Phase II, randomized, double-blind study of two dose levels of arzoxifene in patients with locally advanced or metastatic breast cancer Journal Article


Authors: Buzdar, A.; O'Shaughnessy, J. A.; Booser, D. J.; Pippen, J. E. Jr; Jones, S. E.; Munster, P. N.; Peterson, P.; Melemed, A. S.; Winer, E.; Hudis, C.
Article Title: Phase II, randomized, double-blind study of two dose levels of arzoxifene in patients with locally advanced or metastatic breast cancer
Abstract: Purpose: To select a daily dose of arzoxifene (LY353381), a selective estrogen receptor modulator, for use in future studies in women with locally advanced or metastatic breast cancer who are either potentially tamoxifen sensitive (TS) or tamoxifen refractory (TR). Patients and Methods: This trial was a randomized, double-blind, phase II study of arzoxifene 20 mg (n = 55) and 50 mg (n = 57) in women with advanced or metastatic breast cancer. Patients were randomly assigned to balance for number of metastatic disease sites, prior tamoxifen therapy, and estrogen receptor status. The primary end point was tumor response rate (RR). Secondary end points included clinical benefit rate (CBR), time to progression (TTP), and toxicity. Results: Forty-nine patients were TS and 63 were TR. According to independent review, among TS patients, RR was higher in the 20-mg arm than the 50-mg arm (26.1% v 8.0%), with a longer TTP (8.3 v 3.2 months; P > .05). Among the TR patients, response rate was the same in the 20-mg and 50-mg arms (10.3%) with similar TTP (2.7 and 2.8 months, respectively; P > .05). CBR was higher in the 20-mg arm than in the 50-mg arm among TS patients (39.1% v 20.0%) and TR patients (13.8% v 10.3%). Arzoxifene was well tolerated. Dose-dependent toxicity was not demonstrated. There were no deaths during study. Conclusion: Arzoxifene is effective in the treatment of TS and TR patients with advanced or metastatic breast cancer at the 20-mg and 50-mg dose levels. Toxicities are minimal, and the therapy is tolerated. The 20-mg dose seems to be at least as effective as the 50-mg dose. Accordingly, arzoxifene 20 mg/d was selected for further study in patients with breast cancer. © 2003 by American Society of Clinical Oncology.
Keywords: survival; adult; controlled study; treatment outcome; aged; aged, 80 and over; middle aged; survival analysis; major clinical study; clinical trial; drug tolerability; dose response; drug dose comparison; patient selection; unspecified side effect; metastasis; controlled clinical trial; phase 2 clinical trial; breast cancer; randomized controlled trial; drug administration schedule; tumor markers, biological; drug effect; drug resistance; pathology; dose-response relationship, drug; drug resistance, neoplasm; breast neoplasms; tumor marker; blood; chemistry; breast tumor; tamoxifen; receptors, estrogen; piperidines; antineoplastic agents, hormonal; drug administration; estrogen receptor; double blind procedure; double-blind method; antineoplastic hormone agonists and antagonists; endometrium; piperidine derivative; thiophene derivative; thiophenes; selective estrogen receptor modulator; estrogen receptor modulators; arzoxifene; humans; human; female; priority journal; article
Journal Title: Journal of Clinical Oncology
Volume: 21
Issue: 6
ISSN: 0732-183X
Publisher: American Society of Clinical Oncology  
Date Published: 2003-03-15
Start Page: 1007
End Page: 1014
Language: English
DOI: 10.1200/jco.2003.06.108
PUBMED: 12637464
PROVIDER: scopus
DOI/URL:
Notes: Export Date: 12 September 2014 -- Source: Scopus
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  1. Clifford Hudis
    905 Hudis
  2. Pamela Munster
    30 Munster