Lancet Oncol:转移性黑色素瘤患者:肥胖不再是“催命符”?

2018-03-26 吴星 环球医学

2018年3月,发表在《Lancet Oncol》的一项由美国、澳大利亚、德国和法国科学家进行的回顾性、多队列分析,考察了身体质量指数(BMI)与接受靶向治疗、免疫治疗或化疗的转移性黑色素瘤患者结局的相关性。

2018年3月,发表在《Lancet Oncol》的一项由美国、澳大利亚、德国和法国科学家进行的回顾性、多队列分析,考察了身体质量指数(BMI)与接受靶向治疗、免疫治疗或化疗的转移性黑色素瘤患者结局的相关性。

背景:在多种癌症类型中,肥胖与死亡率的增加相关;但是,黑色素瘤中,肥胖与生存结局之间的相关性尚不明确。本研究的目的是考察使用靶向治疗、免疫治疗或化疗的转移性黑色素瘤患者BMI与无进展生存期或总生存期之间的相关性。

方法:本回顾性研究分析了分配至随机临床试验以及一项患者接受免疫疗法的回顾性研究中,使用靶向治疗、免疫治疗或化疗的独立患者队列。根据BMI,遵循WHO的定义,患者被分为体重偏低、体重正常、体重超重或肥胖。排除无BMI的患者和体重偏低的患者。根据治疗类型和性别分层,主要结局为BMI与无进展生存期或总生存期之间的相关性。在独立队列中进行多变量分析,在混合效果Meta分析中,联合校正风险比,以对BMI于生存结局之间的相关性提供精确估计;用Meta回归分析评估异质性。对随机对照试验中的预定义意向治疗人群以及回归性研究中纳入的全部患者进行分析。

结果:2006年8月8日至2016年1月15日,6个队列共纳入2046例接受靶向治疗、免疫治疗或化疗的转移性黑色素瘤患者。分析中纳入1918例患者。2个队列的患者来自使用靶向治疗的随机对照试验(达帕菲尼联合曲美替尼( [n=599] 和威罗菲尼联合考比替尼[n=240]),2个队列的患者来自接受免疫治疗的队列研究(1项伊匹单抗联合达卡巴嗪的随机对照试验[n=207]和1项使用派姆单抗、纳武单抗或阿特朱单抗治疗的回顾性队列[n=331]),和2个包含化疗患者的队列(2项达卡巴嗪随机对照试验 [n=320和n=221])。在合并分析中,与正常BMI相比,肥胖与转移性黑色素瘤患者生存改善相关(无进展生存的平均校正风险比[HR]为0.77 [95% CI 0.66~0.90],总生存的平均校正风险比为0.74 [0.58~0.95])。肥胖相关生存获益仅限于接受靶向治疗(无进展生存HR 0.72 [0.57~0.91],总生存为0.60 [0.45~0.79])和免疫治疗(HR 0.75 [0.56~1.00]和0.64 [0.47~0.86])的患者。没有观察到与接收化疗存在相关性(无进展生存HR 0.87 [0.65~1.17,相互作用P=0.61],总生存1.03 [0.80~1.34,相互作用P =0.01])。BMI与总生存之间的相关性在使用靶向治疗和免疫治疗的患者中具有性别差异,在男性中存在逆向相关性(HR 0.53 [0.40~0.70]),但在女性中没有相关性(HR 0.85 [0.61~1.18,相互作用P=0.03])。

阐释:结果显示,在转移性黑色素瘤患者中,与BMI正常患者的结局相比,肥胖与无进展生存和总生存改善相关,且这一相关性主要在接受靶向或免疫治疗的男性患者中发现。这些结果提示了转移性黑色素瘤患者未来的临床试验设计,且所发现的巨大获益支持进一步考察这些相关性背后的机制。

