Anti-CD20 monoclonal antibodies in chronic lymphocytic leukemia: from uncertainties to promises

被引:11
|
作者
Bagacean, Cristina [1 ,3 ]
Zdrenghea, Mihnea [3 ,4 ]
Tempescul, Adrian [1 ,5 ]
Cristea, Victor [3 ]
Renaudineau, Yves [1 ,2 ]
机构
[1] European Univ Brittany, Labex IGO, Reseau Epigenet & Reseau Canaux Ion Canc Opole Gr, Res Unit,INSERM,ESPRI,Immunotherpy & Cell Dis ERI, Brest, France
[2] CHRU Morvan, Lab Immunol & Immunotherapy, Brest, France
[3] Iuliu Hatieganu Univ Med & Pharm, 8 Babes St, Cluj Napoca 400012, Romania
[4] Ion Chiricuta Inst Oncol, 34-36 Republ St, Napoca 400015, Romania
[5] CHRU Morvan, Dept Hematol, Brest, France
关键词
CD20; chronic lymphocytic leukemia; immunotherapy; obinutuzumab; ofatumumab; rituximab; B-CELL LYMPHOMA; PNEUMOCYSTIS-JIROVECII PNEUMONIA; NON-HODGKINS-LYMPHOMA; PHASE-II TRIAL; FC-GAMMA-RIIIA; OBINUTUZUMAB GA101; IN-VIVO; PLUS RITUXIMAB; CD20; ANTIBODY; HUMAN IGG1;
D O I
10.2217/imt-2015-0015
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Over the last two decades, anti-CD20 monoclonal antibody (mAb) therapy has improved patient outcome in B-cell malignancies, and confirmed CD20 as an important target in chronic lymphocytic leukemia (CLL). Until recently, the gold standard was based on the utilization of rituximab combined with chemotherapy (fludarabine and cyclophosphamide), but patients often relapse. Next, with our better understanding of mAb engineering, anti-CD20 mAb therapy has evolved with the development of new mAb permitting significant clinical responses by improving pharmacokinetics, safety, activity and immunogenicity. Last but not least, the development of key tumoral tyrosine kinase inhibitors and their association with anti-CD20 mAb is a work in progress with promising results.
引用
收藏
页码:569 / 581
页数:13
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