von Kroge Patricia, Riecke Kerstin, Kornowski Johann, Schmalfeldt Barbara, Müller Volkmar, Laakmann Elena
Department of Gynaecology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Breast Care (Basel). 2025 Apr 14:1-10. doi: 10.1159/000545549.
The development of brain metastases (BM) is an increasing concern for patients with metastatic triple-negative breast cancer (mTNBC). This systematic review aimed to summarize the current evidence regarding systemic treatment options for patients with mTNBC and BM.
A systematic literature review was conducted by searching the database PubMed with the keywords metastatic triple-negative breast cancer," "therapy" and "brain metastases." Articles were screened and included if they focused on the treatment of mTNBC. Both prospective and retrospective clinical trials were eligible for inclusion.
The literature search identified 3,413 articles, of which eight met the inclusion criteria. These studies provided evidence for the treatment of patients with stable BM using sacituzumab govitecan, pembrolizumab combined with chemotherapy, trastuzumab deruxtecan (T-DXd), nab-paclitaxel combined with cisplatin, and talazoparib. No evidence was found for active BM or leptomeningeal metastases.
Based on the current evidence discussed in this review, testing for programmed death-ligand 1 (PD-L1), HER2, including immunohistochemistry (IHC) status as well as germline BRCA 1/2 mutation, should be considered in all mTNBC patients with BM as the results have significant treatment implications. Moreover, PD-L1 expression should be evaluated on primary tumor and (if tissue sample available) reevaluated on BMs if negative on primary BC, to maximize the opportunity for treatment with immune checkpoint inhibitors. Furthermore, if brain tissue is available, HER2 IHC should also be tested in order to evaluate the status switch and to assess the therapeutic effectiveness of treatment with T-DXd. Further targeted agents are urgently needed in order to improve the survival of patients with TNBC and BM.
脑转移(BM)的发生日益成为转移性三阴性乳腺癌(mTNBC)患者关注的问题。本系统评价旨在总结有关mTNBC和BM患者全身治疗选择的现有证据。
通过在PubMed数据库中搜索关键词“转移性三阴性乳腺癌”、“治疗”和“脑转移”进行系统文献回顾。如果文章聚焦于mTNBC的治疗,则进行筛选并纳入。前瞻性和回顾性临床试验均符合纳入标准。
文献检索共识别出3413篇文章,其中8篇符合纳入标准。这些研究为使用戈沙妥珠单抗、帕博利珠单抗联合化疗、曲妥珠单抗德曲妥珠单抗(T-DXd)、白蛋白结合型紫杉醇联合顺铂以及他拉唑帕尼治疗稳定期BM患者提供了证据。未发现针对活动性BM或软脑膜转移的证据。
基于本综述中讨论的现有证据,所有mTNBC和BM患者均应考虑检测程序性死亡配体1(PD-L1)、HER2,包括免疫组化(IHC)状态以及胚系BRCA 1/2突变,因为结果具有重要的治疗意义。此外,应在原发性肿瘤上评估PD-L1表达,并且(如果有组织样本)如果原发性乳腺癌检测为阴性,则应在脑转移瘤上重新评估,以最大程度增加免疫检查点抑制剂治疗的机会。此外,如果有脑组织,还应检测HER2 IHC,以评估状态转换并评估T-DXd治疗的疗效。迫切需要进一步的靶向药物以提高TNBC和BM患者的生存率。