Agrawal Amit, Robertson John F R, Cheung Kwok L, Gutteridge Eleanor, Ellis Ian O, Nicholson Robert I, Gee Julia M W
Division of Breast Surgery, School of Graduate Entry Medicine and Health, Royal Derby Hospital, University of Nottingham, Derby, DE22 3DT, United Kingdom.
Cambridge Breast Unit, Cambridge University Hospitals, Cambridge, CB2 0QQ, United Kingdom.
Int J Cancer. 2016 Jan 1;138(1):146-59. doi: 10.1002/ijc.29682. Epub 2015 Jul 30.
We report the first study of the biological effect of fulvestrant on ER positive clinical breast cancer using sequential biopsies through to progression. Thirty-two locally/systemically advanced breast cancers treated with first-line fulvestrant (250 mg/month) were biopsied at therapy initiation, 6 weeks, 6 months and progression and immunohistochemically-analyzed for Ki67, ER, EGFR and HER2 expression/signaling activity. This series showed good fulvestrant responses (duration of response [DoR] = 25.8 months; clinical benefit = 81%). Ki67 fell (p < 0.001) in 79% of tumours by 6 months and lower Ki67 at all preprogression time-points predicted for longer DoR. ER and PR significantly decreased in all tumours by 6 months (p < 0.001), with some declines in ER (serine 118) phosphorylation and Bcl-2 (p = 0.007). There were modest HER2 increases (p = 0.034, 29% tumours) and loss of any detectable EGFR phosphorylation (p = 0.024, 50% tumours) and MAP kinase (ERK1/2) phosphorylation (p = 0.019, 65% tumours) by 6 months. While ER remained low, there was some recovery of Ki67, Bcl-2 and (weakly) EGFR/MAPK activity in 45-67% patients at progression. Fulvestrant's anti-proliferative impact is related to DoR, but while commonly downregulating ER and indicators of its signaling and depleting EGFR/MAPK signaling in some patients, additional elements must determine response duration. Residual ER at fulvestrant relapse explains reported sensitivity to further endocrine therapies. Occasional modest treatment-induced HER2 and weakly detectable EGFR/HER2/MAPK signaling at relapse suggests targeting of such activity might have value alongside fulvestrant in some patients. However, unknown pathways must drive relapse in most. Ki67 has biomarker potential to predict fulvestrant outcome and as a quantitative measure of response.
我们报告了第一项关于氟维司群对雌激素受体(ER)阳性临床乳腺癌生物学效应的研究,该研究采用连续活检直至疾病进展。对32例接受一线氟维司群(250mg/月)治疗的局部/全身晚期乳腺癌患者在治疗开始时、6周、6个月及疾病进展时进行活检,并对Ki67、ER、表皮生长因子受体(EGFR)和人表皮生长因子受体2(HER2)的表达/信号活性进行免疫组化分析。该系列研究显示氟维司群反应良好(反应持续时间[DoR]=25.8个月;临床获益率=81%)。到6个月时,79%的肿瘤中Ki67下降(p<0.001),在所有疾病进展前时间点Ki67较低预示着更长的DoR。到6个月时,所有肿瘤中的ER和孕激素受体(PR)均显著下降(p<0.001),ER(丝氨酸118)磷酸化和Bcl-2有一些下降(p=0.007)。到6个月时,HER2有适度增加(p=0.034,29%的肿瘤),任何可检测到的EGFR磷酸化丧失(p=0.024,50%的肿瘤)以及丝裂原活化蛋白激酶(ERK1/2)磷酸化丧失(p=0.019,65%的肿瘤)。在疾病进展时,45%-67%的患者中,虽然ER仍较低,但Ki67、Bcl-2和(微弱的)EGFR/丝裂原活化蛋白激酶(MAPK)活性有一些恢复。氟维司群的抗增殖作用与DoR相关,但虽然在一些患者中通常下调ER及其信号传导指标并消耗EGFR/MAPK信号传导,但其他因素必定决定反应持续时间。氟维司群复发时残留的ER解释了报道的对进一步内分泌治疗的敏感性。复发时偶尔出现适度的治疗诱导的HER2以及微弱可检测到的EGFR/HER2/MAPK信号传导表明,在一些患者中,靶向这种活性可能与氟维司群一起具有价值。然而,在大多数情况下,未知途径必定驱动复发。Ki67有作为预测氟维司群治疗结果的生物标志物的潜力,并且作为反应的定量指标。