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w w w . j c o l . o r g . b r

Journal

of

Coloproctology

Original

Article

Is

prevalence

of

colorectal

polyps

higher

in

patients

with

family

history

of

colorectal

cancer?

Sthela

Maria

Murad-Regadas

a,b,

,

Carla

Camila

Rocha

Bezerra

c

,

Ana

Ligia

Rocha

Peixoto

d

,

Francisco

Sérgio

Pinheiro

Regadas

a

,

Lusmar

Veras

Rodrigues

a,e

,

José

Airton

Gonc¸alves

Siebra

c

,

Graziela

Olivia

da

Silva

Fernandes

c

,

Rafael

Aragão

Vasconcelos

c aDepartmentofSurgery,MedicineSchool,UniversidadeFederaldoCeará(UFC),Fortaleza,CE,Brazil

bSectorofAnorectalandPelvicFloorPhysiology,HospitaldasClínicas,MedicineSchool,UniversidadeFederaldoCeará(UFC),

Fortaleza,CE,Brazil

cServiceofColoproctology,HospitalUniversitárioWalterCantídeo,UniversidadeFederaldoCeará(UFC),Fortaleza,CE,Brazil

dServiceofColoproctology,HospitalRegionaldoCariri,JuazeirodoNorte,CE,Brazil

eServiceofColoproctology,MedicineSchool,UniversidadeFederaldoCeará(UFC),Fortaleza,CE,Brazil

a

r

t

i

c

l

e

i

n

f

o

Articlehistory:

Received29December2014 Accepted20February2015 Availableonline10June2015

Keywords:

Colonoscopy Polyps Prevention Colorectalcancer

a

b

s

t

r

a

c

t

Objectives:Toassesstheprevalenceofpolypsinpatientswithafamilyhistoryofcolorectal cancer,incomparisontoasymptomaticindividualswithindicationforscreening.

Methods:Aprospectivestudyinagroupofpatientswhounderwentcolonoscopybetween 2012and2014.Patientsweredividedintotwogroups:GroupI:nofamilyhistoryofcolorectal cancer,andGroupII:withafamilyhistoryinfirst-degreerelatives.Demographic charac-teristics,findingsoncolonoscopy,presence,locationandhistologicaltypeofpolypswere evaluated,comparingthetwogroups.

Results:214patientswereevaluated:162inGroupIand52inGroupII.Thedistributionof patientswithpolypswassimilarinrelationtogender:polypswereevidencedinGroupI in33(20%)femalepatientsvs.10(6%)malepatients(p=1.00);inGroupII,thepresenceof polypswasevidencedin9(17%)femalepatientsvs.2(4%)malepatients(p=1.00).Polypoid lesionswerefoundin54patients(25%),with43(26%)inGroupIand11(21%)inGroupII.The prevalenceofadenomaswassimilarinbothgroups(GroupI=18/37%vs.GroupII=10/50%) (p=0.83).

Conclusion:Inthispreliminarystudy,nocorrelationwasfoundbetweenprevalenceofpolyps andafamilyhistoryofcolorectalcancer.

©2015SociedadeBrasileiradeColoproctologia.PublishedbyElsevierEditoraLtda.All rightsreserved.

Correspondingauthor.

E-mail:smregadas@hospitalsaocarlos.com.br(S.M.Murad-Regadas).

http://dx.doi.org/10.1016/j.jcol.2015.02.010

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A

prevalência

de

pólipos

colorretais

é

mais

elevada

em

pacientes

com

história

familiar

de

câncer

colorretal?

Palavras-chave:

Videocolonoscopia Pólipos

Prevenc¸ão Câncercolorretal

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e

s

u

m

o

Objetivos: Avaliaraprevalênciadepóliposempacientescomhistóriafamiliardecâncer colorretalcomparandocomindivíduosassintomáticoscomindicac¸ãopararastreamento.

