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Acquired Bortezomib Resistance in Multiple Myeloma: From Mechanisms to Strategy.
- Source :
-
Current treatment options in oncology [Curr Treat Options Oncol] 2024 Nov; Vol. 25 (11), pp. 1354-1365. Date of Electronic Publication: 2024 Oct 21. - Publication Year :
- 2024
-
Abstract
- Opinion Statement: Multiple myeloma (MM) is a heterogeneous plasma cell tumor with a survival period of several months to over ten years. Despite the development of various new drugs, MM is still incurable and recurs repeatedly. Bortezomib, a landmark event in the history of MM treatment, has dramatically improved the prognosis of patients with MM. Although proteasome inhibitors (PIs) represented by bortezomib, have greatly prolonged MM survival, unfortunately, almost all MM will develop bortezomib resistance, leading to relapse with a shorter survival. It has been reported that both the tumor microenvironment and myeloma cells drive bortezomib resistance. Multiple treatment methods have been attempted to overcome bortezomib resistance, but unfortunately, there has been no breakthrough. It is believed that the key resistance mechanism has not yet been discovered. A deeper understanding of the mechanism of bortezomib resistance and strategies to overcome it can help identify key resistance mechanisms and further improve the prognosis of MM.<br /> (© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
- Subjects :
- Humans
Proteasome Inhibitors therapeutic use
Proteasome Inhibitors pharmacology
Tumor Microenvironment drug effects
Antineoplastic Combined Chemotherapy Protocols therapeutic use
Prognosis
Multiple Myeloma drug therapy
Multiple Myeloma mortality
Bortezomib therapeutic use
Bortezomib pharmacology
Drug Resistance, Neoplasm
Antineoplastic Agents therapeutic use
Antineoplastic Agents pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1534-6277
- Volume :
- 25
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Current treatment options in oncology
- Publication Type :
- Academic Journal
- Accession number :
- 39432172
- Full Text :
- https://doi.org/10.1007/s11864-024-01273-6