Proteasome inhibitors in mantle cell lymphoma.

Abstract

Mantle cell lymphoma (MCL) represents a subtype of non-Hodgkin's lymphoma (NHL) which has a relatively poor prognosis compared to other forms of NHL. Despite multiple options for cytotoxic chemotherapy, attempts to prolong the survival of patients with this disease have not yet met with success. Consequently, the development of targeted approaches to therapy which minimize toxicities has potentially important implications for MCL. Proteasome inhibitors preferentially kill transformed cells through diverse mechanisms. The proteasome inhibitor bortezomib was initially approved for patients with relapsed or refractory multiple myeloma and now has been approved for relapsed or refractory MCL. The introduction of newer proteasome inhibitors with activity in bortezomib-resistant disease and reduced toxicity profiles may yield further benefits. Multiple ongoing studies are building on the known efficacy of proteasome inhibitors in MCL by evaluating combination regimens involving either cytotoxic or targeted therapies, with the ultimate goal of prolonging survival in this patient population.

• Authors: Beata Holkova, Steven Grant
• Journal: Best practice & research. Clinical haematology (Best Pract Res Clin Haematol) Vol. 25 Issue 2 Pg. 133-41 (Jun 2012) ISSN: 1532-1924 [Electronic] Netherlands
• PMID: 22687449 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Review)
• Copyright: Copyright © 2012 Elsevier Ltd. All rights reserved.

Chemical References

• Antineoplastic Agents
• Boronic Acids
• Oligopeptides
• Protease Inhibitors
• Proteasome Inhibitors
• Pyrazines
• Bortezomib
• carfilzomib

Topics

• Antineoplastic Agents (administration & dosage, therapeutic use)
• Boronic Acids (administration & dosage, therapeutic use)
• Bortezomib
• Clinical Trials as Topic
• Combined Modality Therapy
• Drug Resistance, Neoplasm
• Humans
• Lymphoma, Mantle-Cell (metabolism, mortality, therapy)
• Oligopeptides (administration & dosage, therapeutic use)
• Protease Inhibitors (administration & dosage, therapeutic use)
• Proteasome Inhibitors (administration & dosage, therapeutic use)
• Pyrazines (administration & dosage, therapeutic use)
• Recurrence
• Signal Transduction (drug effects)
• Survival Analysis