Integrating novel agents into the treatment of advanced mycosis fungoides and Sezary syndrome

被引:11
|
作者
Khodadoust, Michael S. [1 ,2 ,4 ]
Mou, Eric [3 ]
Kim, Youn H. [1 ,2 ,5 ]
机构
[1] Stanford Univ, Div Oncol, Stanford, CA USA
[2] Stanford Univ, Dept Dermatol, Stanford, CA USA
[3] Univ Iowa, Div Hematol Oncol Blood & Marrow Transplantat, Iowa City, IA USA
[4] 1701 Page Mill Rd, Palo Alto, CA 94304 USA
[5] 780 Welch Rd,CJ220D, Stanford, CA 94305 USA
关键词
T-CELL LYMPHOMA; BRENTUXIMAB VEDOTIN; PHASE-II; CUTANEOUS LYMPHOMA; PHYSICIANS CHOICE; CLINICAL-EFFICACY; CD30; EXPRESSION; ROMIDEPSIN; MULTICENTER; RESPONSES;
D O I
10.1182/blood.2020008241
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Agents targeting the unique biology of mycosis fungoides and Sezary syndrome are quickly being incorporated into clinical management. With these new therapies, we are now capable of inducing more durable responses and even complete remissions in advanced disease, outcomes which were exceedingly rare with prior therapies. Yet, even this new generation of therapies typically produce objective responses in only a minority of patients. As our therapeutic options increase, we are now challenged with selecting treatments from a growing list of options. To gain the full benefit of these novel agents, we must develop strategies to match treatments for the patients most likely to benefit from them. Here, we consider both the current approaches to treatment selection based on clinical features and the future of molecular biomarker-guided therapy for patients with this heterogeneous disease.
引用
收藏
页码:695 / 703
页数:9
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