dc.contributor.author | Mohammadi, SM | |
dc.contributor.author | Nejad, DM | |
dc.contributor.author | Charoudeh, HN | |
dc.date.accessioned | 2018-08-26T08:57:39Z | |
dc.date.available | 2018-08-26T08:57:39Z | |
dc.date.issued | 2016 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/54597 | |
dc.description.abstract | Considerable advances have been made in treatment of acute lymphoblastic leukemia (ALL) with an overall survival rate of 85% in children, and in great improvement in adults. Despite this improvement and the accessibility of hematopoietic stem cell transplantation, relapsed ALL remains a leading cause of childhood mortality emphasizing the need of new approaches on therapy. Leukemia cells express numerous surface antigens amenable to target therapies, consist of CD20, CD22, and CD19. Monoclonal antibodies which target these antigens have improved the outcomes in B-cell ALL. Rituximab is the best known monoclonal antibody which is routinely used in combination with chemotherapy for treatment of adult B-cell ALL. Monoclonal antibodies including unconjugated and conjugated antibodies to cytotoxic agents for treatment of B-cell ALL are now under investigation. In this article we update the results and current status of investigational monoclonal antibody-based therapies in ALL. أ¯?آ½ 2016, UHOD - Uluslararasi Hematoloji Onkoloji Dergisi. All rights reserved. | |
dc.language.iso | English | |
dc.relation.ispartof | UHOD - Uluslararasi Hematoloji-Onkoloji Dergisi | |
dc.subject | alemtuzumab | |
dc.subject | blinatumomab | |
dc.subject | CD19 antibody | |
dc.subject | CD19 antigen | |
dc.subject | CD20 antigen | |
dc.subject | CD22 antigen | |
dc.subject | CD27 antigen | |
dc.subject | CD34 antigen | |
dc.subject | cell therapy agent | |
dc.subject | chimeric antigen receptor T cell therapy agent | |
dc.subject | chlorambucil | |
dc.subject | coltuximab ravtansine | |
dc.subject | cyclophosphamide | |
dc.subject | denintuzumab mafodotin | |
dc.subject | dexamethasone | |
dc.subject | doxorubicin | |
dc.subject | epratuzumab | |
dc.subject | inotuzumab ozogamicin | |
dc.subject | monoclonal antibody | |
dc.subject | monoclonal antibody CD28 | |
dc.subject | obinutuzumab | |
dc.subject | ofatumumab | |
dc.subject | prednisone | |
dc.subject | rituximab | |
dc.subject | unclassified drug | |
dc.subject | vincristine | |
dc.subject | acute lymphoblastic leukemia | |
dc.subject | apoptosis | |
dc.subject | brain hemorrhage | |
dc.subject | cancer chemotherapy | |
dc.subject | cell therapy | |
dc.subject | clinical trial (topic) | |
dc.subject | complement dependent cytotoxicity | |
dc.subject | drug dose escalation | |
dc.subject | febrile neutropenia | |
dc.subject | fever | |
dc.subject | gene expression | |
dc.subject | headache | |
dc.subject | hematopoietic stem cell transplantation | |
dc.subject | human | |
dc.subject | hyperglycemia | |
dc.subject | hypertransaminasemia | |
dc.subject | immunotherapy | |
dc.subject | leukemia relapse | |
dc.subject | leukopenia | |
dc.subject | mortality rate | |
dc.subject | outcome assessment | |
dc.subject | overall survival | |
dc.subject | phase 1 clinical trial (topic) | |
dc.subject | phase 2 clinical trial (topic) | |
dc.subject | progression free survival | |
dc.subject | Review | |
dc.subject | thrombocytopenia | |
dc.subject | tremor | |
dc.title | Immunotherapy for B-acute lymphoblastic leukemia by focusing on monoclonal antibody and CAR-T-Cell application [Monoklonal antikor ve CAR-T-Cell uygulamasina odakli B-akut lenfoblastik lأ¯?آ½semi ?mmأ¯?آ½noterapisi] | |
dc.type | Article | |
dc.citation.volume | 26 | |
dc.citation.issue | 4 | |
dc.citation.spage | 227 | |
dc.citation.epage | 238 | |
dc.citation.index | Scopus | |
dc.identifier.DOI | https://doi.org/10.4999/uhod.161628 | |