova A, Ferrari P, Riboli E. Meat consumption and colorectal cancer risk: an estimate of attributable and preventable fractions. IARC Sci Publ. 2002;156:223–225.

Larsson SC, Wolk A. Meat consumption and risk of colorectal cancer: a metaanalysis of prospective studies. Int J Cancer. 2006;119:2657– 2664.

Le Marchand L. Meat intake, metabolic genes and colorectal cancer. IARC Sci Publ. 2002;156:481–485.

Santarelli RL, Pierre F, Corpet DE. Processed meat and colorectal cancer: a review of epidemiologic and experimental evidence. Nutr Cancer. 2008;60:131–144.

Riboli E, Norat T. Epidemiologic evidence of the protective effect of fruit and vegetables on cancer risk. Am J Clin Nutr. 2003;78:559S–569S.

Park Y, Hunter DJ, Spiegelman D, et al. Dietary fiber intake and risk of colorectal cancer: a pooled analysis of prospective cohort studies. JAMA. 2005;294:2849–2857.

Schatzkin A, Mouw T, Park Y, et al. Dietary fiber and whole-grain consumption in relation to colorectal cancer in the NIH-AARP Diet and Health Study. Am J Clin Nutr. 2007;85:1353–1360.

Koushik A, Hunter DJ, Spiegelman D, et al. Fruits, vegetables, and colon cancer risk in a pooled analysis of 14 cohort studies. J Natl Cancer Inst. 2007;99:1471–1483.

Asano TK, McLeod RS. Fibra dietética para la prevención de carcinomas y adenomas colorrectales. Oxford: Update Software Ltd; 2008.

Jacobs ET, Lanza E, Alberts DS, et al. Fiber, sex, and colorectal adenoma: results of a pooled analysis. Am J Clin Nutr. 2006;83:343–349.

Millen AE, Subar AF, Graubard BI, et al. Fruit and vegetable intake and prevalence of colorectal adenoma in a cancer screening trial. Am J Clin Nutr. 2007;86:1754–1764.

Norat T, Riboli E. Dairy products and colorectal cancer: a review of possible mechanisms and epidemiological evidence. Eur J Clin Nutr. 2003;57:1–17.

Rodrigo L, Riestra S. Diet and colon cancer. Rev Esp Enferm Dig. 2007;99(4):183–189.

Cho E, Smith-Warner SA, Spiegelman D, et al. Dairy foods, calcium, and colorectal cancer: a pooled analysis of 10 cohort studies. J Natl Cancer Inst. 2004;96:1015–1022.

Sanjoaquin MA, Allen N, Couto E, Roddam AW, Key TJ. Folate intake and colorectal cancer risk: a metaanalytical approach. Int J Cancer.

;113:825–828.

Logan RF, Grainge MJ, Shepherd VC, Armitage NC, Muir KR. Aspirin and folic acid for the prevention of recurrent colorectal adenomas.

Gastroenterology. 2008; 134:29–38.

Cole BF, Baron JA, Sandler RS, et al. Folic acid for the prevention of colorectal adenomas: a randomized clinical trial. JAMA. 2007;297:2351– 2359.

Wactawski-Wende J, Kotchen JM, Anderson GL, et al. Calcium plus vitamin D supplementation and the risk of colorectal cancer. N Engl J Med. 2006;354: 684–696.

Larriba MJ, Valle N, Pálmer HG, et al. The inhibition of Wnt/beta- catenin signalling by 1alfa, 25-dihydroxivitamin D3 is abrogated by Snail in human colon cancer cells. (Artículo) Endocrine-Related Cancer. 2007;14:1–12.

Ding EL, Mehta S, Fawzi WW, Giovannucci EL. Interaction of estrogen therapy with calcium and vitamin D supplementation on colorectal cancer risk: reanalysis of women’s health initiative randomized trial. Int J Cancer. 2008;122: 1690–1694.

