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Blood, 15 June 2005, Vol. 105, No. 12, pp. 4553-4560.
Prepublished online as a Blood First Edition Paper on February 22, 2005; DOI 10.1182/blood-2004-12-4750.


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Submitted December 14, 2004
Accepted February 11, 2005

From Hodgkin's disease to Hodgkin lymphoma: biological insights and therapeutic potential

Daniel Re*, Roman K Thomas, Karolin Behringer, and Volker Diehl

Department I of Internal Medicine, University of Cologne, Cologne, Germany; The Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany; John Reed Laboratory, The Burnham Institute, La Jolla, CA, USA
Department I of Internal Medicine, University of Cologne, Cologne, Germany; The Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany; Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA
Department I of Internal Medicine, University of Cologne, Cologne, Germany
Department I of Internal Medicine, University of Cologne, Cologne, Germany; The Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany

* Corresponding author; email: dre{at}burnham.org.

Reclassification of Hodgkin's disease as Hodgkin's Lymphoma (HL) represents a milestone in the lymphoma field awarding recent insights in the molecular biology of Hodgkin and Reed-Sternberg (H-RS) cells and their environment. This review summarizes antiapoptotic and proproliferative pathways involved in the pathogenesis of this disease with the ultimate goal of translating laboratory knowledge into clinical decision making. The focus is on potential targets and novel drugs, which are discussed in the context of the complex biology of HL. Considering that HL patients are more likely to die from acute and late toxicities than from HL itself, the introduction of targeted, biologically based therapies for HL patients with palliative and eventually curative intention might be justified.


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