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
James P. Wilmot Cancer Center Institute, University of Rochester Medical Center, Rochester, NY;
Charleston Hematology/Oncology Associates, Charleston, SC;
Blood. 2016 May 19;127(20):2411-5. doi: 10.1182/blood-2015-12-683516. Epub 2016 Mar 11.
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.
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。