Blinatumomab: A historical perspective

被引:273
作者
Nagorsen, Dirk [1 ]
Kufer, Peter
Baeuerle, Patrick A.
Bargou, Ralf [2 ]
机构
[1] Amgen Res Munich GmbH, Global Clin Dev, D-81477 Munich, Germany
[2] Univ Hosp Wurzburg, Comprehens Canc Ctr Mainfranken, Dept Internal Med 2, D-97080 Wurzburg, Germany
关键词
BiTE (R); Bispecific antibody; Leukemia; Lymphoma; SINGLE-CHAIN ANTIBODY; MINIMAL RESIDUAL DISEASE; T-CELL-ACTIVATION; B-CELLS; LYMPHOMA; CANCER; THERAPY; LEUKEMIA; RITUXIMAB; LYSIS;
D O I
10.1016/j.pharmthera.2012.07.013
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
For decades, chemotherapy has been the backbone for the treatment of patients with B cell malignancies. Depending on the individual disease, monoclonal antibodies, irradiation and/or hematopoietic stem cell transplantation are added. However, the current standard of care - particularly for patients with relapsed disease - is often not sufficient to achieve durable remissions. A highly promising new drug candidate in late-stage clinical development for treatment of B cell malignancies is blinatumomab (MT103 or AMG 103). This bispecific antibody construct has dual specificity for CD19 and CD3 and belongs to the class of bispecific T cell engager (BiTE (R)) antibodies, which can potentially engage all cytotoxic T cells of a patient for redirected lysis of tumor cells. Here, we review how blinatumomab has so far been pre-clinically and clinically developed for the treatment of patients with non-Hodgkin's lymphoma and acute lymphoblastic leukemia. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:334 / 342
页数:9
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