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Targeted therapies in CLL: mechanisms of resistance and strategies for management

机译:CLL的靶向疗法:耐药机制和治疗策略

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摘要

The therapy of relapsed chronic lymphocytic leukemia (CLL) has changed dramatically in the past year with the regulatory approval of idelalisib and ibrutinib, with other therapeutic small molecules likely to become widely available in the next few years. Although durable remissions are being seen in many patients with these agents, it is becoming apparent that some patients with high genomic risk disease will relapse. Next-generation sequencing in patients as well as in vitro models is affording us the opportunity to understand the biology behind these relapses, which is the first step to designing rational therapies to prevent and treat targeted therapy-resistant CLL. These strategies are critical, as these relapses can be very difficult to manage, and a coordinated effort to put these patients on clinical trials will be required to efficiently determine the optimal therapies for these patients. In this review, we will describe-mechanisms of resistance, both proven and hypothesized, for idelalisib, ibrutinib, and venetoclax, describe patterns of resistance that have been described with ibrutinib, and discuss potential strategies for management of disease resistant to these drugs as well as potential strategies to prevent resistance.
机译:过去一年,随着艾得拉西布和依鲁替尼的监管批准,复发性慢性淋巴细胞白血病(CLL)的治疗发生了巨大变化,其他治疗性小分子药物有望在未来几年中广泛使用。尽管在使用这些药物的许多患者中观察到持久的缓解,但是越来越明显的是,一些具有高基因组风险疾病的患者会复发。患者和体外模型的下一代测序为我们提供了了解这些复发背后生物学的机会,这是设计合理疗法以预防和治疗靶向治疗耐药性CLL的第一步。这些策略至关重要,因为这些复发可能很难控制,需要协调一致的努力使这些患者进入临床试验,才能有效地确定这些患者的最佳疗法。在这篇综述中,我们将描述艾达拉西布,依鲁替尼和委内瑞拉的已证实和假设的耐药机制,描述已用依鲁替尼描述的耐药模式,并讨论治疗这些药物耐药性的潜在策略作为预防抵抗的潜在策略。

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