Métodos: Estudoprospectivorealizadoemumgrupodeindivíduossubmetidosà colono-scopia entre 2012 e 2014. Os pacientes foram distribuídos em dois grupos: Grupo I: semhistóriafamiliardecâncercolorretaleGrupoII:comhistóriafamiliaremparentes de primeiro grau.Avaliaram-se características demográficas,achados na colonoscopia, presenc¸a,localizac¸ãoetipohistológicodospólipos,comparandoosdoisgrupos.

Resultados: Foramavaliados214pacientes,162incluídasnogrupoIe52 nogrupoII.A distribuic¸ãodospacientescompóliposfoisimilaremrelac¸ãoaosexo,sendoevidenciado póliposnoGrupoIem33(20%)pacientesdosexofemininovs.10(6%)masculino(p=1,00) enoGrupoII,presenc¸adepóliposempacientesdosexofemininoem9(17%)vs.2(4%) masculino(p=1,00).Foramencontradaslesõespolipóidesem54pacientes(25%),sendo43 (26%)nogrupoIe11(21%)nogrupoII.Aprevalênciadeadenomasfoisimilaremambosos grupos(GrupoI=18/37%vs.GrupoII=10/50%)(p=0,83).

Conclusão:Nesteestudoinicial,nãofoiencontradacorrelac¸ãoentreaprevalênciadepólipos eohistóricofamiliardecâncercolorretal.

©2015SociedadeBrasileiradeColoproctologia.PublicadoporElsevierEditoraLtda. Todososdireitosreservados.

Introduction

Colorectalcancer(CRC)isthethirdmostcommoncause of cancer worldwidein bothgenders and the second leading causeindevelopedcountries.1InBrazil,theestimated inci-dence for the year 2014 is15.44 and 17.24 new cases per 100,000menandwomen,respectively.2Itiswellestablished thatthegreatmajorityofCRCcases(adenocarcinomas)isdue tobenigntumors(adenomas),aprocessknownas adenoma-carcinomasequence,originallydescribedbyVogelstein.3

Twenty-fivepercentofCRCcasesoccurinindividualswith atleast one first-degree relative (FDR) with a diagnosis of CRCnotassociatedwithaknowngeneticsyndrome.4These individualshave,onaverage,twicetheriskvs.general popu-lation’srisktodevelopCRCintheirlifetime.5

Patients withCRC and their families are candidates for different screeningstrategies, thanksto the increasedrisk ofdevelopingcolorectalcancerandtothepossibilityof pri-maryandsecondaryprevention,allowingforalongersurvival for patients treated in the early stages of this disease.6 Recentstudieshavefavoredcolonoscopyasthebestscreening method,forallowing diagnosis and treatmentofprecursor lesionsandobtainingbiopsiesofsuspiciouslesions.7,8

Currently, the reality of public health in Brazil, espe-cially in Northeast Region, does not allow full access to colonoscopyscreeningtestsforthewholeasymptomatic pop-ulation(includingthosewithafamilyhistory)fromtheageof 40to50yearsonward.

Inthesameline,therearefewstudiesevaluatingthe spe-cificgroupofasymptomaticindividualswithnofamilyhistory. Therefore,studiesareneededtoassesstheprevalenceofthese precursor lesions, aiming to demonstrate, for this popula-tion,thebenefitsofascreeningstrategy.Thisstudyaimsto

assesstheprevalenceofpolypsinpatientswithfamilyhistory ofcolorectalcancer,comparedtoasymptomaticindividuals undergoingcolonoscopywithindicationforascreening pro-cedure.

Methodology

This is a cross-sectional, analytical, prospective, compara-tivestudy,includingasymptomaticpatientswhounderwent screening colonoscopyatthe Hospital Universitário Walter Cantídio,UniversidadeFederaldoCeará(HUWC/UFC)andat theColoproctologyCenter,HospitalSãoCarlos,inthecityof Fortaleza–Ceará,fromJanuary2012toJanuary2014. Partici-pantsweredividedintotwogroups:GroupI–withoutfamily historyofCRC,andGroupII–withafamilyhistoryof spo-radic CRCinFDR.Screeningcolonoscopywasindicatedfor patients agedfrom 50years onwardinasymptomatic indi-vidualswithoutfamilyhistory(GroupI),andforthoseaged from40yearsonward,or10yearsbeforeCRCdiagnosisage inyoungerindividuals,inpatientswithfamilyhistory(Group II).

