revlimid 来那度安 那里怎样能买到正牌卫速安

来那度胺Revlimid,来那度胺说明书,来那度胺价格,香港来那度胺价格,来那度胺规格
【通用名称】
来那度胺Revlimid
【英文名称】
Revlimid(Lenalidomide hard capsules)
【中文名称】
瑞法纳,瑞复美(来那度胺胶囊)
销 商】 香港华特药房咨询:137-255-38-785.
部分英文Revlimid资料(仅供参考)
欧盟扩大来那度胺Revlimid的使用范围包括ASCT
regulators have expanded the scope of Celgene's Revlimid to include its use as
monotherapy for the maintenance treatment of adults with newly diagnosed multiple
myeloma who have undergone autologous stem cell transplantation (ASCT).
According to the firm, Revlimid (lenalidomide) is the first and only licensed treatment
in this setting and thus represents a major advance for those patients who tend
to be younger than the average patient with the incurable blood cancer.
For patients who are newly diagnosed with the condition and eligible for ASCT,
key treatment aims are to delay disease progression and achieve long-term control
over multiple myeloma. As such, these patients typically receive induction therapy
and high-dose chemotherapy with melphalan followed by ASCT.
&This treatment approach has been an established standard of care for over
20 years, but over half of patients who relapse do so within two to three years
of ASCT. Considering that over half of those patients who relapse do so within
2 to 3 years of ASCT, the approval of a maintenance therapy for use after ASCT
that may delay disease progression represents a major advance for these patients,&
Celgene said.
The decision to approve the drug was d on data from two cooperative group-led studies,
CALGB 1001049 and IFM 2005-02, which both had the primary efficacy endpoint of
progression-free survival (PFS) from transplant to the date of disease progression
In the CALGB 100104 trial, after 81.6 months of follow up, median PFS was 56.9
months in the Revlimid arm and 29.4 months in the placebo arm. In the IFM 2005-02
study, after 96.7 months of follow up, median PFS was 44.4 months in the Revlimid
arm versus 23.8 months in the placebo arm.
&We now have an opportunity to enhance immune function and delay disease progression
by controlling residual malignant cells and slowing tumour growth,& said Professor
Michel Attal, executive director of the Institut Universitaire du Cancer Toulouse
Oncopole and Institut Claudius Regaud, France.
&Revlimid has been shown to increase progression-free survival after ASCT
in clinical trials. Having a licensed therapy for use in this very important setting
means we now have the opportunity to delay disease progression by sustaining the
response&.
Around 39,000 people are diagnosed with multiple myeloma and 24,000 die from it
in Europe every year.
Revlimid is also approved as combination therapy for the treatment of patients
not eligible for transplant who are newly diagnosed or those have received at least
one prior therapy.
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S18F.Davies,R.Baz/BloodR;5.In?uenceofdexamethason;Recentevidencesuggeststh;These?ndingsmayhelptoexp;Alternatively,patientsma;Currentavailabledatasugg;withoutantagonizinglenal;DrDav
S18F.Davies,R.Baz/BloodReviews24(5.In?uenceofdexamethasoneonthedualeffectsoflenalidomideRecentevidencesuggeststhatcoadministrationofdexamethasonemayalterthedualeffectsoflenalidomide.9,14,16,17Asmentioned,lenalidomideincombinationwithdexamethasonesynergisticallyinhibitsmyelomacellgrowth,activatescaspases,andinducesapoptosis,14enhancingthetumoricidaleffectsoflenalidomide.However,dexamethasoneappearstoantagonizetheimmune-enhancingeffectoflenalidomidebyinhibitingtheT-andNK-cellcostimulatoryeffectsoflenalidomide.14Speci?cally,dexamethasoneinhibitedlenalidomide-enhancedIL-2productioninprimaryhumanTcells,andinhibitedlenalidomide-mediatedIFN-gandgranzymeBproductioninprimaryhumanNKcellsinadose-dependentmannerinvitro.14These?ndingsmayhelptoexplaintheresultsoftherecentphaseIIItrialinpatientswithnewlydiagnosedMMbyRajkumaretal.,wherelow-dosedexamethasonepluslenalidomidedemonstratedabene?tinearlyOScomparedwithpatientswhoreceivedlenalidomideplushigh-dosedexamethasone.32One-yearOSwas96%(95%CI94C99)inthelow-dosegroupcomparedwith87%(95%CI82C92)inthehigh-dosegroup,and2-yearOSwas87%(95%CI81C93)and75%(95%CI68C93),respectively.Takentogether,resultsfromthepreclinicalstudiesandclinicaltrialsuggestthataregimenoflenalidomidepluslow-dosedexamethasonemayresultinthebestclinicalactivitybyprovidingsynergisticantiproliferativeeffects,butwithoutaffectingtheimmunomodulatoryeffectsoflenalidomide.14AnalternativeexplanationfortheprolongedOSwiththelowerdoseofdexamethasonecouldberelatedtothetolerabilitypro?le.Alowerdosewouldbeassociatedwithabettersafetypro?le,whichmayallowlongertreatmentexposure.Alternatively,patientsmaybene?tfromreceivinglenalidomidealoneorindependentofcorticosteroids.ArecentretrospectivestudyevaluatedtheactivityoflenalidomidemonotherapyinnewlydiagnosedMM.66In17patientstreatedwithlenalidomidewithoutcorticosteroids,theORRwas47%atamedianfollow-upof7months(range1C26).Themediantimeto?rstresponsewas50days(range28C98)andmediantimetobestresponsewas69days(range30C591).Basedonthesepositive?ndings,aphaseIItrialhasbeeninitiatedtoinvestigatetheroleofaresponse-adaptedapproachusingsingle-agentlenalidomideasprimarytherapyforolderpatientswithnewlydiagnosedstandard-riskMM(ClinicalTrials.govidenti?er:NCT.ConclusionsCurrentavailabledatasuggestMMrequirescontinuoustherapytoreducetumorburdenandprolongsurvival.Lenalidomidehastheattributesofanagentthattargetsbothtumorgrowthandconcomitantimmunosuppression,whilebeingwelltoleratedandconvenientforlong-termuse.Lenalidomidehaspotenttumoricidalandimmunomodulatoryeffectsonmyelomacellsandtheirmicroenvironment,whicharethoughttoresultinbothrapidandsustainedcontrolofMMintheclinic.Lenalidomide,incombinationwithdexamethasone,isactiveandgenerallywelltoleratedintherelapsed/refractoryMMsettingandthereisevidencethatcontinuoustreatmentwithlenalidomidemayimproveclinicalresponse.Furthermore,lenalidomideappearstobeeffectiveregardlessofpriorthalidomidetreatment,whichmayre?bined?ndingsfrompreclinicalandclinicalstudiesalsoprovideinsightsintohowtheuseofconcomitantlenalidomideanddexamethasonecanbefurtheroptimized.Theuseoflow-dosedexamethasonemayprovidesynergisticantiproliferativeeffectswithoutantagonizinglenalidomide-mediatedimmuneeffects,whichmayexplaintheearlysurvivalbene?tobservedcomparedwithhigh-dosedexamethasone.Aspreclinicalandclinicalresearchcontinues,additionalinsightsintothedualmechanismofactionoflenalidomidewillbeobtained,whichmayhelptofurthermaximizetheuseoflenalidomideinthetreatmentofMM.7.Con?ictofinterestDrDavieshasservedontheSpeakersBureauforCelgeneCorporationandOrthoBiotechandhasparticipatedinAdvisoryBoardsforCelgene,OrthoBiotech,andNovartis.DrBazhasparticipatedinAdvisoryBoardsfor,andhasreceivedresearchfundingfrom,CelgeneCorporation.AcknowledgementsTheauthorsreceivededitorialsupportfromExcerptaMedicainthepreparationofthismanuscript,fundedbyCelgeneCorporation.Theauthorsarefullyresponsibleforcontentandeditorialdecisionsforthismanuscript.References1.MatsuiW,WangQ,BarberJP,etal.Clonogenicmultiplemyelomaprogenitors,stemcellproperties,anddrugresistance.CancerResC7.2.CookG,CampbellJD.Immuneregulationinmultiplemyeloma:thehost-tumourcon?ict.BloodRevC62.3.Schutt¨P,BrandhorstD,StellbergW,etal.Immuneparametersinmultiplemyelomapatients:in?uenceoftreatmentandcorrelationwithopportunisticinfections.LeukLymphoma0C82.4.AttalM,HarousseauJL,LeyvrazS,etal.Maintenancetherapywiththalidomideimprovessurvivalinpatientswithmultiplemyeloma.Blood9C94.5.Chanan-KhanAA,ChesonBD.LenalidomideforthetreatmentofB-cellmalignancies.JClinOncol4C52.6.KotlaV,GoelS,NischalS,etal.Mechanismofactionoflenalidomideinhematologicalmalignancies.JHematolOncol.7.ChungF,LuJ,PalmerBD,etal.Thalidomidepharmacokineticsandmetaboliteformationinmice,rabbits,andmultiplemyelomapatients.ClinCancerRes9C56.8.ChenN,LauH,KongL,etal.Pharmacokineticsoflenalidomideinsubjectswithvariousdegreesofrenalimpairmentandinsubjectsonhemodialysis.JClinPharmacol6C75.9.HideshimaT,ChauhanD,ShimaY,etal.Thalidomideanditsanalogsovercomedrugresistanceofhumanmultiplemyelomacellstoconventionaltherapy.B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l.SequentialtherapywithIMiD’sinrelapsed-refractorymultiplemyelomapatients[abstract].Blood:Abstract2888.66.BazR,PatelM,Finley-OliverE,etal.Singleagentlenalidomideinnewlydiagnosedmultiplemyeloma:aretrospectiveanalysis.LeukLymphoma5C9.三亿文库包含各类专业文献、中学教育、文学作品欣赏、高等教育、行业资料、应用写作文书、幼儿教育、小学教育、外语学习资料、18来那度胺机制等内容。 
 3.2 来那度胺的作用机制 来那度胺主要通过抑制白介素、α 肿瘤坏死因子来发挥作用[6]。其具有:① 免疫调节作用:来那度胺可通过调整免疫系统中 T 细胞的激活...  抗癌药来那度胺扩大适应症_医药卫生_专业资料。抗癌药来那度胺扩大适应症(来源:医药经济报) 2 月 18 日,FDA 批准扩大 Celgene 公司的抗癌药 Revlimid(来那度...  中国来那度胺行业市场前景调查及投融资战略研究报告
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