Department of Breast and Endocrine Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Cancer. 2011 Aug 15;117(16):3682-90. doi: 10.1002/cncr.25953. Epub 2011 Feb 8.
Sequential administration of paclitaxel plus combined fluorouracil, epirubicin, and cyclophosphamide (P-FEC) is 1 of the most common neoadjuvant chemotherapies for patients with primary breast cancer and produces pathologic complete response (pCR) rates of 20% to 30%. However, a predictor of pCR to this chemotherapy has yet to be developed. The authors developed such a predictor by using a proprietary DNA microarray for gene expression analysis of breast tumor tissues.
Tumor samples were obtained from 84 patients with breast cancer by core-needle biopsy before the patients received P-FEC, and the gene expression profile was analyzed in those samples to construct a classifier for predicting pCR to P-FEC. In addition, the authors analyzed the gene expression profile of tumor tissues that were obtained at surgery from 105 patients with lymph node-negative and estrogen receptor-positive breast cancer who received adjuvant hormone therapy alone to determine the prognostic significance of the classifier.
The 70-gene classifier for predicting pCR to P-FEC was constructed by using the training set (n = 50) and subsequently was validated successfully in the validation set (n = 34), revealing high sensitivity (88%; 95% confidence interval [CI], 47%-100%) and high negative predictive value (93%; 95% CI, 68%-100%). Specificity and positive predictive value were 54% (95% CI, 33%-73%) and 37% (95% CI, 16%-62%), respectively. Among the various parameters (estrogen receptor, progesterone receptor, human epidermal growth factor receptor 2, and Ki-67 status, etc), the 70-gene classifier had the strongest association with pCR (P = .015). In an additional study, genetically assumed complete responders were associated significantly (P = .047) with a poor prognosis.
The 70-gene classifier that was constructed for predicting pCR to P-FEC for breast tumors was successful, with high sensitivity and high negative predictive value. The classifier also appeared to be useful for predicting the prognosis of patients with lymph node-negative and estrogen receptor-positive breast cancer who receive adjuvant hormone therapy alone.
紫杉醇联合氟尿嘧啶、表柔比星和环磷酰胺(P-FEC)序贯治疗是原发性乳腺癌患者最常用的新辅助化疗方案之一,可产生 20%至 30%的病理完全缓解(pCR)率。然而,尚未开发出预测这种化疗 pCR 的指标。作者通过使用专有的 DNA 微阵列对乳腺癌组织的基因表达进行分析,开发了这样的预测指标。
在患者接受 P-FEC 之前,通过核心针活检从 84 名乳腺癌患者中获得肿瘤样本,并对这些样本进行基因表达谱分析,构建预测 P-FEC 对 pCR 的分类器。此外,作者还分析了 105 名接受单独辅助激素治疗的淋巴结阴性和雌激素受体阳性乳腺癌患者手术获得的肿瘤组织的基因表达谱,以确定分类器的预后意义。
通过使用训练集(n=50)构建了预测 P-FEC 对 pCR 的 70 基因分类器,随后在验证集(n=34)中成功验证,显示出高灵敏度(88%;95%置信区间[CI],47%-100%)和高阴性预测值(93%;95%CI,68%-100%)。特异性和阳性预测值分别为 54%(95%CI,33%-73%)和 37%(95%CI,16%-62%)。在各种参数(雌激素受体、孕激素受体、人表皮生长因子受体 2、Ki-67 状态等)中,70 基因分类器与 pCR 相关性最强(P=0.015)。在一项额外的研究中,基因假设的完全缓解者与预后不良显著相关(P=0.047)。
用于预测乳腺癌 P-FEC 对 pCR 的 70 基因分类器成功,具有高灵敏度和高阴性预测值。该分类器似乎也可用于预测接受单独辅助激素治疗的淋巴结阴性和雌激素受体阳性乳腺癌患者的预后。