Demographic characteristics such as age, gender, body massindex(BMI)andfamilyhistoryofCRC,aswellasdata obtainedwithcolonoscopy(qualityofcolonpreparation[good, optimal or bad]), progression of the device until reaching cecum(fullexamination),presenceofpolyps,and histopatho-logicalexamination(histologytypeforpolyps).Thestudywas approvedbytheEthicsCommitteeofHospitalUniversitário WalterCantídio.

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geneticsyndromethatarguablyincreasesCRCrisk; individ-ualswithahistoryofcolorectalsurgeryforanycause;witha diagnosisofinflammatoryboweldisease(IBD); immunosup-pressedindividuals,orwithsymptomsrelatedtocolorectal disorderswereexcluded.

Foranevaluationofnumericalvariables,Studentt,Fisher andChi-squaredtestswereused.Thestatisticalsignificance levelwassetatp<0.05.

Results

Atotalof214patientswereincluded:47(22%)maleand167 (78%)female.Asfortheassessmentofbodymassindex(BMI), 87 (40%) were eutrophic,67 (31%) with overweight and 60 (28%)were obese patients. In 183 (86%) colonoscopies,the colonwasvisualizedinitsentirety,andagoodandoptimal preparationwasdescribedin62%oftests.In54(25%) proce-dures,atotalof69colonicpolypswerefound.Thelocalization ofthepolypswas:rectum(18/26%polyps),ascendingcolon (12/17%polyps),descendingcolon(11/16%polyps),andcecum, transversecolonandsigmoid(10/14.5%10/14.5%8/12%polyps, respectively).

Fromthetotalof214individuals,162(76%)wereincludedin GroupI(meanage,56years;ofthese,125(77%)werefemale.In GroupII,52(24%)patientswereincluded(meanage,54years);

ofthese,42(81%)werefemale.Nostatisticaldifferencewas notedbetweengroups,regardingageandgender(Table1).

Colonoscopyandhistopathologyfindings

InGroupI,polypswereseenin43(26%)ofthe162examined patients.InGroupII,from52examinationsperformed,polyps werefoundin11(21%)patients,withoutstatisticaldifference betweengroups(p=0.47).Thelocationofthepolypsincolonic areaswassimilarinbothgroups(Table1).

Astogender,thedistributionofpatientswithpolypswas similar;inGroupI,polypswereevidencedin33(20%)female vs.10 (6%)malepatients(p=1.00).InGroupII,polypswere evidencedin9(17%)femalevs.2(4%)malepatients(p=1.00). Whencomparinggroups,nodifferencewasidentifiedinterms ofprevalenceofpolypsbygender,asfollows:malegenderin GroupIvs.GroupII(10/6%vs.2/4%,p=1.00)andfemalegender inGroupIvs.GroupII(33/20%vs.9/17%,p=0.68)(Table2).The meansizeofpolypsinGroupIwas0.4cm,whileinGroupII was0.3cm.

AstothehistologyofpolypsinGroupI,inthose43patients withpolyps,atotalof49polypswasdemonstrated,as fol-lows:18(37%)adenomatous,23(47%)hyperplasticand8(16%) inflammatorypolyps.InGroupII, atotalof20 polypswere identifiedin11patientswithpositivecolonoscopyfor pres-ence ofpolyps, as follows: 9(45%) adenomatous, 10 (50%)

Table1–Characteristicsofpatientscomparinggroupswithfamilyhistoryvs.nofamilystoryforcolorectalcancer.

WithnofamiliarhistoryofCRC WithapositivefamiliarhistoryforCRC p

GroupI GroupII

n(%) n(%)

Age 56±12 54±10 0.60

Gender

Male 37(23%) 10(19%) 0.70

Female 125(77%) 42(81%)

Presenceofpolyps 43(26%) 11(21%) 0.47

Locationofpolyps

Caecum 8(16%) 2(10%) 0.71

Ascendingcolon 8(16%) 4(20%) 0.73

Transversecolon 7(15%) 3(15%) 1.00

Descendingcolon 8(16%) 3(15%) 1.00

Sigmoid 5(10%) 3(15%) 0.68

Rectum 13(27%) 5(25%) 1.00

Totalnumberofpatients 162(76%) 52(24%)

CRC,colorectalcancer.

