» Articles » PMID: 32622530

Receptor Discordance and Phenotype Change in Metastatic Breast Cancer

Overview
Journal Asian J Surg
Publisher Elsevier
Specialty General Surgery
Date 2020 Jul 6
PMID 32622530
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Background: changes may occur in tumor phenotype and receptor status during the progression of breast cancer. Discordance between primary and metastases has implications for further treatment and prognosis.

Methods: 185 patients confirmed breast cancer metastasis were retrospectively analyzed during 1999-2019. All the pathological assessments of receptors and phenotypes of both primaries and metastases were recorded.

Results: rates of receptor discordance were 18.65%, 30.57%, and 16.06% for ER, PR, and HER2, respectively and 31.62% for phenotype change. Patients with ER discordance experienced a worse OS and PMS, and those with ER loss had worse PMS compared with ER positive concordance. Patients with PR discordance experienced poorer OS and loss of PR positivity also had decreased OS and PMS when comparing with PR positive concordance. There was also significantly poorer PMS of hormon receptor (HR) discordance than HR positive concordance. In phenotype change, the luminal A type concordance group showed better PMS result.

Conclusions: this study demonstrated that discordance in subtype and receptor status between primary and metastatic lesions ultimately affects the survival and has a potential impact on treatment options.

Citing Articles

NUPR1 contributes to endocrine therapy resistance by modulating BIRC5 expression and inducing luminal B-ERBB2 subtype-like characteristics in estrogen receptor-positive breast cancer cells.

Lee C, Lin Y, Chang Y, Chen P, Lin K, Yeh T J Cancer. 2025; 16(5):1694-1708.

PMID: 39991577 PMC: 11843241. DOI: 10.7150/jca.105425.


Breast biomarkers evolution between primary and distant metastasis: incidence and significance.

Khedr M, Gandhi S, Roy A, Alharbi M, George A, Attwood K Histopathology. 2024; 86(5):793-804.

PMID: 39687980 PMC: 11903192. DOI: 10.1111/his.15387.


Study of Biomarker Discordance between Primary and Recurrent Sites and its Clinical Implications in Metastatic Breast Cancer : A Single Institutional Study from India.

Shanthala S, Amirtham U, Gopal C, N S, Jacob L, Babu G South Asian J Cancer. 2024; 13(2):90-98.

PMID: 38919661 PMC: 11196144. DOI: 10.1055/s-0043-1775807.


Retrospective analysis of estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor-2 (HER2), Ki67 changes and their clinical significance between primary breast cancer and metastatic tumors.

Qi G, Zhang X, Gai X, Yan X PeerJ. 2024; 12:e17377.

PMID: 38766488 PMC: 11102064. DOI: 10.7717/peerj.17377.


Dynamic whole-body [F]FES PET/CT increases lesion visibility in patients with metastatic breast cancer.

Pedersen M, Munk O, Dias A, Steffensen J, Moller A, Johnsson A EJNMMI Res. 2024; 14(1):24.

PMID: 38436824 PMC: 10912074. DOI: 10.1186/s13550-024-01080-y.