Literature DB >> 3285486

Studies of high-dose megestrol acetate: potential applications in cachexia.

J Aisner1, N S Tchekmedyian, N Tait, H Parnes, M Novak.   

Abstract

Cachexia can be a severe problem in the management of patients with cancer and other illnesses because it produces an ever-increasing spiral of anorexia, undernutrition, loss of tissue mass, muscle wasting, and increased susceptibility to infection and treatment toxicity. Megestrol acetate has been observed to produce weight gain in patients with hormone-sensitive tumors and has recently been noted to produce a similar degree of weight gain in those with hormone insensitive tumors. A review of our experience in a phase I-II study of escalating doses of megestrol acetate for advanced breast cancer revealed that weight gain occurred in more than 80% of all treated patients and in 90% of those patients who received treatment for 6 or more weeks. The median maximum weight gain was 5.5 kg, with a range of -5.6 to 44 kg. Subjective improvement in appetite occurred in most patients. These data provided the impetus for a series of further studies of the role of megestrol acetate in the control of cachexia, including a randomized study in cancer cachexia, AIDS cachexia, and anorexia nervosa. In addition, a number of laboratory trials seeking the mechanism of action have been initiated, as well as whole-animal studies to define the compartment of increased weight. Our data and the preliminary observation of weight gain in patients with hormone insensitive tumors suggest that megestrol acetate has a potential role in producing a possibly dose-related subjective improvement and an increase in appetite and weight. Further research is necessary to understand the mechanism of appetite stimulation and anabolic effect.

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Year:  1988        PMID: 3285486

Source DB:  PubMed          Journal:  Semin Oncol        ISSN: 0093-7754            Impact factor:   4.929


  8 in total

1.  Pharmacological interference with tissue hypercatabolism in tumour-bearing rats.

Authors:  L Tessitore; P Costelli; F M Baccino
Journal:  Biochem J       Date:  1994-04-01       Impact factor: 3.857

Review 2.  Pharmacologic circumvention of multidrug resistance.

Authors:  J M Ford; W N Hait
Journal:  Cytotechnology       Date:  1993       Impact factor: 2.058

3.  Megestrol acetate reverses multidrug resistance and interacts with P-glycoprotein.

Authors:  G F Fleming; J M Amato; M Agresti; A R Safa
Journal:  Cancer Chemother Pharmacol       Date:  1992       Impact factor: 3.333

Review 4.  Nutritional and anti-inflammatory interventions in chronic heart failure.

Authors:  Kamyar Kalantar-Zadeh; Stefan D Anker; Tamara B Horwich; Gregg C Fonarow
Journal:  Am J Cardiol       Date:  2008-06-02       Impact factor: 2.778

Review 5.  Cancer cachexia.

Authors:  M J Tisdale
Journal:  Br J Cancer       Date:  1991-03       Impact factor: 7.640

6.  Effect of megestrol acetate on weight loss induced by tumour necrosis factor alpha and a cachexia-inducing tumour (MAC16) in NMRI mice.

Authors:  S A Beck; M J Tisdale
Journal:  Br J Cancer       Date:  1990-09       Impact factor: 7.640

7.  Alterations in serum lipolytic activity of cancer patients with response to therapy.

Authors:  S A Beck; P Groundwater; C Barton; M J Tisdale
Journal:  Br J Cancer       Date:  1990-11       Impact factor: 7.640

8.  Reversal effects of nomegestrol acetate on multidrug resistance in adriamycin-resistant MCF7 breast cancer cell line.

Authors:  J Li; L Z Xu; K L He; W J Guo; Y H Zheng; P Xia; Y Chen
Journal:  Breast Cancer Res       Date:  2001-04-02       Impact factor: 6.466

  8 in total

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