ACTR-64. PHASE 2 STUDY OF SYM004 FOR ADULT PATIENTS WITH RECURRENT GLIOBLASTOMA (GBM)

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Conference Paper

BACKGROUND Sym004, a recombinant antibody mixture binding specifically to the epidermal growth factor receptor (EGFR), contains two mouse-human chimeric IgG1 monoclonal antibodies (mAbs) binding to non-overlapping epitopes on the extracellular domain III of EGFR. It induces highly efficient internalization and degradation of EGFR on cancer cells. In solid tumors, the phase 2 Sym004 dose is 18 mg/kg intravenously every 2 weeks. Results of a phase 2 trial in recurrent GBM are reported. METHODS Eligible patients are adults with recurrent GBM; EGFR amplified (>15% of cells exhibiting >5 copies of EGFR loci); ≤3 prior progressions; ≥4 weeks after chemotherapy, or study drug; ≥12 weeks after radiation; adequate organ function; and KPS ≥70%. Patients received Sym004 18 mg/kg IV every 2 weeks and imaging every 8 weeks. Bevacizumab naïve (cohort 1) and bevacizumab failure (cohort 2) patients were enrolled. RESULTS As of 5/26/2017, 24 patients have been treated on study (cohort 1: 17 patients; cohort 2: 7 patients). Grade 3 or higher adverse events (AEs) possibly related to study include: fatigue (grade 3, n=1); skin infection (grade 3, n=1); hypokalemia (grade 3, n=1); and dry skin (grade 3, n=1). Adverse events of special interest are: rash (grade 3, n=3; grade 2, n=7; grade 1, n=12) and hypomagnesemia (grade 1, n=18). Eighteen patients experienced disease progression within 2 months of initiating treatment, but three patients remained stable for at least six months. CONCLUSION Because of the low frequency of significant cutaneous toxicity and hypomagnesia observed in our phase 2 trial evaluating GBM patients, AEs generally associated with anti-tumor response to anti-EGFR mAbs, we are increasing the dose administered to 24 mg/kg to evaluate whether increased efficacy may be observed. Data on the new dose will be presented.

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Cited Authors

  • Desjardins, A; Randazzo, D; Peters, KB; Johnson, MO; Massey, W; Herndon, JE; McSherry, F; Lipp, ES; Nadler, P; Horak, ID; Friedman, HS

Duke Contributors

Published Date

  • November 6, 2017

Published In

Volume / Issue

  • 19 / suppl_6

Start / End Page

  • vi14 - vi14

Published By

Electronic International Standard Serial Number (EISSN)

  • 1523-5866

International Standard Serial Number (ISSN)

  • 1522-8517

Digital Object Identifier (DOI)

  • 10.1093/neuonc/nox168.052

Conference Name

  • 22nd Annual Scientific Meeting and Education Day of the Society for Neuro-Oncology

Conference Location

  • San Francisco, CA

Conference Start Date

  • November 16, 2017

Conference End Date

  • November 19, 2017