Weingarten MA, Zalmanovici A, Yaphe J. Dietary calcium supplementation for preventing colorectal cancer and adenomatous polyps. Cochrane Database Syst Rev. 2008:CD003548.

Gorham ED, Garland CF, Garland FC, et al. Vitamin D and prevention of colorectal cancer. J Steroid Biochem Mol Biol. 2005;97:179–194.

Gorham ED, Garland CF, Garland FC, et al. Optimal vitamin D status for colorectal cancer prevention: a quantitative meta analysis. Am J Prev Med. 2007; 32:210–216.

Bjelakovic G, Nikolova D, Simonetti RG, Gluud C. Antioxidant supplements for preventing gastrointestinal cancers. Cochrane Database Syst Rev. 2008:CD004183.

Mannisto S, Yaun SS, Hunter DJ, et al. Dietary carotenoidsand risk of colorectal cancer in a pooled analysis of 11 cohort studies. Am J Epidemiol. 2007;165: 246–255.

Bjelakovic G, Nagorni A, Nikolova D, Simonetti RG, Bjelakovic M, Gluud C. Meta-analysis: antioxidant supplements for primary and secondary prevention of colorectal adenoma. Aliment Pharmacol Ther. 2006;24:281–291.

IARC Working Group on the Evaluation of Cancer-Preventive Agents. Weight control and physical activity. IARC Sci Publ. 2002.

Samad AK, Taylor RS, Marshall T, Chapman MA. A meta-analysis of the associationof physical activity with reduced risk of colorectal cancer. Colorectal Dis. 2005;7:204–213.

Moghaddam AA, Woodward M, Huxley R. Obesity and risk of colorectal cancer: a metaanálisis of 31 studies with 70,000 events. Cancer Epidemiol Biomarkers Prev. 2007;16:2533–2547.

Larsson SC, Wolk A. Obesity and colon and rectal cancer risk: a meta- analysis of prospective studies. Am J Clin Nutr. 2007;86:556–565.

Renehan AG, Tyson M, Egger M, Heller RF, Zwahlen M. Body-mass index and incidence of cancer: a systematic review and meta-analysis of prospective observational studies. Lancet. 2008;371:569–578.

Pischon T, Lahmann PH, Boeing H, et al. Body size and risk of colon and rectal cancer in the European Prospective Investigation Into Cancer and Nutrition(EPIC). J Natl Cancer Inst. 2006;98:920–931.

Pisani P. Hyper-insulinaemia and cancer, meta-analyses of epidemiological studies. Arch Physiol Biochem. 2008;114:63–70.

Cho E, Smith-Warner SA, Ritz J, et al. Alcohol intake and colorectal cancer: a pooled analysis of 8 cohort studies. Ann Intern Med. 2004;140:603–613.

Moskal A, Norat T, Ferrari P, Riboli E. Alcohol intake and colorectal cancer risk: a dose–response meta-analysis of published cohort studies. Int J Cancer. 2007;120: 664–671.

Giovannucci E. An updated review of the epidemiological evidence that cigarette smoking increases risk of colorectal cancer. Cancer Epidemiol Biomarkers Prev. 2001;10:725–731.

Kuper H, Boffetta P, Adami HO. Tobacco use and cancer causation: association by tumour type. J Intern Med. 2002;252:206–224.

Botteri E, Iodice S, Raimondi S, Maisonneuve P, Lowenfels AB. Cigarette smoking and adenomatouspolyps: a meta-analysis. Gastroenterology. 2008;134: 388–395.

Paskett ED, Reeves KW, Rohan TE, et al. Association between cigarette smoking and colorectal cancer in the women’s health initiative. J Natl Cancer Inst. 2007;99:1729–1735.

Hooker CM, Gallicchio L, Genkinger JM, Comstock GW, Alberg AJ. A prospective cohort study of rectal cancer risk in relation to active cigarette smoking and passive smoke exposure. Ann Epidemiol. 2008;18:28–35.

Asano TK, McLeod RS. Non steroidal anti-inflammatory drugs (NSAID) and aspirin for preventing colorectal adenomas and carcinomas. Cochrane Database Syst Rev. 2004:CD004079.

