首页> 外文期刊>Journal of Clinical Oncology >PAM50 Risk of Recurrence Score Predicts 10-Year Distant Recurrence in a Comprehensive Danish Cohort of Postmenopausal Women Allocated to 5 Years of Endocrine Therapy for Hormone Receptor-Positive Early Breast Cancer
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PAM50 Risk of Recurrence Score Predicts 10-Year Distant Recurrence in a Comprehensive Danish Cohort of Postmenopausal Women Allocated to 5 Years of Endocrine Therapy for Hormone Receptor-Positive Early Breast Cancer

机译:PAM50复发评分的风险预测,在综合丹麦群体综合妇女综合妇女群体分配给荷尔蒙受体阳性早期乳腺癌5年的综合丹麦群体中的10年遥远复发

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PurposeThe PAM50-based Prosigna risk of recurrence (ROR) score has been validated in randomized clinical trials to predict 10-year distant recurrence (DR). The value of Prosigna for predicting DR was examined in a comprehensive nationwide Danish cohort consisting of postmenopausal women with hormone receptor-positive early breast cancer treated with 5 years of endocrine therapy alone.Patients and MethodsUsing the population-based Danish Breast Cancer Cooperative Group database, follow-up data were collected on all patients diagnosed from 2000 through 2003 who, by nationwide guidelines, were treated with endocrine therapy for 5 years. Primary tumor blocks from 2,740 patients were tested with Prosigna and, after determination of human epidermal growth factor receptor 2 (HER2) status, data from 2,558 hormone receptor-positive/HER2-negative samples were analyzed, including 1,395 node-positive patients. Fine and Gray models were applied to determine the prognostic value of ROR for DR.ResultsMedian follow-up for recurrence was 9.2 years. Twenty-six percent of the node-positive patients were classified as low ROR (n = 359) with a DR risk of 3.5% (95% confidence interval [CI], 1.9% to 6.1%) versus a DR risk of 22.1% (95% CI, 18.6% to 25.8%) at 10 years for patients classified as high ROR (n = 648). Node-negative patients classified as low and high ROR had a risk of DR of 5.0% (95% CI, 2.9% to 8.0%) and 17.8% (95% CI, 14.0% to 22.0%), respectively. Luminal B tumors (n = 947; DR risk, 18.4% [95% CI: 15.7% to 21.3%]) had a significantly worse outcome than luminal A tumors (n = 1,474,;DR risk, 7.6% [95% CI: 6.1% to 9.2%]; P .001).ConclusionProsigna ROR score improved the prediction of outcome in this nationwide Danish population. In a real-world setting, Prosigna can reliably identify node-negative patients and a significant proportion of patients with one to three positive nodes who can be spared treatment with adjuvant chemotherapy. (C) 2018 by American Society of Clinical Oncology
机译:PMOSethe PAM50的PROSIGNA复发(ROR)评分的风险已被验证在随机临床试验中,以预测10年的远程复发(DR)。在全国范围的丹麦队列中审查了ProSigna预测博士的价值,该丹麦队列由单独的患有激素受体阳性早期乳腺癌的绝经后患者组成,用5年的内分泌治疗治疗。患者和方法是丹麦乳腺癌合作组数据库,在2000年至2003年诊断的所有患者上收集了后续数据,通过全国范围内的指南,持续5年的内分泌治疗治疗。从2,740名患者的原发性肿瘤嵌段用ProSigna测试,并在测定人表皮生长因子受体2(HER2)状态后,分析了来自2,558个激素受体阳性/ HER2阴性样品的数据,包括1,395名Node阳性患者。应用精细和灰色模型来确定ROR的预后价值.Resultsme​​dian的再次发生的后续行动为9.2年。将26%的节点阳性患者分类为低ROR(n = 359),博士风险为3.5%(95%置信区间[CI],1.9%至6.1%)与博士风险22.1%( 95%CI,10年为18.6%至25.8%,患者分类为高ror(n = 648)。分类为低压和高rOR的节点阴性患者的风险为5.0%(95%CI,2.9%至8.0%)和17.8%(95%CI,14.0%至22.0%)。 Luminal B肿瘤(n = 947;危险博士,18.4%[95%CI:15.7%至21.3%])具有比腔肿瘤更差的结果明显更差(n = 1,474,;博士风险,7.6%[95%CI: 6.1%至9.2%]; p& .001).ConclusionProSigna ROR评分改善了全国丹麦人群的结果预测。在真实世界的环境中,ProSigna可以可靠地识别节点阴性患者和大量比例的患者一到三个阳性节点,他们可以用佐剂化疗进行备受治疗。 (c)2018年美国临床肿瘤学会

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