曲妥珠单抗德鲁司康治疗 HER2 低乳腺癌脑转移瘤的疗效:病例报告。

Zeni Kharel, Sarah Stanford, Lauryn E Hemminger, Tyler Schmidt, Sara J Hardy, Jason Zittel, Nimish A Mohile, Ajay Dhakal
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引用次数: 0

摘要

我们报告了曲妥珠单抗德鲁司康(T-DXd)在治疗人类表皮生长因子受体 2 (HER2) 低、ID 型左侧乳腺癌 (LMD) (脑脊液 [CSF] 细胞学阳性,脑积水是唯一的异常影像学发现)方面的疗效,以及一种名为 CNSide™ 的新型微流控平台在诊断和监测方面的应用。乳腺癌 LMD 与预后不良有关,目前缺乏有效的治疗方法。我们的病例突出了与乳腺癌 LMD 治疗和监测相关的两个关键方面。首先,根据脑脊液恶性细胞的免疫细胞化学(IHC)数据选择了 T-DXd,随访显示 T-DXd 对治疗 HER2 低的 LMD 有效。虽然 T-DXd 在治疗转移性 HER2 低乳腺癌方面的疗效已经得到证实,但据我们所知,我们的病例是首次证明 T-DXd 在治疗 HER2 低乳腺癌 LMD 方面的疗效。其次,由于这是 1D 型 LMD,中枢神经系统(CNS)和中枢神经系统外都没有明确的可测量放射性疾病,因此我们采用了一种新型微流控 CSF 检测方法来监测疾病反应。在我们的病例中,这种新型检测方法的效果优于标准 CSF 细胞学检测。目前急需开发 CSF 肿瘤细胞评估工具,以超越传统 CSF 细胞学的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of trastuzumab deruxtecan in treating HER2-low breast cancer leptomeningeal metastasis: a case report.

accepted at SABCS 2023, poster presented at SABCS 2023We report the efficacy of trastuzumab deruxtecan (T-DXd) in treating human epidermal growth factor receptor 2 (HER2) low, type ID leptomeningeal breast cancer (LMD) (with positive cerebrospinal fluid [CSF] cytology and hydrocephalus as the only abnormal imaging finding) and the diagnostic and monitoring utilization of a novel microfluidic platform called CNSide™. Breast cancer LMD is associated with poor prognosis, and effective treatments are lacking. Our case highlights two crucial aspects related to the treatment and monitoring of breast cancer LMD. First, T-DXd was chosen based on immunocytochemistry (IHC) data from CSF malignant cells and follow-up revealed effectiveness of T-DXd in treating HER2-low LMD. While the efficacy of T-DXd has been established in treating metastatic HER2-low breast cancer, our case represents, to our knowledge, the first demonstration of T-DXd's effectiveness in HER2-low breast cancer LMD. Second, since this is type 1D LMD with absence of unequivocal measurable radiological disease in both the central nervous system (CNS) and extra-CNS, we employed a novel microfluidic CSF assay to monitor disease response. This novel assay outperformed standard CSF cytology in our case. There is an urgent need to develop CSF tumor cell assessment tool that surpasses the capabilities of conventional CSF cytology.

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