Table2–Prevalenceofpolypsdistributedbetweengendersingroupswithnofamilyhistoryvs.familystoryofcolorectal cancer.

Totalnumberofpatients Withoutpolyps Gender Withpolyps Gender

GroupI

162 27 M 10 M

92 F 33 F

GroupII

52 08 M 02 M

33 F 09 F

M,male;F,female.

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Table3–Histologicalsubtypesofpolypscomparinggroupswithvs.withoutfamilyhistoryofcolorectalcancer.

Patientsn(%) Adenomatousn(%) Hyperplasticn(%) Inflammatoryn(%) Polypsna(%)

GroupI 43(26%) 18(37%) 23(47%) 08(16%) 49(71%)

GroupII 11(21%) 09(45%) 10(50%) 01(5%) 20(29%)

p=0.83.

a Insometests,morethanonepolypectomywasperformed,whichjustifiestheincreasednumberofhistologicalresultswhencomparedto

thenumberofexamswithpolyp.

hyperplasticand1(5%)inflammatorypolyps,withno statisti-callysignificantdifference(p=0.83)betweengroups(Table3).

Discussion

TheriskofdevelopingCRCisof5%,withanincreasedriskfor peoplewhohavecloserelativeswithCRC,especiallyif diag-nosedatanearlyage.10,11 Dependingonthe familyhistory andthepresenceofaninheritedmutationforCRC,therisk variabilityforthisneoplasiacanreachupto70%.11Screening programs,includingcolonoscopy,inindividualswithfamilial CRCaswellasinthepopulationingeneral,reducethe inci-denceofneoplasiaandappeartopreventCRCmortality.7,12,13 Thereisstillmuchdiscussiontodetermineiftheprevalence andfrequencyofadenomasinindividualswithafamily his-toryofCRCarehigherthaninthegeneralpopulation.14–17

Thisstudyevaluatedtheprevalenceofpolypsin asymp-tomatic patients with CRC history in first-degree relatives (GroupI)andcompareditsfindingsvs.anasymptomatic pop-ulationwithnofamilyhistory(GroupII)whoperformedtheir firstexaminationwithindicationforscreeningpurposes.It hasbeen shownthatthe distributionofpolypswassimilar inbothgroups,andnoevidenceofacorrelationwasfound betweenthe number ofpolyps and patients’ gender, since thedistributionofthepolypswassimilarinacomparisonof femalevs.malegenderinbothgroups.Thelargestnumber ofpolypsinfemales wasproportional tothe greater num-berofwomeninthegeneralpopulationstudied,justifyingthe similarityofdistributionofpolypsbygender.

Inthisstudy,“familyhistory”wasconsideredasthe pres-enceofadiagnosisofCRCinfirst-degreerelatives,including the patient’s father, mother and children.18 Using this cri-terion,thedistribution ofpolypsand the histologicaltype, including adenomatous polyps, were also similar in both groups.

Byanalyzingthedataobtained,itwasobservedthatthe numberofwomenundergoingpreventiveproceduresisstill higherthanthatinmen,whichcanbeexplainedbymen’s historicalresistancetoseekmedicalservicesandalsoby prej-udicesrelatedtocolonoscopyproceduresinmen.

Itwasalsoobservedthatthegroupwithapositivefamily historyforCRC(GroupII)presentedalowermeanage(54vs. 56years),whencomparedtothegroupwithnofamilyhistory (GroupI),butthisfindinghadnostatisticalsignificance,even withtheadviceforstartingthescreeningprocedure10years beforethe ageofthatrelativewhowasdiagnosedwiththe disease.

