scispace - formally typeset
Journal ArticleDOI

Fulvestrant ('Faslodex')--a new treatment option for patients progressing on prior endocrine therapy.

C Morris, +1 more
- 01 Dec 2002 - 
- Vol. 9, Iss: 4, pp 267-276
Reads0
Chats0
TLDR
Fulvestrant has recently gained US Food and Drug Administration approval for the treatment of hormone receptor-positive metastatic breast cancer in postmenopausal women with disease progression following antiestrogen therapy and these new hormonal treatments expand the choice of endocrine therapy for women with advanced breast cancer.
Abstract
Since its introduction more than 30 years ago, tamoxifen has been the most widely used endocrine therapy for the treatment of women with advanced breast cancer. More recently, a number of alternative endocrine treatments have been developed, including several selective estrogen receptor modulators (SERMs), aromatase inhibitors (AIs) and, most recently, fulvestrant ('Faslodex'). Fulvestrant is an estrogen receptor (ER) antagonist, which, unlike the SERMs, has no known agonist (estrogenic) effect and downregulates the ER protein. Tamoxifen is effective and well tolerated, although the non-steroidal AIs, anastrozole and letrozole, are more effective treatments for advanced disease than tamoxifen. Fulvestrant has recently gained US Food and Drug Administration approval for the treatment of hormone receptor-positive metastatic breast cancer in postmenopausal women with disease progression following antiestrogen therapy. In two global phase III clinical trials fulvestrant was at least as effective and as equally well tolerated as anastrozole for the treatment of postmenopausal women with advanced and metastatic breast cancer. In a retrospective analysis of the combined data from these trials, mean duration of response was significantly greater for fulvestrant compared with anastrozole. These new hormonal treatments expand the choice of endocrine therapy for women with advanced breast cancer and offer new options for sequencing and combining treatments.

read more

Content maybe subject to copyright    Report

Citations
More filters
Journal ArticleDOI

Novel Biphenyl Amines Inhibit Oestrogen Receptor (ER)-α in ER-Positive Mammary Carcinoma Cells.

TL;DR: In this paper, the activity of adamantanyl-tethered-biphenyl amines (AMTA) as oestrogen receptor alpha (ERα) modulating ligands is reported.
Journal ArticleDOI

Effect of Berry Extracts and Bioactive Compounds on Fulvestrant (ICI 182,780) Sensitive and Resistant Cell Lines

TL;DR: In this paper, two berry extracts (Jamun-EJAE and red raspberry-RRE) and their bioactive compounds (Delphinidin-Del and Ellagic acid-EA) were tested to inhibit cell proliferation with or without a sub-lethal dose of ICI in various breast cancer cell lines.
Journal ArticleDOI

Reproductive expression dynamics and comparative toxicological perspective of beta estrogen receptor gene in the male wall lizard, Podarcis sicula Rafinesque, 1810 (Chordata: Reptilia)

TL;DR: The potential use of Podarcis sicula as a model for human testis development and maturation is explored, as well as esr2 expression for toxicological screening in one-testis gonadectomy is explored.
Journal ArticleDOI

The fight against tamoxifen resistance in breast cancer therapy: a new target in the battle?

TL;DR: It is now clear that aromatase inhibitors are the preferred first line therapy for all stages of breast cancer in post-menopausal women, whether they have had previous tamoxifen exposure or resistance.
Patent

Detection of esr1 amplification in breast cancer

TL;DR: In this paper, an in-vitro method of identifying a tumor resulting from a proliferative breast disease as responsive to anti-estrogen treatment is proposed. But the method is not suitable for the case of non-cancerous individuals.
References
More filters
Journal ArticleDOI

The Functional Assessment of Cancer Therapy scale: development and validation of the general measure.

TL;DR: The FACT-G meets or exceeds all requirements for use in oncology clinical trials, including ease of administration, brevity, reliability, validity, and responsiveness to clinical change.
Journal ArticleDOI

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.

TL;DR: Anastrozole is an effective and well tolerated endocrine option for the treatment of postmenopausal patients with hormone-sensitive early breast cancer and longer follow-up is required before a final benefit:risk assessment can be made.
Journal Article

A potent specific pure antiestrogen with clinical potential.

TL;DR: The properties of ICI 182,780 identify this pure antiestrogen as a prime candidate with which to evaluate the potential therapeutic benefits of complete estrogen withdrawal in endocrine-responsive human breast cancer.
Journal ArticleDOI

Endometrial Cancer in Tamoxifen-Treated Breast Cancer Patients: Findings From the National Surgical Adjuvant Breast and Bowel Project (NSABP) B-14

TL;DR: Risk of endometrial cancer increases following tamoxifen therapy for invasive breast cancer; however, net benefit greatly outweighs risk, and tamoxIFen treatment for breast cancer should continue.
Related Papers (5)