Andre Fabrice, Hatzis Christos, Anderson Keith, Sotiriou Christos, Mazouni Chafika, Mejia Jaime, Wang Bailiang, Hortobagyi Gabriel N, Symmans W Fraser, Pusztai Lajos
Breast Cancer Unit and Translational Research Unit, UPRES03535, Institut Gustave Roussy, Villejuif, France.
Clin Cancer Res. 2007 Apr 1;13(7):2061-7. doi: 10.1158/1078-0432.CCR-06-2078.
The clinical outcome for patients with breast cancer is influenced by the metastatic competence of the cancer and its sensitivity to endocrine therapy and chemotherapy. A molecular marker may be prognostic of outcome or predictive of response to therapy, or a combination of both.
We examined separately the prognostic and predictive values of tau mRNA expression in estrogen receptor (ER)-positive primary breast cancers in three patient cohorts. We used gene expression data from 209 untreated patients to assess the pure prognostic value of tau, data from 267 patients treated with adjuvant tamoxifen to assess predictive value for endocrine therapy, and data from 82 patients treated with preoperative paclitaxel followed by 5-fluorouracil, doxorubicin, and cyclophosphamide (paclitaxel/FAC) to assess predictive value for chemotherapy response. Wilcoxon rank sum test was used to compare tau expression between different outcome groups.
Higher tau mRNA expression showed borderline nonsignificant association with better prognosis in the absence of systemic adjuvant therapy. Higher tau mRNA expression was significantly associated with no recurrence (at 5 and 10 years, P = 0.005 and P = 0.05, respectively) in patients treated with tamoxifen, indicating a predictive value for endocrine therapy. Tau expression was significantly lower in patients who achieved pathologic complete response to paclitaxel/FAC chemotherapy (P < 0.001).
This study suggests that high tau mRNA expression in ER-positive breast cancer indicates an endocrine-sensitive but chemotherapy-resistant disease. In contrast, low tau expression identifies a subset of ER-positive cancers that have poor prognosis with tamoxifen alone and may benefit from taxane-containing chemotherapy.
乳腺癌患者的临床结局受癌症转移能力及其对内分泌治疗和化疗的敏感性影响。分子标志物可能对结局具有预后价值或对治疗反应具有预测价值,或两者兼具。
我们在三个患者队列中分别研究了雌激素受体(ER)阳性原发性乳腺癌中tau mRNA表达的预后和预测价值。我们使用来自209例未经治疗患者的基因表达数据评估tau的纯预后价值,来自267例接受他莫昔芬辅助治疗患者的数据评估内分泌治疗的预测价值,以及来自82例接受术前紫杉醇继以5-氟尿嘧啶、多柔比星和环磷酰胺(紫杉醇/FAC)治疗患者的数据评估化疗反应的预测价值。采用Wilcoxon秩和检验比较不同结局组之间的tau表达。
在无全身辅助治疗的情况下,较高的tau mRNA表达与较好的预后呈临界无显著关联。在接受他莫昔芬治疗的患者中,较高的tau mRNA表达与无复发显著相关(5年和10年时,P分别为0.005和0.05),表明对内分泌治疗具有预测价值。在对紫杉醇/FAC化疗达到病理完全缓解的患者中,tau表达显著较低(P<0.001)。
本研究提示,ER阳性乳腺癌中高tau mRNA表达表明为内分泌敏感但化疗耐药的疾病。相反,低tau表达确定了一部分ER阳性癌症,这些癌症单独使用他莫昔芬预后较差,可能从含紫杉烷的化疗中获益。