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In parallel with these therapeutic advances, elegant laboratory-based studies have employed cutting edge science to explore the basic biology of Hodgkin lymphoma, verifying the power of these techniques to yield major insights into neoplastic biology. Laser-capture single-cell dissection followed by demonstration of monoclonal immunoglobulin gene rearrangement and stable p53 gene mutational status in primary and relapsed specimens clarified both the neoplastic and B-cell origin of Hodgkin lymphoma. Immunophenotyping with internationally validated cluster designation markers separated Hodgkin lymphoma into classic and nodular lymphocyte predominant subtypes. Epidemiologic and virologic studies combined to provide novel insights into the basic and neoplastic biology of Epstein-Barr virus. Characterization of the interconnected signaling pathways within Hodgkin cells and between Hodgkin cells and their microenvironment, with their distortions of normal antigen feedback loops and inappropriate blockage of apoptosis and evasion of immunologically mediated cell destruction, has illuminated our thinking about oncogene expression, cytokine action, immunologic regulation, and immune cell networks.
Hodgkin lymphoma has evolved from frequently fatal to imminently curable in the practice lifetime of many still active hematologists. As a medical student, I helped care for a patient dying of her first recurrence. As an oncology fellow, I warned patients they had to choose between being cured and fathering children. Today patients who required treatment through two relapses bring me pictures of their children and grandchildren. These extraordinary changes characterize the recent history of Hodgkin lymphoma, a history in which hematologists have played a major role.
Footnotes
See the related ASH 50th Anniversary Review articles under the LYMPHOMA AND MYELOMA section of the publication ASH 50th Anniversary Reviews: A Salute to the American Society of Hematology.
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