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10.2147/OTT.S70524

http://scihub22266oqcxt.onion/10.2147/OTT.S70524
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C4485855!4485855!26170691
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suck abstract from ncbi


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pmid26170691      Onco+Targets+Ther 2015 ; 8 (ä): 1567-74
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  • Profile of blinatumomab and its potential in the treatment of relapsed/refractory acute lymphoblastic leukemia #MMPMID26170691
  • Ribera JM; Ferrer A; Ribera J; Genescà E
  • Onco Targets Ther 2015[]; 8 (ä): 1567-74 PMID26170691show ga
  • The CD19 marker is expressed on the surface of normal and malignant immature or mature B-cells. On the other hand, immunotherapy involving T-cells is a promising modality of treatment for many neoplastic diseases including leukemias and lymphomas. The CD19/CD3-bispecific T-cell-engaging (BiTE®) monoclonal antibody blinatumomab can transiently engage cytotoxic T-cells to CD19+ target B-cells inducing serial perforin-mediated lysis. In the first clinical trial, blinatumomab showed efficacy in non-Hodgkin?s lymphomas, but the most important trials have been conducted in relapsed/refractory (R/R) acute lymphoblastic leukemia (ALL) and in ALL with minimal residual disease. Encouraging reports on the activity of blinatumomab in R/R Philadelphia chromosome-negative B-cell precursor ALL led to its approval by the US Food and Drug Administration on December 3, 2014 after an accelerated review process. This review focuses on the profile of blinatumomab and its activity in R/R ALL.
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