Literature DB >> 19441873

Exemestane: a review of its use in postmenopausal women with breast cancer.

Emma D Deeks1, Lesley J Scott.   

Abstract

Exemestane (Aromasin) is an orally active steroidal irreversible inactivator of the aromatase enzyme indicated as an adjuvant treatment in postmenopausal women with estrogen receptor-positive early-stage breast cancer following 2-3 years of adjuvant treatment with tamoxifen, and for the treatment of advanced breast cancer in postmenopausal women whose disease has progressed following tamoxifen or other antiestrogen therapy. Exemestane is effective for the treatment of postmenopausal women with early-stage or advanced breast cancer. In early-stage disease, switching to exemestane for 2-3 years after 2-3 years of adjuvant tamoxifen treatment was more effective in prolonging disease-free survival than continuing tamoxifen therapy, although it was not associated with an overall survival benefit, except in those with estrogen receptor-positive or unknown receptor status disease when nodal status, hormone replacement therapy (HRT) and chemotherapy use were adjusted for. Moreover, preliminary data suggest that the efficacy of exemestane is generally no different to that of tamoxifen in the primary adjuvant treatment of early-stage breast cancer, although exemestane may be better in prolonging the time to distant recurrence. In advanced disease, exemestane showed equivalent efficacy to megestrol in patients with disease refractory to tamoxifen and an efficacy not significantly different from that of fulvestrant in those refractory to a nonsteroidal aromatase inhibitor. Available data, some of which are limited, suggest exemestane is also effective in the first-line hormonal treatment of advanced breast cancer in postmenopausal women. Exemestane is generally well tolerated, although the potential bone fracture risk of the drug requires further investigation. Results from directly comparative trials indicating the efficacy, tolerability and bone fracture risk of exemestane relative to third-generation aromatase inhibitors and other agents in both early-stage and advanced disease, as well as the optimal sequence of endocrine therapies, are awaited with interest. In the meantime, switching to exemestane should be considered in postmenopausal women who have received 2-3 years of adjuvant tamoxifen treatment for early-stage breast cancer, and is an emerging treatment option for postmenopausal women with advanced breast cancer refractory to one or more antiestrogen therapies.

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Year:  2009        PMID: 19441873     DOI: 10.2165/00003495-200969070-00007

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  71 in total

1.  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.

Authors:  M Kaufmann; E Bajetta; L Y Dirix; L E Fein; S E Jones; N Zilembo; J L Dugardyn; C Nasurdi; R G Mennel; J Cervek; C Fowst; A Polli; E di Salle; A Arkhipov; G Piscitelli; L L Miller; G Massimini
Journal:  J Clin Oncol       Date:  2000-04       Impact factor: 44.544

2.  Effect of exemestane on the lipidemic profile of post-menopausal operable breast cancer patients following 5-7 years of adjuvant tamoxifen: preliminary results of the ATENA substudy.

Authors:  C Markopoulos; M Chrissochou; A Michailidou; E Tzoracoleftherakis; G Xepapadakis; J Papadiamantis; J Misitzis; V Zobolas; D Bafaloukos; H Gogas
Journal:  Anticancer Drugs       Date:  2005-09       Impact factor: 2.248

3.  Pharmacoeconomic analysis of adjuvant therapy with exemestane, anastrozole, letrozole or tamoxifen in postmenopausal women with operable and estrogen receptor-positive breast cancer.

Authors:  J M Gil; C Rubio-Terrés; A Del Castillo; P González; F Canorea
Journal:  Clin Transl Oncol       Date:  2006-05       Impact factor: 3.405

4.  High activity and tolerability demonstrated for exemestane in postmenopausal women with metastatic breast cancer who had previously failed on tamoxifen treatment.

Authors:  S Kvinnsland; G Anker; L Y Dirix; J Bonneterre; A M Prove; N Wilking; J P Lobelle; O Mariani; E di Salle; A Polli; G Massimini
Journal:  Eur J Cancer       Date:  2000-05       Impact factor: 9.162

5.  Changes in bone turnover and in bone mass in women with breast cancer switched from tamoxifen to exemestane.

Authors:  S Gonnelli; A Cadirni; C Caffarelli; R Petrioli; A Montagnani; M B Franci; B Lucani; G Francini; R Nuti
Journal:  Bone       Date:  2006-08-14       Impact factor: 4.398

Review 6.  Exemestane for breast cancer prevention: a feasible strategy?

