File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1111/his.14767
- Scopus: eid_2-s2.0-85137182645
- PMID: 35945680
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Marker assessments in ER-positive breast cancers: old markers, new applications?
Title | Marker assessments in ER-positive breast cancers: old markers, new applications? |
---|---|
Authors | |
Keywords | breast cancer immunohistochemistry oestrogen receptor targeted therapy |
Issue Date | 2023 |
Citation | Histopathology, 2023, v. 82, n. 2, p. 218-231 How to Cite? |
Abstract | Evaluation of oestrogen receptor (ER) expression by immunostaining is essential in the pathological assessment of breast cancer. Its expression is intercorrelated with clinicopathological features, molecular typing, and treatment selection. The development of novel therapeutic agents related to ER status, the recent ASCO introduction of an ER-low positive category of breast cancers, and the ever-increasing plethora of diagnostic and theragnostic markers call for a timely update. In this article we aim to review the clinicopathological features of ER-positive breast cancers, with an emphasis on ER-low positive breast cancers, and a focus on updating the (i) assessment, reporting and interpretation of ER immunohistochemical (IHC) staining, (ii) correlations of ER status with other diagnostic and theragnostic markers, and (iii) implications for treatment selection and response. In the face of the developments in IHC and molecular techniques and targeted therapy, ER immunostaining is still expected to remain as the core component of prognostic and theragnostic assessment of breast cancers. |
Persistent Identifier | http://hdl.handle.net/10722/343391 |
ISSN | 2023 Impact Factor: 3.9 2023 SCImago Journal Rankings: 1.392 |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Li, Joshua J.X. | - |
dc.contributor.author | Tse, Gary M. | - |
dc.date.accessioned | 2024-05-10T09:07:43Z | - |
dc.date.available | 2024-05-10T09:07:43Z | - |
dc.date.issued | 2023 | - |
dc.identifier.citation | Histopathology, 2023, v. 82, n. 2, p. 218-231 | - |
dc.identifier.issn | 0309-0167 | - |
dc.identifier.uri | http://hdl.handle.net/10722/343391 | - |
dc.description.abstract | Evaluation of oestrogen receptor (ER) expression by immunostaining is essential in the pathological assessment of breast cancer. Its expression is intercorrelated with clinicopathological features, molecular typing, and treatment selection. The development of novel therapeutic agents related to ER status, the recent ASCO introduction of an ER-low positive category of breast cancers, and the ever-increasing plethora of diagnostic and theragnostic markers call for a timely update. In this article we aim to review the clinicopathological features of ER-positive breast cancers, with an emphasis on ER-low positive breast cancers, and a focus on updating the (i) assessment, reporting and interpretation of ER immunohistochemical (IHC) staining, (ii) correlations of ER status with other diagnostic and theragnostic markers, and (iii) implications for treatment selection and response. In the face of the developments in IHC and molecular techniques and targeted therapy, ER immunostaining is still expected to remain as the core component of prognostic and theragnostic assessment of breast cancers. | - |
dc.language | eng | - |
dc.relation.ispartof | Histopathology | - |
dc.subject | breast cancer | - |
dc.subject | immunohistochemistry | - |
dc.subject | oestrogen receptor | - |
dc.subject | targeted therapy | - |
dc.title | Marker assessments in ER-positive breast cancers: old markers, new applications? | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1111/his.14767 | - |
dc.identifier.pmid | 35945680 | - |
dc.identifier.scopus | eid_2-s2.0-85137182645 | - |
dc.identifier.volume | 82 | - |
dc.identifier.issue | 2 | - |
dc.identifier.spage | 218 | - |
dc.identifier.epage | 231 | - |
dc.identifier.eissn | 1365-2559 | - |