Profile of belinostat for the treatment of relapsed or refractory peripheral T-cell lymphoma

被引:14
作者
Bodiford, Andrew [1 ]
Bodge, Megan [1 ]
Talbott, Mahsa S. [1 ]
Reddy, Nishitha M. [2 ]
机构
[1] Vanderbilt Univ, Med Ctr, Dept Pharm, Nashville, TN USA
[2] Vanderbilt Univ, Med Ctr, Div Hematol & Oncol, Nashville, TN USA
关键词
histone deacetylase inhibitor; pharmacokinetics; cutaneous T-cell lymphoma; HISTONE DEACETYLASE INHIBITOR; PHASE-II TRIAL; SOLID TUMORS; TRANSPLANTATION; PXD101; VORINOSTAT; MECHANISMS; EXPRESSION; THERAPIES; CANCER;
D O I
10.2147/OTT.S59269
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The peripheral T-cell lymphomas are a rare and heterogeneous group of mature T-cell lymphomas with limited available therapies. The outcome of frontline chemotherapy regimens has been disappointing, with a long-term survival of only 20%-30%. There is an urgent need to optimize induction therapy by incorporating novel agents that target the dysregulated pathways. Histone deacetylase inhibitors that induce acetylation of histones and enhance apoptosis have shown promising activity. In this article, we summarize the role of histone deacetylase inhibitors and specifically discuss pharmacokinetics, efficacy, and toxicity of the recently US Food and Drug Administration-approved agent belinostat for its use in patients with relapsed/refractory peripheral T-cell lymphoma.
引用
收藏
页码:1971 / 1977
页数:7
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