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在新辅助多西他赛、阿霉素和环磷酰胺化疗前,通过粗针活检获得的乳腺癌基因表达谱与常规预后标志物相关,可用于识别预测性特征。

Gene expression profiles of breast cancer obtained from core cut biopsies before neoadjuvant docetaxel, adriamycin, and cyclophoshamide chemotherapy correlate with routine prognostic markers and could be used to identify predictive signatures.

作者信息

Rody A, Karn T, Gätje R, Kourtis K, Minckwitz G, Loibl S, Munnes M, Ruckhäberle E, Holtrich U, Kaufmann M, Ahr A

机构信息

Department of Obstetrics and Gynecology, J.-W.-Goethe-University, Frankfurt, Germany.

出版信息

Zentralbl Gynakol. 2006 Apr;128(2):76-81. doi: 10.1055/s-2006-921508.

Abstract

BACKGROUND

Neoadjuvant administration of chemotherapy provides a unique opportunity to monitor response to treatment in breast cancer and assesses response exactly. Global gene expression profiling by microarrays has been used as a valuable tool for the identification of prognostic and predictive marker genes. Even though this technology is now wide spread and relatively standardized, there are only few data available which compare established parameters with expression values to determine reliability of this method. Therefore we analyzed gene expression data of pretreatment biopsies of breast cancer patients and compared them with the results of the immunohistochemical receptor expression for ER/ PR and Her-2, as well as FISH testing for HER-2 amplification. We analyzed the change of expression of these markers before and after neoadjuvant chemotherapy. Furthermore we evaluated the predictive significance of prognostic gene signatures as described by Sorlie, van't Veer and Ahr for response to neoadjuvant chemotherapy.

METHODS

Pretherapeutic core biopsies were obtained from 70 patients undergoing neoadjuvant TAC chemotherapy within the GEPARTRIO-trial. Samples were characterized according to standard pathology including ER, PR and HER2 IHC and amount of cancer cells. Only biopsies with more than 80 % tumor cells were considered for further examination. RNA was isolated and expression profiling performed using Affymetrix Hg U133 Arrays (22 500 genes). GeneData's Expressionist software was used for bioinformatic analyses.

RESULTS

More than two thirds of the biopsies yielded sufficient amounts (> 5 microg) of RNA for expression profiling and high quality data were obtained for 50 samples. Unsupervised clustering broadly revealed a correlation with hormone receptor status. When ER-alpha, PR and HER2 as analyzed by immunohistochemistry were compared to the corresponding mRNA data from gene chips more than 90 % concordance was observed. We could observe a switch of receptor expression for ER, PR or HER-2 from positive to negative and vice versa in 16/35 cases (45.7 %) and 5/22 cases (22.7 %) respectively. The prognostic marker sets of Sorlie, van't Veer and Ahr could not discriminate responders from non-responders in our patient group.

CONCLUSIONS

Our results demonstrate that reliable expression profiles can be achieved by using limited amounts of tissue obtained during neoadjuvant chemotherapy. Microarray data capture conventional prognostic markers but might contain additional informative gene sets correlated with treatment outcome. Prognostic marker sets are not suitable to predict tumor response in the neoadjuvant setting, suggesting the necessity of class prediction methods to identify marker sets predictive for the type of therapy used.

摘要

背景

新辅助化疗提供了一个独特的机会来监测乳腺癌对治疗的反应并准确评估反应情况。通过微阵列进行的全基因组表达谱分析已被用作鉴定预后和预测性标记基因的重要工具。尽管这项技术目前已广泛应用且相对标准化,但仅有少量数据可用于比较既定参数与表达值以确定该方法的可靠性。因此,我们分析了乳腺癌患者治疗前活检组织的基因表达数据,并将其与雌激素受体(ER)/孕激素受体(PR)和人表皮生长因子受体2(Her-2)的免疫组化受体表达结果以及Her-2扩增的荧光原位杂交(FISH)检测结果进行比较。我们分析了新辅助化疗前后这些标记物表达的变化。此外,我们评估了Sorlie、van't Veer和Ahr所描述的预后基因特征对新辅助化疗反应的预测意义。

方法

在GEPARTRIO试验中,从70例接受新辅助TAC化疗的患者中获取治疗前的核心活检组织。根据标准病理学对样本进行特征分析,包括ER、PR和HER2免疫组化以及癌细胞数量。仅考虑肿瘤细胞比例超过80%的活检组织进行进一步检查。提取RNA并使用Affymetrix Hg U133阵列(22500个基因)进行表达谱分析。使用GeneData的Expressionist软件进行生物信息学分析。

结果

超过三分之二的活检组织产生了足够量(>5微克)的RNA用于表达谱分析,并且为50个样本获得了高质量数据。无监督聚类大致显示出与激素受体状态的相关性。当将免疫组化分析的ER-α、PR和HER2与基因芯片相应的mRNA数据进行比较时,观察到超过90%的一致性。我们分别在16/35例(45.7%)和5/22例(22.7%)病例中观察到ER、PR或HER-2受体表达从阳性转为阴性或反之亦然。在我们的患者组中,Sorlie、van't Veer和Ahr的预后标记集无法区分反应者与无反应者。

结论

我们的结果表明,使用新辅助化疗期间获取的有限组织量可实现可靠的表达谱。微阵列数据捕获了传统的预后标记物,但可能包含与治疗结果相关的其他信息基因集。预后标记集不适用于预测新辅助治疗环境中的肿瘤反应,这表明需要分类预测方法来识别对所用治疗类型具有预测性的标记集。

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