Integrating novel systemic therapies for the treatment of mycosis fungoides and Sezary syndrome

被引:7
|
作者
Prince, H. Miles [1 ]
Querfeld, Christiane [2 ]
机构
[1] Univ Melbourne, Epworth Healthcare & Sir Peter MacCallum Dept Onc, 140 Clarendon St, East Melbourne, Vic, Australia
[2] City Hope Natl Med Ctr, Natl Med Ctr, Beckman Res Inst, 1500 E Duarte Rd, Duarte, CA 91010 USA
关键词
Cutaneous; T cell; Lymphoma; Sezary; Novel agents; Biological agents; T-CELL LYMPHOMA; BONE-MARROW-TRANSPLANTATION; LOW-DOSE METHOTREXATE; PHASE-II TRIAL; INTERNATIONAL-SOCIETY; CUTANEOUS-LYMPHOMAS; INTERFERON ALPHA-2A; BRENTUXIMAB VEDOTIN; DENILEUKIN DIFTITOX; PROGNOSTIC-FACTORS;
D O I
10.1016/j.beha.2018.07.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Novel systemic therapies are generally prescribed to patients with advanced-stage disease or those with early-stage disease refractory to skin-directed therapies. In general, systemic chemotherapy should be reserved for patients who fail to respond to biological agents. Such biological agents include interferon alfa, bexarotene, histone deacetylase inhibitors (vorinostat, romidepsin), brentuximab vedotin and mogamulizumab. Extracorporeal photopheresis is particularly effective for patients with Sezary Syndrome. Allogeneic transplantation is becoming increasing used for younger patients. Novel agents in advanced development include the monoclonal antibody IPH4102, duvelisib, and the new modified formulation of denileukin diftitox. The choice of agents for patients is typically a balance of patient factors (age, co-morbidities, geographic location), relative efficacy and toxicity.
引用
收藏
页码:322 / 335
页数:14
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