Division of Pulmonary, and Critical Care Medicine, Department of Medicine, Stanford University, Stanford, CA, USA.
Department of Chemistry, Yonsei University, Seoul, Korea.
Cancer Res Treat. 2023 Jul;55(3):1048-1052. doi: 10.4143/crt.2022.1529. Epub 2023 Jan 31.
Poly(ADP-ribose) polymerase inhibitors have been shown dramatic responses in patients with BRCAness. However, clinical studies have been limited to breast cancer patients with germline mutations. Here, we describe a patient with metastatic breast cancer who had a rare BRCA1 somatic mutation (BRCA1 c.4336G>T (p.E1446*)) detected by cell-free DNA analysis after failing standard therapies. This tier III variant of unknown significance was predicted to be a pathogenic variant in our assessment, leading us to consider off-label treatment with olaparib. The patient responded well to olaparib for several months, with a decrease in allele frequency of this BRCA1 somatic mutation in cell-free DNA. Olaparib resistance subsequently developed with an increase in the allele frequency and new BRCA1 reversion mutations. To our knowledge, this is the first report confirming BRCA1 c.4336G>T (p.E1446*) as a mutation sensitive to olaparib in breast cancer and describing the dynamic changes in the associated mutations using liquid biopsy.
聚(ADP-核糖)聚合酶抑制剂在具有 BRCAness 的患者中显示出显著的反应。然而,临床研究仅限于携带种系突变的乳腺癌患者。在这里,我们描述了一名转移性乳腺癌患者,该患者在标准治疗失败后通过游离 DNA 分析检测到罕见的 BRCA1 体细胞突变(BRCA1 c.4336G>T (p.E1446*))。在我们的评估中,这种三级意义不明的变体被预测为致病性变体,这促使我们考虑使用奥拉帕利进行非适应证治疗。该患者对奥拉帕利治疗反应良好,几个月后,游离 DNA 中该 BRCA1 体细胞突变的等位基因频率下降。随后奥拉帕利耐药出现,等位基因频率增加,新出现 BRCA1 回复突变。据我们所知,这是首例报道证实 BRCA1 c.4336G>T (p.E1446*) 是乳腺癌中对奥拉帕利敏感的突变,并描述了使用液体活检的相关突变的动态变化。