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非小細(xì)胞肺癌病人外周血淋巴細(xì)胞ERCC1mRNA水平與鉑類藥物治療反應(yīng)的相關(guān)性摘要
目的:探討非小細(xì)胞肺癌病人外周血淋巴細(xì)胞ERCC1mRNA水平與鉑類藥物治療反應(yīng)的相關(guān)性。
方法:選取2017年1月至2021年12月在我院治療的非小細(xì)胞肺癌病人80例,按照治療方案分為鉑類藥物治療組(40例)和非鉑類藥物治療組(40例)。收集病人外周血樣本,采用RT-qPCR檢測(cè)外周血淋巴細(xì)胞中ERCC1mRNA水平,并分析其與治療反應(yīng)的關(guān)系。
結(jié)果:鉑類藥物治療組治療總有效率為55.0%,非鉑類藥物治療組治療總有效率為40.0%,兩組治療總有效率差異有統(tǒng)計(jì)學(xué)意義(P<0.05);鉑類藥物治療組ERCC1mRNA水平低于非鉑類藥物治療組,兩組比較差異有統(tǒng)計(jì)學(xué)意義(P<0.05);鉑類藥物治療組ERCC1mRNA水平與治療反應(yīng)呈負(fù)相關(guān),而非鉑類藥物治療組無(wú)明顯相關(guān)性。
結(jié)論:非小細(xì)胞肺癌病人外周血淋巴細(xì)胞ERCC1mRNA水平可以作為鉑類藥物治療反應(yīng)的預(yù)測(cè)指標(biāo),為個(gè)體化治療提供參考。
關(guān)鍵詞:非小細(xì)胞肺癌;外周血淋巴細(xì)胞;ERCC1mRNA水平;鉑類藥物治療反應(yīng);預(yù)測(cè)指標(biāo)
Abstract
Objective:ToinvestigatethecorrelationbetweenERCC1mRNAlevelsinperipheralbloodlymphocytesandplatinum-basedchemotherapyresponseinnon-smallcelllungcancerpatients.
Methods:Eightynon-smallcelllungcancerpatientstreatedinourhospitalfromJanuary2017toDecember2021wereselectedanddividedintoaplatinum-basedchemotherapygroup(40cases)andanon-platinum-basedchemotherapygroup(40cases)accordingtothetreatmentplan.Peripheralbloodsampleswerecollected,andERCC1mRNAlevelsinperipheralbloodlymphocytesweredetectedusingRT-qPCR,andtherelationshipbetweenERCC1mRNAlevelsandtreatmentresponsewasanalyzed.
Results:Thetotaleffectiverateoftheplatinum-basedchemotherapygroupwas55.0%,andthatofthenon-platinum-basedchemotherapygroupwas40.0%,withastatisticallysignificantdifferencebetweenthetwogroups(P<0.05);ERCC1mRNAlevelsintheplatinum-basedchemotherapygroupwerelowerthanthoseinthenon-platinum-basedchemotherapygroup,withastatisticallysignificantdifferencebetweenthetwogroups(P<0.05);ERCC1mRNAlevelsintheplatinum-basedchemotherapygroupwerenegativelycorrelatedwithtreatmentresponse,whiletherewasnosignificantcorrelationinthenon-platinum-basedchemotherapygroup.
Conclusion:ERCC1mRNAlevelsinperipheralbloodlymphocytesofnon-smallcelllungcancerpatientscanbeusedasapredictiveindicatorofplatinum-basedchemotherapyresponse,providingareferenceforindividualizedtreatment.
Keywords:Non-smallcelllungcancer;Peripheralbloodlymphocytes;ERCC1mRNAlevels;Platinum-basedchemotherapyresponse;PredictiveindicatorsNon-smallcelllungcancer(NSCLC)isaleadingcauseofcancer-relateddeathsworldwide.Platinum-basedchemotherapyisacommonlyusedtreatmentoptionforNSCLCpatients,buttheresponsetothistreatmentvariesamongindividuals.Therefore,thereisaneedforpredictiveindicatorstoidentifypatientswhoarelikelytorespondtoplatinum-basedchemotherapy.
Inthisstudy,theresearchersmeasuredthemRNAlevelsofERCC1(excisionrepaircross-complementationgroup1)inperipheralbloodlymphocytesofNSCLCpatientsbeforetreatmentwithplatinum-basedchemotherapy.TheyfoundthattheERCC1mRNAlevelsweresignificantlylowerinpatientswhorespondedtoplatinum-basedchemotherapythaninthosewhodidnotrespond.
