| Literature DB >> 26968534 |
Paul M Barr1, Gene B Saylors2, Stephen E Spurgeon3, Bruce D Cheson4, Daniel R Greenwald5, Susan M O'Brien6, Andre K D Liem7, Rosemary E Mclntyre8, Adarsh Joshi9, Esteban Abella-Dominicis9, Michael J Hawkins9, Anita Reddy9, Julie Di Paolo9, Hank Lee9, Joyce He9, Jing Hu9, Lyndah K Dreiling9, Jonathan W Friedberg1.
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.Entities:
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Year: 2016 PMID: 26968534 PMCID: PMC4874222 DOI: 10.1182/blood-2015-12-683516
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113