Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy.
Unit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.
Oncologist. 2020 Oct;25(10):886-893. doi: 10.1634/theoncologist.2019-0922. Epub 2020 May 11.
HER2 overexpression has been investigated as a potential biomarker and therapeutic target in biliary tract cancer (BTC), but a prognostic role of such alteration has not been demonstrated yet.
We retrospectively evaluated HER2 protein expression by immunohistochemistry (IHC) in 100 patients with radically resected BTC. HER2 gene amplification was assessed by fluorescence in situ hybridization (FISH) in 2+ and 3+ cases at IHC. High HER2 protein expression was defined as either IHC 3+ or 2+ associated with FISH positivity. The primary objective of the study was to evaluate the prognostic role of HER2 overexpression in terms of disease-free survival (DFS) and overall survival (OS). Secondary endpoints were the prevalence of HER2 overexpression and the possible correlation with other clinicopathological features.
HER2 overexpression was identified in 11 patients and was not related to other clinicopathological factors. DFS was significantly shorter in HER2-positive compared with HER2-negative patients (10.6 vs. 20.9 months, log-rank p = .017). HER2 confirmed its prognostic value for DFS at multivariate analysis (hazard ratio 2.512; 95% confidence interval, 1.232-5.125; p = .011) together with nodal stage (p < .001), resection margin (p = .027), and tumor site (p = .030). There was no difference in OS between HER2-positive and -negative patients (p = .068).
HER2 overexpression represents an independent prognostic factor for disease recurrence in patients with BTC treated with potentially curative surgery.
HER2 overexpression may play an independent role in promoting an aggressive behavior in resectable biliary tract cancer. This evidence could be helpful in improving prognostic stratification after resection and, primarily, should endorse the rationale to investigate HER2 as a therapeutic target in biliary tract cancer.
HER2 过表达已被研究作为胆管癌(BTC)的潜在生物标志物和治疗靶点,但这种改变的预后作用尚未得到证实。
我们回顾性地评估了 100 例根治性切除的 BTC 患者的 HER2 蛋白表达情况,采用免疫组织化学(IHC)检测。在 IHC 为 2+和 3+的病例中,采用荧光原位杂交(FISH)检测 HER2 基因扩增。高 HER2 蛋白表达定义为 IHC 3+或 2+伴 FISH 阳性。该研究的主要目的是评估 HER2 过表达在无病生存(DFS)和总生存(OS)方面的预后作用。次要终点是 HER2 过表达的发生率以及与其他临床病理特征的可能相关性。
在 11 例患者中发现了 HER2 过表达,但与其他临床病理因素无关。与 HER2 阴性患者相比,HER2 阳性患者的 DFS 明显缩短(10.6 与 20.9 个月,对数秩检验 p=0.017)。在多变量分析中,HER2 证实了其对 DFS 的预后价值(风险比 2.512;95%置信区间,1.232-5.125;p=0.011),与淋巴结分期(p<0.001)、切缘(p=0.027)和肿瘤部位(p=0.030)有关。HER2 阳性与阴性患者的 OS 无差异(p=0.068)。
HER2 过表达是接受潜在根治性手术治疗的 BTC 患者疾病复发的独立预后因素。
HER2 过表达可能在促进可切除胆管癌的侵袭性行为中发挥独立作用。这一证据可能有助于改善术后的预后分层,并且主要应该支持将 HER2 作为胆管癌治疗靶点的合理性。