Korean J Hematol.  2012 Mar;47(1):8-16. 10.5045/kjh.2012.47.1.8.

Treatment strategies for Hodgkin lymphoma recurring following autologous hematopoietic stem cell transplantation

Affiliations
  • 1Department of Internal Medicine, University of Washington School of Medicine, Seattle, WA, USA.
  • 2Division of Medical Oncology, University of Washington, Fred Hutchinson Cancer Research Center, Seattle, WA, USA. agopal@u.washington.edu

Abstract

Hodgkin lymphoma (HL) represents one of the great success stories in hematology going from a uniformly fatal disease, to one that is curable in the vast majority of cases. Despite this success, some patients experience relapse. To address this unmet need a variety of agents, classes of drugs, and strategies have demonstrated activity in HL recurring after autologous hematopoietic stem cell transplantation. These include chemotherapeutics (gemcitabine-based combinations, bendamustine), histone deacetylase (HDAC) inhibitors (panobinostat), immunomodulatory agents (lenalidomide), mTOR inhiobitors (everolimus), monoclonal antibodies (rituximab), and antibody-drug conjugates (brentuximab vedotin) as well the potential of long-term disease control via allogeneic transplantation. Such advances reflect our increased understanding of the biology of HL and hold promise for continued improved outcomes for those suffering with this condition.

Keyword

Hodgkin lymphoma; Antibody drug conjugates; allogeneic transplant; HDAC inhibitor; IMID; mTOR

MeSH Terms

Antibodies, Monoclonal
Biology
Hematology
Hematopoietic Stem Cell Transplantation
Hematopoietic Stem Cells
Histone Deacetylases
Hodgkin Disease
Humans
Recurrence
Stress, Psychological
Transplantation, Homologous
Antibodies, Monoclonal
Histone Deacetylases

Figure

  • Fig. 1 Proposed Mechanism of Action of Brentuximab Vedotin Antibody Drug Conjugate (ADC). Depiction of CD30 ligation by ADC followed by CD30-ADC internalization, lysosomal cleavage of linker and intracellular release of anti-tubulin agent MMAE leading to cell cycle arrest and apoptosis. Abbreviation: RS, Reed-Sternberg.


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