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Prediction of Response to Neoadjuvant Chemotherapy: New Biomarker Approaches and Concepts

机译:预测对新辅助化疗的反应:新的生物标志物方法和概念

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About 10-25% of breast cancer patients achieve a pathologically confirmed complete response after neoadjuvant chemotherapy. Tissue samples of pretreatment core biopsies are a valuable resource for translational research aiming towards predictive biomarkers for selecting patients who are likely to benefit from neoadjuvant therapy. The German Breast Group (GBG) and the AGO-B Group (AGO = Working Group Gynecological Oncology) have extensive experience in conducting neoadjuvant clinical trials. Technologies as immunohisto-chemistry on tissue microarrays and standardized reverse transcription-polymerase chain reaction (RT-PCR) approaches on formalin-fixed paraffin-embedded samples allow high-throughput investigation of protein and mRNA biomarkers. With these approaches, we could demonstrate that molecular tumor subtypes and immu-nological infiltrates are valuable and independent predictors of therapy response. New biomarkers such as poly(ADP-ribose) polymerase (PARP) might be useful for the prediction of response to conventional and new targeted therapies. This review summarizes current research projects focusing on biomarker discovery in the neoadjuvant setting.
机译:约10-25%的乳腺癌患者在新辅助化疗后达到病理确认的完全缓解。预处理核心活组织检查的组织样本是转化研究的宝贵资源,其目的在于预测生物标志物,以选择可能从新辅助治疗中受益的患者。德国乳房小组(GBG)和AGO-B小组(AGO =妇科肿瘤工作组)在进行新辅助临床试验方面具有丰富的经验。组织微阵列上的免疫组织化学技术和福尔马林固定石蜡包埋样品上的标准化逆转录-聚合酶链反应(RT-PCR)方法可以对蛋白质和mRNA生物标记物进行高通量研究。通过这些方法,我们可以证明分子肿瘤亚型和免疫学浸润是治疗反应的有价值且独立的预测因子。新的生物标记物,例如聚(ADP-核糖)聚合酶(PARP),可用于预测对常规和新靶向疗法的反应。这篇综述总结了当前专注于新辅助环境中生物标志物发现的研究项目。

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