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Management of Angioimmunoblastic T-Cell Lymphoma (AITL) and other T Follicular Helper Cell lymphomas (TFH PTCL)
被引:5
|作者:
Ma, Helen
[1
]
O'Connor, Owen A.
[2
]
Marchi, Enrica
[2
]
机构:
[1] Univ Calif Irvine, Div Hematol Oncol, Long Beach, CA USA
[2] Univ Virginia, Div Hematol Oncol, Charlottesville, VA USA
关键词:
Angioimmunoblastic T-cell lymphoma (AITL)&
nbsp;
Nodal PTCL with T Follicular Helper Phenotype (PTCL TFH);
Epigenetic Modifiers;
EPSTEIN-BARR-VIRUS;
PIVOTAL PHASE-II;
OPEN-LABEL;
B-CELLS;
IMMUNOBLASTIC LYMPHADENOPATHY;
MUTATIONAL LANDSCAPE;
CD30;
EXPRESSION;
SINGLE-AGENT;
PRALATREXATE;
MULTICENTER;
D O I:
10.1053/j.seminhematol.2021.03.001
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Despite the remarkable improvements in the treatment and outcome of patients with aggressive B-cell lymphoma, the peripheral T-cell lymphomas (PTCL) continue to carry a poor prognosis with the presently available treatment options. The PTCL are very rare diseases that account for only 10,0 0 0 to 15,0 0 0 new cases per year in the United States. The World Health Organization's 2016 classification describes 29 distinct subtypes of PTCL, thus making these both rate and incredibly heterogenous. The 2 most common forms of PTCL, for example, peripheral T-cell lymphoma-not otherwise specified and angioimmunoblastic T-cell lymphoma , have an incidence of only 2500 and 1800 cases per year respectively, in the United States (c) 2021 Elsevier Inc. All rights reserved.
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页码:95 / 102
页数:8
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