2024.V1版NCCN指南更新:乳腺癌用药选择.docx

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1、2024.V1版NCCN指南更新:乳腺癌用药选择2024年1月25日,乳腺癌NCCN指南更新至2024.V1版,此次药物治疗方面的更新主要涉及化疗药物的选择和剂量的调整,具体更新内容如下。并且本文汇总了最新版乳腺癌NCCN指南推荐的靶向、免疫药及方案选择,仅供参考。01、术前/辅助治疗方案HER2阴性的三阴性乳腺癌(TNBC)其他推荐方案调整:紫杉醇+卡钳(不同给药方式)调整为2A类证据多西他赛+卡钳删除“仅用于新辅助治疗”,调整为2A类证据National Comprehensive Cancer Network-NCCN Guidelines Version 1.2024 Invasive

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11、mab(ctgocy1)1pgMg.trb(cWfloryifUWuIMCfUlnCkcumMfc: DocoUxoiCyclaphospIwnkSetrastuzumab ACfollowedTIrMtuzumabh(doxorbcincyc*opbopmMIoIIowmIbyPyplutrMtuamb.vhou38us) ACIollowodbyTbtrastuzumabpoclitax4trastuzumabPortUZUfnabh AdotrMtuzutnabmtantin(TDM-1)(duvlMttmgOrtfy)OtherRconwnnxlbtrastuzumab(doxorub

12、clrVcyclophopamktofoHcwdbydocUxdtrMtuzumb)ACt/odbydoc*taxlbtrMummbXrtMZUrnt(donJbklnGeoph*p3nMfoowmlbydocCax4PcWU3QoMMuzumabprtuzumbAddHIonaICoidratlonforThoMReceivingProprattvodjuvMThra”(BlxVL3)HER2阴性乳腺癌其他推荐方案给药剂量调整:多西他赛+卡钳(46个周期),删除“仅限术前”NCCNNeCN GwddDea IndexTab工 o* * CortclU*a Doxoruttan 60 mfn1

13、 rv 0 1,CyCiOPho6 amide 600 j*n N dey 1 CCydeevery2idaystx 4 cycftn CFoBowedby PaCRW 80 BBay IhlVSUBOOEAlyQ 12weM CctAbineZftenance therapy严 MO mg3 PO *ice daiy OndSyB 1-28 Oycted CVery 2B day for 11Car.EPrgCrl1mgfrrfvday1.CydOPhaH)horned830mgn*rday10QrBdevery21Osfor8cyclesTACChomothorapytDocctvci75

14、mgfrntIVds1Doiorubian50mgffIVday1.Cydopt*hawS9SOOmgfrneIVdBy1OCycirtevery21(toysfor6cydrHERZNO9athUMfUlifICertainCrcumtancoMt Aa v*C4nmeaclaa ar caf4ry 2A mfeM rhrM rtfcatBtm*mQmQfimwc*rcMnBiPv*cipBUnscAji3wck6CMdBINVI5OF9HER2阳性乳腺癌首选方案调整:新增TDMT方案,剂量每日3.6mgkg,21天一个疗程,共14个疗程NCCNColensiveNCCNGuidelines

15、Version1.2024InvasiveBreastCancerPBMfMr(Vw*tof 1Z wa*aW Tfuruna 4 mgfQfVwlMf(l 00M Qf PJun*n. m99 Z v(y2i d* m ba IMd to*VQ Z 60Mon & pUx Z 9ca*t 1 yo V* IV or 17, OReDWid, Dec*Ml 79 Jbo0M(M Cywy2l etof6ey tn Nturat 8 ngM Wg 1.ruvwfrM0 2 rv,i:FLtd*Wwf*MWrWerotwr*nMVq02全身治疗方案ER和/或PR阳性复发不可切除(局部或区域)或IV

16、期(Ml)乳腺癌其他推荐治疗方案调整:修改第二条:选择性ER下调剂(氟维司群)+非俗体芳香化酶抑制剂(阿那曲哇、来曲嘎)(1类),删除氟维司群的“1类推荐”iv.NCCNGuidelinesVersion1.2024弑黑kInvasiveBreastCancer复发性不可切除(局部或区域)或IV期(Ml)疾病靶向治疗和相关生物标志物检测调整:新增任何亚型的生物标志物检测:胚系BRCAl或BRCA2突变,胚系测序,FDA批准用药为奥拉帕利、他拉理帕利,NCCN指南的证据类别为1类,NCCN指南推荐为首选方案HR阳性/HER2阴性的生物标志物检测修订为:PIK3CA或AKTl激活突变或PTEN突变

17、;NGS检测的样本类型修改为:血液或如果血液阴性则使用肿瘤组织National Comprehensive Cancer Network*其他检测的样本类型修改NCCNNCCNGuidelinesVersion1.2024InvasiveBreastCancerTARGETEDTHERAPIESANDASSoClATEDBIOMARKERTESTINGFORRECURRENTUNRESECTALE(LOCALORREGIONAL)ORSTAGEIV(M1DISEASEBINVO 6 OF 14BiomerkersAwocietedwitFDA-ApprovedTr*pBfttCncrS*Jt*

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20、药物:卡培他滨150Omg口服,每日两次,第1-7天和第1521天,每28天循环NCCNNational Comprehensive Cancer NetworkeNCCN Guidelines Version 1.2024 Invasive Breast CancerNCCN Gtxlelnes ItxtexTbte of Contents DtscusoDOSING: SYSTEMIC THERAPY REGIMENS FOR RECURRENT UNRESECTABLE (LOCAL OR REGIONAL) OR STAGE IV (M1) DISEASEHER2NgJtv Rggim

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23、 28 day*DocU,su WMOOmmlrV 则 1 CyM p 21 Sy.DocetaMl17 36 m9to1, IV weeitar6waeKst)A0wM ty 2*mM* rMM*Mt AKMimtnound pcltx4,t1t.IOOmotn1Of Q5m9*nvrdVyl.M H Cye0fnIiVdeyl Cyi40mg*nl IVtoy 1 Cyded every 21 OeyB Scuarab govttc*wtfy(ICf TMBC Cr HR*HER2)2x3 IOmgftg N onde)s 1 and 8, CyM wery 21 Odyt-FaHHrMt

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25、2Vondys1 MS Cyded Mry 21CefboplMinteItiu(ViM)Ound pcUx CMtOpUIin AUC 2 IVonOtyt 1 M 8 XfttfYWMXXMK125mgn IVonUy1 W8 Cycled Mry 21 dytOtfboPiMinZlKAl j3 PKtUitf 17MDO mgn IVdey 1 CarbopKmAUC 6IV dr 1 Cycled every 21 daysB PttCiUid l00mgf and *wwtatan erf f* cncr 9tf* and ta tnaea9eTMrt tfaM0Mldtocaa

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27、r BnAMltfMa C*N*kaFCOTlVUCO ,taal Mi *l C e9aMB9t * *BMMMCLCOntinUedBINV-Q8 OF 14现将2O24.V1版乳腺癌NCCN指南推荐的靶向、免疫药物及使用方案汇总如下:Ol术前/辅助治疗方案HER2阴性首选方案:奥拉帕利,如果基因检测为胚系BRCAl/2突变高危的三阴性乳腺癌(TNBC):术前帕博利珠单抗+卡伯+紫杉醇,随后术前帕博利珠单抗+环磷酰胺+阿霉素或表柔比星,随后辅助帕博利珠单抗脚注:c.以下情况考虑加用奥拉帕利辅助治疗1年,胚系BRCAI/2突变且:三阴性乳腺癌(TNBC),如果1)pT2或)pNl辅助化疗后,

28、或2)新辅助化疗后残留病灶。*HR阳性,HER2阴性,如果1)辅助化疗后4个阳性淋巴结(2A类),或2)术前治疗后残留病变和临床分期、病理分期、雌激素受体状态和肿瘤分级(CPS+EG)评分3。辅助奥拉帕利可与内分泌治疗同时使用。d.OlympiA研究中的患者未接受卡培他滨治疗,因此没有先后顺序或一种方案优于另一种的证据。e.High-risk高危标准包括1111I期TNBC。辅助帕博利珠单抗(2A类)的使用可能需要个体化。NCCNNational Comprehensive Cancer NetworkNCCN Guidelines Version 1.2024 Invasive Breast

29、 CancerPreoperativezadjuvanttherapyregimens*7rgfemnslkdIngUblIorHER2rwgtZSsmmaeMCMegOry1xcptwhrindicated)wnUMdIntd)uv Ifdo 0 Cf 9 5 nb(rd AMmjfi* Uxanes 0t. docouxM WtxttUtod Ior WGCK PJKKeXOl orHER2-mtl一ProfgrrOdRagimana:D”)followedorpreceded百WMkIy(cBUxlbTCfva!andrrubAcnofttDkublci.foMowodbv*diuvat

30、KMfnbroliJyQTNBCandresidualdoasoafterProOPerativtherapywithtaxan.alkyiator*,andanlhrcyclin*baMdchomothorapy:CpocitabinoUmIuIInJrtainClrCUmtSncc Dos-dnsAC(doxorubicinyclophophmkS) AC(doxorubkincydophosphamid)every3WMkS(category2B) CMF(CyclophosphamidezmethotrexateznuofouraciI) ACfollowedWMkIypcStaxlb

31、 Capocltabino(maintenancetrapyforTNBCafteraduvantCbomothOraPy)OtMrRecommecxSedRgit: ACfollowed5docUxlvy3wksb EC(prubidrVcyclophosphamd) TAC(d8mRcMgProprUv3AQuMtTrpy(BVL3HER2阳性首选方案:紫杉醇+曲妥珠单抗TCH(多西他赛/卡粕/曲妥珠单抗)TCHP(多西他赛/卡铛/曲妥珠单抗/帕妥珠单抗)如果术前治疗后无残留病灶或未接受术前治疗:使用曲妥珠单抗(1类)士帕妥珠单抗完成长达一年的抗HER2靶向治疗如果术前治疗后残留病灶:单独

32、使用恩美曲妥珠单抗(T-DMI)(I类)o如果因毒性停用恩美曲妥珠单抗(T-DMl),则使用曲妥珠单抗(1类)帕妥珠单抗完成一年的治疗。如果初始淋巴结阳性,采用曲妥珠单抗+帕妥珠单抗(1类)在某些情况下使用:多西他赛+环磷酰胺+曲妥珠单抗AC序贯T+曲妥珠单抗(阿霉素/环磷酰胺序贯紫杉醇+曲妥珠单抗,多种方案)AC序贯T+曲妥珠单抗+帕妥珠单抗(阿霉素/环磷酰胺序贯紫杉醇十曲妥珠单抗+帕妥珠单抗,多种方案)来那替尼(仅辅助治疗)紫杉醇+曲妥珠单抗+帕妥珠单抗恩美曲妥珠单抗(T-DMD(仅辅助治疗)其他推荐方案:AC序贯多西他赛+曲妥珠单抗(阿霉素+环磷酰胺序贯多西他赛+曲妥珠单抗)AC序贯多西他赛+曲妥珠单抗+帕妥珠单抗(阿霉素/环

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