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EHA 2018 | Phase I study of the synergistic effects of CC-122 and obinutuzumab

By Sara Valente

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Jean-Marie MichotJean-Marie Michot

Jul 13, 2018


On Friday 15th June an oral abstract session took place at the 23rd congress of the European Hematology Association (EHA). Abstract S104 was presented by Jean-Marie Michot, Institute Gustave Roussy, Villejuif, France, on the drug CC-122, which is a novel cereblon-modulating agent used in combination with obinutuzumab in patients with relapsed/refractory (R/R) non-Hodgkin lymphoma (NHL).

CC-122 targets Cereblon and induces degradation of Aiolos and Ikaros that has a dual effect; tumoricidal effects of ISGs (IRF7 and OAS) and T- and NK-cell activation.

Study Overview

  • The initial part of the study was a dose escalation followed by dose expansion
  • The recommended dose for the dose expansion was 3 mg CC-122 + obinutuzumab divided into two cohorts of patients with follicular lymphoma (FL). The FL-1 cohort had R/R CD20+ disease and were lenalidomide-treated. The FL-2 cohort had R/R CD20+ disease and were lenalidomide-naïve
  • The primary endpoint of the study was to assess the safety and tolerability of CC-122 with obinutuzumab. To identify the non-tolerated dose, maximum tolerated dose (MTD), and the recommended phase II dose
  • The secondary endpoints included; preliminary efficacy, overall response rate (ORR) and progression-free survival (PFS)

Key Findings

  • The best ORR:
    • Diffuse large B-cell lymphoma (DLBCL) (n = 19) = 47%
    • FL + MZL (n = 30) = 77%
  • Median PFS:
    • DLBCL = 4.7 months (95% CI, 1.8–13.8)
    • FL + MZL = 16.6 months (95% CI, 5.4–not reached)

Safety

  • The most frequent Grade 3/4 adverse events were neutropenia (55%) and thrombocytopenia (22%)
  • 1 patient had a grade 5 tumor flare reaction/tumor lysis syndrome (dose 4 mg CC-122 + obinutuzumab)

The study found that the recommended dose of CC-122 for future clinical studies was 3 mg with obinutuzumab. This combination demonstrated a high response rate for patients with FL. Additionally, the adverse events during this study were manageable with no unexpected toxicities.

Expert Opinion

Jean-Marie MichotJean-Marie Michot

References