Department of Biology, Centre Eugène Marquis, Unicancer, Rennes, France.
Department of Medical Oncology, Centre Eugène Marquis, Unicancer, Rennes, France.
Mol Oncol. 2024 Nov;18(11):2714-2729. doi: 10.1002/1878-0261.13592. Epub 2024 Jan 29.
Erb-b2 receptor tyrosine kinase 2 (ERBB2)-activating mutations are therapeutically actionable alterations found in various cancers, including metastatic breast cancer (MBC). We developed multiplex digital PCR assays to detect and quantify ERBB2 mutations in circulating tumor DNA from liquid biopsies. We studied the plasma from 272 patients with hormone-receptor-positive, human epidermal growth factor receptor 2-negative (HR+/HER2-) MBC to detect 17 ERBB2 mutations using a screening assay. The assay was developed on the three-color Crystal dPCR™ naica® platform with a two-step strategy for precise mutation identification. We found that nine patients (3.3%) harbored at least one ERBB2 mutation. The mutation rate was higher in patients with lobular histology (5.9%) compared to invasive breast carcinoma of no special type (2.6%). A total of 12 mutations were found with the following frequencies: L755S (25.00%), V777L (25.00%), S310Y (16.67%), L869R (16.67%), S310F (8.33%), and D769H (8.33%). Matched tumor samples from six patients identified the same mutations with an 83% concordance rate. In summary, our highly sensitive multiplex digital PCR assays are well suited for plasma-based monitoring of ERBB2 mutational status in patients with MBC.
表皮生长因子受体 2 酪氨酸激酶 2(ERBB2)激活突变是存在于多种癌症中的治疗靶点改变,包括转移性乳腺癌(MBC)。我们开发了多重数字 PCR 检测方法,以检测和定量液体活检中循环肿瘤 DNA 中的 ERBB2 突变。我们对 272 例激素受体阳性、人表皮生长因子受体 2 阴性(HR+/HER2-)MBC 患者的血浆进行了研究,使用一种筛选检测方法检测了 17 种 ERBB2 突变。该检测方法是在三通道 Crystal dPCR™ naica®平台上开发的,采用两步策略进行精确的突变鉴定。我们发现 9 名患者(3.3%)至少携带一种 ERBB2 突变。具有小叶状组织学特征的患者(5.9%)的突变率高于非特殊类型浸润性乳腺癌(2.6%)。总共发现了 12 种突变,其频率如下:L755S(25.00%)、V777L(25.00%)、S310Y(16.67%)、L869R(16.67%)、S310F(8.33%)和 D769H(8.33%)。对 6 名患者的匹配肿瘤样本进行了鉴定,相同突变的一致性为 83%。总之,我们的高灵敏度多重数字 PCR 检测方法非常适合用于监测 MBC 患者血浆中 ERBB2 突变状态。