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idelalisib与entospletinib的2期研究:肺炎限制了复发难治性慢性淋巴细胞白血病和非霍奇金淋巴瘤的联合治疗。

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

作者信息

Barr Paul M, Saylors Gene B, Spurgeon Stephen E, Cheson Bruce D, Greenwald Daniel R, O'Brien Susan M, Liem Andre K D, Mclntyre Rosemary E, Joshi Adarsh, Abella-Dominicis Esteban, Hawkins Michael J, Reddy Anita, Di Paolo Julie, Lee Hank, He Joyce, Hu Jing, Dreiling Lyndah K, Friedberg Jonathan W

机构信息

James P. Wilmot Cancer Center Institute, University of Rochester Medical Center, Rochester, NY;

Charleston Hematology/Oncology Associates, Charleston, SC;

出版信息

Blood. 2016 May 19;127(20):2411-5. doi: 10.1182/blood-2015-12-683516. Epub 2016 Mar 11.

Abstract

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 www.clinicaltrials.gov as #NCT01796470.

摘要

尽管针对B细胞受体信号传导的药物在复发的慢性淋巴细胞白血病(CLL)和非霍奇金淋巴瘤(NHL)治疗中取得了改变实践的结果,但它们需要长期给药且反应不完全。鉴于与磷脂酰肌醇3-激酶δ和脾酪氨酸激酶抑制具有协同临床前活性,这项2期研究评估了idelalisib和entospletinib联合用药的安全性和疗效。符合条件的复发或难治性CLL或NHL患者对每种药物进行了患者内剂量递增。中位治疗暴露时间为10周,CLL或滤泡性淋巴瘤患者分别有60%和36%达到客观缓解。然而,该研究因18%的患者出现治疗中出现的肺炎(12例中有11例严重)而提前终止。尽管大多数患者通过支持措施和全身用类固醇恢复,但发生了2例死亡,归因于治疗中出现的肺炎。发生肺炎的患者中,干扰素-γ和白细胞介素6、7和8随时间增加。未来新型联合用药的研究应采用纳入药效学/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,以试图验证预测反应和毒性的生物标志物。该试验在www.clinicaltrials.gov上注册为#NCT01796470。

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