Clinically used breast cancer markers such as estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2 are unstable throughout tumor progression - PubMed (original) (raw)
. 2012 Jul 20;30(21):2601-8.
doi: 10.1200/JCO.2011.37.2482. Epub 2012 Jun 18.
Affiliations
- PMID: 22711854
- DOI: 10.1200/JCO.2011.37.2482
Clinically used breast cancer markers such as estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2 are unstable throughout tumor progression
Linda Sofie Lindström et al. J Clin Oncol. 2012.
Abstract
PURPOSE To investigate whether hormonal receptors and human epidermal growth factor receptor 2 (HER2) change throughout tumor progression, because this may alter patient management. PATIENTS AND METHODS The study cohort included female patients with breast cancer in the Stockholm health care region who relapsed from January 1, 1997, to December 31, 2007. Either biochemical or immunohistochemical (IHC)/immunocytochemical (ICC) methods were used to determine estrogen receptor (ER), progesterone receptor (PR), and HER2 status, which was then confirmed by fluorescent in situ hybridization for IHC/ICC 2+ and 3+ status. Results ER (459 patients), PR (430 patients), and HER2 (104 patients) from both primary tumor and relapse were assessed, revealing a change in 32.4% (McNemar's test P < .001), 40.7% (P < .001), and 14.5% (P = .44) of patients, respectively. Assessment of ER (119 patients), PR (116 patients), and HER2 (32 patients) with multiple (from two to six) consecutive relapses showed an alteration in 33.6%, 32.0%, and 15.7% of patients, respectively. A statistically significant differential overall survival related to intraindividual ER and PR status in primary tumor and relapse (log-rank P < .001) was noted. In addition, women with ER-positive primary tumors that changed to ER-negative tumors had a significant 48% increased risk of death (hazard ratio, 1.48; 95% CI, 1.08 to 2.05) compared with women with stable ER-positive tumors. CONCLUSION Patients with breast cancer experience altered hormone receptor and HER2 status throughout tumor progression, possibly influenced by adjuvant therapies, which significantly influences survival. Hence, marker investigations at relapse may potentially improve patient management and survival.
Similar articles
- Discordant expression of hormone receptors and HER2 in breast cancer. A retrospective comparison of primary tumors with paired metachronous recurrences or metastases.
Arapantoni-Dadioti P, Valavanis C, Gavressea T, Tzaida O, Trihia H, Lekka I. Arapantoni-Dadioti P, et al. J BUON. 2012 Apr-Jun;17(2):277-83. J BUON. 2012. PMID: 22740206 - HER2 status in hormone receptor positive premenopausal primary breast cancer adds prognostic, but not tamoxifen treatment predictive, information.
Rydén L, Landberg G, Stål O, Nordenskjöld B, Fernö M, Bendahl PO. Rydén L, et al. Breast Cancer Res Treat. 2008 May;109(2):351-7. doi: 10.1007/s10549-007-9660-2. Epub 2007 Jul 18. Breast Cancer Res Treat. 2008. PMID: 17636399 Clinical Trial. - Discordances in ER, PR and HER2 receptors after neoadjuvant chemotherapy in breast cancer.
van de Ven S, Smit VT, Dekker TJ, Nortier JW, Kroep JR. van de Ven S, et al. Cancer Treat Rev. 2011 Oct;37(6):422-30. doi: 10.1016/j.ctrv.2010.11.006. Epub 2010 Dec 21. Cancer Treat Rev. 2011. PMID: 21177040 Review. - Biological subtypes of breast cancer: current concepts and implications for recurrence patterns.
Cadoo KA, Fornier MN, Morris PG. Cadoo KA, et al. Q J Nucl Med Mol Imaging. 2013 Dec;57(4):312-21. Q J Nucl Med Mol Imaging. 2013. PMID: 24322788 Review.
Cited by
- Detection, significance and potential utility of circulating tumor cells in clinical practice in breast cancer (Review).
Rusnáková DŠ, Aziri R, Dubovan P, Jurík M, Mego M, Pinďák D. Rusnáková DŠ, et al. Oncol Lett. 2024 Oct 17;29(1):10. doi: 10.3892/ol.2024.14756. eCollection 2025 Jan. Oncol Lett. 2024. PMID: 39492933 Free PMC article. Review. - Hypoxia-induced epigenetic regulation of breast cancer progression and the tumour microenvironment.
Capatina AL, Malcolm JR, Stenning J, Moore RL, Bridge KS, Brackenbury WJ, Holding AN. Capatina AL, et al. Front Cell Dev Biol. 2024 Aug 30;12:1421629. doi: 10.3389/fcell.2024.1421629. eCollection 2024. Front Cell Dev Biol. 2024. PMID: 39282472 Free PMC article. Review. - A case report of breast cancer metastasis to the bladder from invasive ductal carcinoma.
Hou T, Shen G, Hu X, Bai T, He H, Zhang Z, Bao W, Tian R, Yu X, Sun T, Ding X, Wang X, Zhang Y. Hou T, et al. Ann Med Surg (Lond). 2024 Jul 11;86(9):5529-5534. doi: 10.1097/MS9.0000000000002352. eCollection 2024 Sep. Ann Med Surg (Lond). 2024. PMID: 39238959 Free PMC article. - Receptor Discordance in Metastatic Breast Cancer; a review of clinical and genetic subtype alterations from primary to metastatic disease.
Dowling GP, Keelan S, Cosgrove NS, Daly GR, Giblin K, Toomey S, Hennessy BT, Hill ADK. Dowling GP, et al. Breast Cancer Res Treat. 2024 Oct;207(3):471-476. doi: 10.1007/s10549-024-07431-6. Epub 2024 Aug 1. Breast Cancer Res Treat. 2024. PMID: 39090418 Free PMC article. Review. - Evolving Management of Breast Cancer in the Era of Predictive Biomarkers and Precision Medicine.
Afzal MZ, Vahdat LT. Afzal MZ, et al. J Pers Med. 2024 Jul 3;14(7):719. doi: 10.3390/jpm14070719. J Pers Med. 2024. PMID: 39063972 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous