Abstract | INTRODUCTION: Patients with relapsed or refractory diffuse large B-cell lymphoma (R/R DLBCL) require further treatment options, especially in cases that cannot tolerate stem cell transplant or cytotoxic chemotherapy. CD19 has emerged as an attractive target in B-cell malignancy and is the subject of several therapeutic strategies. The anti-CD19, humanized, monoclonal antibody tafasitamab (MOR208) has an engineered, modified Fc region with increased affinity for Fcγ receptors, leading to increased cytotoxicity via natural killer cells and macrophages (antibody-dependent cellular cytotoxicity and antibody-dependent cell-mediated phagocytosis) in a promising approach. AREAS COVERED: The development of tafasitamab is reviewed, together with the pharmacokinetics and clinical experience of tafasitamab in R/R DLBCL; clinical data have led to FDA approval and inclusion in NCCN treatment guidelines for tafasitamab in combination with lenalidomide in this indication. EXPERT OPINION:
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Authors | Gilles Salles, Monika Długosz-Danecka, Hervé Ghesquières, Wojciech Jurczak |
Journal | Expert opinion on biological therapy
(Expert Opin Biol Ther)
Vol. 21
Issue 4
Pg. 455-463
(04 2021)
ISSN: 1744-7682 [Electronic] England |
PMID | 33554668
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
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Chemical References |
- Antibodies, Monoclonal, Humanized
- tafasitamab
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Topics |
- Antibodies, Monoclonal, Humanized
- Antineoplastic Combined Chemotherapy Protocols
- Hematopoietic Stem Cell Transplantation
- Humans
- Lymphoma, Large B-Cell, Diffuse
(drug therapy)
- Transplantation, Autologous
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