Brentuximab vedotin in anaplastic large cell lymphoma

被引:5
|
作者
Skarbnik, Alan P. Z. [2 ]
Smith, Mitchell R. [1 ]
机构
[1] Fox Chase Canc Ctr, Lymphoma Serv, Philadelphia, PA 19111 USA
[2] Fox Chase Canc Ctr, Dept Med Oncol, Philadelphia, PA 19111 USA
关键词
ALCL; ALK; anaplastic large cell lymphoma; antibody-drug conjugate; brentuximab vedotin; CD30; MMAE; non-Hodgkin lymphoma; SGN-35; T-cell lymphoma; NON-HODGKINS-LYMPHOMA; FRANKFURT-MUNSTER GROUP; KI-1; LYMPHOMA; DISEASE; EXPRESSION; CHILDHOOD; FEATURES; RECEPTOR; KINASE; CANCER;
D O I
10.1517/14712598.2012.673578
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
Introduction: Brentuximab vedotin, a novel anti-CD30 antibody-drug conjugate, delivers a cytotoxic agent into CD30(+) cells. CD30 expression is characteristic of anaplastic large cell lymphoma (ALCL) and Hodgkin lymphoma (HL). Areas covered: We reviewed data on brentuximab vedotin, focusing on ALCL and discuss pharmacology, clinical trials leading to approval and future research directions. Systemic ALCL, 3% of adult NHL, is characterized by large anaplastic CD30+ cells. The fusion protein NPM-ALK, when present in systemic ALCL, confers better prognosis, although even ALK- patients with IPI score >= 3 are high-risk. For patients with systemic ALCL, 25 - 45% relapse after frontline therapy, and > 50% of patients will relapse following high-dose chemotherapy with autologous stem-cell support. There has been no standard therapy for relapsed/refractory systemic ALCL. Brentuximab vedotin, combines a monoclonal antibody targeted to CD30 with a microtubule disrupting agent and was recently approved for treatment of patients with systemic ALCL that is refractory or relapsed after at least one multiagent chemotherapy regimen. Expert opinion: Brentuximab vedotin provides targeted therapy to CD30(+) lymphomas, including ALCL and HL, with high response rates and manageable toxicity, predominantly myelosuppression and peripheral neuropathy.
引用
收藏
页码:633 / 639
页数:7
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