Authors:  Per E Lønning
Journal:  Clin Cancer Res       Date:  2005-01-15       Impact factor: 12.531

7.  Anastrozole alone or in combination with tamoxifen versus tamoxifen alone for adjuvant treatment of postmenopausal women with early breast cancer: first results of the ATAC randomised trial.

Authors:  M Baum; A U Budzar; J Cuzick; J Forbes; J H Houghton; J G M Klijn; T Sahmoud
Journal:  Lancet       Date:  2002-06-22       Impact factor: 79.321

Review 8.  Update on aromatase inhibitors in breast cancer.

Authors:  Richard E Gould; Agustin A Garcia
Journal:  Curr Opin Obstet Gynecol       Date:  2006-02       Impact factor: 1.927

9.  Double-blind, randomized placebo controlled trial of fulvestrant compared with exemestane after prior nonsteroidal aromatase inhibitor therapy in postmenopausal women with hormone receptor-positive, advanced breast cancer: results from EFECT.

Authors:  Stephen Chia; William Gradishar; Louis Mauriac; Jose Bines; Frederic Amant; Miriam Federico; Luis Fein; Gilles Romieu; Aman Buzdar; John F R Robertson; Adam Brufsky; Kurt Possinger; Pamela Rennie; Francisco Sapunar; Elizabeth Lowe; Martine Piccart
Journal:  J Clin Oncol       Date:  2008-03-03       Impact factor: 44.544

10.  Management of arthralgias associated with aromatase inhibitor therapy.

Authors:  C Thorne
Journal:  Curr Oncol       Date:  2007-12       Impact factor: 3.677

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  15 in total

1.  Bilateral Optic Disc Swelling Following Anastrozole Therapy.

Authors:  Oscar Jim Michael Coppes; Rimas V Lukas; Gini F Fleming; Jeffrey Nichols; Meaghan Tenney; Jacqueline Bernard
Journal:  Neuroophthalmology       Date:  2014-09-19

Review 2.  Breast and prostate cancer: more similar than different.

Authors:  Gail P Risbridger; Ian D Davis; Stephen N Birrell; Wayne D Tilley
Journal:  Nat Rev Cancer       Date:  2010-02-11       Impact factor: 60.716

3.  Pain in long-term breast cancer survivors: frequency, severity, and impact.

Authors:  Mark P Jensen; Hao-Yuan Chang; Yeur-Hur Lai; Karen L Syrjala; Jesse R Fann; Julie R Gralow
Journal:  Pain Med       Date:  2010-06-08       Impact factor: 3.750

Review 4.  Fulvestrant: a review of its use in the management of hormone receptor-positive metastatic breast cancer in postmenopausal women.

Authors:  Jamie D Croxtall; Kate McKeage
Journal:  Drugs       Date:  2011-02-12       Impact factor: 9.546

5.  Characterization of 17-dihydroexemestane glucuronidation: potential role of the UGT2B17 deletion in exemestane pharmacogenetics.

Authors:  Dongxiao Sun; Gang Chen; Ryan W Dellinger; Arun K Sharma; Philip Lazarus
Journal:  Pharmacogenet Genomics       Date:  2010-10       Impact factor: 2.089

Review 6.  Adverse reactions to targeted and non-targeted chemotherapeutic drugs with emphasis on hypersensitivity responses and the invasive metastatic switch.

Authors:  Brian A Baldo; Nghia H Pham
Journal:  Cancer Metastasis Rev       Date:  2013-12       Impact factor: 9.264

Review 7.  Current medical treatment of estrogen receptor-positive breast cancer.

Authors:  Franco Lumachi; Davide A Santeufemia; Stefano Mm Basso
Journal:  World J Biol Chem       Date:  2015-08-26

8.  Relevance of anti-inflammatory and antioxidant activities of exemestane and synergism with sulforaphane for disease prevention.

Authors:  Hua Liu; Paul Talalay
Journal:  Proc Natl Acad Sci U S A       Date:  2013-11-04       Impact factor: 11.205

9.  Aromatase inhibitors associated musculoskeletal disorders and bone fractures in postmenopausal breast cancer patients: a result from Chinese population.

Authors:  Lu Xu; Jue Wang; Dan-Dan Xue; Wei He
Journal:  Med Oncol       Date:  2014-07-24       Impact factor: 3.064

10.  Impact of UGT2B17 Gene Deletion on the Pharmacokinetics of 17-Hydroexemestane in Healthy Volunteers.

Authors:  Shanly M Chen; Daniel H Atchley; Michael A Murphy; Bill J Gurley; Landry K Kamdem
Journal:  J Clin Pharmacol       Date:  2015-12-31       Impact factor: 3.126

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