Literature DB >> 3161613

Endocrine effects of medroxyprogesterone acetate: relation between plasma levels and suppression of adrenal steroids in patients with breast cancer.

H van Veelen, P H Willemse, D T Sleijfer, W J Sluiter, H Doorenbos.   

Abstract

The elimination of adrenal steroids by adrenalectomy or medical treatment has been one of the mainstays in the palliative treatment of patients with disseminated breast cancer. Recently, the effects of progestins on adrenal function has become the subject of renewed interest. To find a relation between plasma levels of medroxyprogesterone acetate (MPA) and adrenal suppression in breast cancer patients, we compared a group of 41 postmenopausal patients with disseminated or inoperable breast cancer, treated with oral MPA, with a control group of 28 postmenopausal breast cancer patients without treatment. To obtain MPA plasma levels in the lower range, 13 patients initially received 300 mg of MPA daily (Group 1), six of whom were subsequently treated with 600 mg (Group 2). Group 3 comprised 37 patients treated with 900 mg of MPA. All of the parameters studied varied widely. Only in Group 3 patients were the MPA levels higher and the levels of cortisol, androstenedione, DHAS, and estrone lower than those in Group 1 patients. All steroid levels in Group 3 were significantly below control values. Considering all data, a negative but weak correlation was found between MPA levels and cortisol (R = -0.55), androstenedione (R = -0.58), and dehydro-epi-androsterone sulfate (R = -0.40), but not for MPA and estrone, indicating better adrenal suppression by higher MPA dosage and plasma levels. However, suppressed cortisol concentrations did not predict sufficient MPA dosage in all patients because low cortisol was not always associated with high MPA levels. A positive relation existed between the levels of androstenedione and estrone, which shows that suppression of these adrenal androgens may result in suppression of plasma estrone. This may be of additional therapeutic benefit in breast cancer patients.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 3161613

Source DB:  PubMed          Journal:  Cancer Treat Rep        ISSN: 0361-5960


  7 in total

1.  Dose response evaluation. Use of plasma concentration confidence intervals as a tool to predict optimal drug dose ratio.

Authors:  P E Lønning
Journal:  Clin Pharmacokinet       Date:  1993-07       Impact factor: 6.447

2.  Medroxyprogesterone acetate inhibits the proliferation of estrogen- and progesterone-receptor negative MFM-223 human mammary cancer cells via the androgen receptor.

Authors:  R Hackenberg; T Hawighorst; A Filmer; A H Nia; K D Schulz
Journal:  Breast Cancer Res Treat       Date:  1993       Impact factor: 4.872

3.  Medroxyprogesterone acetate: steady-state pharmacokinetics bioequivalence of two oral formulations.

Authors:  K Pollow; R Kreienberg; N Di Pietro
Journal:  J Cancer Res Clin Oncol       Date:  1989       Impact factor: 4.553

4.  Androgen and glucocorticoid receptor-mediated inhibition of cell proliferation by medroxyprogesterone acetate in ZR-75-1 human breast cancer cells.

Authors:  R Poulin; D Baker; D Poirier; F Labrie
Journal:  Breast Cancer Res Treat       Date:  1989-03       Impact factor: 4.872

5.  Adrenal failure in patients with breast carcinoma after long-term treatment of cyclic alternating oestrogen progesterone.

Authors:  V Hug; S Kau; G N Hortobagyi; L Jones
Journal:  Br J Cancer       Date:  1991-03       Impact factor: 7.640

6.  Adjuvant high-dose medroxyprogesterone acetate for early breast cancer: 13 years update in a multicentre randomized trial.

Authors:  C Focan; M Beauduin; E Salamon; J de Greve; G de Wasch; J P Lobelle; F Majois; A Tagnon; J Tytgat; S van Belle; R Vandervellen; A Vindevoghel
Journal:  Br J Cancer       Date:  2001-07-06       Impact factor: 7.640

7.  The effects of low and high dose medroxyprogesterone acetate on sex steroids and sex hormone binding globulin in postmenopausal breast cancer patients.

Authors:  M Dowsett; A Lal; I E Smith; S L Jeffcoate
Journal:  Br J Cancer       Date:  1987-03       Impact factor: 7.640

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.