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Prostate cancer biomarkers: Are we hitting the mark?

机译:前列腺癌生物标志物:我们达到目标了吗?

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Purpose Localised prostate cancer diagnosis and management is increasingly complex due to its heterogeneous progression and prognostic subgroups. Pitfalls in current screening and diagnosis have prompted the search for accurate and invasive molecular and genetic biomarkers for prostate cancer. Such tools may be able to distinguish clinically significant cancers from less aggressive variants to assist with prostate cancer risk stratification and guide decisions and healthcare algorithms. We aimed to?provide a comprehensive review of the current prostate cancer biomarkers available and in development. Methods MEDLINE and EMBASE databases searches were conducted to identify articles pertaining to the use of novel biomarkers for prostate cancer. Results A growing number of novel biomarkers are currently under investigation. Such markers include urinary biomarkers, serology-based markers or pathological tissue assessments of molecular and genetic markers. While limited clinical data is present for analysis, early results appear promising. Specifically, a combination of serum and urinary biomarkers (Serum PSA + Urinary PCA3 + Urinary TMPRSS2-ERG fusion) appears to provide superior sensitivity and specificity profiles compared to traditional diagnostic approaches (AUC 0.88). Conclusion The accurate diagnosis and risk stratification of prostate cancer is critical to ensure appropriate intervention. The development of non-invasive biomarkers can add to the information provided by current screening practices and allows for individualised risk stratification of patients. The use of these biomarkers appears to increase the sensitivity and specificity of diagnosis of prostate cancer. Further studies are necessary to define the appropriate use and time points of each biomarker and their effect on the management algorithm of prostate cancer.
机译:目的由于其异质性进展和预后亚组,局部前列腺癌的诊断和管理越来越复杂。当前的筛查和诊断中的缺陷促使人们寻找前列腺癌的准确和侵入性的分子和遗传生物标记。这样的工具可能能够将临床上重要的癌症与侵略性较低的变体区分开来,以帮助进行前列腺癌风险分层,并指导决策和医疗算法。我们旨在对当前可用的和正在开发中的前列腺癌生物标记物进行全面审查。方法对MEDLINE和EMBASE数据库进行搜索,以鉴定与使用新型生物标志物治疗前列腺癌有关的文章。结果目前正在研究越来越多的新型生物标志物。此类标记包括尿液生物标记,基于血清学的标记或分子和遗传标记的病理组织评估。尽管目前有限的临床数据可用于分析,但早期结果似乎很有希望。具体而言,与传统诊断方法(AUC 0.88)相比,血清和尿液生物标志物(血清PSA +尿液PCA3 +尿液TMPRSS2-ERG融合蛋白)的组合似乎具有更高的敏感性和特异性。结论前列腺癌的准确诊断和危险分层对于确保适当的干预至关重要。非侵入性生物标志物的开发可以增加当前筛查实践提供的信息,并可以对患者进行个体化风险分层。这些生物标志物的使用似乎增加了诊断前列腺癌的敏感性和特异性。需要进一步的研究来定义每种生物标志物的适当用途和时间点及其对前列腺癌治疗算法的影响。

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