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Blood:CD19 CAR-T细胞免疫疗法有助于难治性/复发性滤泡性淋巴瘤患者获得持久的缓解

2019-06-26 MedSci MedSci原创

在初次化学免疫治疗后早期复发的、难治性的或存在组织学转化(tFL)的滤泡性淋巴瘤(FL)患者的无进展存活期和总体生存期有限。近日,Alexandre V. Hirayama等人在《Blood》杂志上发表了其对21位复发性/难治性(R/R)FL(8位)和tFL(13位)患者的长期随访结果。这21位患者均参与了采用环磷酰胺和氟达拉滨淋巴细胞清除+输注2x106/kg CD19导向的嵌合抗原受体修饰的T

在初次化学免疫治疗后早期复发的、难治性的或存在组织学转化(tFL)的滤泡性淋巴瘤(FL)患者的无进展存活期和总体生存期有限。近日,Alexandre V. Hirayama等人在《Blood》杂志上发表了其对21位复发性/难治性(R/R)FL(8位)和tFL(13位)患者的长期随访结果。

这21位患者均参与了采用环磷酰胺和氟达拉滨淋巴细胞清除+输注2x106/kg CD19导向的嵌合抗原受体修饰的T细胞(CAR-T)的1/2期临床试验。

FL患者和tFL患者的完全缓解(CR)率分别为88%和46%。截止中位随访24个月时,所有获得CR的FL患者仍处于缓解状态。中位随访38个月时,tFL患者的中位缓解持续时间为10.2个月。

FL患者和tFL患者细胞因子释放综合征的发生率分别是50%和39%,神经毒性的发生率分别是50%和23%,无重度副反应事件发生。CAR-T细胞的体内扩增/持久性在FL和tFL患者之间没有显著差异。

总而言之,CD19 CAR-T细胞免疫疗法对临床侵袭性的R/R滤泡性淋巴瘤成年患者非常有效,无论是否发生转化,大部分FL患者的病情均得到持久的缓解。

原始出处:

Alexandre V. Hirayama, et al. High Rate of Durable Complete Remission in Follicular Lymphoma after CD19 CAR-T cell Immunotherapy. Blood 2019 :blood.2019000905; doi: https://doi.org/10.1182/blood.2019000905

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    2020-04-21 仁者大医
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time=2019-06-28, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=1629095, encodeId=7e5116290958e, content=<a href='/topic/show?id=c92340e325' target=_blank style='color:#2F92EE;'>#CAR-T细胞免疫疗法#</a>, beContent=null, objectType=article, channel=null, level=null, likeNumber=67, replyNumber=0, topicName=null, topicId=null, topicList=[TopicDto(id=4073, encryptionId=c92340e325, topicName=CAR-T细胞免疫疗法)], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=bdd121300695, createdName=andy2094, createdTime=Fri Jun 28 13:10:00 CST 2019, time=2019-06-28, status=1, ipAttribution=)]
    2019-06-28 dingxiaobo
  8. 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time=2019-06-28, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=1629095, encodeId=7e5116290958e, content=<a href='/topic/show?id=c92340e325' target=_blank style='color:#2F92EE;'>#CAR-T细胞免疫疗法#</a>, beContent=null, objectType=article, channel=null, level=null, likeNumber=67, replyNumber=0, topicName=null, topicId=null, topicList=[TopicDto(id=4073, encryptionId=c92340e325, topicName=CAR-T细胞免疫疗法)], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=bdd121300695, createdName=andy2094, createdTime=Fri Jun 28 13:10:00 CST 2019, time=2019-06-28, status=1, ipAttribution=)]
    2019-06-28 freve
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中心点:基础血小板计数、LDH和淋巴细胞耗竭方案均会影响CD19 CAR-T细胞治疗后获得MRD阴性的完全缓解的患者的无事件存活期。CD19 CAR-T细胞治疗后进行同种异体HCT,患者耐受性好,还有望延长患者的无事件存活期。摘要:特异性表达CD19嵌合抗原受体(CAR)的自体T细胞可提高复发性/难治性急性B淋巴细胞白血病(B-ALL)患者的微小残留病阴性的完全缓解(MRD-CR)率。但是,与CA

Allogene与Servier宣布FDA批准ALLO-501的IND

Allogene是一家临床阶段生物技术公司,与其开发合作伙伴Servier(一家独立的国际制药公司)合作,率先开发了一种抗CD19的同种异体CAR-T(ALLO-501)癌症治疗药物,Allogene与Servier近日宣布美国食品和药品监督管理局(FDA)已批准ALLO-501的研究性新药申请(IND)用于治疗复发/难治性非霍奇金淋巴瘤(NHL)患者。

2019 EHA:TG Therapeutics的抗CD47 / CD19双特异性抗体TG-1801临床前抗淋巴瘤作用显著

第 24 届欧洲血液学协会(EHA)年会上,TG Therapeutics宣布推出TG-1801的临床前数据。TG-1801是一种抗CD47 / CD19的双特异性抗体,可选择性地靶向CD19 + B细胞上的CD47,并阻断成熟B细胞上的CD47-SIRPα介导的'不要吃我'的自我保护信号,来发挥抗肿瘤的作用。

Autolus的下一代CAR-T细胞疗法更加安全有效

英国生物技术公司Autolus正在开发下一代更安全,但同样有效的嵌合抗原受体(CAR)-T细胞疗法。该公司本周在美国癌症研究协会(AACR)上发布了其公司开发的CD19 CAR-T细胞疗法AUTO1治疗急性淋巴细胞白血病(ALL)成人患者的新数据。

Immunity:发现改善化学治疗抗肿瘤效果新机制

肿瘤是一种基因病,但并非是遗传的。它是指细胞在致癌因素作用下,基因发生了改变,失去对其生长的正常调控,导致单克隆性异常增生而形成的新生物。全身免疫抑制极大地影响化学治疗抗肿瘤作用。2019年2月12日,由浙江大学医学院蔡志坚&王建莉组成的团队在Immunity上发表了题为“Specific Decrease inB-Cell-Derived Extracellular Vesicles Enhan

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