Di Palma Silvana, Koliou Panagiotis, Simonovic Alex, Costa Daniela, Faulkes Catherine, Kobutungi Brenda, Paterson Felicity, Horsnell Jonathan David, Pakzad Farrokh, Irvine Tracey, Partlett Polly, Clayton Elizabeth, Collins Nadine
Department of Cellular Pathology, Berkshire & Surrey Pathology Services, The Royal Surrey Hospital NHS Foundation Trust, University of Surrey, Egerton Road, Guildford GU2 7XX, UK.
Department of Oncology, The Royal Surrey Hospital NHS Foundation Trust, Egerton Road, Guildford GU2 7XX, UK.
Int J Mol Sci. 2024 Feb 23;25(5):2616. doi: 10.3390/ijms25052616.
The APIS Breast Cancer Subtyping Kit is an mRNA-based assessment of the seven parameters including three biomarkers routinely assessed in all the newly diagnosed breast cancers (BC), oestrogen receptor (ER), progesterone receptor (PR) and HER-2 and an additional four genes that create a novel proliferation signature, MKI67, PCNA, CCNA2 and KIF23. Taken together, the data are used to produce a molecular subtype for every sample. The kit was evaluated against the current standard protocol of immunohistochemistry (IHC) and/or in situ hybridisation (ISH) in breast cancer patients. The data were presented at the weekly breast multidisciplinary team (MDT) meeting. A total of 98 consecutive cases of pre-operative breast cancer core biopsies and two core biopsies of nodal metastases yielding 100 cases were assessed. IHC and APIS results were available for 100 and 99 cases. ER was concordant in 97% cases, PR was concordant in 89% and HER-2 results were concordant with IHC/ISH in 100% of the cases. Ki-67 IHC was discordant in 3% of cases when compared with MK167 alone but discordant in 24% when compared with the four-gene proliferation signature. In conclusion, our study indicates that the APIS Breast Cancer Subtyping Kit is highly concordant when compared to the results produced for ER/PR/HER-2 by IHC and/or ISH. The assay could play a role in the routine assessment of newly diagnosed breast cancer (BC) specimens.
APIS乳腺癌亚型分型试剂盒是一种基于mRNA的检测方法,可评估七个参数,包括在所有新诊断乳腺癌(BC)中常规检测的三个生物标志物,即雌激素受体(ER)、孕激素受体(PR)和HER-2,以及另外四个可产生新的增殖特征的基因,即MKI67、PCNA、CCNA2和KIF23。综合这些数据可用于为每个样本生成分子亚型。该试剂盒在乳腺癌患者中与当前的免疫组织化学(IHC)和/或原位杂交(ISH)标准方案进行了评估。数据在每周的乳腺多学科团队(MDT)会议上进行了汇报。共评估了98例连续的术前乳腺癌核心活检病例以及2例淋巴结转移的核心活检病例,共100例。100例和99例分别有IHC和APIS结果。ER在97%的病例中结果一致,PR在89%的病例中一致,HER-2结果与IHC/ISH在100%的病例中一致。单独与MK167相比时,Ki-67 IHC在3%的病例中结果不一致,但与四基因增殖特征相比时,在24%的病例中结果不一致。总之,我们的研究表明,与IHC和/或ISH检测ER/PR/HER-2的结果相比,APIS乳腺癌亚型分型试剂盒具有高度一致性。该检测方法可在新诊断乳腺癌(BC)标本的常规评估中发挥作用。