Abstract
The influence of steroid hormone receptors on response rate to endocrine therapy in 85 patients with metastatic breast cancer was determined in a retrospective study. We have previously reported that estrogen receptor status has an overwhelming influence on predicting response to therapy when compared to other prognostic variables. In the present study, we expand our analysis to include the results of progesterone, androgen, and glucocorticoid receptors. Of 18 patients whose tumors contained progesterone receptor, 11 responded to endocrine therapy, compared to 8 of 26 patients with low or absent progesterone receptor. Progesterone receptor increased the predictive index of the estrogen receptor in a group of patients who had received no prior therapy, but it did not help in patients who had received prior endocrine therapy. None of four patients whose tumors were estrogen receptor negative but progesterone receptor positive responded to endocrine therapy. At the present time, there are trends suggesting a possible association between androgen and glucocorticoid receptor and response to endocrine therapy. These trends are apparent only with a cutoff value of 10 fmol/mg cytoplasmic protein, and the distributions of androgen and glucocorticoid receptor values for responders and nonresponders are not significantly different. Knowledge of androgen receptor status does not increase the predictive index in estrogen receptor-positive tumors or estrogen receptor-negative tumors. Glucocorticoid receptor positivity may increase the predictive index in estrogen receptor-positive tumors, but not in estrogen receptor-negative tumors.
| Original language | English |
|---|---|
| Pages (from-to) | 1973-1979 |
| Number of pages | 7 |
| Journal | Cancer Research |
| Volume | 39 |
| Issue number | 6 I |
| State | Published - Dec 1 1979 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Cancer Research
- Oncology
Cite this
Relationship between the progesterone, androgen, and glucocorticoid receptor and response rate to endocrine therapy in metastatic breast cancer. / Lippman, Marc E; Lippman, M. E.; Thompson, E. B.; Simon, R.; Barlock, A.; Green, L.; Huff, K. K.; Do, H. M.; Aitken, S. C.; Warren, R.
In: Cancer Research, Vol. 39, No. 6 I, 01.12.1979, p. 1973-1979.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Relationship between the progesterone, androgen, and glucocorticoid receptor and response rate to endocrine therapy in metastatic breast cancer
AU - Lippman, Marc E
AU - Lippman, M. E.
AU - Thompson, E. B.
AU - Simon, R.
AU - Barlock, A.
AU - Green, L.
AU - Huff, K. K.
AU - Do, H. M.
AU - Aitken, S. C.
AU - Warren, R.
PY - 1979/12/1
Y1 - 1979/12/1
N2 - The influence of steroid hormone receptors on response rate to endocrine therapy in 85 patients with metastatic breast cancer was determined in a retrospective study. We have previously reported that estrogen receptor status has an overwhelming influence on predicting response to therapy when compared to other prognostic variables. In the present study, we expand our analysis to include the results of progesterone, androgen, and glucocorticoid receptors. Of 18 patients whose tumors contained progesterone receptor, 11 responded to endocrine therapy, compared to 8 of 26 patients with low or absent progesterone receptor. Progesterone receptor increased the predictive index of the estrogen receptor in a group of patients who had received no prior therapy, but it did not help in patients who had received prior endocrine therapy. None of four patients whose tumors were estrogen receptor negative but progesterone receptor positive responded to endocrine therapy. At the present time, there are trends suggesting a possible association between androgen and glucocorticoid receptor and response to endocrine therapy. These trends are apparent only with a cutoff value of 10 fmol/mg cytoplasmic protein, and the distributions of androgen and glucocorticoid receptor values for responders and nonresponders are not significantly different. Knowledge of androgen receptor status does not increase the predictive index in estrogen receptor-positive tumors or estrogen receptor-negative tumors. Glucocorticoid receptor positivity may increase the predictive index in estrogen receptor-positive tumors, but not in estrogen receptor-negative tumors.
AB - The influence of steroid hormone receptors on response rate to endocrine therapy in 85 patients with metastatic breast cancer was determined in a retrospective study. We have previously reported that estrogen receptor status has an overwhelming influence on predicting response to therapy when compared to other prognostic variables. In the present study, we expand our analysis to include the results of progesterone, androgen, and glucocorticoid receptors. Of 18 patients whose tumors contained progesterone receptor, 11 responded to endocrine therapy, compared to 8 of 26 patients with low or absent progesterone receptor. Progesterone receptor increased the predictive index of the estrogen receptor in a group of patients who had received no prior therapy, but it did not help in patients who had received prior endocrine therapy. None of four patients whose tumors were estrogen receptor negative but progesterone receptor positive responded to endocrine therapy. At the present time, there are trends suggesting a possible association between androgen and glucocorticoid receptor and response to endocrine therapy. These trends are apparent only with a cutoff value of 10 fmol/mg cytoplasmic protein, and the distributions of androgen and glucocorticoid receptor values for responders and nonresponders are not significantly different. Knowledge of androgen receptor status does not increase the predictive index in estrogen receptor-positive tumors or estrogen receptor-negative tumors. Glucocorticoid receptor positivity may increase the predictive index in estrogen receptor-positive tumors, but not in estrogen receptor-negative tumors.
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UR - http://www.scopus.com/inward/citedby.url?scp=0018769728&partnerID=8YFLogxK
M3 - Article
C2 - 445396
AN - SCOPUS:0018769728
VL - 39
SP - 1973
EP - 1979
JO - Journal of Cancer Research
JF - Journal of Cancer Research
SN - 0099-7013
IS - 6 I
ER -