Literature DB >> 354147

High dose medroxyprogesterone acetate (MPA) treatment in metastatic carcinoma of the breast: a dose-response evaluation.

G R Cuna, A Calciati, M R Strada, C Bumma, L Campio.   

Abstract

The results of controlled clinical trial that used high doses of medroxyprogesterone acetate (MPA) in the treatment of metastatic breast cancer are reported. Two treatment reigmens were used: regimen A, 500 mg daily with a total dose of 30 g; regimen B, 1,000 mg daily with a total dose of 60 g. The overall response rates were similar, with no statistically significant difference between the two treated groups. Regimen A (lower dosage group) reached a remission rate of 44%, whereas regimen B (higher dosage group) had a remission rate of 41%. The mean duration of response was 8 months with regimen A and 9 months with regimen B. The advantages of the lower dosage regimen as opposed to the higher dosage regimen of MPA in the treatment of advanced breast cancer are discussed.

Entities:  

Keywords:  Breast Cancer; Cancer; Clinical Research; Comparative Studies; Contraception; Contraceptive Agents, Female--administraction and dosage; Contraceptive Agents, Female--side effects; Contraceptive Agents, Progestin--administraction and dosage; Contraceptive Agents, Progestin--side effects; Contraceptive Agents--administraction and dosage; Contraceptive Agents--side effects; Developed Countries; Diseases; Europe; Family Planning; Italy; Mediterranean Countries; Medroxyprogesterone Acetate--administraction and dosage; Medroxyprogesterone Acetate--side effects; Neoplasms; Research Methodology; Southern Europe; Studies; Treatment

Mesh:

Substances:

Year:  1978        PMID: 354147     DOI: 10.1177/030089167806400204

Source DB:  PubMed          Journal:  Tumori        ISSN: 0300-8916


  16 in total

Review 1.  Clinical significance of differences in bioavailability of medroxyprogesterone acetate preparations.

Authors:  A D Stockdale; A Y Rostom
Journal:  Clin Pharmacokinet       Date:  1989-03       Impact factor: 6.447

2.  A phase I/II study of high-dose megestrol acetate in the treatment of metastatic breast cancer.

Authors:  H L Parnes; J S Abrams; N S Tchekmedyian; N Tait; J Aisner
Journal:  Breast Cancer Res Treat       Date:  1991-08       Impact factor: 4.872

3.  On the role of additive hormone monotherapy with tamoxifen, medroxyprogesterone acetate and aminoglutethimide, in advanced breast cancer.

Authors:  E Petru; D Schmähl
Journal:  Klin Wochenschr       Date:  1987-10-15

4.  High-dose medroxyprogesterone acetate in breast cancer resistant to endocrine and cytotoxic therapy.

Authors:  M De Lena; C Brambilla; P Valagussa; G Bonadonna
Journal:  Cancer Chemother Pharmacol       Date:  1979       Impact factor: 3.333

Review 5.  Current status of high dose progestin treatment in advanced breast cancer.

Authors:  W Mattsson
Journal:  Breast Cancer Res Treat       Date:  1983       Impact factor: 4.872

Review 6.  Endocrine therapy for advanced breast cancer: a review.

Authors:  H B Muss
Journal:  Breast Cancer Res Treat       Date:  1992       Impact factor: 4.872

7.  Oral medroxyprogesterone acetate in the treatment of metastatic breast cancer.

Authors:  G N Hortobagyi; A U Buzdar; D Frye; H Y Yap; V Hug; K Pinnamaneni; G Fraschini; H C Halvorson; G R Blumenschein
Journal:  Breast Cancer Res Treat       Date:  1985       Impact factor: 4.872

8.  Comparative pharmacokinetics of medroxyprogesterone acetate administered by oral and intramuscular routes.

Authors:  M Salimtschik; H T Mouridsen; J Loeber; E Johansson
Journal:  Cancer Chemother Pharmacol       Date:  1980       Impact factor: 3.333

9.  Medroxyprogesterone acetate (MAP) plasma levels after multiple high-dose administration in advanced cancer patients.

Authors:  C M Camaggi; E Strocchi; M Giovannini; B Angelelli; B Costanti; E Zebini; P Ferrari; F Pannuti
Journal:  Cancer Chemother Pharmacol       Date:  1983       Impact factor: 3.333

10.  [High dose medroxyprogesteroneacetate in metastasizing breast cancer: correlations between course of the disease and hormone profiles].

Authors:  H E Wander; C Blossey; J Köbberling; G A Nagel
Journal:  Klin Wochenschr       Date:  1983-06-01
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