Vendrell Julie A, Solassol Jérôme, Győrffy Balázs, Vilquin Paul, Jarlier Marta, Donini Caterina F, Gamba Laurent, Maudelonde Thierry, Rouanet Philippe, Cohen Pascale A
Univ Lyon, Université Claude Bernard Lyon 1, INSERM U1052, CNRS 5286, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Département de Pathologie et Oncobiologie, Laboratoire de Biologie des Tumeurs Solides, CHU Montpellier, University of Montpellier, Montpellier, France.
Front Pharmacol. 2019 Jan 25;9:1581. doi: 10.3389/fphar.2018.01581. eCollection 2018.
is a candidate oncogene with a wide variety of deleterious functions in breast cancer. Here, we aimed at investigating in a pilot prospective study the association between mRNA expression levels and the clinical response to neoadjuvant endocrine therapy (ET) in postmenopausal ER-positive (ER+) breast cancer patients. Core surgical biopsy samples before treatment initiation and post-treatment were obtained from 68 patients, and Ki-67 values measured by immunohistochemistry (IHC) were used to identify responders ( = 59) and non-responders ( = 9) after 4 months of ET. We report for the first time that high mRNA expression level measured by RT-qPCR in the initial tumor samples (pre-treatment) is associated with poor response to neoadjuvant ET. Indeed, the clinical positive response rate in patients with low expression levels was significantly higher than that in those with high expression levels ( = 0.027). Additionally, a retrospective analysis evaluating expression levels in primary breast tumor of ER+/HER2-/LN0 breast cancer patients treated with adjuvant ET enabled the identification of poorer responders prone to earlier relapse ( = 0.013), while did not retain any prognostic value in the ER+/HER2-/LN0 breast cancer patients who did not receive any treatment. Altogether, these data suggest that expression might be predictive of clinical response to ET.
是一种在乳腺癌中具有多种有害功能的候选癌基因。在此,我们旨在通过一项前瞻性试点研究,调查绝经后雌激素受体阳性(ER+)乳腺癌患者中mRNA表达水平与新辅助内分泌治疗(ET)临床反应之间的关联。在治疗开始前和治疗后,从68例患者中获取核心手术活检样本,并使用免疫组织化学(IHC)测量的Ki-67值来识别ET治疗4个月后的反应者(n = 59)和无反应者(n = 9)。我们首次报告,通过RT-qPCR在初始肿瘤样本(治疗前)中测量的高mRNA表达水平与新辅助ET反应不佳相关。事实上,低表达水平患者的临床阳性反应率显著高于高表达水平患者(P = 0.027)。此外,一项回顾性分析评估了接受辅助ET治疗的ER+/HER2-/LN0乳腺癌患者原发性乳腺肿瘤中的表达水平,结果发现反应较差且易于早期复发的患者(P = 0.013),而在未接受任何治疗的ER+/HER2-/LN0乳腺癌患者中没有保留任何预后价值。总之,这些数据表明表达可能预测ET的临床反应。