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Assistant Professor of Pharmacy Practice Oncology, School of Pharmacy, Texas Tech Health Sciences Center, Lubbock, TX
Pharmacy Practice Resident, School of Pharmacy, Texas Tech Health Sciences Center
Reprints: Brad L Stanford PharmD BCOP, School of Pharmacy, Texas Tech Health Sciences Center, 3601 4th St., MS 8162, Lubbock, TX 79430-8162, FAX 806/743-4209, brad.stanford{at}ttuhsc.edu
OBJECTIVE: To review the pharmacology, pharmacokinetics, and place of bortezomib in the therapy of multiple myeloma (MM).
DATA SOURCES: A MEDLINE search was conducted (1985May 2003). Meeting abstracts, bibliographies from identified articles, and the package insert were also used. Search terms were bortezomib, multiple myeloma, Velcade, PS-341, LDP-341, MLNM341, and proteasome inhibitor.
STUDY SELECTION AND DATA EXTRACTION: All published information relevant to the clinical activity of bortezomib in MM was considered. All human clinical studies, with an emphasis on Phase II trials, were selected.
DATA SYNTHESIS: Current therapy for MM yields significant, although temporary, responses. Bortezomib is a novel anticancer agent with significant activity in relapsed and refractory MM.
CONCLUSIONS: Although the clinical trial data are incomplete, bortezomib offers a novel therapeutic modality for patients with MM who would otherwise have few options.
Key Words: bortezomib, LDP-341, MLNM341, multiple myeloma, proteasome inhibitor, PS-341, Velcade
Published Online, October 29, 2003. www.theannals.com, DOI 10.1345/aph.1D262
THIS ARTICLE IS APPROVED FOR CONTINUING EDUCATION CREDIT
ACPE
UNIVERSAL PROGRAM NUMBER: 407-000-03-038-H01
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