Novel treatment strategies for patients with relapsed classical Hodgkin lymphoma
- PMID: 20828898
- PMCID: PMC3181220
- DOI: 10.1016/j.blre.2010.08.003
Novel treatment strategies for patients with relapsed classical Hodgkin lymphoma
Abstract
The treatment of patients with relapsed and refractory Hodgkin lymphoma (HL), especially those who relapse after autologous stem cell transplantation, remains challenging. Patients with HL whose disease relapses after stem cell transplantation are rarely cured with current treatment modalities, and have a median survival of less than 3 years. Since no new drugs have been approved by the FDA for HL in more than three decades, there is a clear unmet medical need for drug development for this patient population. New treatment strategies that are based on targeting oncogenic signaling pathways are currently explored. This review will focus on emerging new treatment modalities that are currently under investigation for patients with relapsed classical HL.
Copyright © 2010 Elsevier Ltd. All rights reserved.
Conflict of interest statement
Conflict of interest statement
A. Younes declares the following conflicts of interest:
Research funding and honoraria from Genetech.
Research funding and honoraria from SBIO.
Research funding and honoraria from Novartis.
Research funding and honoraria from Seattle Genetics.
A. Jona has no conflicts of interest to declare.
References
-
- Jemal A, Siegel R, Ward E, Hao Y, Xu J, Thun MJ. Cancer Statistics, 2009. CA Cancer J Clin. 2009;59:225–249. - PubMed
-
- Horning S, Fanale MSd. Defining a population of Hodgkin lymphoma patients for novel therapeutics: an international effort [abstract] Ann Oncol. 2008;20:118.
-
- Buglio D, Georgakis G, A Y. Novel small-molecule therapy of Hodgkin lymphoma. Expert Rev Anticancer Ther. 2007;7:735–740. - PubMed
-
- Kuppers R. The biology of Hodgkin’s lymphoma. Nat Rev Cancer. 2009;9:15–17. - PubMed
-
- Younes A, Carbone A. CD30/CD30 ligand and CD40/ CD40 ligand in malignant lymphoid disorders. Int J Biol Markers. 1999;14:135–143. - PubMed
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