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

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.

Publication types

  • Clinical Trial, Phase II

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Class I Phosphatidylinositol 3-Kinases / antagonists & inhibitors
  • Cytokines / metabolism
  • Early Termination of Clinical Trials
  • Female
  • Humans
  • Indazoles / administration & dosage
  • Indazoles / adverse effects*
  • Leukemia, Lymphocytic, Chronic, B-Cell / drug therapy*
  • Leukemia, Lymphocytic, Chronic, B-Cell / enzymology
  • Lymphoma, Non-Hodgkin / drug therapy*
  • Lymphoma, Non-Hodgkin / enzymology
  • Male
  • Middle Aged
  • Neoplasm Proteins / antagonists & inhibitors
  • Pneumonia / chemically induced*
  • Protein Kinase Inhibitors / administration & dosage
  • Protein Kinase Inhibitors / adverse effects*
  • Purines / administration & dosage
  • Purines / adverse effects*
  • Pyrazines / administration & dosage
  • Pyrazines / adverse effects*
  • Quinazolinones / administration & dosage
  • Quinazolinones / adverse effects*
  • Salvage Therapy*
  • Syk Kinase / antagonists & inhibitors

Substances

  • 6-(1H-indazol-6-yl)-N-(4-morpholinophenyl)imidazo(1,2-a)pyrazin-8-amine
  • Cytokines
  • Indazoles
  • Neoplasm Proteins
  • Protein Kinase Inhibitors
  • Purines
  • Pyrazines
  • Quinazolinones
  • Class I Phosphatidylinositol 3-Kinases
  • PIK3CD protein, human
  • SYK protein, human
  • Syk Kinase
  • idelalisib

Associated data

  • ClinicalTrials.gov/NCT01796470