Adult T-cell leukemia-lymphoma: current treatment strategies and novel immunological approaches
被引:2
|
作者:
Tanosaki, Ryuji
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机构:
Natl Canc Ctr, Pathol & Clin Lab, Div Med, Chuo Ku, Tokyo 1040045, JapanNatl Canc Ctr, Pathol & Clin Lab, Div Med, Chuo Ku, Tokyo 1040045, Japan
Tanosaki, Ryuji
[1
]
Tobinai, Kensei
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机构:
Natl Canc Ctr, Hematol & Stem Cell Transplantat Div, Chuo Ku, Tokyo 1040045, JapanNatl Canc Ctr, Pathol & Clin Lab, Div Med, Chuo Ku, Tokyo 1040045, Japan
Tobinai, Kensei
[2
]
机构:
[1] Natl Canc Ctr, Pathol & Clin Lab, Div Med, Chuo Ku, Tokyo 1040045, Japan
[2] Natl Canc Ctr, Hematol & Stem Cell Transplantat Div, Chuo Ku, Tokyo 1040045, Japan
adult T cell leukemia lymphoma;
graft versus ATL effects;
graft versus HTLV 1 effects;
hematopoietic stem cell transplantation;
human T cell lymphotropic virus type I;
IFN alpha;
reduced intensity stem cell transplantation;
treatment;
zidovudine;
BONE-MARROW-TRANSPLANTATION;
TOTAL-BODY IRRADIATION;
PHASE-I TRIAL;
VIRUS TYPE-1;
MONOCLONAL-ANTIBODY;
COMPLETE RESPONSE;
INTERFERON-ALPHA;
LONG-TERM;
LEUKEMIA/LYMPHOMA;
COMBINATION;
D O I:
10.1586/EHM.10.73
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Adult T-cell leukemia lymphoma (ATL) is a peripheral T-cell malignancy closely associated with human T-cell lymphotropic virus type I infection Clinically ATL is classified into four subtypes acute, lymphoma chronic and smoldering type Although the prognosis of chronic and smoldering-type ATL is relatively good that of patients with acute- or lymphoma-type ATL still remains extremely poor Zidovudine/IFN-alpha therapy seems to be promising although its efficacy has not yet been confirmed in well-designed prospective studies High-dose chemotherapy with the support of autologous transplantation does not improve outcome Allogeneic stem cell transplantation is promising and approximately 40% of aggressive ATL patients are expected to survive long-term although transplantation-related mortality is as high as 40-50% Stem cell transplantation using reduced-intensity conditioning is also effective and safer with graft-versus-ATL and graft-versus-human T-cell lymphotropic virus type I effects observed after transplantation Novel approaches including new agents such as purine nucleoside phosphorylase inhibitors and histone deacetylase inhibitors or targeted immunotherapy using antichemokine receptor-4 antibody or dendritic cell/peptide vaccine are also warranted