Combination of Targeted Drugs to Control Chronic Lymphocytic Leukemia: Harnessing the Power of New Monoclonal Antibodies in Combination With Ibrutinib

P. Cramer, P. Langerbeins, M. Hallek
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引用次数: 4

Abstract

AbstractThe landscape of treatment for chronic lymphocytic leukemia is rapidly changing at present. Considerable improvement has been achieved with the introduction of the anti-CD20 antibodies, and chemoimmunotherapy has now become an established standard for patients without the high-risk features del(17p)/TP53 mutation. Also, the outcome of patients with these adverse genetic aberrations was dramatically improved with the introduction of the kinase inhibitors ibrutinib and idelalisib. Different combinations of these and additional novel agents are currently evaluated in clinical trials. The combination of the Bruton tyrosine kinase inhibitor ibrutinib with an anti-CD20 antibody is an attractive option, because both drugs act synergistically: ibrutinib redistributes the CLL cells from their homing organs to the peripheral blood, and obinutuzumab eliminates the leukemic cells in the blood with particular efficiency. Adding the Bcl-2 antagonist venetoclax could further intensify the treatment of CLL. This combination might hold the potential to achieve a deep remission with an eradication of residual CLL cells and thus lead to long-term remissions of CLL.
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联合靶向药物控制慢性淋巴细胞白血病:利用新型单克隆抗体联合伊鲁替尼的力量
摘要目前慢性淋巴细胞白血病的治疗前景正在迅速变化。随着抗cd20抗体的引入,已经取得了相当大的改善,并且化学免疫治疗现在已经成为没有del(17p)/TP53突变高风险特征的患者的既定标准。此外,随着激酶抑制剂伊鲁替尼和ideelalisib的引入,这些不良遗传畸变患者的预后得到了显着改善。这些药物和其他新型药物的不同组合目前正在临床试验中进行评估。布鲁顿酪氨酸激酶抑制剂依鲁替尼与抗cd20抗体的组合是一个有吸引力的选择,因为这两种药物协同作用:依鲁替尼将CLL细胞从它们的归管器官重新分配到外周血,而obinutuzumab以特别的效率消除血液中的白血病细胞。加入Bcl-2拮抗剂venetoclax可进一步强化CLL的治疗。这种组合可能有潜力通过根除残留的CLL细胞实现深度缓解,从而导致CLL的长期缓解。
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