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Androgen receptor in advanced breast cancer: is it useful to predict the efficacy of anti-estrogen therapy?

机译:晚期乳腺癌中的雄激素受体:预测抗雌激素治疗的功效是否有用?

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Androgen receptor (AR) is widely expressed in breast cancer (BC) but its role in estrogen receptor (ER)-positive tumors is still controversial. The AR/ER ratio has been reported to impact prognosis and response to antiestrogen endocrine therapy (ET). We assessed whether AR in primary tumors and/or matched metastases is a predictor of efficacy of first-line ET in advanced BC. Patients who had received first-line ET (2002–2011) were recruited, while those given concomitant chemotherapy or trastuzumab or pretreated with >?2 lines of chemotherapy were excluded. ER, progesterone receptor (PgR), Ki67 and AR expression were assessed by immunohistochemistry, and HER2 mainly by fluorescent in-situ hybridization. Cut-offs of 1 and 10% immunostained cells were used to categorize AR expression. Among 102 evaluable patients, biomarkers were assessed in primary tumors in 70 cases and in metastases in 49, with 17 patients having both determinations. The overall concordance rate between primary tumors and metastases was 64.7% (95% CI 42%-87.4%) for AR status. AR status did not affect TTP significantly, whereas PgR and Ki67 status did. AR/PgR ≥0.96 was associated with a significantly shorter TTP (HR?=?1.65, 95% CI 1.05-2.61, p?=?0.028). AR status in primary tumors or metastases was not associated with progressive disease (PD) as best response. In contrast, Ki67?≥?20% and PgR
机译:雄激素受体(AR)在乳腺癌(BC)中广泛表达,但其在雌激素受体(ER)阳性肿瘤中的作用仍存在争议。据报道,AR / ER比会影响抗雌激素内分泌治疗(ET)的预后和反应。我们评估了原发肿瘤和/或匹配转移中的AR是否是一线ET在晚期BC中疗效的预测指标。招募了接受一线ET(2002-2011)的患者,而同时接受化疗或曲妥珠单抗或经≥2行化疗预处理的患者除外。 ER,孕激素受体(PgR),Ki67和AR表达通过免疫组织化学评估,而HER2主要通过荧光原位杂交进行评估。使用1%和10%免疫染色细胞的临界值对AR表达进行分类。在102例可评估患者中,对70例原发肿瘤和49例转移瘤中的生物标志物进行了评估,其中17例均具有上述两项测定。 AR状态下,原发肿瘤与转移之间的总体一致性率为64.7%(95%CI 42%-87.4%)。 AR状态对TTP的影响不明显,而PgR和Ki67状态对TTP的影响却很大。 AR / PgR≥0.96与TTP明显缩短有关(HR≤1.65,95%CI 1.05-2.61,p≤0.028)。原发性肿瘤或转移的AR状态与最佳反应与进展性疾病(PD)无关。相反,Ki67≥≥20%,PgR <≥10%显示与PD的统计学显着相关性是最佳反应。在晚期BC中,AR表达似乎无法预测ET的疗效,而Ki67和PgR对其效果产生更大的影响。

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