Itwas expectedabigger difference betweenmean ages whencomparingthetwogroups.Thisfindingmayreflectthe

lackofinformationandthedifficultyofmonitoringprograms targetedtothisriskgroupinNortheastRegionofthiscountry. Twenty-sixpercentofindividuals withnofamily history ofCRC(GroupI)underwentpolypectomy,whichisin agree-mentwiththeliterature,althoughthispercentagecanvary between17and21%,eventuallyreachingupto50%,depending ontheagegroupinquestion.6,10Inthegroupwithapositive family historyforCRC(GroupII),21% hadpolypsdetected, withnostatisticaldifferencevs.GroupI.Theseresultswere similartothosedescribedbyZandonáetal.,19whoevaluated patientswithafamilyhistoryofcolorectalcancercompared withpatientsundergoingcolonoscopywithawide rangeof indications, showinga percentage of18% of polypsin the groupwithapositivefamilyhistoryand14%inthepopulation withanindicationforcolonoscopicevaluation.

In a multicenter study, the histology revealed that 37.5% of polyps were adenomatous, mostof them tubular adenomas.6,10InananalysisoftypesofpolypsinGroupsIand II,ourdataweresimilar(37%and45%ofadenomatouspolyps, respectively). Corroborating the results of this study, Zan-donáetal.19confirmedthattherewasnostatisticaldifference intheprevalenceofadenomatouspolyps,whencomparing patients with a positive family history for CRC vs. symp-tomatic patients and/or individuals with an indicationfor colonoscopy.

Astothelocationofpolyps,itisknownthatan examina-tionofthedistalcolon(rectum,sigmoidcolon,anddescending colon)candetect60–80%ofthepolyps.6Inthisstudy, approxi-mately54%ofthepolypswerelocatedinleftcolonandrectum inbothgroups,whichisinagreementwiththeliterature. How-ever,itisimportanttonotethatwhenoneevaluatesonlythe rectum andsigmoid, thispercentageofpolypdetection, or evenofmalignantlesiondetection,canfallto40%.8Thesedata reinforcetheimportanceofafullcolonoscopy,andnotonlya flexiblerectosigmoidoscopy,asamethodofdetectingpolyps andforpreventionofCRC.Studiesshowthatcolonoscopyis consideredthemethodofchoiceforearlydetectionof colo-rectalcancer.6,20 However,thisisnotamethodavailablein allservices,notcoveringevenallpatientswithindicationsfor thistypeofassessment.

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obtained,aswellasforcomparisonwithotherreference cen-ters.

Conclusion

Inthispreliminarystudy,nocorrelationbetweenthe preva-lenceofpolypsandpresenceofafamilyhistoryforCRCwas evidenced,since the prevalenceand distributionof polyps accordingtogenderandhistologicsubtypeofthisgroupwere similartothepopulationofpatientswithnofamilyhistory, whowereexaminedwithanindicationforCCRscreening.

Conflicts

of

interest

Theauthorsdeclarenoconflictsofinterest.

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1. Habr-GamaA,KissDR,PerezRO.CâncerdoColon,doRetoe doÂnus.In:ClínicaCirúrgica.SãoPaulo:Manole;2008.p. 849–99.

2. MinistériodaSaúdeInstitutoNacionaldoCâncer,Brasil. EstimativadeincidênciaemortalidadeporcâncernoBrasil; 2014.Availablefrom:http://www.inca.gov.br[accessed 03.02.14].

3. FearonER,VogelsteinB.Ageneticmodelforcolorectal tumorigenesis.Cell.1990;61:759–67.

4. GordonPH.Malignantneoplasmsofthecolon.In:Nivatvongs S,GordonPH,editors.Principlesandpracticeofsurgeryfor thecolon,rectumandanus.NewYork:InformaHealthcare; 2007.p.490–2.

5. WilschutJA,SteyerbergEW,vanLeerdamME,

Lansdorp-VogelaarI,HabbemaJD,vanBallegooijenM.How muchcolonoscopyscreeningshouldberecommendedto individualswithvariousdegreesoffamilyhistoryof colorectalcancer?Cancer.2011;117:4166–74.

