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Abstract Details

Avelumab in Newly Diagnosed Glioblastoma Multiforme-the SEJ Study
Neuro-oncology
P2 - Poster Session 2 (8:00 AM-9:00 AM)
13-014
To determine the safety and efficacy of avelumab when added to standard therapy in patients with newly diagnosed glioblastoma multiforme.

 Glioblastoma Multiforme (GBM) has well documented systemic and local immunosuppressive mechanisms to escape immune surveillance and grow. GBM tumor cells as well as the microglia within it have a high PD-L1 surface expression which may make it susceptible to anti-PD-L1 antagonism and ADCC with avelumab therapy. Standard combination temozolomide/radiotherapy is associated with a median survival of 14.6 months and a median progression free survival of 6.9 months.

This is a single center, phase 2, open label study of avelumab 10 mg/kg Q2W for 156 weeks duration in patients receiving standard therapy for newly diagnosed GBM. Thirty patients will be entered into the study within 3 weeks of completing combined radiotherapy/temozolomide.  Here, we report the results of the second interim analysis which was completed when the first 20 patients completed 52 or more  weeks or an end of study visit.

Recrutement was completed in September 2019. As per data cut off of 02-2020 patient follow-up will range from 6 months to 26 months. Preliminary pathological biomarker analysis as well as efficacy and safety results are pending and will be presented at the meeting.
is pending
Authors/Disclosures
Francois H. Jacques, MD (Clinique Neuro-Outaouais)
PRESENTER
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file