Background: In nongastric gastrointestinal (GI) cancers, HER2-positive (HER2+) disease is not common. In breast cancer, HER2 status is associated with increased risk of brain metastases and response to HER2-targeted therapy. The purpose of this project was to compare HER2 status in GI cancer brain metastases versus matched prior sites of disease in order to determine if HER2+ disease is more common intracranially.
Materials and methods: We identified 28 patients with GI cancer who had craniotomy for brain metastases between 1999 and 2017 with intracranial metastatic tissue available at Massachusetts General Hospital. Twenty-four patients also had tissue from a prior site of disease. Fluorescence in situ hybridization (FISH) and immunohistochemistry (IHC) for HER2 were performed on all samples. A tumor was defined as HER2+ if it had 3+ staining by IHC or amplification by FISH.
Results: A prior site of disease (including intracranial metastases) was HER2+ for 13% of evaluable patients: 3 of 11 patients with colorectal cancer and no patients with esophageal or pancreatic cancer. The most recent brain metastases were HER2+ for 32% of patients: 2 of 3 esophageal squamous cell carcinomas, 3 of 10 esophageal adenocarcinomas (ACs), 3 of 14 colorectal ACs, and 1 of 1 pancreatic AC. Only 37.5% of patients with HER2+ brain metastasis had concordant HER2+ prior tissue (κ = 0.38, p = .017).
Conclusion: In this cohort of patients with GI cancer with brain metastases, HER2+ status was more common intracranially compared with prior sites of disease. These findings suggest that testing HER2 in patients with GI cancer with brain metastases may lead to additional therapeutic options, regardless of HER2 status in previously examined tissue.
Implications for practice: HER2 amplification is a well-known driver of oncogenesis in breast cancer, with associated increased risk of brain metastases and response to HER2-directed therapy. In nongastric gastrointestinal (GI) cancers, HER2 amplification is not common and consequently is infrequently tested. The current study shows that brain metastases in patients with GI primary malignancies have a relatively high likelihood of being HER2 positive despite HER2 amplification or overexpression being less commonly found in matched tissue from prior sites of disease. This suggests that regardless of prior molecular testing, patients with GI cancer with brain metastases who have tissue available are likely to benefit from HER2 assessment to identify potential novel therapeutic options.
背景。在非胃肠 (GI) 癌症中,HER2 阳性 (HER2+) 疾病并不常见。在乳腺癌中,HER2 状态与脑转移风险增加和 HER2 靶向治疗反应相关。该项目的目的是将胃肠癌脑转移中的 HER2 状态与相匹配的先前疾病部位进行比较,以确定 HER2+ 疾病是否更常见于颅内。
材料和方法。我们确定了 28 名患有胃肠癌的患者,这些患者于 1999 年至 2017 年间进行了脑转移开颅术,颅内转移组织存放于马萨诸塞州综合医院。有二十四名患者之前患病部位的组织也可获得。我们对所有样本进行了针对 HER2 的荧光原位杂交 (FISH) 和免疫组织化学 (IHC) 检测。如果肿瘤通过 IHC 出现 3+ 染色或通过 FISH 扩增,则将肿瘤定义为 HER2+。
结果。对于 13% 的可评估患者,先前的疾病部位(包括颅内转移)为 HER2+:11 例患者中有 3 例患有结肠直肠癌,且没有患有食管癌或胰腺癌的患者。对于 32% 的患者,最近的脑转移是 HER2+:3 例食管鳞状细胞癌病例中有 2 位患者,10 例食管腺癌 (AC) 病例中有 3 位患者,14 例结直肠腺癌病例中有 3 位患者,以及 1 例胰腺癌中的 1 位患者。只有 37.5% 的 HER2+ 脑转移患者具有与先前组织一致的 HER2+ (κ = 0.38, p = 0.017)。
结论。在这组患有脑转移的胃肠癌患者中,与先前的疾病部位相比,HER2+ 状态在颅内更常见。这些研究结果表明,对患有脑转移的胃肠癌患者进行 HER2 检测可能会产生其他治疗选择,无论先前检查的组织中 HER2 状态如何。
对实践的启示:HER2 扩增是众所周知的乳腺癌中癌发生的驱动因素,与脑转移的风险增加和对 HER2 定向治疗的反应有关。在非胃肠 (GI) 癌症中,HER2 扩增并不常见,因此很少进行检测。目前的研究表明,胃肠原发性恶性肿瘤患者的脑转移具有相对较高的 HER2 阳性可能性,尽管 HER2 扩增或过表达在先前疾病部位的匹配组织中较少见。这表明,无论先前的分子检测如何,具有可用组织的患有脑转移的胃肠癌患者可能受益于 HER2 评估,以确定潜在的新治疗选择。
Keywords: Biomarker; Brain metastases; Gastrointestinal cancer; HER2.
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