Combination Therapy of Bortezomib with Novel Targeted Agents: An Emerging Treatment Strategy

被引:84
作者
Wright, John J. [1 ]
机构
[1] NCI, Invest Drug Branch, Canc Therapy Evaluat Program, Div Canc Treatment & Diag, Bethesda, MD 20892 USA
关键词
PROTEASOME INHIBITOR BORTEZOMIB; MULTIPLE-MYELOMA CELLS; HISTONE DEACETYLASE INHIBITORS; LYMPHOCYTIC-LEUKEMIA CELLS; MIMETIC GX15-070 OBATOCLAX; UNFOLDED PROTEIN RESPONSE; CANCER-THERAPY; LUNG-CANCER; FLAVOPIRIDOL INTERACT; MONOCLONAL-ANTIBODY;
D O I
10.1158/1078-0432.CCR-09-2882
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Clinical trials evaluating combinations of targeted agents with bortezomib, the first-in-class proteasome inhibitor, have been initiated, with the objective of enhancing its single agent activity in hematologic malignancies (myeloma, mantle cell lymphoma), as well as expanding its efficacy in solid tumors. In most cases, preclinical studies have provided a supportive rationale for designing these doublet combination studies. Novel, small molecule-targeted agents being investigated with bortezomib in clinical trials include protein deacetylase inhibitors, kinase inhibitors, farnesyltransferase inhibitors, heat-shock protein 90 inhibitors, pan-Bcl-2 family inhibitors, and other classes of targeted inhibitors. Preliminary clinical data, available from a number of ongoing trials, suggest that most of these combinations are well tolerated and some have promising clinical efficacy that will require subsequent confirmation. Translational studies, conducted as part of the trials, may provide important insights into the putative mechanism of action delineated by preclinical studies of the combinations. The emergence of novel proteasome inhibitors may also expand the opportunities for optimizing these combination therapies. There is potential for an increasingly broad clinical trials program to investigate this therapeutic approach in a range of tumor types, as well as to consider additional agents in sequence or in combination. Clin Cancer Res; 16(16); 4094-104. (C) 2010 AACR.
引用
收藏
页码:4094 / 4104
页数:11
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