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Adult T-Cell Leukemia/Lymphoma
被引:57
|作者:
Mehta-Shah, Neha
Ratner, Lee
Horwitz, Steven M.
机构:
[1] Washington Univ, St Louis, MO USA
[2] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
关键词:
VIRUS TYPE-I;
RECEPTOR GENE REARRANGEMENTS;
NORTH-AMERICAN PATIENTS;
LEUKEMIA-LYMPHOMA;
INTERFERON-ALPHA;
PHASE-II;
TRANSPLANTATION;
HTLV-1;
TYPE-1;
COMBINATION;
D O I:
10.1200/JOP.2017.021907
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Adult T-cell lymphoma/leukemia (ATL) is a rare T-cell lymphoproliferative neoplasm caused by human T-lymphotrophic virus 1. In its more common, aggressive forms, ATL carries one of the poorest prognoses of the non-Hodgkin lymphomas. The disease has clinical subtypes (ie, acute, lymphoma, chronic, and smoldering forms) defined by the presenting features, and therefore, the clinical course can vary. For the smoldering and lower-risk chronic forms, combinations involving antiviral therapies have shown some success. However, in many patients, the more indolent forms will evolve into the more aggressive subtypes. In the more aggressive acute, lymphoma, and higher-risk chronic forms, the literature supports initial treatment with combination chemotherapy followed by allogeneic transplantation as a potentially curative approach. Recently, mogamulizumab and lenalidomide have shown promise in the treatment of ATL. With better understanding of the molecular drivers of this disease, we hope that the therapeutic landscape will continue to expand.
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页码:487 / +
页数:7
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