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Outcomes of CLL patients treated with sequential kinase inhibitor therapy: a real world experience.连续激酶抑制剂治疗 CLL 患者的结果:真实世界经验。
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Clonal evolution in patients with chronic lymphocytic leukaemia developing resistance to BTK inhibition.慢性淋巴细胞白血病患者对 BTK 抑制产生耐药性后的克隆进化。
Nat Commun. 2016 May 20;7:11589. doi: 10.1038/ncomms11589.
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Ibrutinib as Initial Therapy for Patients with Chronic Lymphocytic Leukemia.伊布替尼作为慢性淋巴细胞白血病患者的初始治疗方法。
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Complex karyotype is a stronger predictor than del(17p) for an inferior outcome in relapsed or refractory chronic lymphocytic leukemia patients treated with ibrutinib-based regimens.对于接受基于伊布替尼方案治疗的复发或难治性慢性淋巴细胞白血病患者,复杂核型比17号染色体短臂缺失(del(17p))更能预示不良预后。
Cancer. 2015 Oct 15;121(20):3612-21. doi: 10.1002/cncr.29566. Epub 2015 Jul 20.
5
Etiology of Ibrutinib Therapy Discontinuation and Outcomes in Patients With Chronic Lymphocytic Leukemia.伊布替尼治疗中断的病因及慢性淋巴细胞白血病患者的结局。
JAMA Oncol. 2015 Apr;1(1):80-7. doi: 10.1001/jamaoncol.2014.218.
6
Hypermorphic mutation of phospholipase C, γ2 acquired in ibrutinib-resistant CLL confers BTK independency upon B-cell receptor activation.在依鲁替尼耐药的慢性淋巴细胞白血病中获得的磷脂酶Cγ2的超形态突变赋予B细胞受体激活对布鲁顿酪氨酸激酶的独立性。
Blood. 2015 Jul 2;126(1):61-8. doi: 10.1182/blood-2015-02-626846. Epub 2015 May 13.
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Selinexor is effective in acquired resistance to ibrutinib and synergizes with ibrutinib in chronic lymphocytic leukemia.塞利尼索对依鲁替尼获得性耐药有效,并在慢性淋巴细胞白血病中与依鲁替尼协同作用。
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Three-year follow-up of treatment-naïve and previously treated patients with CLL and SLL receiving single-agent ibrutinib.初治和既往接受过治疗的慢性淋巴细胞白血病(CLL)和小淋巴细胞淋巴瘤(SLL)患者接受单药伊布替尼治疗的三年随访
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Outcomes of patients with chronic lymphocytic leukemia after discontinuing ibrutinib.停用依鲁替尼后慢性淋巴细胞白血病患者的预后
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10
Ibrutinib for previously untreated and relapsed or refractory chronic lymphocytic leukaemia with TP53 aberrations: a phase 2, single-arm trial.伊布替尼用于既往未治疗及复发或难治的伴有TP53畸变的慢性淋巴细胞白血病:一项2期单臂试验
Lancet Oncol. 2015 Feb;16(2):169-76. doi: 10.1016/S1470-2045(14)71182-9. Epub 2014 Dec 31.

我如何治疗依鲁替尼难治性慢性淋巴细胞白血病。

How I manage ibrutinib-refractory chronic lymphocytic leukemia.

作者信息

Woyach Jennifer A

机构信息

Division of Hematology, Department of Internal Medicine, The Ohio State University, Columbus, OH.

出版信息

Blood. 2017 Mar 9;129(10):1270-1274. doi: 10.1182/blood-2016-09-693598. Epub 2017 Jan 17.

DOI:10.1182/blood-2016-09-693598
PMID:28096090
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5345730/
Abstract

The introduction of the Bruton tyrosine kinase (BTK) inhibitor ibrutinib has dramatically changed the management of chronic lymphocytic leukemia (CLL). Although responses have been durable in the majority of patients, relapses do occur, especially in the high-risk patient population. Most relapses occur as the result of acquired mutations in BTK and PLCG2, which may facilitate success with alternative targeted therapies. As outcomes after ibrutinib relapse have been reported to be poor, specific strategies are needed for this patient population. Here, I discuss the diagnosis and management of ibrutinib-refractory CLL. The focus will be on common clinical scenarios that can be mistaken for relapse and how to accurately determine which patients are relapsing. Because there is no established standard of care, I discuss currently available options for standard therapy and existing clinical data. I also discuss new agents with the potential to be effective in patients refractory to ibrutinib. Finally, I discuss strategies for long-term disease control in this patient population.

摘要

布鲁顿酪氨酸激酶(BTK)抑制剂依鲁替尼的引入极大地改变了慢性淋巴细胞白血病(CLL)的治疗方式。尽管大多数患者的反应持久,但复发确实会发生,尤其是在高危患者群体中。大多数复发是由BTK和PLCG2的获得性突变导致的,这可能有助于采用替代靶向疗法取得成功。由于依鲁替尼复发后的预后据报道较差,因此需要针对该患者群体制定特定策略。在此,我将讨论依鲁替尼难治性CLL的诊断和管理。重点将放在可能被误诊为复发的常见临床情况以及如何准确确定哪些患者正在复发。由于尚无既定的标准治疗方案,我将讨论目前可用的标准治疗选择和现有临床数据。我还将讨论有可能对依鲁替尼难治的患者有效的新型药物。最后,我将讨论该患者群体长期疾病控制的策略。