Flossmann E, Rothwell PM. Effect of aspirin on long-term risk of colorectal cancer: consistent evidence from randomised and observational studies. Lancet. 2007;369:1603–1613.

Wang YP, Wang Q , Gan T, Pan T, Yang JL. Non-steroidal anti- inflammatory agents for chemoprevention of colorectal polyps: a meta- analysis. Zhonghua Nei Ke Za Zhi. 2004;43:10–12.

Arber N, Eagle CJ, Spicak J, et al. Celecoxib for the prevention of colorectal adenomatous polyps. N Engl J Med. 2006;355:885–895.

Bertagnolli MM, Eagle CJ, Zauber AG, et al. Celecoxib for the prevention of sporadic colorectal adenomas. N Engl J Med. 2006;355:873–884.

Baron JA, Sandler RS, Bresalier RS, et al. A randomized trial of rofecoxib for the chemoprevention of colorectal adenomas. Gastroenterology. 2006;131:1674–1682.

Rostom A, Dube C, Lewin G, et al. Nonsteroidal anti-inflammatory drugs and cyclooxygenase-2 inhibitors for primary prevention of colorectal cancer: a systematic review prepared for the U.S. Preventive Services Task Force. Ann Intern Med. 2007;146:376–389.

Bonovas S, Filioussi K, Flordellis CS, Sitaras NM. Statins and the risk of colorectal cancer: a meta-analysis of 18 studies involving more than 1.5 million patients. J Clin Oncol. 2007;25:3462–3468.

Hebert-Croteau N. A meta-analysis of hormone replacement therapy and colon cancer in women. Cancer Epidemiol Biomarkers Prev. 1998;7:653–659.

Nanda K, Bastian LA, Hasselblad V, Simel DL. Hormone replacement therapy and the risk of colorectal cancer: a meta-analysis. Obstet Gynecol. 1999;93: 880–888.

Beral V, Banks E, Reeves G, Appleby P. Use of HRT and the subsequent risk of cancer. J Epidemiol Biostat. 1999;4:191–210.

Grodstein F, Newcomb PA, Stampfer MJ. Postmenopausal hormone therapy and the risk of colorectal cancer: a review and meta-analysis. Am J Med. 1999;106: 574–582.

Rossouw JE, Anderson GL, Prentice RL, et al. Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results from the women’s health initiative randomized controlled trial. JAMA. 2002;288:321–333.

Heiss G, Wallace R, Anderson GL, et al. Health risks and benefits 3 years after stopping randomized treatment with estrogen and progestin. JAMA.2008;299:1036–1045.

Hulley S, Furberg C, Barrett-Connor E, et al. Noncardiovascular disease outcomes during 6.8 years of hormone therapy: Heart and Estrogen/progestin Replacement Study follow-up (HERS II). JAMA. 2002;288:58–66.

Norrelund N, Norrelund H. Colorectal cancer and polyps in patients aged 40 years and over who consult a GP with rectal bleeding. Fam Pract. 1996;13: 160–165.

Mandel JS, Church TR, Ederer F, Bond JH. Colorectal cancer mortality: effectiveness of biennial screening for fecal occult blood. J Natl Cancer Inst. 1999;91:434–437.

Mandel JS, Church TR, Bond JH, et al. The effect of fecal screening on the incidence of colorectal cancer. N Engl J Med. 2000;343:1603– 1607.

Weller D, Coleman D, Robertson R, et al. The UK colorectal cancer screening pilot: results of the second round of screening in England. Br J Cancer. 1007;97:1601–1605.

Lindholm E, Brevinge H, Haglind E. Survival benefit in a randomized clinical trial of faecal occult blood screening for colorectal cancer. Br J Surg. 2008;95:1029–1036.

Burch JA, Soares-Weiser K, St John DJ, et al. Diagnostic accuracy of faecal occult blood tests used in screening for colorectal cancer: a systematic review. J Med Screen. 2007;14:132–115.

