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Phase 2 study of idelalisib and entospletinib: pneumonitis limits combination therapy in relapsed refractory CLL and NHL

机译:艾达拉西布和恩替普替尼的2期研究:肺炎限制了复发难治性CLL和NHL的联合治疗

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摘要

Although agents targeting B-cell receptor signaling have provided practice-changing results in relapsed chronic lymphocytic leukemia (CLL) and non-Hodgkin lymphoma (NHL), they require prolonged administration and provide incomplete responses. Given synergistic preclinical activity with phosphatidylinositol 3-kinase δ and spleen tyrosine kinase inhibition, this phase 2 study evaluated the safety and efficacy of the combination of idelalisib and entospletinib. Eligible patients with relapsed or refractory CLL or NHL underwent intrapatient dose escalation with each agent. With a median treatment exposure of 10 weeks, 60% and 36% of patients with CLL or follicular lymphoma, respectively, achieved objective responses. However, the study was terminated early because of treatment-emergent pneumonitis in 18% of patients (severe in 11 of 12 cases). Although most patients recovered with supportive measures and systemic steroids, 2 fatalities occurred and were attributed to treatment-emergent pneumonitis. Increases of interferon-γ and interleukins 6, 7, and 8 occurred over time in patients who developed pneumonitis. Future studies of novel combinations should employ conservative designs that incorporate pharmacodynamics/biomarker monitoring. These investigations should also prospectively evaluate plasma cytokine/chemokine levels in an attempt to validate biomarkers predictive of response and toxicity. This trial was registered at as #.
机译:尽管靶向B细胞受体信号转导的药物在复发性慢性淋巴细胞白血病(CLL)和非霍奇金淋巴瘤(NHL)中提供了改变实践的结果,但它们需要延长给药时间并提供不完全的应答。鉴于与磷脂酰肌醇3激酶δ和脾酪氨酸激酶抑制作用具有协同的临床前活性,该2期研究评估了依达拉西布和恩替普列替尼联合使用的安全性和有效性。符合条件的复发性或难治性CLL或NHL患者需接受每种药物的患者剂量递增。中位治疗时间为10周,分别有60%和36%的CLL或滤泡性淋巴瘤患者达到了客观反应。但是,由于治疗中出现的肺炎在18%的患者中严重(在12例中有11例中),该研究提前终止。尽管大多数患者通过支持措施和全身性类固醇康复,但有2例死亡发生,并归因于治疗性肺炎。随着时间的流逝,发生肺炎的患者中干扰素-γ和白介素6、7和8的增加。新型组合的未来研究应采用结合药效学/生物标志物监测的保守设计。这些研究还应前瞻性评估血浆细胞因子/趋化因子水平,以尝试验证可预测反应和毒性的生物标志物。该试用版注册为#。

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