6. LevinB,LiebermanDA,McFarlandB,SmithRA,BrooksD, AndrewsKS,etal.Screeningandsurveillancefortheearly detectionofcolorectalcancerandadenomatouspolyps2008 ajointguidelinefromtheAmericanCancerSociety,theUS Multi-SocietyTaskForceonColorectalCancer,andthe AmericanCollegeofRadiology.CACancerJClin. 2008;58(3):130–60.

7. WinaverSJ,ZauberAG,HoMN,O’BrienMJ,GottliebLS, SternbergSS,etal.PreventionofColorectalCancer’by

colonoscopicpolypectomy.TheNationalPolypStudy Work-group.NEnglJMed.1993;329:1977–81.

8.LiebermanDA,WeissDG,BondJH,AhnenDJ,GarewalH, ChejfecG.Useofcolonoscopytoscreenasymptomaticadults forcolorectalcancer.NEnglJMed.2000;343(3):162–8.

9.VasenHF,WatsonP,MecklinJ-P,LynchHT.Newclinical criteriaforhereditarynonpolyposiscolorectalcancer(HNPCC, Lynchsyndrome)proposedbytheInternationalCollaborative GrouponHNPCC.Gastroenterology.1999;116:1453–6.

10.MengesM,FischingerJ,GärtnerB,GeorgT,WoerdehoffD, MaierM,etal.Screeningcolonoscopyin40-to50-year-old first-degreerelativesofpatientswithcolorectalcanceris efficient:acontrolledmulticentrestudy.IntJColorectalDis. 2006;21:301–7.

11.FuchsCS,GiovanniEL,ColditzGA,HunterDJ,SpeizerFE, WillettWC.Familyhistoryincreasestheriskofcolorectal cancer.Gastroenterology.1995;109:1015–7.

12.JärvinenHJ,MecklinJ-P,SistonenP.Screeningreduces colorectalcancerrateinfamilieswithhereditary nonpolyposiscolorectalcancer.Gastroenterology. 1995;108:1405–11.

13.JärvinenHJ,AarnioM,MustonenH,Aktan–CollanK,Aaltonen LA,PeltomäkiP,etal.Controlled15-yeartrialonscreeningfor colorectalcancerinhereditarynonpolyposiscolorectal cancer.Gastroenterolgy.2000;118:829–34.

14.LanspaJS,LynchHT,SmyrkTC,StrayhornP,WatsonP,Lynch JF,etal.ColorectaladenomasintheLynchsyndromes. Resultsofacolonoscopyscreeningprogram.

Gastroenterology.1990;98:1117–22.

15.JassJR,StewartSM.Evolutionofhereditarynon-polyposis colorectalcancer.Gut.1992;33:783–6.

16.PonzdeLeonM,DellaCasaG,BenattiP,PercesepeA,di GregorioC,FanteR,etal.Frequencyandtypeofcolorectal tumorsinasymptomatichigh-riskindividualsinfamilies withhereditarynonpolyposiscolorectalcancer.Cancer EpidemiolBiomarkPrev.1998;7:639–41.

17.JassJR,StewartSM,StewartJ,LaneMR.Hereditary non-polyposiscolorectalcancer—morphologies,genesand mutations.MutatRes.1994;3(10):125–33.

18.PuenteGutierrezJ,MarinMorenoMA,DomınguezJimenezJL, BernalBlancoE,DíazIglesiasJM.Effectivenessofa

colonoscopicscreeningprogrammeinfirst-degreerelatives ofpatientswithcolorectalcancer.ColorectalDis.2011;13: 145–53.

19.ZandonáB,DeCarvalhoLP,SchimedtJ,KoppeDC,Koshimizu RT,MallmannACM.Prevalênciadeadenomascolorretaisem pacientescomhistóriafamiliarparacâncercolorretal.Rev brasColoproctol.2001;13:147–54.

Imagem

Table 1 – Characteristics of patients comparing groups with family history vs. no family story for colorectal cancer.
Table 3 – Histological subtypes of polyps comparing groups with vs. without family history of colorectal cancer.

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