Literature DB >> 2987601

[Megestrol acetate in various doses in the treatment of metastatic breast carcinoma--clinical and endocrinologic studies].

H E Wander, H C Blossey, G A Nagel, D Emrich.   

Abstract

Both medroxyprogesterone acetate (MPA) and megestrol acetate (MA) are effective in the treatment of metastatic breast cancer. Although the dose-dependent mode of actions of MPA have been extensively clarified, there is still some uncertainty regarding the mode of actions and dosage of MA. Thirty-three patients with metastatic breast cancer were treated with various dosages of MA under a phase-II study. Eight patients were given 200 mg, 9 X 400 mg, 10 X 600 mg and 6 X 800 mg MA daily per os. The LH, FSH, TBI, T3, T4, TSH, ACTH, aldosterone, testosterone, prolactin and cortisol levels were determined regularly during treatment to enable the investigation of the pharmacodynamics of MA. A complete remission was achieved in two patients, a partial remission in seven patients and there was no change in eight patients (total responder rate 51.5%). The clinical and endocrine changes therefore suggest that the dose-dependent mode of actions of MPA and MA are identical. Equivalent dosages of MPA are 1000-1500 mg per os and of MA 160-200 mg. Furthermore, similar relationships between the endocrine changes and remission behaviour of MA and MPA have been observed. Persisting tumour remissions are inevitable under cortisol suppression and normal prolactin, aldosterone and ACTH levels.

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Year:  1985        PMID: 2987601     DOI: 10.1007/bf01731974

Source DB:  PubMed          Journal:  Klin Wochenschr        ISSN: 0023-2173


  16 in total

1.  Assessment of response to therapy in advanced breast cancer: a project of the Programme on Clinical Oncology of the International Union Against Cancer, Geneva, Switzerland.

Authors:  J L Hayward; P P Carbone; J C Heuson; S Kumaoka; A Segaloff; R D Rubens
Journal:  Cancer       Date:  1977-03       Impact factor: 6.860

2.  [Study of a protein binding method for the determination of plasma corticoids].

Authors:  J Köbberling
Journal:  Z Klin Chem Klin Biochem       Date:  1972-02

Review 3.  Megestrol acetate.

Authors:  R Canetta; S Florentine; H Hunter; L Lenaz
Journal:  Cancer Treat Rev       Date:  1983-09       Impact factor: 12.111

4.  [Hyperprolactinemia in metastasizing breast cancer].

Authors:  G A Nagel; H E Wander; H C Blossey
Journal:  Schweiz Med Wochenschr       Date:  1981-12-12

5.  Progestin therapy of breast cancer: comparison of agents.

Authors:  B A Stoll
Journal:  Br Med J       Date:  1967-08-05

6.  The effect of medroxyprogesterone acetate on the pituitary-adrenal axis.

Authors:  L Hellman; K Yoshida; B Zumoff; J Levin; J Kream; D K Fukushima
Journal:  J Clin Endocrinol Metab       Date:  1976-05       Impact factor: 5.958

7.  Progesterone receptor level as a predictor of response to megestrol acetate in advanced breast cancer: a retrospective study.

Authors:  P A Johnson; P D Bonomi; K M Anderson; J M Wolter; L D Bacon; A H Rossof; S G Economou
Journal:  Cancer Treat Rep       Date:  1983 Jul-Aug

8.  Estrogen, androgen, glucocorticoid, and progesterone receptors in progestin-induced regression of human breast cancer.

Authors:  F A Teulings; H A van Gilse; M S Henkelman; H Portengen; J Alexieva-Figusch
Journal:  Cancer Res       Date:  1980-07       Impact factor: 12.701

9.  Danazol inhibition of steroidogenesis in the human corpus luteum.

Authors:  R L Barbieri; R Osathanondh; K J Ryan
Journal:  Obstet Gynecol       Date:  1981-06       Impact factor: 7.661

10.  Effect of megestrol acetate (Megace) on steroid metabolism and steroid-protein binding in the human prostate.

Authors:  J Geller; J Albert; S Geller; D Lopez; T Cantor; S Yen
Journal:  J Clin Endocrinol Metab       Date:  1976-11       Impact factor: 5.958

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