Fulvestrant versus anastrozole for the treatment of advanced breast carcinoma: a prospectively planned combined survival analysis of two multicenter trials.
dc.contributor.author | Howell, Anthony | |
dc.contributor.author | Pippen, John | |
dc.contributor.author | Elledge, Richard M | |
dc.contributor.author | Mauriac, Louis | |
dc.contributor.author | Vergote, Ignace | |
dc.contributor.author | Jones, Stephen E | |
dc.contributor.author | Come, Steven E | |
dc.contributor.author | Osborne, C Kent | |
dc.contributor.author | Robertson, John F R | |
dc.date.accessioned | 2009-07-22T10:32:46Z | |
dc.date.available | 2009-07-22T10:32:46Z | |
dc.date.issued | 2005-07-15 | |
dc.identifier.citation | Fulvestrant versus anastrozole for the treatment of advanced breast carcinoma: a prospectively planned combined survival analysis of two multicenter trials. 2005, 104 (2):236-9 Cancer | en |
dc.identifier.issn | 0008-543X | |
dc.identifier.pmid | 15937908 | |
dc.identifier.doi | 10.1002/cncr.21163 | |
dc.identifier.uri | http://hdl.handle.net/10541/74886 | |
dc.description.abstract | BACKGROUND: Fulvestrant is an estrogen receptor antagonist with no agonist effects. In the second-line treatment of advanced breast carcinoma, fulvestrant was shown previously to be as effective as the third-generation aromatase inhibitor, anastrozole, in terms of time to disease progression and objective response rates. The authors reported the overall survival results from these studies. METHODS: A prospectively planned, combined, overall survival analysis was performed, including data from two Phase III trials that compared the efficacy and tolerability of fulvestrant (250 mg monthly; n = 428) with anastrozole (1 mg daily; n = 423) in the treatment of postmenopausal women with advanced breast carcinoma who had disease progression after receipt of previous endocrine treatment. RESULTS: At an extended median follow-up of 27.0 months (range, 0-66.9 months), 319 (74.5%) patients in the fulvestrant group and 322 (76.1%) patients in the anastrozole group had died. Prolonged survival was observed with both drugs, with 10-20% of patients still alive > 5 years after randomization. The median overall survival was similar between treatments, being 27.4 months and 27.7 months in fulvestrant and anastrozole-treated patients, respectively (hazards ratio, 0.98; 95% confidence interval, 0.84-1.15; P = 0.809). Fulvestrant continued to be well tolerated, and was associated with a significantly lower incidence of joint disorders compared with anastrozole (P = 0.0234). CONCLUSIONS: The current analysis showed that fulvestrant was similar to anastrozole with respect to overall survival in the second-line treatment of postmenopausal women with advanced breast carcinoma. | |
dc.language.iso | en | en |
dc.subject | Breast Cancer | en |
dc.subject | Oestrogen Antagonists | en |
dc.subject.mesh | Antineoplastic Agents, Hormonal | |
dc.subject.mesh | Aromatase Inhibitors | |
dc.subject.mesh | Breast Neoplasms | |
dc.subject.mesh | Disease-Free Survival | |
dc.subject.mesh | Double-Blind Method | |
dc.subject.mesh | Estradiol | |
dc.subject.mesh | Estrogen Antagonists | |
dc.subject.mesh | Female | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Nitriles | |
dc.subject.mesh | Postmenopause | |
dc.subject.mesh | Survival Analysis | |
dc.subject.mesh | Survival Rate | |
dc.subject.mesh | Triazoles | |
dc.title | Fulvestrant versus anastrozole for the treatment of advanced breast carcinoma: a prospectively planned combined survival analysis of two multicenter trials. | en |
dc.type | Article | en |
dc.contributor.department | Department of Medical Oncology, Cancer Research UK, Christie Hospital, Manchester, United Kingdom. maria.parker@christie-tr.nwest.nhs.uk | en |
dc.identifier.journal | Cancer | en |
html.description.abstract | BACKGROUND: Fulvestrant is an estrogen receptor antagonist with no agonist effects. In the second-line treatment of advanced breast carcinoma, fulvestrant was shown previously to be as effective as the third-generation aromatase inhibitor, anastrozole, in terms of time to disease progression and objective response rates. The authors reported the overall survival results from these studies. METHODS: A prospectively planned, combined, overall survival analysis was performed, including data from two Phase III trials that compared the efficacy and tolerability of fulvestrant (250 mg monthly; n = 428) with anastrozole (1 mg daily; n = 423) in the treatment of postmenopausal women with advanced breast carcinoma who had disease progression after receipt of previous endocrine treatment. RESULTS: At an extended median follow-up of 27.0 months (range, 0-66.9 months), 319 (74.5%) patients in the fulvestrant group and 322 (76.1%) patients in the anastrozole group had died. Prolonged survival was observed with both drugs, with 10-20% of patients still alive > 5 years after randomization. The median overall survival was similar between treatments, being 27.4 months and 27.7 months in fulvestrant and anastrozole-treated patients, respectively (hazards ratio, 0.98; 95% confidence interval, 0.84-1.15; P = 0.809). Fulvestrant continued to be well tolerated, and was associated with a significantly lower incidence of joint disorders compared with anastrozole (P = 0.0234). CONCLUSIONS: The current analysis showed that fulvestrant was similar to anastrozole with respect to overall survival in the second-line treatment of postmenopausal women with advanced breast carcinoma. |