Whitlock EP, Lin JS, Liles E, Beil TL, Fu R. Screening for colorectal cancer:a targeted, updated systematic review for the U.S. Preventive Services Task Force. Ann Intern Med. 2008;149:135–144.

Allison JE, Sakoda LC, Levin TR, et al. Screening for colorectal neoplasms with new fecal occult blood tests: update on performance characteristics. J Natl Cancer Inst. 2007;99:1462–1470.

van Rossum LG, van Rijn AF, Laheij RJ, et al. Random comparison of guaiac and immunochemical fecal occult blood tests for colorectal cancer in a screening population. Gastroenterology. 2008;135:82–90.

Smith A, Young GP, Cole SR, Bampton P. Comparison of a brush- samplingfecal immunochemical test for hemoglobin with a sensitive guaiac-based fecal occult blood test in detection of colorectal neoplasia. Cancer. 2006;107:2152–2159.

Fraser CG, Matthew CM, Mowat NA, Wilson JA, Carey FA, Steele RJ. Immunochemicaltesting of individuals positive for guaiac faecal occult blood test in a screening programme for colorectal cancer: an observational study. Lancet Oncol. 2006;7:127–131.

Fraser CG, Mathew CM, Mowat NA, Wilson JA, Carey FA, Steele RJ. Evaluation of a card collection-based faecal immunochemical test in screening for colorectal cancer using a two-tier reflex approach. Gut. 2007;56:1415–1418.

Levin B, Lieberman DA, McFarland B, et al. Screening and surveillance for the early detection of colorectal cancer and adenomatous polyps, 2008: a joint guideline from the American Cancer Society, the US Multi-Society Task Force on Colorectal Cancer, and the American College of Radiology. Gastroenterology. 2008;134:1570–1595.

Whitlock EP, Lin JS, Liles E, Beil TL, Fu R. Screening for colorectal cancer: a targeted, updated systematic review for the U.S. Preventive Services Task Force. Ann Intern Med. 2008;149:638-58.

Zubero MB, Arana-Arri E, Pijoan JI, Portillo I, Idigoras I, López- Urrutia A, et al. Population-based colorectal cancer screening: comparison of two fecal occult blood test. Front Pharmacol.2014;4:175.

Grobbee EJ, Van der Vlugt M, Van Vuuren A, Stroobants AK, Didden P, Mundt MW, et al. Comparison of OCSensor and FOBGold in population- based colorectal cancer screening based on FIT. Gastroenterology. 2015;148:S-160.

Chiu HM, Lee YC, Chou C, Wu MS. Comparison of one-day and- plasm by fecal immunochemical test. Preliminary results from a population-based randomized controlled trial. Gastroenterology. 2015;148:S-742.

Schreuders EH, Van Roon AH, Nieuwenburg SA, Grobbee EJ, Kapidzic A, Van Vuuren A, et al. Third round of two-sample immunochemical fecal occult blood test screening in the Netherlands. Gastroenterology. 2015;148:S-759.

Auge JM, Pellise M, Escudero JM, Hernández C, Andreu M, Grau according to fecal hemoglobin concentration in a colorectal cancer screening program. Gastroenterology. 2014;147:628-36.

Wieten E, Grobbee EJ, Hansen BE, Bruno MJ, Kuipers EJ, Lansdorp- Vogelaar I, et al. Positive predictive value increases with age in a FIT- based colorectal cancer screening program. Gastroenterology. 2015;148:S-760.

Grobbee EJ, Stoop EM, De Wijkerslooth TR, Lansdorp-Vogelaar I, Bossuyt PM, Dekker E, et al. FIT-based colorectal cancer screening: do we need to tailor screening for men and women? Gastroenterology. 2015;148:S-757-8.

Van der Meulen MP, Kapidzic A, Van Leerdam ME, Van der Steen A, Kuipers EJ, Spaander MC, et al. Do men and women need to be screened differently with faecal immunochemical testing? A cost-effectiveness analysis. Gastroenterology. 2015;148:S-758.

