Oestrogen-receptor status and endocrine therapy of breast cancer: response rates and status stability
- PMID: 7459239
- PMCID: PMC2010491
- DOI: 10.1038/bjc.1981.8
Oestrogen-receptor status and endocrine therapy of breast cancer: response rates and status stability
Abstract
The concentration of cellular oestrogen receptor (RE) was measured in both the soluble and nuclear-pellet fractions of biopsies from 1,000 breast cancers. Data suggest that functional steroid RE is always in equilibrium between the soluble and nuclear fractions. However, biopsies from only one-third of patients contained detectable amounts of high-affinity RE in both fractions. Thirty patients out of 42 (71%) whose biopsies contained RE in both fractions, showed objective remission after receiving some form of hormonal manipulation as sole treatment. Response rates in the other categories ranged from 9% for those whose biopsies contained no detectable RE to 24% for those who displayed soluble RE alone. The presence of RE in both fractions of primary disease, whereas RE-negativity was maintained during progression from primary to secondary disease. Other aspects of RE status in relation to stage of disease are analysed.
PIP: Both the soluble and pellet RE (estrogen receptor) status of 1000 patients with breast cancers were measured. Functional steroid RE was found to be always in equilibrium between the soluble and nuclear fractions. Detectable amounts of high affinity RE in both fractions were seen in biopsies from only 1/3 of patients. 30 out of 42 patients (71%) whose biopsies contained RE in both fractions exhibited objective remission following hormonal manipulation as sole treatment. Response rates in other categories ranged from 9% for those whose biopsies had no detectable RE to 24% for those who exhibited soluble RE alone. RE presence in both fractions of primary disease was found to be an unreliable index of RE status in subsequent secondary disease while RE negativity was maintained during progression from primary to secondary disease. Other aspects of RE status in relation to stage of disease are analyzed.
Similar articles
-
Soluble and nuclear oestrogen receptor status in human breast cancer in relation to prognosis.Br J Cancer. 1981 Jan;43(1):67-71. doi: 10.1038/bjc.1981.9. Br J Cancer. 1981. PMID: 7459240 Free PMC article.
-
Expression of the oestrogen regulated pNR-2 mRNA in human breast cancer: relation to oestrogen receptor mRNA levels and response to tamoxifen therapy.Br J Cancer. 1990 Jan;61(1):32-8. doi: 10.1038/bjc.1990.8. Br J Cancer. 1990. PMID: 2153395 Free PMC article.
-
Activated oestrogen receptors in breast cancer and response to endocrine therapy.Eur J Cancer Clin Oncol. 1984 Jan;20(1):41-6. doi: 10.1016/0277-5379(84)90032-4. Eur J Cancer Clin Oncol. 1984. PMID: 6537914
-
Oestrogen and progesterone receptor determinations in breast cancer: technology and biology.Cancer Surv. 1986;5(3):505-25. Cancer Surv. 1986. PMID: 3555780 Review.
-
Steroid hormone receptors in the management of human breast cancer.Ann Clin Res. 1980 Oct;12(5):202-7. Ann Clin Res. 1980. PMID: 7015982 Review.
Cited by
-
Breast cancer: a comparison of response to endocrine therapy and oestrogen excretion patterns including unusual metabolites.Br J Cancer. 1981 Nov;44(5):670-4. doi: 10.1038/bjc.1981.252. Br J Cancer. 1981. PMID: 6274375 Free PMC article.
-
cDNA transfection followed by the isolation of a MCF-7 breast cell line resistant to tamoxifen in vitro and in vivo.Br J Cancer. 1993 Dec;68(6):1088-96. doi: 10.1038/bjc.1993.486. Br J Cancer. 1993. PMID: 8260359 Free PMC article.
-
Epidermal growth factor receptor (EGFr); results of a 6 year follow-up study in operable breast cancer with emphasis on the node negative subgroup.Br J Cancer. 1991 Jan;63(1):146-50. doi: 10.1038/bjc.1991.30. Br J Cancer. 1991. PMID: 1846551 Free PMC article.
-
Measurement of oestrogen receptor mRNA levels in human breast tumours.Br J Cancer. 1988 Nov;58(5):600-5. doi: 10.1038/bjc.1988.267. Br J Cancer. 1988. PMID: 2851309 Free PMC article.
-
Chemotherapy of breast cancer.Med Oncol Tumor Pharmacother. 1984;1(3):169-92. doi: 10.1007/BF02934139. Med Oncol Tumor Pharmacother. 1984. PMID: 6400037 Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical