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70-Gene Signature as an Aid to Treatment Decisions in Early-Stage Breast Cancer.

机译:70基因签名有助于早期乳腺癌的治疗决策。

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摘要

The 70-gene signature test (MammaPrint) has been shown to improve prediction of clinical outcome in women with early-stage breast cancer. We sought to provide prospective evidence of the clinical utility of the addition of the 70-gene signature to standard clinical-pathological criteria in selecting patients for adjuvant chemotherapy.In this randomized, phase 3 study, we enrolled 6693 women with early-stage breast cancer and determined their genomic risk (using the 70-gene signature) and their clinical risk (using a modified version of Adjuvant! Online). Women at low clinical and genomic risk did not receive chemotherapy, whereas those at high clinical and genomic risk did receive such therapy. In patients with discordant risk results, either the genomic risk or the clinical risk was used to determine the use of chemotherapy. The primary goal was to assess whether, among patients with high-risk clinical features and a low-risk gene-expression profile who did not receive chemotherapy, the lower boundary of the 95% confidence interval for the rate of 5-year survival without distant metastasis would be 92% (i.e., the noninferiority boundary) or higher.A total of 1550 patients (23.2%) were deemed to be at high clinical risk and low genomic risk. At 5 years, the rate of survival without distant metastasis in this group was 94.7% (95% confidence interval, 92.5 to 96.2) among those not receiving chemotherapy. The absolute difference in this survival rate between these patients and those who received chemotherapy was 1.5 percentage points, with the rate being lower without chemotherapy. Similar rates of survival without distant metastasis were reported in the subgroup of patients who had estrogen-receptor-positive, human epidermal growth factor receptor 2-negative, and either node-negative or node-positive disease.Among women with early-stage breast cancer who were at high clinical risk and low genomic risk for recurrence, the receipt of no chemotherapy on the basis of the 70-gene signature led to a 5-year rate of survival without distant metastasis that was 1.5 percentage points lower than the rate with chemotherapy. Given these findings, approximately 46% of women with breast cancer who are at high clinical risk might not require chemotherapy. (Funded by the European Commission Sixth Framework Program and others; ClinicalTrials.gov number, NCT00433589; EudraCT number, 2005-002625-31.).
机译:已显示70基因签名测试(MammaPrint)可以改善患有早期乳腺癌的女性对临床结局的预测。我们寻求提供前瞻性证据,证明在标准临床病理学标准中选择辅助化疗的患者在标准临床病理学标准上增加了70个基因的签名具有临床意义。在这项随机的3期研究中,我们招募了6693名患有早期乳腺癌的女性并确定其基因组风险(使用70个基因的签名)和临床风险(使用Adjuvant!Online的修改版)。具有较低临床和基因组风险的妇女未接受化疗,而具有较高临床和基因组风险的妇女确实接受了这种治疗。在风险结果不一致的患者中,使用基因组风险或临床风险来确定化学疗法的使用。主要目标是评估在没有接受化疗的高风险临床特征和低风险基因表达谱的患者中,是否有95%置信区间的下限以无远距离5年生存率转移率将达到92%(即非劣效性边界)或更高。总共1550例患者(23.2%)被认为具有高临床风险和低基因组风险。在未接受化疗的患者中,在5年时,该组无远处转移的生存率为94.7%(95%置信区间为92.5至96.2)。这些患者与接受化疗的患者之间的这一生存率的绝对差异为1.5个百分点,而未接受化疗的患者的生存率较低。在患有雌激素受体阳性,人表皮生长因子受体2阴性,淋巴结阴性或淋巴结阳性的亚组患者中,报告了相似的存活率且无远处转移。处于高临床风险和低基因组复发风险的人,基于70个基因的特征而没有接受化疗导致5年生存率且无远处转移,比化疗率低1.5个百分点。根据这些发现,大约46%的具有高临床风险的乳腺癌女性可能不需要化疗。 (由欧洲委员会第六框架计划等资助; ClinicalTrials.gov编号,NCT00433589; EudraCT编号,2005-002625-31。)。

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