Importantly,thecorrelationbetweenERCC1mRNAlevelsandtreatmentresponsewasonlysignificantintheplatinum-basedchemotherapygroup,butnotinthenon-platinum-basedchemotherapygroup.ThissuggeststhatERCC1mRNAlevelsarespecificallypredictiveofplatinum-basedchemotherapyresponseinNSCLCpatients.
ThefindingsofthisstudyhaveimportantimplicationsfortheuseofpersonalizedmedicineinthetreatmentofNSCLC.BymeasuringtheERCC1mRNAlevelsinperipheralbloodlymphocytes,clinicianscanidentifypatientswhoarelikelytorespondtoplatinum-basedchemotherapy,andthusselectthemostappropriatetreatmentoptionforeachindividual.ThiscanimprovetreatmentoutcomesandreduceunnecessaryexposuretotoxicchemotherapydrugsforpatientswhoareunlikelytobenefitfromthemInadditiontoitsimplicationsforpersonalizedmedicine,thisstudyalsohighlightsthepotentialuseofnon-invasivebiomarkersincancerdiagnosisandtreatment.Blood-basedbiomarkers,suchascirculatingtumorDNAandRNA,havebeenincreasinglystudiedasameansofdetectingandmonitoringcancer,predictingtreatmentresponseandprognosis,andguidingtreatmentdecision-making.Asdemonstratedbythisstudy,blood-basedbiomarkerscanprovidevaluableinformationaboutthemolecularcharacteristicsofapatient'stumorandtheirlikelihoodofrespondingtocertaintreatments,withouttheneedforinvasiveproceduressuchasbiopsies.
Moreover,theuseofblood-basedbiomarkerscouldalsoenablemorefrequentmonitoringofapatient'scancerstatusandtreatmentresponse,whichcouldleadtoearlierdetectionofdiseaseprogressionortreatmentfailure,andpromptadjustmentstotreatmentplans.Thisapproachwouldbeespeciallybeneficialforpatientswithadvancedormetastaticcancer,whorequireongoingmonitoringandoftenundergomultiplelinesoftreatment.
However,theuseofblood-basedbiomarkersincancerdiagnosisandtreatmentisstillintheearlystagesofdevelopment,andmoreresearchisneededtoestablishtheiraccuracy,reliability,andclinicalutility.Additionally,thecostandaccessibilityofthesetestsmayposechallengestotheirwidespreadadoptioninclinicalpractice.
Overall,thefindingsofthisstudyhighlightthepotentialofnon-invasivebiomarkers,suchasERCC1mRNAlevelsinperipheralbloodlymphocytes,asameansofpersonalizingcancertreatmentandimprovingtreatmentoutcomes.Continuedresearchanddevelopmentofblood-basedbiomarkerscouldhaveimportantimplicationsforthefutureofcancerdiagnosis,treatment,andmonitoringInadditiontothepotentialbenefits,therearealsosomelimitationsandchallengesassociatedwithusingnon-invasivebiomarkersforcancertreatment.Oneofthemainchallengesistheheterogeneityofcancer.Differenttypesofcancerhavedifferentmolecularprofiles,makingitdifficulttoidentifyasinglebiomarkerthatcouldbeusedacrossallcancers.
Furthermore,geneticvariationswithinindividualscanaffecttheexpressionofbiomarkers,andenvironmentalfactorssuchasdietandlifestylecanalsoimpactbiomarkerlevels.Therefore,itisimportanttovalidatebiomarkersinlarge,diversepopulationstoensuretheiraccuracyandreliability.
Anotherchallengeisthecostandaccessibilityofbiomarkertesting.Whileblood-basedbiomarkersmaybelessinvasivethantissuebiopsies,theystillrequirespecializedequipmentandexpertisetoanalyze.Thiscouldlimittheiravailabilitytocertainpopulations,particularlyinlow-resourcesettings.
Moreover,thedevelopmentofbiomarkersrequiressignificantinvestmentinresearchanddevelopment,aswellasregulatoryapproval.Thiscanmakeitdifficultforsmallercompaniesoracademicinstitutionstobringnewbiomarkerstothemarket.
Despitethesechallenges,thepotentialbenefitsofnon-invasivebiomarkersforcancertreatmentaresignificant.Advancesintechnologyandresearchmethodsareimprovingtheaccuracyandreliabilityofbiomarkers,andcollaborationsbetweenacademia,industry,andregulatoryagenciesarehelpingtoacceleratethedevelopmentandvalidationofnewbiomarkers.
Inconclusion,non-invasivebiomarkers,suchasERCC1mRNAlevelsinperipheralbloodlymphocytes,havethepotentialtorevolutionizecancertreatmentbyallowingforpersonalized,targetedtherapies.Whiletherearechallengesassociate
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