Novel agents in development for peripheral T-cell lymphoma
- PMID: 20359580
- DOI: 10.1053/j.seminhematol.2010.01.014
Novel agents in development for peripheral T-cell lymphoma
Abstract
Though peripheral T-cell lymphoma (PTCL) is an area of significant unmet therapeutic need, a number of new treatment options are available for patients, especially those with relapsed or refractory disease. A plethora of drugs are now in development for PTCL, but drugs that truly target novel disease biology are noticeably absent. Combinations of T-cell centric agents could produce novel platforms of therapy to replace the relatively ineffective CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone)-based regimens. Among agents with T-cell activity are the folate analog pralatrexate, histone deacetylase inhibitors (HDACi) like romidepsin, the proteasome inhibitor bortezomib, the immunomodulatory agent lenalidomide, the purine nucleoside phosphorylase (PNP) inhibitor forodesine, the nucleoside analog gemcitabine, and BH3-only mimetics like ABT-263 and ABT-737.
Copyright 2010. Published by Elsevier Inc.
Similar articles
-
Clinical trials for human T-cell lymphotropic virus type I-associated peripheral T-cell lymphoma in Japan.Semin Hematol. 2010 Apr;47 Suppl 1:S5-7. doi: 10.1053/j.seminhematol.2010.01.015. Semin Hematol. 2010. PMID: 20359583 Review.
-
Therapeutic options in relapsed or refractory peripheral T-cell lymphoma.Cancer Treat Rev. 2014 Oct;40(9):1080-8. doi: 10.1016/j.ctrv.2014.08.001. Epub 2014 Aug 24. Cancer Treat Rev. 2014. PMID: 25199959 Review.
-
Novel therapies for peripheral T-cell non-Hodgkin's lymphomas.Curr Opin Hematol. 2009 Jul;16(4):299-305. doi: 10.1097/MOH.0b013e32832ad69a. Curr Opin Hematol. 2009. PMID: 19367159 Review.
-
Relapsed refractory nodal peripheral T-cell lymphoma with follicular helper T-cell phenotype was initially resistant to pralatrexate and confirmed to be unresponsive to subsequent forodesine, but responded to re-instituted pralatrexate.J Clin Exp Hematop. 2020;60(1):26-28. doi: 10.3960/jslrt.18031. J Clin Exp Hematop. 2020. PMID: 32224563 Free PMC article. No abstract available.
-
Combined proteasome and histone deacetylase inhibition: A promising synergy for patients with relapsed/refractory multiple myeloma.Leuk Res. 2010 Sep;34(9):1111-8. doi: 10.1016/j.leukres.2010.04.001. Epub 2010 May 15. Leuk Res. 2010. PMID: 20472288 Review.
Cited by
-
Novel therapeutics for aggressive non-Hodgkin's lymphoma.J Clin Oncol. 2011 May 10;29(14):1876-84. doi: 10.1200/JCO.2010.32.7171. Epub 2011 Apr 11. J Clin Oncol. 2011. PMID: 21483007 Free PMC article. Review.
-
Antagonism of inhibitors of apoptosis proteins reveals a novel, immune response-based therapeutic approach for T-cell lymphoma.Blood Adv. 2021 Oct 26;5(20):4003-4016. doi: 10.1182/bloodadvances.2020003955. Blood Adv. 2021. PMID: 34474469 Free PMC article.
-
Noninvasive phosphorus magnetic resonance spectroscopic imaging predicts outcome to first-line chemotherapy in newly diagnosed patients with diffuse large B-cell lymphoma.Acad Radiol. 2013 Sep;20(9):1122-9. doi: 10.1016/j.acra.2013.04.013. Acad Radiol. 2013. PMID: 23931426 Free PMC article.
-
Interplay between proteasome inhibitors and NF-κB pathway in leukemia and lymphoma: a comprehensive review on challenges ahead of proteasome inhibitors.Cell Commun Signal. 2024 Feb 8;22(1):105. doi: 10.1186/s12964-023-01433-5. Cell Commun Signal. 2024. PMID: 38331801 Free PMC article. Review.
-
Update: peripheral T-cell lymphomas.Curr Hematol Malig Rep. 2011 Dec;6(4):222-30. doi: 10.1007/s11899-011-0100-3. Curr Hematol Malig Rep. 2011. PMID: 21953415 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous