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CLIN CANCER RES:新辅助多西他赛联合去势治疗对高风险前列腺癌基因组学和转录组学的影响

2017-11-18 MedSci MedSci原创

多西他赛联合去势治疗已成为转移性前列腺癌的标准治疗方式。近期进行的临床试验CALGB 90203主要的目的观察这一治疗方式在疾病早期的临床效果。在临床试验中获得的标本为探索多西他赛联合去势治疗的分子反应及可能的分子标志提供了机会。CLIN CANCER RES近期发表了一篇文章,研究了这一问题。

多西他赛联合去势治疗已成为转移性前列腺癌的标准治疗方式。近期进行的临床试验CALGB 90203主要的目的观察这一治疗方式在疾病早期的临床效果。在临床试验中获得的标本为探索多西他赛联合去势治疗的分子反应及可能的分子标志提供了机会。CLIN CANCER RES近期发表了一篇文章,研究了这一问题。

作者评估了CALGB 90203临床试验中纳入的52例患者的临床数据、穿刺活检标本和根治性切除后标本。通过病理、DNA测序和表达分析研究前列腺癌中与侵袭和耐药相关通路的变化。研究表明,最常见的改变包括TMPRSS2-ERG融合(n=32),TP53突变或缺失(n=11),PTEN缺失(n=6),FOXA1(n=6)和SPOP(n=4)突变,治疗后的标本中并未显着增加。作者并未观察到AR扩增或突变。治疗后的肿瘤AR信号抑制情况不同,AR和AR-V7表达以及一些神经内分泌基因表达上调。

文章最后认为,该研究数据表明对新辅助治疗后前列腺癌进行靶向基因和转录测序是可行的。治疗后发现的治疗反应异质性和分子异常为寻找可能的耐药标志提供了新的思路。

原始出处:
Himisha Beltran,Alexander W.Wyatt,et al.Impact of Therapy on Genomics and Transcriptomics in High-Risk Prostate Cancer Treated with Neoadjuvant Docetaxel and Androgen Deprivation Therapy.CLIN CANCER RES.November 2017 doi:10.1158/1078-0432.CCR-17-1034

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    2018-01-24 mjldent
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雄激素受体(AR)是前列腺癌预防和治疗的经典靶标。但是,有研究表明雌激素和它们的受体同样涉及到了前列腺癌发展和肿瘤恶化。最近,有研究人员回顾了最近的实验和临床数据,从而来阐释雌激素和它们的受体对前列腺致瘤和肿瘤恶化产生作用的病理机制。研究发现,雌激素受体(ERβ)是人类前列腺中最普遍的ER,然而雌激素受体(ERα)的分布限制在前列腺上皮基底细胞和基质细胞中。在高等级前列腺上皮内瘤(HGPIN)中,

Scand J Urol:爱沙尼亚前列腺发生率、死亡率和生存趋势分析

最近,有研究人员进行了旨在分析爱沙尼亚前列腺癌(PCa)发生率、死亡率和生存长期趋势的研究,并且特别关注了年龄和阶段参数。研究人员分别从爱沙尼亚癌症登记处和死亡原因登记处获得了1995年到2014年的PCa发生案例数据和有关的死亡数据,并利用连接点回归评估了发生和死亡比例的每年变化趋势。研究人员还推算出了5年的相对生存率(RSRs),并通过年龄和阶段对发生率和生存进行了分析。研究发现,2010-2

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高风险前列腺癌可以由病人的格林森得分(GS)、前列腺特异性抗原水平(PSA)和临床T(cT)阶段进行确定,但是由于该病的异质性,一个新的标记是需要的。最近,有研究人员评估了在患有高风险前列腺癌病人中,是否由穿刺活检确定的前列腺导管内癌(IDC-P)是无进展自由生存(PFS)和癌症特异生存(CSS)的不良预后参数。研究人员回顾性的评估了1991年到2005年经历根治性前列腺癌切除术的患有高风险前列腺

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