Abstract
Introduction of the proteasome inhibitor bortezomib (Velcade, Millennium Pharmaceuticals, The Takeda Oncology Company, Cambridge, MA) has substantially improved outcomes for patients with multiple myeloma (MM), and has become one of the cornerstones of current anti-myeloma treatment regimens. However, with the introduction of bortezomib it has become clear that peripheral neuropathy (PN) is one of the most frequent, potentially disabling, nonhematologic complications of bortezomib, often requiring dose modification or discontinuation, with a potential negative impact on clinical endpoints and quality of life. To find a balance between maximal benefit of bortezomib treatment, while maintaining quality of life, it is necessary to minimize toxicity. Here, we discuss all aspects of bortezomib-induced peripheral neuropathy (BiPN), and elaborate on the mechanisms underlying the development of BiPN. Semin Hematol 49:249-257. (C) 2012 Elsevier Inc. All rights reserved.
Original language | Undefined/Unknown |
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Pages (from-to) | 249-257 |
Number of pages | 9 |
Journal | Seminars in Hematology |
Volume | 49 |
Issue number | 3 |
DOIs | |
Publication status | Published - 2012 |
Research programs
- EMC MM-02-41-03
- EMC MM-03-44-06
- EMC OR-01-86-13