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化疗一线方案后复发 CLL 的治疗方法。

Approaches for relapsed CLL after chemotherapy-free frontline regimens.

机构信息

CLL Program, Leukemia Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

出版信息

Hematology Am Soc Hematol Educ Program. 2020 Dec 4;2020(1):10-17. doi: 10.1182/hematology.2020000168.

Abstract

Novel agents, including Bruton's tyrosine kinase inhibitors (BTKi; ibrutinib, acalabrutinib), venetoclax, and phosphatidylinositol 3-kinase inhibitors (PI3Ki; idelalisib, duvelisib), have fundamentally changed the chronic lymphocytic leukemia (CLL) treatment landscape, allowing for a chemotherapy-free paradigm for many. Randomized trials that demonstrated efficacy of these agents in the relapsed/refractory setting rarely included patients with prior novel agent exposure. Herein, we review available data, including single-arm prospective studies and retrospective cohorts, on outcomes for novel agent approaches after novel agent exposure. We examine data for subsequent treatment options in 3 specific scenarios: (1) progression of disease while receiving BTKi, (2) progression of disease after discontinuation of BTKi for intolerance, and (3) after treatment with venetoclax. Data are most robust for venetoclax-based regimens after progression on BTKi. For patients who experience progression of disease after discontinuation of BTKi for intolerance, venetoclax-based regimens and retreatment with BTKi (depending on severity of initial intolerance) are 2 data-driven options. After frontline venetoclax/obinutuzumab, subsequent treatment approaches depend on whether patients experience progression of disease during or after discontinuation of their fixed duration frontline regimen and whether venetoclax/obinutuzumab was discontinued for intolerance. After progression of disease while on venetoclax, we recommend BTKi as second-line therapy. For patients who experience progression after completion or premature discontinuation (because of intolerance) of fixed duration venetoclax/obinutuzumab, either BTKi or retreatment with venetoclax (with aggressive supportive care if prior intolerance) are reasonable considerations. Subsequent lines of therapy in these scenarios include PI3Ki and consideration of cellular therapies. Finally, clinical trial enrollment for interested patients in any line of therapy is recommended.

摘要

新型药物,包括布鲁顿酪氨酸激酶抑制剂(BTKi;依鲁替尼、阿卡替尼)、维奈托克和磷脂酰肌醇 3-激酶抑制剂(PI3Ki;idelalisib、duvelisib),彻底改变了慢性淋巴细胞白血病(CLL)的治疗格局,使许多患者不再需要接受化疗。在复发/难治性环境中证明这些药物疗效的随机试验很少包括先前接触过新型药物的患者。在此,我们回顾了现有数据,包括单臂前瞻性研究和回顾性队列研究,以了解新型药物暴露后新型药物方法的结果。我们检查了在 3 种特定情况下新型药物治疗后后续治疗选择的数据:(1)接受 BTKi 时疾病进展,(2)因不耐受而停止 BTKi 后疾病进展,以及(3)接受维奈托克治疗后。BTKi 进展后使用维奈托克的方案数据最为可靠。对于因不耐受而停止 BTKi 后疾病进展的患者,维奈托克为基础的方案和 BTKi 的再治疗(取决于初始不耐受的严重程度)是 2 种数据驱动的选择。在一线维奈托克/奥滨尤妥珠单抗治疗后,后续治疗方法取决于患者在固定疗程一线治疗期间或之后是否发生疾病进展,以及是否因不耐受而停止维奈托克/奥滨尤妥珠单抗治疗。在维奈托克治疗期间疾病进展后,我们建议使用 BTKi 作为二线治疗。对于完成或因不耐受(因不耐受)提前停止固定疗程维奈托克/奥滨尤妥珠单抗的患者,BTKi 或维奈托克再治疗(如果之前不耐受,应积极支持治疗)是合理的考虑因素。在这些情况下,后续的治疗方案包括 PI3Ki,并考虑细胞疗法。最后,建议任何治疗线的感兴趣的患者参加临床试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d50e/7727527/094b3421cf24/bloodbook-2020-10-absf1.jpg

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