How I treat adult T-cell leukemia/lymphoma

Author:

Bazarbachi Ali1,Suarez Felipe2,Fields Paul3,Hermine Olivier2

Affiliation:

1. Department of Internal Medicine, American University of Beirut, Beirut, Lebanon;

2. Centre Nationale de Recherche Scientifique Unité Mixte de Recherche 8147 and Department of Hematology, Necker Hospital, Paris Descartes University, Paris, France; and

3. Department of Haematology, Guys and St Thomas Hospital, Kings Health Partners, London, United Kingdom

Abstract

AbstractAdult T-cell leukemia/lymphoma (ATL) is an aggressive malignancy of mature activated T cells caused by human T-cell lymphotropic virus type I. ATL carries a bad prognosis because of intrinsic chemoresistance and severe immunosuppression. In acute ATL, Japanese trials demonstrated that although combinations of chemotherapy improved response rate, they failed to achieve a significant impact on survival. Patients with chronic and smoldering ATL have a better prognosis, but long-term survival is poor when these patients are managed with a watchful-waiting policy or with chemotherapy. Recently, a worldwide meta-analysis revealed that the combination of zidovudine and IFN-α is highly effective in the leukemic subtypes of ATL and should be considered as standard first-line therapy in that setting. This combination has changed the natural history of the disease through achievement of significantly improved long-term survival in patients with smoldering and chronic ATL as well as a subset of patients with acute ATL. ATL lymphoma patients still benefit from chemotherapy induction with concurrent or sequential antiretroviral therapy with zidovudine/IFN. To prevent relapse, clinical trials assessing consolidative targeted therapies such as arsenic/IFN combination or novel monoclonal antibodies are needed. Finally, allogeneic BM transplantation should be considered in suitable patients.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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