Bortezomib is a dipeptide boronic acid derivative and proteasome inhibitor used to treat multiple myeloma and mantle cell lymphoma. The 26S proteasome is a protein complex that degrades ubiquitinated proteins in the ubiquitin-proteasome pathway: reversible inhibition of the 26S proteasome, leading to cell cycle arrest and apoptosis of cancer cells, is thought to be the main mechanism of action of bortezomib. However, multiple mechanisms may be involved in the anticancer activity of bortezomib.
Bortezomib was first synthesized in 1995. In May 2003, bortezomib became the first anticancer proteasome inhibitor that was approved by the FDA under the trade name VELCADE. Phase I, II, III, and IV clinical trials are undergoing to investigate the therapeutic efficacy of bortezomib in leukemia, myasthenia gravis, systemic lupus erythematosus, rheumatoid arthritis, and solid tumours.
Bortezomib is indicated for the treatment of adults with multiple myeloma or mantle cell lymphoma.
Purchase Cancer Group - Paducah, Paducah, Kentucky, United States
MBCCOP - Meharry Medical College - Nashville, Nashville, Tennessee, United States
Baptist Regional Cancer Center at Baptist Riverside, Knoxville, Tennessee, United States
Dana-Farber Cancer Institute, Boston, Massachusetts, United States
Hæmatologisk afdeling L Amtssygehuset i Herlev, Herlev, Denmark
Medicinklin, sekt för hematologi, Norrlands Universitetssjukhus, Umeå, Sweden
University Hospital Lund, Lund, Sweden
MD Anderson Cancer Network, Houston, Texas, United States
Institut Bergonie, Bordeaux, France
CHU Dijon, Dijon, France
CHU Purpan, Toulouse, France
Thomas Jefferson University, Philadelphia, Pennsylvania, United States
Stay informed with timely notifications on clinical trials, regulatory changes, and research advancements related to this medication.