Literature DB >> 3158449

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

C M Camaggi, E Strocchi, B Costanti, P Beghelli, P Ferrari, F Pannuti.   

Abstract

Administration of medroxyprogesterone acetate IP in advanced cancer with peritoneal metastases and ascitic effusion generates considerably higher drug plasma levels than those observed after PO or IM treatment. Comparison of areas under the time-concentration curves (AUC) with reference to the three administration routes indicates that after oral administration only 0.2%-17.4% (mean 5.7%; SD 3.77; 40 patients) of the administered dose is absorbed; after IM treatment a daily absorption of 0.7%-7.7% (mean 2.5%; SD 1.66; 30 patients) of the administered dose per injection site was computed.

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Year:  1985        PMID: 3158449     DOI: 10.1007/bf00258122

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


  9 in total

1.  Pharmacokinetic observations on medroxyprogesterone acetate administered orally and intravaginally.

Authors:  A Victor; E D Johansson
Journal:  Contraception       Date:  1976-09       Impact factor: 3.375

2.  Medroxyprogesterone acetate, estradiol, FSH and LH in peripheral blood after intramuscular administration of Depo-ProveraR to women.

Authors:  S Jeppsson
Journal:  Contraception       Date:  1976-10       Impact factor: 3.375

3.  Plasma medroxyprogesterone acetate levels following intramuscular or oral administration in patients with endometrial adenocarcinoma.

Authors:  T Laatikainen; U Nieminen; H Adlercreutz
Journal:  Acta Obstet Gynecol Scand       Date:  1979       Impact factor: 3.636

4.  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

5.  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

6.  Medroxyprogesterone acetate (MPA) plasma levels after oral and intramuscular administration in a long-term study.

Authors:  I Hesselius; E D Johansson
Journal:  Acta Obstet Gynecol Scand Suppl       Date:  1981

7.  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

8.  Pharmacokinetics of medroxyprogesterone acetate administered by oral and intramuscular route.

Authors:  J Løber; H T Mouridsen; M Salimtschik; E Johansson
Journal:  Acta Obstet Gynecol Scand Suppl       Date:  1981

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

  9 in total
  3 in total

Review 1.  Clinical pharmacokinetics of endocrine agents used in advanced breast cancer.

Authors:  P E Lønning; E A Lien; S Lundgren; S Kvinnsland
Journal:  Clin Pharmacokinet       Date:  1992-05       Impact factor: 6.447

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.  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

  3 in total

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