Advances in Immunotherapy for the Treatment of Cutaneous T-Cell Lymphoma

被引:4
|
作者
Pelcovits, Ari [1 ,2 ]
Ollila, Thomas A. [1 ,2 ]
Olszewski, Adam J. [1 ,2 ,3 ]
机构
[1] Brown Univ, Dept Med, Alpert Med Sch, Providence, RI USA
[2] Rhode Isl Hosp, Div Hematol Oncol, Providence, RI USA
[3] Brown Univ, Rhode Isl Hosp, Dept Med, Alpert Med Sch, George Bldg, Ste 310, 593 Eddy St, Providence, RI 02903 USA
来源
关键词
cutaneous T-cell lymphoma; Sezary syndrome; immunotherapy; brentuximab vedotin; VERSUS-HOST-DISEASE; PHASE-II TRIAL; BRENTUXIMAB VEDOTIN; SEZARY-SYNDROME; MYCOSIS-FUNGOIDES; MONOCLONAL-ANTIBODY; DENILEUKIN DIFTITOX; ANTI-CCR4; ANTIBODY; SYSTEMIC TREATMENT; OPEN-LABEL;
D O I
10.2147/CMAR.S330908
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cutaneous T-Cell Lymphoma (CTCL) is a heterogenous disease that consists of distinct clinicopathologic entities and presentations requiring a unique and expert approach to management. The most common subtype is mycosis fungoides, in which local disease has an excellent prognosis and is often managed with topical therapy alone. More extensive cutaneous involvement as well as involvement of lymph nodes and the peripheral blood (Sezary syndrome) require systemic therapies. Recent years have brought an expansion of therapeutic options, specifically with immune-based approaches that were developed using the knowledge gained regarding the biology and molecular pathology of CTCL. Previous systemic therapies such as retinoids, histone deacetylase inhibitors, and chemotherapeutic agents come with significant toxicity and only short-term response. Newer agents such as mogamulizumab and brentuximab vedotin use a targeted immune-based approach leading to longer periods of response with less systemic toxicity. While still in its infancy, the use of immune checkpoint inhibitors such as nivolumab and pembrolizumab appears promising, and while their current clinical application is limited, early data suggest possible future areas for research of immune manipulation to treat CTCL. Herein, we review these novel immune-based treatment strategies, their superiority over prior systemic options, and the ongoing need for further research and clinical trial enrollment.
引用
收藏
页码:989 / 998
页数:10
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