Hammershøi Madsen Anna Martha, Løvendahl Eefsen Rikke Helene, Nielsen Dorte, Kümler Iben
Department of Oncology 54 B1 Herlev Hospital University of Copenhagen, Herlev Ringvej 75, DK-2730, Copenhagen, Denmark.
Breast J. 2024 Jul 11;2024:9083055. doi: 10.1155/2024/9083055. eCollection 2024.
Triple-negative breast cancer (TNBC) is a subgroup of breast cancer characterized by the absence of estrogen and the human epidermal 2 receptor and also a lack of targeted therapy options. Chemotherapy has so far been the only approved treatment option, and patients with metastatic cancer have a dismal prognosis with a median overall survival (OS) of approximately 14 months. Identification of druggable targets for metastatic TNBC is therefore of special interest.
A systematic search was performed, to review the existing evidence on targeted therapies in metastatic TNBC.
A total of 37 phase 2/3 studies were identified, evaluating 29 different targeted agents. In this review, results on progression free survival (PFS) and OS are presented.
In most of the studies included, no improvement was observed for neither PFS nor OS; however, a few studies did show improvement with targeted agents and have led to new treatment options in subgroups of patients. The antibody drug conjugate, sacituzumab govitecan, demonstrated superior PFS and OS in comparison to chemotherapy. Immunotherapy with checkpoint inhibitors such as atezolizumab and pembrolizumab is now recommended as a first-line treatment option for patients with expression a PD-L1 positive tumor. Finally, the poly adenosine diphosphate-ribose polymerase (PARP) inhibitors talazoparib and olaparib are recommended, as first-line treatment options in patients with metastatic breast cancer and a germline BRCA mutation, but an immune checkpoint inhibitor should be considered for the subset of these patients who are PD-L1 positive.
三阴性乳腺癌(TNBC)是乳腺癌的一个亚组,其特征是缺乏雌激素和人表皮生长因子2受体,并且也缺乏靶向治疗选择。迄今为止,化疗一直是唯一被批准的治疗选择,转移性癌症患者的预后很差,中位总生存期(OS)约为14个月。因此,确定转移性TNBC的可药物靶向具有特殊意义。
进行了系统检索,以综述关于转移性TNBC靶向治疗的现有证据。
共确定了37项2/3期研究,评估了29种不同的靶向药物。在本综述中,展示了无进展生存期(PFS)和总生存期(OS)的结果。
在纳入的大多数研究中,未观察到PFS和OS有改善;然而,一些研究确实显示靶向药物有改善,并为部分患者亚组带来了新的治疗选择。抗体药物偶联物赛托珠单抗戈维汀与化疗相比,显示出更好的PFS和OS。对于肿瘤表达PD-L1阳性的患者,现在推荐使用阿替利珠单抗和帕博利珠单抗等检查点抑制剂进行免疫治疗作为一线治疗选择。最后,聚腺苷二磷酸核糖聚合酶(PARP)抑制剂他拉唑帕尼和奥拉帕尼被推荐作为转移性乳腺癌且有胚系BRCA突变患者的一线治疗选择,但对于这些患者中PD-L1阳性的亚组,应考虑使用免疫检查点抑制剂。