Siltuximab for multicentric Castleman disease

被引:17
|
作者
Liu, Yi-Chang [1 ,2 ,3 ]
Stone, Katie [1 ]
van Rhee, Frits [1 ]
机构
[1] Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA
[2] Kaohsiung Med Univ, Coll Med, Fac Med, Kaohsiung 807, Taiwan
[3] Kaohsiung Med Univ Hosp, Dept Hematol Oncol, Kaohsiung 807, Taiwan
关键词
Castleman disease; IL-6; monoclonal antibody; siltuximab; targeted therapy; ANTI-INTERLEUKIN-6; MONOCLONAL-ANTIBODY; MULTIPLE-MYELOMA; VIRAL INTERLEUKIN-6; PHASE-I; RECEPTOR; RITUXIMAB; ANTI-IL-6; IL-6; EFFICACY; PATIENT;
D O I
10.1586/17474086.2014.946402
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dysregulated secretion of IL-6 plays a pivotal role in the pathogenesis of Castleman disease (CD), a rare lymphoproliferative disorder. In contrast to unicentric CD for which surgery is considered the treatment of choice, there is no standard therapeutic approach for multicentric CD (MCD). Siltuximab (trade name: Sylvant, formerly known as CNTO 328) is a chimeric monoclonal antibody with high binding affinity for human IL-6. In a recent randomized placebo-controlled Phase II trial, subjects with HIV-negative, HHV8-negative MCD who received siltuximab demonstrated a significantly higher rate of durable tumor and symptomatic response with a tolerable safety profile, leading to its approval for the treatment of HIV-negative HHV8-negative MCD by the US FDA and the European Commission in April and May 2014, respectively. This article will cover the current treatment options of MCD, the drug profile of siltuximab and future directions in the management of MCD.
引用
收藏
页码:545 / 557
页数:13
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