Reclassification of early stage breast cancer into treatment groups by combining the use of immunohistochemistry and microarray analysis

dc.contributor.authorGrant, Kathleen A.en_ZA
dc.contributor.authorMyburgh, Ettienne J.en_ZA
dc.contributor.authorMurray, Elizabethen_ZA
dc.contributor.authorPienaar, Fredrieka M.en_ZA
dc.contributor.authorKidd, Martinen_ZA
dc.contributor.authorWright, Colleen A.en_ZA
dc.contributor.authorKotze, Maritha J.en_ZA
dc.date.accessioned2021-03-10T08:29:05Z
dc.date.available2021-03-10T08:29:05Z
dc.date.issued2019
dc.descriptionCITATION: Grant, K. A., et al. 2019. Reclassification of early stage breast cancer into treatment groups by combining the use of immunohistochemistry and microarray analysis. South African Journal of Science, 115(3/4), Art. #5461, doi:10.17159/sajs.2019/5461.
dc.descriptionThe original publication is available at http://sajs.co.za
dc.description.abstractENGLISH ABSTRACT: Immunohistochemistry (IHC) is routinely used to approximate breast cancer intrinsic subtypes, which were initially discovered by microarray analysis. However, IHC assessment of oestrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor receptor-2 (HER2) status, is a poor surrogate of molecular subtype. Therefore, MammaPrint/BluePrint (MP/BP) microarray gene expression profiling is increasingly used to stratify breast cancer patients into different treatment groups. In this study, ER/PR status, as reported by standard IHC and single-gene mRNA analysis using TargetPrint, was compared with molecular subtyping to evaluate the combined use of MP/BP in South African breast cancer patients. Pathological information of 74 ER/PR positive, HER2 negative tumours from 73 patients who underwent microarray testing, were extracted from a central breast cancer genomics database. The IHC level was standardised by multiplying the intensity score (0–3) by the reported proportion of positively stained nuclei, giving a score of 0–300. Comparison between mRNA levels and IHC determination of ER/PR status demonstrated a significant correlation (p<0.001) for both receptors (ER: 0.34 and PR: 0.54). Concordance was shown in 61 (82%) cases and discordance in 13 (18%) of the 74 tumours tested. Further stratification by MP/BP identified 49 (66.2%) Luminal A, 21 (28.4%) Luminal B and 4 (5.4%) Basal-like tumours. Neither IHC nor TargetPrint could substitute BP subtyping, which measures the functional integrity of ER and can identify patients with false-positive tumours who are resistant to hormone therapy. These findings support the implementation of a pathology-supported genetic testing approach combining IHC and microarray gene profiling for definitive prognostic and predictive treatment decision-making in patients with early stage breast cancer.en_ZA
dc.description.urihttps://www.sajs.co.za/article/view/5461
dc.description.versionPublishers version
dc.format.extent6 pagesen_ZA
dc.identifier.citationGrant, K. A., et al. 2019. Reclassification of early stage breast cancer into treatment groups by combining the use of immunohistochemistry and microarray analysis. South African Journal of Science, 115(3/4), Art. #5461, doi:10.17159/sajs.2019/5461
dc.identifier.issn1996-7489 (online)
dc.identifier.issn0038-2353 (print)
dc.identifier.otherdoi:10.17159/sajs.2019/5461
dc.identifier.urihttp://hdl.handle.net/10019.1/109634
dc.language.isoen_ZAen_ZA
dc.publisherAcademy of Science of South Africaen_ZA
dc.rights.holderAuthors retain copyrighten_ZA
dc.subjectOestrogen receptoren_ZA
dc.subjectBreast -- Canceren_ZA
dc.subjectMicroarrays, DNAen_ZA
dc.subjectImmunohistochemistryen_ZA
dc.titleReclassification of early stage breast cancer into treatment groups by combining the use of immunohistochemistry and microarray analysisen_ZA
dc.typeArticleen_ZA
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