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    2018-10-31 sunylz
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    2018-09-27 howi
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06:50:21 CST 2018, time=2018-03-28, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=300222, encodeId=9adc30022259, content=不错耶.学习了, beContent=null, objectType=article, channel=null, level=null, likeNumber=42, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=3b2c1627329, createdName=owlhealth, createdTime=Tue Mar 27 17:15:05 CST 2018, time=2018-03-27, status=1, ipAttribution=)]
    2018-12-06 minlingfeng
  4. 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06:50:21 CST 2018, time=2018-03-28, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=300222, encodeId=9adc30022259, content=不错耶.学习了, beContent=null, objectType=article, channel=null, level=null, likeNumber=42, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=3b2c1627329, createdName=owlhealth, createdTime=Tue Mar 27 17:15:05 CST 2018, time=2018-03-27, status=1, ipAttribution=)]
    2018-04-10 1215ce8am69暂无昵称

    学习了.谢谢;-)

    0

  5. 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  6. 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  8. 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  9. 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06:50:21 CST 2018, time=2018-03-28, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=300222, encodeId=9adc30022259, content=不错耶.学习了, beContent=null, objectType=article, channel=null, level=null, likeNumber=42, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=3b2c1627329, createdName=owlhealth, createdTime=Tue Mar 27 17:15:05 CST 2018, time=2018-03-27, status=1, ipAttribution=)]
    2018-03-28 jihuaijun1112

    学习学习学习

    0

  10. 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    2018-03-27 owlhealth

    不错耶.学习了

    0

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免疫检查点抑制剂显著改变了转移性黑色素瘤患者的治疗选择。但是部分患者仍然对治疗没有反应。回顾性数据表明ipilimumab在NY-ESO-1阳性的黑素瘤患者中具有更高的临床益处

全新分子MK-8353显示出对黑色素瘤的治疗希望

近日,在一项早期临床试验中,旨在阻断晚期黑色素瘤和其他肿瘤中过度活化的细胞生长信号的在研化合物显示出了良好的治疗前景。作为该项目的研究者,北卡罗来纳大学的Stergios Moschos博士及其同事公布了第一阶段的结果,在这项多中心试验中,研究者们招募了含有BRAF或RAS基因突变的黑色素瘤和其他肿瘤患者,共涉及26例患者,对患者使用新型化合物MK-8353进行治疗,该化合物旨在阻断驱动耐药性黑色

Nature:红头发的人易得黑色素瘤被揭密

红发人占全球人口的1-2%,但占英国民众的比例约6%。他们携带了2个黑色素突变基因,导致白皮肤、雀斑和红色头发的出现。人们普遍认为,皮肤过多接受紫外线的照射会增加DNA破坏的风险。但是并不是每个人的DNA都容易被紫外线破坏。红头发和白皮肤的民众较为敏感,他们的DNA容易受到紫外线破坏。过去认为,红色头发民众的突变黑色素基因生成黑色素的能力降低,进而保护皮肤免受紫外线伤害的能力降低。 一提到红头发

白血病药物的重新使用能够预防黑色素瘤的转移

一项最新研究的数据显示,重新使用治疗白血病的药物(ABL激酶抑制剂)有望预防黑色素瘤转移。该研究显示癌症促进基因ABL激酶的激活与黑素瘤中促转移性组织蛋白酶(pro-metastatic cathepsins)的分泌正向相关。组织蛋白酶能够降解蛋白质并在癌细胞中高度表达,肿瘤细胞将这些蛋白酶释放到细胞微环境中,这些酶“咀嚼”了肿瘤周围的纤维基质,进而使肿瘤细胞更容易地进入血液和淋巴系统并转移到身体

Mol Cell:可不敢乱吃膳食补充剂了!硫酸软骨素竟会促进特定肿瘤生长,并导致耐药性

《分子细胞》杂志近期出了一项新研究,按说已经挺安全的硫酸软骨素,居然也是个要小心的对象!

Nat Commun:黑色素瘤耐药机制研究取得突破性进展

近日,西安交大生命学院线粒体生物医学研究所和前沿院转化医学研究中心等单位合作,发现了一种新的基于磷酸化与SUMO化修饰的SOX10转录活性调控机制,揭示了ERK1/2/SOX10/FOXD3/ERBB3信号通路在人黑色素瘤对RAF抑制剂的适应性耐药发生过程中的作用。这一突破性的进展将会极大地促进以SOX10为靶点提高黑色素瘤的治疗效果方面的研究。