Pidilizumab in the treatment of diffuse large B-cell lymphoma

被引:28
作者
Bryan, Locke J. [1 ]
Gordon, Leo I. [1 ]
机构
[1] Northwestern Univ, Div Hematol Oncol, Chicago, IL 60611 USA
关键词
diffuse large B-cell lymphoma; monoclonal antibody; non-Hodgkin lymphoma; programmed death-1; pidilizumab; PROGRAMMED DEATH-1; MONOCLONAL-ANTIBODY; T-CELLS; PD-1; EXPRESSION; BLOCKADE; TRANSPLANTATION; LYMPHOCYTES; REGRESSION; TOLERANCE;
D O I
10.1517/14712598.2014.942637
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Introduction: The programmed death-1 (PD-1) immune checkpoint pathway is an emerging target in the treatment of hematologic malignancies. Pidilizumab is an mAb that binds to PD-1 and is a safe and well-tolerated therapy. Recent data have shown clinical activity utilizing this strategy in diffuse large B-cell lymphoma (DLBCL). Areas covered: The role of PD-1 expression in hematologic malignancies is explored. Recent clinical trials including the results of a Phase I trial in hematologic malignancies and a Phase II trial of pidilizumab following autologous hematopoietic stem-cell transplant (AHSCT) are reviewed. Expert opinion: We review data that suggest that PD-1 is a promising target in the treatment and management of DLBCL. Changes in immune subsets following administration of pidilizumab are felt to represent on-target responses. The improvement in progression-free survival (PFS) following AHSCT supports a response to therapy. Importantly, the improvement in PFS for patients with positive FDG-PET/CT following AHSCT indicating residual disease further supports direct activity of pidilizumab in DLBCL.
引用
收藏
页码:1361 / 1368
页数:8
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