dc.contributor.author | Safdari, Y | |
dc.contributor.author | Ahmadzadeh, V | |
dc.contributor.author | Farajnia, S | |
dc.date.accessioned | 2018-08-26T07:26:39Z | |
dc.date.available | 2018-08-26T07:26:39Z | |
dc.date.issued | 2016 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/46797 | |
dc.description.abstract | Expression of CD20 antigen by the most of transformed B cells is believed to be the driving force for targeting this molecule by using anti-CD20 monoclonal antibodies. While it is true that most lymphoma/leukemia patients can be cured, these regimens are limited by the emergence of treatment resistance. Based on these observations, development of anti-CD20 monoclonal antibodies and combination therapies have been recently proposed, in particular with the aim to optimize the cytotoxic activity. Here we outline a range of new experimental agents concerning the CD20 positive B-cell tumors which provide high benefit from conventional therapy. | |
dc.language.iso | English | |
dc.relation.ispartof | INVESTIGATIONAL NEW DRUGS | |
dc.subject | B-cell malignancies | |
dc.subject | CD20 antigen | |
dc.subject | Antibody-based therapeutics | |
dc.subject | Combination therapy | |
dc.title | CD20-targeting in B-cell malignancies: novel prospects for antibodies and combination therapies | |
dc.type | Review | |
dc.citation.volume | 34 | |
dc.citation.issue | 4 | |
dc.citation.spage | 497 | |
dc.citation.epage | 512 | |
dc.citation.index | Web of science | |
dc.identifier.DOI | https://doi.org/10.1007/s10637-016-0349-4 | |