Bessa X, Álvarez-Urturi C, Hernández C, Auge JM, Grau J, Buron A, et al. Lower risk of high-risk adenoma and colorectal cancer among patients with a previous negative result from a fecal immunochemical test for colorectal cancer. Data on second round screening. Gastroenterology. 2015;148:S-748.

Zauber AG, Winawer SJ, O’Brien MJ, Lansdorp-Vogelaar I, Van Ballegooijen M, Hankey BF, et al. Colonoscopic polypectomy and long- term prevention of colorectal-cancer deaths. N Engl J Med. 2012;366:687-96.

Samadder NJ, Curtin K, Pappas L, Boucher KM, Mineau GP, Smith K, et al. Risk of developing colorectal cancer following a negative colonoscopy: a population-based study in Utah. Gastroenterology. 2015;148:S-138.

Kaminski MF, Regula J, Kraszewska E, Polkowski M, Wojciechowska U, Didkowska J, et al. Quality indicators for colonoscopy and the risk of interval cancer. N Engl J Med. 2010;362:1795-803.

Corley DA, Jensen CD, Marks AR, Zhao WK, Lee JK, Doubeni CA, et al. Adenoma detection rate and risk of colorectal cancer and death. N Engl J Med. 2014;370:1298-306.

Kaminski MF, Polkowski M, Kraszewska E, Rupinski M, Butruk E, Regula J. A risk score to facilitate informed decision-making about colonoscopy screening. Gastroenterology. 2015;144:S-603.

Kaminski MF, Rupinski M, Wieszczy P, Wojciechowska U, Didkowska J, Kraszewska E, et al. Effect of adenoma detection rate improvement on the risk of colorectal cancer and death. Gastroenterology. 2015;148:S-189.

IJspeert JE, Vermeulen L, Meijer GA, Dekker E. Serrated neoplasia- role in colorectal carcinogenesis and clinical implications. Nat Rev Gastroenterol Hepatol. 2015;12:401-9.

Shelby ES, Cirri H, Tuck M, Brenner DE, Baron JA, Crockett SD. Advanced serrated polyps are variably detected and are associated with a high rate of synchronous neoplasia: results from a large multi-center crosssectional study. Gastrointest Endosc. 2015;81:AB258.

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.

Zauber AG, Lansdorp-Vogelaar I, Wilschut J, Knudsen AB, van Ballegooijen M, Kuntz KM. Cost-Effectiveness of DNA Stool Testing to Screen for Colorectal Cancer. AHRQ Technology Assessment Program. Agency for Health Research and Quality; 2007.

Traverso G, Shuber A, Levin B, et al. Detection of APC mutations in fecal DNA from patients with colorectal tumors. N Engl J Med. 2002;346:311–320.

Traverso G, Shuber A, Olsson L, et al. Detection of proximal colorectal cancers through analysis of faecal DNA. Lancet. 2002;359:403– 404.

Dong SM, Traverso G, Johnson C, et al. Detecting colorectal cancer in stool with the use of multiple genetic targets. J Natl Cancer Inst. 2001;93:858–865.

Itzkowitz SH, Jandorf L, Brand R, et al. Improved fecal DNA test for colorectal cancer screening. Clin Gastroenterol Hepatol. 2007;5:111–117.

Haug U, Brenner H. New stool tests for colorectal cancer screening: a systematic review focusing on performance characteristics and practicalness. Int J Cancer. 2005;117:169–176.

Propuesta de estrategia en cáncer del sistema nacional de salud. Madrid: Ministerio de Sanidad y Consumo; 2006.

Plan Oncológico de la Comunidad Valenciana 2007-2010. Valencia: Conselleria de Sanitat. Generalitat Valenciana; 2007.

Descripción del cribado del cáncer en España. Proyecto DESCRIC. Informes de Evaluación de Tecnologías Sanitarias AATRM Núm.2006/01.

Published

2017-09-22