Division of Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Institute of Human Genetics, Diagnostic and Research Center for Molecular Biomedicine (Austria), Medical University of Graz, Graz, Austria.
Br J Cancer. 2022 Feb;126(3):456-463. doi: 10.1038/s41416-021-01601-9. Epub 2021 Nov 9.
The benefit of alpelisib in hormone-receptor-positive (HR+) metastatic breast cancer patients provided clinical evidence for the increasing importance of PIK3CA testing. We performed a comparison of liquid biopsy and tissue-based detection of PIK3CA mutations.
PIK3CA hotspot mutation analysis using a high-resolution SiMSen-Seq assay was performed in plasma from 93/99 eligible patients with HR+/HER2- breast cancer. Additionally, mFAST-SeqS was used to estimate the tumour fractions in plasma samples. In 72/93 patients, matched tissue was available and analysed using a customised Ion Torrent panel.
PIK3CA mutations were detected in 48.6% of tissue samples and 47.3% of plasma samples, with identical PIK3CA mutation detected in 24/72 (33.3%) patients both in tissue and plasma. In 10 (13.9%) patients, mutations were only found in plasma, and in 6 (8.3%) patients, PIK3CA mutations found in tissue were not detectable in ctDNA. In 49/93 plasma samples without detectable PIK3CA mutations, 22 (44.9%) samples had elevated tumour fractions, implying true negative results.
SiMSen-Seq-based detection of PIK3CA mutations in plasma shows advantageous concordance with the tissue analyses. A combination with an untargeted approach for detecting ctDNA fractions may confirm a negative PIK3CA result and enhance the performance of the SiMSen-Seq test.
在激素受体阳性(HR+)转移性乳腺癌患者中,阿培利司的获益为越来越重视 PIK3CA 检测提供了临床证据。我们对液体活检和基于组织的 PIK3CA 突变检测进行了比较。
使用高分辨率 SiMSen-Seq 测定法对 99 例符合条件的 HR+/HER2-乳腺癌患者的血浆进行 PIK3CA 热点突变分析。此外,还使用 mFAST-SeqS 估计血浆样本中的肿瘤分数。在 72/93 例患者中,有匹配的组织可用,并使用定制的 Ion Torrent 面板进行分析。
组织样本中检测到 48.6%的 PIK3CA 突变,血浆样本中检测到 47.3%,24/72(33.3%)例患者的组织和血浆中均检测到相同的 PIK3CA 突变。在 10 例(13.9%)患者中,仅在血浆中发现突变,在 6 例(8.3%)患者中,在组织中发现的 PIK3CA 突变在 ctDNA 中无法检测到。在 49/93 例未检测到 PIK3CA 突变的血浆样本中,有 22 例(44.9%)样本的肿瘤分数升高,提示为真正的阴性结果。
基于 SiMSen-Seq 的血浆 PIK3CA 突变检测与组织分析具有有利的一致性。与检测 ctDNA 分数的非靶向方法相结合,可能会确认 PIK3CA 结果为阴性,并提高 SiMSen-Seq 检测的性能。