Literature DB >> 11091543

Benefits of Medroxyprogesterone Acetate (MPA) in Advanced or Recurrent Breast Cancer with Higher Serum Concertration.

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Abstract

The efficacy of medroxyprogesterone acetate (MPA) therapy in controlling progressive measurable metastatic breast cancer was assessed in 61 patients. In addition serum MPA concentrations were measured by high performance liquid chromatography (HPLC) and subjective effects of treatment were monitored. Overall 24 patients (39.3%) achieved an objective response(2 complete responses [ CR ] and 22 partial responses [ PR ]). There was no significant relationships between response to therapy and menopausal status, metastatic sites, previous therapy, histological type, or disease-free interval. Patients with estrogen (ER) and progesterone (PgR) receptor-positive tumors responded more frequently. Significant differences in serum MPA concentrations were seen between responders and non-responders, objective tumor shrinkage being seen in patients with serum levels in excess of 55 ng/ml. There were few cases responding to the therapy with serum MPA concentrations lower than 25 ng/ml. The serum MPA levels significantly correlated with an improvement in the performance status and survival. Patients with serum MPA concentrations lower than 25 ng/ml had significantly poorer survival. There was a significant relationship between MPA level and dose per area of boby surface (mg/ m(2)) in cases with CR or PR or no change (NC). However, the serum levels of patients with progressive disease despite therapy were lower than the expected levels based on the body surface area. This study demonstrated that serum MPA concentration is a determining factor for therapeutic benefit in advanced or recurrent breast cancer.

Entities:  

Year:  1995        PMID: 11091543     DOI: 10.1007/BF02966952

Source DB:  PubMed          Journal:  Breast Cancer        ISSN: 1340-6868            Impact factor:   4.239


  16 in total

1.  Comparison of mass spectrometry and radioimmunoassay to measure medroxyprogesterone acetate in patients with endometrial cancer.

Authors:  J Kärkkäinen; E Vesterinen; U H Stenman; H Adlercreutz; U Nieminen; O Widholm
Journal:  Eur J Cancer       Date:  1990       Impact factor: 9.162

2.  Plasma concentrations of medroxyprogesterone acetate and megesterol acetate during long-term follow-up in patients treated for metastatic breast cancer.

Authors:  A A Miller; R Becher; C G Schmidt
Journal:  J Cancer Res Clin Oncol       Date:  1988       Impact factor: 4.553

3.  Angiogenic activity of rat mammary carcinomas induced by 7,12-dimethylbenz[a]anthracene and its inhibition by medroxyprogesterone acetate: possible involvement of antiangiogenic action of medroxyprogesterone acetate in its tumor growth inhibition.

Authors:  T Oikawa; A Hiragun; Y Yoshida; H Ashino-Fuse; T Tominaga; T Iwaguchi
Journal:  Cancer Lett       Date:  1988-12-01       Impact factor: 8.679

4.  High dose versus low dose medroxyprogesterone acetate: a randomized trial in advanced breast cancer.

Authors:  C J Gallagher; F Cairnduff; I E Smith
Journal:  Eur J Cancer Clin Oncol       Date:  1987-12

5.  Pharmacokinetics and pharmacodynamics of medroxyprogesterone acetate in advanced breast cancer patients.

Authors:  M C Etienne; G Milano; M Frenay; N Renee; E Francois; A Thyss; M Schneider; M Namer
Journal:  J Clin Oncol       Date:  1992-07       Impact factor: 44.544

6.  Lack of correlations between plasma concentration of medroxyprogesterone acetate, hypothalamic-pituitary function, and tumour response in patients with advanced breast cancer.

Authors:  D W Hedley; M Christie; R P Weatherby; I D Caterson
Journal:  Cancer Chemother Pharmacol       Date:  1985       Impact factor: 3.333

7.  Medroxyprogesterone acetate: variation in serum concentrations achieved with three commercially available preparations.

Authors:  A D Stockdale; D Chapman; G P Mould; A Y Rostom
Journal:  Cancer Treat Rep       Date:  1987-09

8.  Oral versus im administration of high-dose medroxyprogesterone acetate in pretreated patients with advanced breast cancer.

Authors:  L Beex; J Burghouts; J van Turnhout; W Breed; H Hillen; A Holdrinet; G Boetius; G Hoogendoorn; W Doesburg; M Verhulst
Journal:  Cancer Treat Rep       Date:  1987-12

9.  Pharmacokinetic approach to the selection of dose schedules for medroxyprogesterone acetate in clinical oncology.

Authors:  V Tamassia; A Battaglia; F Ganzina; A M Isetta; G Sacchetti; F Cavalli; A Goldhirsch; K Brunner; G Bernardo; G Robustelli della Cuna
Journal:  Cancer Chemother Pharmacol       Date:  1982       Impact factor: 3.333

10.  Medroxyprogesterone acetate pharmacokinetics following oral high-dose administration in humans: a bioavailability evaluation of a new MPA tablet formulation.

Authors:  E D Johansson; P B Johansen; S N Rasmussen
Journal:  Acta Pharmacol Toxicol (Copenh)       Date:  1986-05
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