Literature DB >> 8494706

A double blind placebo controlled trial of medroxyprogesterone acetate (MPA) in cancer cachexia.

S Downer1, S Joel, A Allbright, H Plant, L Stubbs, D Talbot, M Slevin.   

Abstract

Patients with breast cancer treated with MPA often report an improvement in appetite. Similar appetite stimulation is seen in patients treated with some corticosteroids, but MPA has a potential advantage over these drugs in that it does not exert a catabolic effect. MPA (100 mg tds orally) has therefore been compared with placebo in 60 patients with advanced malignant disease. Twenty-one patients in the MPA group and 20 in the placebo group were receiving chemotherapy. Patients were treated for 6 weeks and were assessed at weeks 0, 3 and 6 for appetite, energy, mood and pain using visual analogue scales. Nutritional status was assessed by the measurement of serum proteins and anthropometrics. Karnofsky score was recorded as a measure of performance status. There was a significant improvement in appetite in the MPA group between weeks 0 (pre-study) and 3 (P = 0.0002) and 0 and 6 (P = 0.015). There was no significant improvement in appetite in the placebo group. Supporting this finding was the significant increase in serum thyroid binding pre-albumin and retinol binding protein in the MPA group between weeks 0 and 3 and 0 and 6 (P = 0.023 and P = 0.039 respectively). These two parameters showed no significant change in the placebo group. There was no change in anthropometric measurements, weight, performance status, energy, mood or pain in either group. These data indicate that there was a significant increase in appetite in anorexic patients with advanced cancer treated with MPA which was reflected in increases in rapid turnover proteins reported to reflect nutritional status. However, this apparent increase in appetite did not result in improved weight, performance status, energy levels, mood or relief of pain. Further studies to investigate the effect of higher doses of MPA are indicated.

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Year:  1993        PMID: 8494706      PMCID: PMC1968469          DOI: 10.1038/bjc.1993.202

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  15 in total

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  8 in total

Review 1.  Managing cancer-related anorexia/cachexia.

Authors:  G Mantovani; A Macciò; E Massa; C Madeddu
Journal:  Drugs       Date:  2001       Impact factor: 9.546

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Authors:  B Gagnon; E Bruera
Journal:  Drugs       Date:  1998-05       Impact factor: 9.546

3.  Medroxyprogesterone acetate enhances in vivo and in vitro antibody production.

Authors:  M Vermeulen; P Pazos; C Lanari; A Molinolo; R Gamberale; J R Geffner; M Giordano
Journal:  Immunology       Date:  2001-09       Impact factor: 7.397

4.  Multidrug-resistant recurrent breast cancer which responded to medroxyprogesterone acetate showing a remarkable improvement in the quality of life: report of a case and the role of team medical care.

Authors:  T Kurihara; Y Higashi; K Suemasu; T Tabei; S Ishiguro; Y Iino; Y Morishita; F Takeda
Journal:  Surg Today       Date:  1998       Impact factor: 2.549

Review 5.  Pharmacological treatments for fatigue associated with palliative care.

Authors:  Martin Mücke; Henning Cuhls; Vera Peuckmann-Post; Ollie Minton; Patrick Stone; Lukas Radbruch
Journal:  Cochrane Database Syst Rev       Date:  2015-05-30

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Authors:  J H Heimdal; H J Aarstad; A Aakvaag; J Olofsson
Journal:  Eur Arch Otorhinolaryngol       Date:  1997       Impact factor: 3.236

7.  Medroxyprogesterone acetate inhibits interleukin 6 secretion from KPL-4 human breast cancer cells both in vitro and in vivo: a possible mechanism of the anticachectic effect.

Authors:  J Kurebayashi; S Yamamoto; T Otsuki; H Sonoo
Journal:  Br J Cancer       Date:  1999-02       Impact factor: 7.640

8.  Medroxyprogesterone Acetate Decreases Th1, Th17, and Increases Th22 Responses via AHR Signaling Which Could Affect Susceptibility to Infections and Inflammatory Disease.

Authors:  Marie-Pierre Piccinni; Letizia Lombardelli; Federica Logiodice; Ornela Kullolli; Enrico Maggi; Marylynn S Barkley
Journal:  Front Immunol       Date:  2019-04-03       Impact factor: 7.561

  8 in total

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