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HTLV-1-Associated T-cell Diseases

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Part of the book series: Contemporary Hematology ((CH))

Abstract

Adult T-cell leukemia-lymphoma (ATL) is a distinct peripheral T-lymphocytic malignancy etiologically associated with human T-cell lymphotropic virus type I. The diversity in clinical features and prognosis of patients with this disease has led to its subtype classification into four categories, acute, lymphoma, chronic, and smoldering types. The chronic or smoldering subtypes are considered indolent and are usually managed with watchful-waiting until disease progression. Patients with acute or lymphoma subtypes generally have a very poor prognosis due to multidrug-resistance of ATL cells, a large tumor burden with multi-organ failure, hypercalcemia, and/or frequent infectious complications due to a profound T-cell immunodeficiency. A treatment strategy based on the clinical subtypes, prognostic factors, and response to initial therapy is suggested including watchful-waiting approach, intensive chemotherapy, interferon-α zidobudine therapy, allogeneic hematopoietic stem cell transplantation, and targeted-therapies. Several new agent-trials for ATL are ongoing and in preparation, including a defucosylated humanized anti-CC chemokine receptor 4 monoclonal antibody, IL2-fused with diphtheria toxin, histone deacetylase inhibitors, a purine nucleoside phosphorylase inhibitor, a proteasome inhibitor, and lenalidomide.

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Tsukasaki, K., Tobinai, K. (2013). HTLV-1-Associated T-cell Diseases. In: Foss, F. (eds) T-Cell Lymphomas. Contemporary Hematology. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-62703-170-7_8

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