Literature DB >> 6293627

Suppression of estrogens with aminoglutethimide and hydrocortisone (medical adrenalectomy) as treatment of advanced breast carcinoma: a review.

R J Santen.   

Abstract

Fifty to sixty percent of postmenopausal women with estrogen receptor positive metastatic breast cancer respond objectively to surgical ablation of the pituitary or adrenal glands. Several investigators have recently developed medical alternatives to surgical ablative therapy for these patients. This review describes one of these strategies, the inhibition of estrogen synthesis with the enzyme inhibitor aminoglutethimide (AG). Aminoglutethimide blocks several cytochrome P-450-mediated steroid hydroxylation steps including those required for cholesterol to pregnenolone conversion and for the aromatization of androgens to estrogens. In women with metastatic carcinoma, a regimen including 1,000 mg of AG and 40 mg of hydrocortisone as replacement glucocorticoid was administered daily. Clinical studies revealed a 32% objective response rate to AG-HC in unselected patients, and a 52% response in women with estrogen receptor positive tumors. Randomized trials revealed that AG-HC produced objective regression as frequently as surgical adrenalectomy (Ag-HC + 53% vs. surgical adrenalectomy (43%, p = NS), and as surgical hypophysectomy (AG-HC 47% vs. hypox 21%, p + NS). Comparison of AG-HC administration with antiestrogen treatment suggested an equal rate of response to either therapy. Preliminary data document responses to AG in antiestrogen-resistant patients. Current studies do not allow precise recommendations regarding the sequence of use of antiestrogens and AG-HC.

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Year:  1981        PMID: 6293627     DOI: 10.1007/bf01806259

Source DB:  PubMed          Journal:  Breast Cancer Res Treat        ISSN: 0167-6806            Impact factor:   4.872


  53 in total

1.  Compensatory increase in TSH secretion without effect on prolactin secretion in patients treated with aminoglutethimide.

Authors:  R J Santen; S A Wells; N Cohn; L M Demers; R I Misbin; E L Foltz
Journal:  J Clin Endocrinol Metab       Date:  1977-10       Impact factor: 5.958

2.  Ovarian dysfunction associated with an anticonvulsant drug.

Authors:  R Cash; M A Petrini; A J Brough
Journal:  JAMA       Date:  1969-05-19       Impact factor: 56.272

3.  Aminoglutethimide and advanced breast cancer [proceedings].

Authors:  R C Mason; U Chetty; W R Miller; R A Hawkins; A P Forrest
Journal:  Biochem Soc Trans       Date:  1980-06       Impact factor: 5.407

4.  Medical adrenalectomy with aminoglutethimide: clinical studies in postmenopausal patients with metastatic breast carcinoma.

Authors:  S A Wells; R J Santen; A Lipton; D E Haagensen; E J Ruby; H Harvey; W G Dilley
Journal:  Ann Surg       Date:  1978-05       Impact factor: 12.969

5.  24-Hour secretory pattern of dehydroisoandrosterone and dehydroisoandrosterone sulfate.

Authors:  R S Rosenfeld; B J Rosenberg; D K Fukushima; L Hellman
Journal:  J Clin Endocrinol Metab       Date:  1975-05       Impact factor: 5.958

6.  Aromatization of androstenedione by isolated human hairs.

Authors:  H U Schweikert; L Milewich; J D Wilson
Journal:  J Clin Endocrinol Metab       Date:  1975-03       Impact factor: 5.958

Review 7.  Current status of estrogen and progesterone receptors in breast cancer.

Authors:  W L McGuire; K B Horwitz; O H Pearson; A Segaloff
Journal:  Cancer       Date:  1977-06       Impact factor: 6.860

8.  Serum aminoglutethimide levels: studies of serum half-life, clearance, and patient compliance.

Authors:  F T Murray; S Santner; E Samojlik; R J Santen
Journal:  J Clin Pharmacol       Date:  1979 Nov-Dec       Impact factor: 3.126

9.  A randomized trial comparing surgical adrenalectomy with aminoglutethimide plus hydrocortisone in women with advanced breast cancer.

Authors:  R J Santen; T J Worgul; E Samojlik; A Interrante; A E Boucher; A Lipton; H A Harvey; D S White; E Smart; C Cox; S A Wells
Journal:  N Engl J Med       Date:  1981-09-03       Impact factor: 91.245

10.  Medical adrenalectomy and plasma steroids in advanced breast carcinoma.

Authors:  H H Newsome; P W Brown; J J Terz; W Lawrence
Journal:  Surgery       Date:  1978-01       Impact factor: 3.982

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  7 in total

1.  Aromatase inhibition causes increased amplitude, but not frequency, of hypothalamic-pituitary output in normal women.

Authors:  Alexander Kucherov; Alex J Polotsky; Marie Menke; Barbara Isaac; Beth McAvey; Erkan Buyuk; Andrew P Bradford; Cheryl Hickmon; Beatrice Babbs; Sarah Berga; Tammy Loucks; Nanette Santoro
Journal:  Fertil Steril       Date:  2011-02-26       Impact factor: 7.329

Review 2.  Mechanisms of action of aminoglutethimide as endocrine therapy of breast cancer.

Authors:  P E Lønning; S Kvinnsland
Journal:  Drugs       Date:  1988-06       Impact factor: 9.546

3.  Aminoglutethimide treatment in advanced breast cancer: an efficient therapy as a late endocrine alternative in a sequential therapeutic approach.

Authors:  S Kvinnsland; O Dahl
Journal:  Breast Cancer Res Treat       Date:  1983       Impact factor: 4.872

Review 4.  Aromatase expression and regulation in breast and endometrial cancer.

Authors:  Hong Zhao; Ling Zhou; Anna Junjie Shangguan; Serdar E Bulun
Journal:  J Mol Endocrinol       Date:  2016-04-11       Impact factor: 5.098

Review 5.  New experimental models for aromatase inhibitor resistance.

Authors:  Shiuan Chen; Selma Masri; Yanyan Hong; Xin Wang; Sheryl Phung; Yate-Ching Yuan; Xiwei Wu
Journal:  J Steroid Biochem Mol Biol       Date:  2007-05-24       Impact factor: 4.292

6.  Alterations in the metabolism of oestrogens during treatment with aminoglutethimide in breast cancer patients. Preliminary findings.

Authors:  P E Lønning; S Kvinnsland; T Thorsen; P M Ueland
Journal:  Clin Pharmacokinet       Date:  1987-12       Impact factor: 6.447

Review 7.  Aromatase inhibition 2013: clinical state of the art and questions that remain to be solved.

Authors:  Per Eystein Lønning; Hans Petter Eikesdal
Journal:  Endocr Relat Cancer       Date:  2013-06-24       Impact factor: 5.678

  7 in total

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