Abstract |
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®) 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.
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Authors | Dirk Nagorsen, Peter Kufer, Patrick A Baeuerle, Ralf Bargou |
Journal | Pharmacology & therapeutics
(Pharmacol Ther)
Vol. 136
Issue 3
Pg. 334-42
(Dec 2012)
ISSN: 1879-016X [Electronic] England |
PMID | 22940266
(Publication Type: Journal Article, Review)
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Copyright | Copyright © 2012 Elsevier Inc. All rights reserved. |
Chemical References |
- Antibodies, Bispecific
- blinatumomab
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Topics |
- Animals
- Antibodies, Bispecific
(administration & dosage, chemistry, therapeutic use)
- Clinical Trials as Topic
- Humans
- Lymphoma, Large B-Cell, Diffuse
(drug therapy)
- Lymphoma, Mantle-Cell
(drug therapy)
- Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
(drug therapy)
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