Department of Surgery, Washington University School of Medicine St. Louis, 660 South Euclid Avenue, Campus Box 8109, St. Louis, MO 63110, USA.
Breast Cancer Res Treat. 2010 Oct;123(3):691-9. doi: 10.1007/s10549-009-0664-y. Epub 2009 Dec 6.
Several gene expression profiles have been reported to predict breast cancer response to neoadjuvant chemotherapy. These studies often consider breast cancer as a homogeneous entity, although higher rates of pathologic complete response (pCR) are known to occur within the basal-like subclass. We postulated that profiles with higher predictive accuracy could be derived from a subset analysis of basal-like tumors in isolation. Using a previously described "intrinsic" signature to differentiate breast tumor subclasses, we identified 50 basal-like tumors from two independent clinical trials associated with gene expression profile data. 24 tumor data sets were derived from a 119-patient neoadjuvant trial at our institution and an additional 26 tumor data sets were identified from a published data set (Hess et al. J Clin Oncol 24:4236-4244, 2006). The combined 50 basal-like tumors were partitioned to form a 37 sample training set with 13 sequestered for validation. Clinical surveillance occurred for a mean of 26 months. We identified a 23-gene profile which predicted pCR in basal-like breast cancers with 92% predictive accuracy in the sequestered validation data set. Furthermore, distinct cluster of patients with high rates of cancer recurrence was observed based on cluster analysis with the 23-gene signature. Disease-free survival analysis of these three clusters revealed significantly reduced survival in the patients of this high recurrence cluster. We identified a 23-gene signature which predicts response of basal-like breast cancer to neoadjuvant chemotherapy as well as disease-free survival. This signature is independent of tissue collection method and chemotherapeutic regimen.
已经有几个基因表达谱被报道可以预测乳腺癌对新辅助化疗的反应。这些研究通常将乳腺癌视为同质实体,尽管基底样亚型的病理完全缓解(pCR)率更高。我们假设,从单独的基底样肿瘤亚组分析中可以得出具有更高预测准确性的谱。我们使用先前描述的“内在”特征来区分乳腺癌亚型,从与基因表达谱数据相关的两项独立临床试验中鉴定了 50 个基底样肿瘤。24 个肿瘤数据集来自我们机构的一项 119 例新辅助试验,另外 26 个肿瘤数据集来自已发表的数据集(Hess 等人,J Clin Oncol 24:4236-4244, 2006)。合并的 50 个基底样肿瘤被分割形成一个 37 个样本的训练集,其中 13 个被隔离用于验证。平均临床监测时间为 26 个月。我们确定了一个 23 基因谱,该谱可预测基底样乳腺癌的 pCR,在隔离验证数据集中具有 92%的预测准确性。此外,基于 23 基因特征的聚类分析观察到了具有高癌症复发率的患者明显不同的聚类。对这三个聚类的无病生存分析显示,高复发聚类患者的生存明显降低。我们确定了一个 23 基因签名,可以预测基底样乳腺癌对新辅助化疗的反应以及无病生存。该特征独立于组织采集方法和化疗方案。