Literature DB >> 15701884

Endocrine therapy trials of aromatase inhibitors for breast cancer in the adjuvant and prevention settings.

James N Ingle1.   

Abstract

The recent past has witnessed the appearance of substantial data relating to endocrine therapy of breast cancer. In the adjuvant therapy setting in early breast cancer, several large, well-conducted, randomized, double-blind clinical trials have provided evidence for the value of the third-generation aromatase inhibitors (AI) anastrozole, exemestane, and letrozole. The three major studies to date [i.e., Arimidex, tamoxifen alone, or in combination (ATAC), International Exemestane Study (IES), and letrozole after 5 years of tamoxifen (MA.17)] evaluated three different populations of women from the standpoints of duration of prior tamoxifen and thus time since the treatment of the primary breast cancer. A consistent pattern of improvement in disease-free survival was seen whether the control arm was tamoxifen (ATAC and IES) or placebo following tamoxifen (MA.17). From a toxicity standpoint, the major findings with the AIs were a decreased incidence of thromboembolic events and endometrial cancers but an increase in musculoskeletal complaints and potential for decreasing bone density. The last issue should be clarified with ongoing studies addressing the impact of the three AIs on bone density and fractures. In summary, based on ATAC, IES, and MA.17, respectively, the following conclusions can be drawn relating to postmenopausal women with hormone receptor positive early breast cancer: anastrozole is a reasonable choice for initial endocrine adjuvant therapy, exemestane should be considered for women who have received 2 to 3 years of tamoxifen, and letrozole should be considered for those who have completed about 5 years of tamoxifen. In the prevention setting, tamoxifen has been evaluated in multiple trials involving >28,000 women and, despite clear evidence of benefit, the level of acceptance of this agent by women seems to be low. Two recently developed prevention trials, IBIS 2 and MAP.3, involve the study of aromatase inhibitors against a placebo control rather than tamoxifen. Whereas the recent adjuvant trials have established the value of the third-generation aromatase inhibitors in early-stage breast cancer, the marked reductions in contralateral breast cancers seen in these trials suggest they will be of value in the prevention setting in women at increased risk of developing the disease.

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Year:  2005        PMID: 15701884

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  9 in total

1.  Circadian and melatonin disruption by exposure to light at night drives intrinsic resistance to tamoxifen therapy in breast cancer.

Authors:  Robert T Dauchy; Shulin Xiang; Lulu Mao; Samantha Brimer; Melissa A Wren; Lin Yuan; Muralidharan Anbalagan; Adam Hauch; Tripp Frasch; Brian G Rowan; David E Blask; Steven M Hill
Journal:  Cancer Res       Date:  2014-08-01       Impact factor: 12.701

2.  Variation in anastrozole metabolism and pharmacodynamics in women with early breast cancer.

Authors:  James N Ingle; Aman U Buzdar; Daniel J Schaid; Matthew P Goetz; Anthony Batzler; Mark E Robson; Donald W Northfelt; Janet E Olson; Edith A Perez; Zeruesenay Desta; Randy A Weintraub; Clark V Williard; David A Flockhart; Richard M Weinshilboum
Journal:  Cancer Res       Date:  2010-03-30       Impact factor: 12.701

Review 3.  Modulation of estrogen synthesis and metabolism by phytoestrogens in vitro and the implications for women's health.

Authors:  Majorie B M van Duursen
Journal:  Toxicol Res (Camb)       Date:  2017-09-08       Impact factor: 3.524

4.  Progesterone receptor isoform-specific promoter methylation: association of PRA promoter methylation with worse outcome in breast cancer patients.

Authors:  Thushangi N Pathiraja; Priya B Shetty; Jaroslav Jelinek; Rong He; Ryan Hartmaier; Astrid L Margossian; Susan G Hilsenbeck; Jean-Pierre J Issa; Steffi Oesterreich
Journal:  Clin Cancer Res       Date:  2011-04-01       Impact factor: 12.531

Review 5.  The NSABP Study of Tamoxifen and Raloxifene (STAR) trial.

Authors:  Victor G Vogel
Journal:  Expert Rev Anticancer Ther       Date:  2009-01       Impact factor: 4.512

6.  Functional genetic polymorphisms in the aromatase gene CYP19 vary the response of breast cancer patients to neoadjuvant therapy with aromatase inhibitors.

Authors:  Liewei Wang; Katarzyna A Ellsworth; Irene Moon; Linda L Pelleymounter; Bruce W Eckloff; Yvette N Martin; Brooke L Fridley; Gregory D Jenkins; Anthony Batzler; Vera J Suman; Saranya Ravi; J Michael Dixon; William R Miller; Eric D Wieben; Aman Buzdar; Richard M Weinshilboum; James N Ingle
Journal:  Cancer Res       Date:  2010-01-01       Impact factor: 12.701

7.  Effects of estrogen on breast cancer development: Role of estrogen receptor independent mechanisms.

Authors:  Wei Yue; Ji-Ping Wang; Yuebai Li; Ping Fan; Guijian Liu; Nan Zhang; Mark Conaway; Hongkun Wang; Kenneth S Korach; Wayne Bocchinfuso; Richard Santen
Journal:  Int J Cancer       Date:  2010-10-15       Impact factor: 7.396

8.  Pharmacogenetics and pharmacogenomics of endocrine agents for breast cancer.

Authors:  James N Ingle
Journal:  Breast Cancer Res       Date:  2008-12-18       Impact factor: 6.466

9.  Morphological and Functional Changes in Skin of Adult Male Rats Chronically Treated with Letrozole, a Nonsteroidal Inhibitor of Cytochrome P450 Aromatase.

Authors:  Kamila Misiakiewicz-Has; Alicja Zawiślak; Anna Pilutin; Agnieszka Kolasa-Wołosiuk; Paweł Szumilas; Ewa Duchnik; Barbara Wiszniewska
Journal:  Acta Histochem Cytochem       Date:  2020-09-08       Impact factor: 1.938

  9 in total

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