Literature DB >> 12038879

Aromatase inhibitors and inactivators for breast cancer therapy.

Per E Lønning1.   

Abstract

Aromatase inhibitors and inactivators are increasingly important to the therapy of advanced breast cancer in postmenopausal women. These compounds are also currently being evaluated in the adjuvant setting and may have potential in breast cancer prevention. In addition to the recent clinical results, experimental research with development of aromatase 'knockout' mice as well as certain clinical observations in individuals lacking this enzyme have deepened our understanding of estrogens outside of the field of reproduction. Such information should help us to further develop this type of therapy in breast cancer and, in particular, extend our understanding of the lack of complete cross-resistance between aromatase inhibitors and inactivators. Clinically, third-generation aromatase inhibitors and inactivators have shown superiority compared with conventional treatment in advanced postmenopausal breast cancer with respect to second-line (tamoxifen failures) as well as first-line therapy. The fact that tamoxifen is noncurative in metastatic disease but improves long-term survival in the adjuvant setting suggests that even modest improvements in therapy of advanced disease may be translated into survival benefits in patients with early disease. In addition, these novel compounds with lack of complete cross-resistance extend the scope of using sequential treatment options to maximise the duration of optimal endocrine therapy in metastatic breast cancer disease.

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Year:  2002        PMID: 12038879     DOI: 10.2165/00002512-200219040-00003

Source DB:  PubMed          Journal:  Drugs Aging        ISSN: 1170-229X            Impact factor:   3.923


  202 in total

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Authors:  J Geisler; S Detre; H Berntsen; L Ottestad; B Lindtjørn; M Dowsett; P Einstein Lønning
Journal:  Clin Cancer Res       Date:  2001-05       Impact factor: 12.531

2.  Dose-related endocrine effects and pharmacokinetics of oral and intramuscular 4-hydroxyandrostenedione in postmenopausal breast cancer patients.

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Journal:  Cancer Res       Date:  1989-03-01       Impact factor: 12.701

3.  Exemestane is superior to megestrol acetate after tamoxifen failure in postmenopausal women with advanced breast cancer: results of a phase III randomized double-blind trial. The Exemestane Study Group.

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Journal:  J Clin Oncol       Date:  2000-04       Impact factor: 44.544

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Journal:  J Steroid Biochem       Date:  1977-08       Impact factor: 4.292

5.  Impact of tamoxifen on the pharmacokinetics and endocrine effects of the aromatase inhibitor letrozole in postmenopausal women with breast cancer.

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Journal:  Clin Cancer Res       Date:  1999-09       Impact factor: 12.531

6.  Anastrozole versus tamoxifen as first-line therapy for advanced breast cancer in 668 postmenopausal women: results of the Tamoxifen or Arimidex Randomized Group Efficacy and Tolerability study.

Authors:  J Bonneterre; B Thürlimann; J F Robertson; M Krzakowski; L Mauriac; P Koralewski; I Vergote; A Webster; M Steinberg; M von Euler
Journal:  J Clin Oncol       Date:  2000-11-15       Impact factor: 44.544

Review 7.  Progestins in breast cancer treatment. A review.

Authors:  S Lundgren
Journal:  Acta Oncol       Date:  1992       Impact factor: 4.089

8.  Control of aromatase activity in breast cancer cells: the role of cytokines and growth factors.

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Journal:  J Steroid Biochem Mol Biol       Date:  1993-03       Impact factor: 4.292

9.  Effect of tamoxifen on bone mineral density measured by dual-energy x-ray absorptiometry in healthy premenopausal and postmenopausal women.

Authors:  T J Powles; T Hickish; J A Kanis; A Tidy; S Ashley
Journal:  J Clin Oncol       Date:  1996-01       Impact factor: 44.544

10.  A link between breast cancer and local estrogen biosynthesis suggested by quantification of breast adipose tissue aromatase cytochrome P450 transcripts using competitive polymerase chain reaction after reverse transcription.

Authors:  S E Bulun; T M Price; J Aitken; M S Mahendroo; E R Simpson
Journal:  J Clin Endocrinol Metab       Date:  1993-12       Impact factor: 5.958

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  3 in total

Review 1.  Clinical pharmacokinetics of aromatase inhibitors and inactivators.

Authors:  Per Lønning
Journal:  Clin Pharmacokinet       Date:  2003       Impact factor: 6.447

Review 2.  Breast cancer management: quality-of-life and cost considerations.

Authors:  Davide Radice; Alberto Redaelli
Journal:  Pharmacoeconomics       Date:  2003       Impact factor: 4.981

3.  The Lineage Determining Factor GRHL2 Collaborates with FOXA1 to Establish a Targetable Pathway in Endocrine Therapy-Resistant Breast Cancer.

Authors:  Kimberly J Cocce; Jeff S Jasper; Taylor K Desautels; Logan Everett; Suzanne Wardell; Thomas Westerling; Robert Baldi; Tricia M Wright; Kendall Tavares; Alex Yllanes; Yeeun Bae; Jeremy T Blitzer; Craig Logsdon; Daniel P Rakiec; David A Ruddy; Tiancong Jiang; Gloria Broadwater; Terry Hyslop; Allison Hall; Muriel Laine; Linda Phung; Geoffrey L Greene; Lesley-Ann Martin; Sunil Pancholi; Mitch Dowsett; Simone Detre; Jeffrey R Marks; Gregory E Crawford; Myles Brown; John D Norris; Ching-Yi Chang; Donald P McDonnell
Journal:  Cell Rep       Date:  2019-10-22       Impact factor: 9.423

  3 in total

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