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在循环肿瘤 DNA 中检测到不常见的种系 BRCA 突变的治疗耐药性转移性乳腺癌中奥拉帕利的疗效。

Efficacy of Olaparib in Treatment-Refractory, Metastatic Breast Cancer with Uncommon Somatic BRCA Mutations Detected in Circulating Tumor DNA.

机构信息

Division of Pulmonary, and Critical Care Medicine, Department of Medicine, Stanford University, Stanford, CA, USA.

Department of Chemistry, Yonsei University, Seoul, Korea.

出版信息

Cancer Res Treat. 2023 Jul;55(3):1048-1052. doi: 10.4143/crt.2022.1529. Epub 2023 Jan 31.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b84/10372606/3c0e8534e079/crt-2022-1529f1.jpg

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