Literature DB >> 6224604

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

C M Camaggi, E Strocchi, M Giovannini, B Angelelli, B Costanti, E Zebini, P Ferrari, F Pannuti.   

Abstract

Medroxyprogesterone acetate plasma levels were measured in advanced cancer patients after multiple PO or IM administration (500, 1000, 2000, 3000, 4000, and 5000 mg/day PO and 500, 1000, 2000 mg/day IM for 30 days). After PO administration, the plasma concentration rises quickly and plateau level is reached in 4-10 days. Discontinuation of the treatment produces a fast decay (t1/2 = 62.4 h) of the drug levels. When medroxyprogesterone acetate is given IM plasma levels, steadily increase and after drug discontinuation no noticeable decay is observed for at least 6 months; plateau plasma levels are about three times higher than after the corresponding PO treatment. Extremely high interpatient variation in bioavailability is present with both administration routes. These data may well rationalize the results of previous clinical trials and will help in planning treatment schedules.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6224604     DOI: 10.1007/bf00257410

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  12 in total

1.  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

2.  Interaction between steroids and a uterine progestogen specific binding macromolecule.

Authors:  J L McGuire; C D Bariso; A P Shroff
Journal:  Biochemistry       Date:  1974-01-15       Impact factor: 3.162

3.  GLC determination of medroxyprogesterone acetate in plasma.

Authors:  D G Kaiser; R G Carlson; K T Kirton
Journal:  J Pharm Sci       Date:  1974-03       Impact factor: 3.534

4.  Prospective, randomized clinical trial of two different high dosages of medroxyprogesterone acetate (MAP) in the treatment of metastatic breast cancer.

Authors:  F Pannuti; A Martoni; A R Di Marco; E Piana; F Saccani; G Becchi; G Mattioli; F Barbanti; G A Marra; W Persiani; L Cacciari; F Spagnolo; D Palenzona; G Rocchetta
Journal:  Eur J Cancer       Date:  1979-04       Impact factor: 9.162

5.  Medroxyprogesterone acetate (MAP) plasma levels after simultaneous oral and intramuscular administration in cancer patients.

Authors:  F Pannuti; C M Camaggi; E Strocchi; M Giovannini; N Canova; G Murari
Journal:  Cancer Chemother Pharmacol       Date:  1982       Impact factor: 3.333

6.  Measurement of medroxyprogesterone acetate (Provera ) by radioimmunoassay.

Authors:  J C Cornette; K T Kirton; G W Duncan
Journal:  J Clin Endocrinol Metab       Date:  1971-09       Impact factor: 5.958

7.  A radioimmunoassay for serum medroxyprogesterone acetate.

Authors:  K Shrimanker; B N Saxena; K Fotherby
Journal:  J Steroid Biochem       Date:  1978-04       Impact factor: 4.292

8.  Medroxyprogesterone acetate (MAP) relative bioavailability after single high-dose administration in cancer patients.

Authors:  F Pannuti; C M Camaggi; E Strocchi; M Giovannini; A R Di Marco; B Costanti
Journal:  Cancer Treat Rep       Date:  1982-12

9.  The pharmacokinetics of high-dose medroxyprogesterone acetate (MPA) in the therapy of advanced breast cancer.

Authors:  H C Blossey; H H Bartsch; D Kanne; J Koebberling; G A Nagel
Journal:  Cancer Chemother Pharmacol       Date:  1982       Impact factor: 3.333

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

Authors:  G R Cuna; A Calciati; M R Strada; C Bumma; L Campio
Journal:  Tumori       Date:  1978-04-30
View more
  9 in total

Review 1.  Rare diseases. 1. Lymphangioleiomyomatosis: clinical features, management and basic mechanisms.

Authors:  S Johnson
Journal:  Thorax       Date:  1999-03       Impact factor: 9.139

Review 2.  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

3.  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

4.  In vivo assessment of the regulation of transforming growth factor alpha, epidermal growth factor (EGF), and EGF receptor in the human endometrium by medroxyprogesterone acetate.

Authors:  Fernando M Reis; Cintia Lhullier; Maria Isabel Edelweiss; Poli Mara Spritzer
Journal:  J Assist Reprod Genet       Date:  2005-01       Impact factor: 3.412

5.  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

6.  Medroxyprogesterone acetate (MAP) and tamoxifen (TMX) plasma levels after simultaneous treatment with 'low' TMX and 'high' MAP doses.

Authors:  C M Camaggi; E Strocchi; N Canova; B Costanti; F Pannuti
Journal:  Cancer Chemother Pharmacol       Date:  1985       Impact factor: 3.333

7.  Medroxyprogesterone acetate bioavailability after high-dose intraperitoneal administration in advanced cancer.

Authors:  C M Camaggi; E Strocchi; B Costanti; P Beghelli; P Ferrari; F Pannuti
Journal:  Cancer Chemother Pharmacol       Date:  1985       Impact factor: 3.333

8.  Medroxyprogesterone acetate plasma pharmacokinetics after intravenous administration in rabbits.

Authors:  F Pannuti; C M Camaggi; E Strocchi; R Comparsi
Journal:  Cancer Chemother Pharmacol       Date:  1987       Impact factor: 3.333

9.  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

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.