Literature DB >> 2259928

Weight changes in women with metastatic breast cancer treated with megestrol acetate: a comparison of standard versus high-dose therapy.

J M Cruz1, H B Muss, J K Brockschmidt, G W Evans.   

Abstract

One hundred seventy-two patients with advanced breast cancer were randomized to receive 160 or 800 mg megestrol acetate per day. Patients were monitored monthly for weight, blood pressure, performance status, edema, measurement of clinically evident lesions, and toxicities. Pretreatment characteristics were similar in both arms. Weight gain was the most commonly seen side effect, with 52% of patients gaining in excess of 10 lb and 28% gaining more than 20 lb. Median weight gain for standard-dose treatment was 5 lb compared with 18 lb for high-dose treatment. There was no dose modification for excessive weight gain in any of the patients receiving the standard dose but doses were modified in 15% of those receiving high-dose megestrol acetate. Weight gains for both groups were analyzed at 30, 90, and 180 days after study entry. Treatment arm, age, prior therapy, response to prior endocrine therapy, race, performance status, dominant disease site, and number of disease sites were included in the analysis. At 30 days, patients taking high-dose megestrol acetate had a mean weight gain of 2.5 lb whereas patients taking the standard dose had stable weights. Factors predictive of weight gain were younger age (P = .0012) and fewer disease sites (P = .017). At 90 and 180 days, patients taking high-dose megestrol acetate had consistently gained more weight than those taking the standard dose (9.0 and 16.0 lb v 2.5 and 9.0 lb, respectively). Significant covariables were treatment arm (P = .0006) and younger age (P = .0211). Probability of gaining 20 lb was dependent only on treatment dose (P = .0002), and median time to a 20-lb weight gain was 217 days. Increases in systolic and diastolic blood pressures were seen in both groups, but the differences were not significant. Megestrol acetate is associated with weight gain in women with advanced breast cancer, and the amount of weight gained correlates directly with dose of megestrol acetate, length of treatment, and age of patient.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2259928

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


  6 in total

Review 1.  A review of the drug treatment of cachexia associated with cancer.

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

Review 2.  Comprehensive pharmacology and clinical efficacy of aromatase inhibitors.

Authors:  V C Njar; A M Brodie
Journal:  Drugs       Date:  1999-08       Impact factor: 9.546

Review 3.  Is the pharmacological treatment of cancer cachexia possible?

Authors:  E Bruera
Journal:  Support Care Cancer       Date:  1993-11       Impact factor: 3.603

Review 4.  Anorexia: aetiology, epidemiology and management in older people.

Authors:  David R Thomas
Journal:  Drugs Aging       Date:  2009       Impact factor: 3.923

5.  Pharmacokinetic evaluation of two different formulations of megestrol acetate in patients with advanced malignancies.

Authors:  C M Camaggi; E Strocchi; A Martoni; C Zamagni; N Cacciari; G Robustelli della Cuna; L Pavesi; M Tedeschi; A Silva; F Pannuti
Journal:  Cancer Chemother Pharmacol       Date:  1995       Impact factor: 3.333

6.  Pharmacokinetics, pharmacological and anti-tumour effects of the specific anti-oestrogen ICI 182780 in women with advanced breast cancer.

Authors:  A Howell; D J DeFriend; J F Robertson; R W Blamey; L Anderson; E Anderson; F A Sutcliffe; P Walton
Journal:  Br J Cancer       Date:  1996-07       Impact factor: 7.640

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.