ANN ONCOL:蛋白结合型紫杉醇联合卡铂或吉西他滨治疗转移性三阴性乳腺癌

2018-08-25 MedSci MedSci原创

转移性三阴性乳腺癌侵袭性强,往往预后较差。tnAcity试验评估了蛋白结合型紫杉醇联合卡铂(nab-P/C),蛋白结合型紫杉醇联合吉西他滨(nab-P/G)和吉西他滨联合卡铂(G/C)作为一线疗法治疗转移性三阴性乳腺癌患者的安全性和有效性。

转移性三阴性乳腺癌侵袭性强,往往预后较差。tnAcity试验评估了蛋白结合型紫杉醇联合卡铂(nab-P/C),蛋白结合型紫杉醇联合吉西他滨(nab-P/G)和吉西他滨联合卡铂(G/C)作为一线疗法治疗转移性三阴性乳腺癌患者的安全性和有效性。

病理诊断为三阴性乳腺癌且未接受过化疗的患者按1:1:1分入三组。Ⅱ期主要的研究终点为无进展生存,次要研究终点包括总缓解率,总生存,开始6个周期接受双重了疗法患者的比例以及安全性。最终共纳入191例患者。研究结果表明,nab-P/C组的无进展生存显着优于nab-P/G组和G/C组。nab-P/C组的总生存率数字上高于nab-P/G组和G/C组。nab-P/C组,nab-P/G组和G/C组的总缓解率分别为73%,39%和44%。在nab-P/C组,nab-P/G组和G/C组中,开始6个周期接受双重治疗的患者比例分别为64%,56%和50%。≥3级不良反应主要为血液学不良反应。

文章最后认为,一线nab-P/C治疗转移性三阴性乳腺癌具有活性,与nab-P/G和G/C相比无进展生存显着改善。

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  5. 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    2018-11-12 minlingfeng
  6. 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  7. 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  8. 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    2018-08-27 xlysu
  9. 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    2018-08-26 kafei

    学习了谢谢

    0

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科学家们发现了一种对抗难以治疗的乳腺癌的新方法,从而引发了一项新的药物计划,旨在开发针对这种疾病的新型靶向疗法。由英国慈善机构Breast Cancer Now资助的研究人员发现,阻断KIFC1基因的作用对三阴性乳腺癌有效的同时健康细胞不受伤害。该基因是研究人员发现的37个新基因中最有前途的一种,研究人员发现三阴性乳腺癌与该基因有关,当沉默的时候,抑制肿瘤细胞的生长,但对正常细胞没有影响,从而提供

CLIN CANCER RES:新辅助卡铂和多西他赛治疗的三阴性乳腺癌患者的病理缓解情况

三阴性乳腺癌(TNBC)需要可靠的能够预测新辅助化疗(NACT)反应的预测标志物。CLIN CANCER RES近期发表了一篇文章,评估TNBCtype-4分类在接受新辅助卡铂和多西他赛(Tcb)治疗的三阴性乳腺癌患者中预测治疗反应的能力。

Nat Med:“靶向化疗”成为可能—卡铂用于治疗BRCA1/2突变及BRCAness表型三阴性乳腺癌的III期TNT研究

BRCA1/2突变胚系突变在TNBC中的检出率约为10%,BRCA突变细胞对铂类药物具有很高的敏感性。在早期的新辅助研究中,发现铂类单药能使BRCA突变乳腺癌的pCR率提高到60%以上;TBCRC009研究亦显示了其在BRCA突变的晚期乳腺癌中的作用。但尚缺乏大型临床试验对其进行验证。TNT研究作为一项对比卡铂与多西他赛在BRCA1/2突变及BRCAness表型三阴性乳腺癌患者中的有效性研究,填补

依地福新可防止乳腺癌细胞在大脑中的激活

近日,研究人员使用计算机模型证明现有的用于白血病患者治疗的药物依地福新,依地福新可以阻断转移到大脑的三阴性乳腺癌细胞的激活。

PNAS:TDP43可以作为三阴性乳腺癌治疗的潜在靶标

三阴性乳腺癌(TNBC)是一类恶性程度较高的乳腺癌分型。相对于其他类型的乳腺癌,三阴性乳腺癌表现出转移率高、细胞增殖快和预后差等特征。目前缺乏三阴型乳腺癌的成功靶向药物。

Signal Transduct Target Ther:靶向MUC1-C可抑制三阴性乳腺癌中的BCL2A1

B细胞淋巴瘤2相关蛋白A1(BCL2A1)是抗细胞凋亡蛋白BCL-2家族的成员,是导致抗癌药物治疗抗性的主要因素,但是目前还没有针对BCL2A1的药物。MUC1-C癌蛋白在三阴性乳腺癌(TNBCs)细胞中异常表达,诱导上皮-间质转化(EMT)并促进抗癌药物抗性。本研究表明,在TNBCs细胞中靶向MUC1-C可导致BCL2A1表达的下调。结果显示,MUC1-C通过NF-κBp65介导的机制激活BCL