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分子亚型为晚期前列腺癌的精准医疗提供了可能性。

[Molecular subtypes provide possibilities for precision medicine in a advanced prostate cancer].

作者信息

Wikström Pernilla, Bergh Anders, Josefsson Andreas, Thysell Elin, Welén Karin

机构信息

professor i tumörbiologi, institutionen för medicinsk biovetenskap, Umeå universitet.

senior professor, patologi , institutionen för medicinsk biovetenskap, Umeå universitet.

出版信息

Lakartidningen. 2024 Apr 24;121:23179.

Abstract

Increased molecular knowledge makes it possible to consider not only genetic defects but also expression profiles for precision medicine in advanced prostate cancer. Several prognostic and treatment-predictive classifiers for prostate cancer have been described, such as Prolaris, OncotypeDx, Decipher, Prostatype, PAM50, PCS1-2, and MetA-C, which all build upon transcript profiles. In research studies, the MetA-C classifier has shown clear prognostic information for patients with metastatic disease, in relation to outcome after androgen receptor targeting therapies, and so has immunohistochemical evaluation of tumor cell proliferation (Ki67) and PSA expression. Unfortunately, methods within clinical routine today do not allow molecular subclassification of prostate cancer. To enable comparison of the most promising treatment-predictive biomarkers and to evaluate the health economic value of implementing such precision medicine for prostate cancer, a prospective study is being planned as a joint initiative in Sweden that aims to evaluate and validate biomarkers and to establish a study platform for adaptive biomarker-driven clinical trials (sprintr.se).

摘要

分子知识的增加使得在晚期前列腺癌的精准医疗中不仅可以考虑基因缺陷,还可以考虑表达谱。已经描述了几种用于前列腺癌的预后和治疗预测分类器,如Prolaris、OncotypeDx、Decipher、Prostatype、PAM50、PCS1-2和MetA-C,它们都基于转录谱构建。在研究中,MetA-C分类器已显示出与雄激素受体靶向治疗后的结果相关的、对转移性疾病患者的明确预后信息,肿瘤细胞增殖(Ki67)的免疫组化评估和PSA表达也是如此。不幸的是,当今临床常规中的方法不允许对前列腺癌进行分子亚分类。为了能够比较最有前景的治疗预测生物标志物,并评估实施这种前列腺癌精准医疗的健康经济价值,瑞典正在计划一项前瞻性研究,作为一项联合倡议,旨在评估和验证生物标志物,并建立一个用于适应性生物标志物驱动的临床试验的研究平台(sprintr.se)。

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