Evidence mapPaperPMID 39499201Full record

Trial reportClinical cancer research : an official journal of the American Association for Cancer Research2024

Pilot Trial of Perampanel on Peritumoral Hyperexcitability in Newly Diagnosed High-grade Glioma.

Steven Tobochnik, Michael S Regan, Maria K C Dorotan, Dustine Reich, Emily Lapinskas, Md Amin Hossain, Sylwia Stopka, David M Meredith, Sandro Santagata, Melissa M Murphy and 10 more

Abstract readClinical Trial
In one paragraph

Trial report in Clinical cancer research : an official journal of the American Association for Cancer Research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Review
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  15. Elevated glioma-related cortical glutamateBrain communications · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors.

Steven Tobochnik *Department of Neurology, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0001-9071-8398
Michael S Regan *Department of Neurosurgery, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0001-5252-2829
Maria K C DorotanDepartment of Neurology, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0002-0073-4982
Dustine ReichWeill Cornell Medical College, New York, New York.ORCID 0000-0001-7284-9538
Emily LapinskasDepartment of Neurology, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0001-9860-3544
Md Amin HossainDepartment of Neurosurgery, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0001-7136-503X
Sylwia StopkaDepartment of Neurosurgery, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0003-3761-6899
David M MeredithDepartment of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0002-7054-8624
Sandro SantagataDepartment of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0002-7528-9668
Melissa M MurphyDepartment of Neurology, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0009-0000-7548-743X
Omar ArnaoutDepartment of Neurosurgery, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0003-3890-8615
Wenya Linda BiDepartment of Neurosurgery, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0002-4635-0247
E Antonio ChioccaDepartment of Neurosurgery, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0001-5183-1670
Alexandra J GolbyDepartment of Neurosurgery, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0001-8461-9561
Michael A MooneyDepartment of Neurosurgery, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0001-5428-051X
Timothy R SmithDepartment of Neurosurgery, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0009-0003-0691-7530
Keith L LigonDepartment of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0002-7733-600X
Patrick Y WenDepartment of Medical Oncology, Center for Neuro-Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-0774-7700
Nathalie Y R AgarDepartment of Neurosurgery, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0003-3149-3146
Jong Woo LeeDepartment of Neurology, Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0001-5283-7476

Funding

TRD 3 - Enabling Technologies for Intraprocedural GuidanceP41EB028741 · NIBIB · BRIGHAM AND WOMEN'S HOSPITAL · 2022 to 2025
$6.8M
Targeted Therapies for GliomaP50CA165962 · BRIGHAM AND WOMEN'S HOSPITAL · 2025 to 2025
$2.4M
Dana-Farber Cancer Institute (DFCI)National Cancer Institute (NCI) P50CA165962National Cancer Institute (NCI) U54CA210180National Institute of Biomedical Imaging and Bioengineering (NIBIB) P41EB015898NCI NIH HHS P50 CA165962NCI NIH HHS U54 CA210180NIBIB NIH HHS P41 EB015898NIBIB NIH HHS P41 EB028741U.S. Department of Veterans Affairs (VA) V1CDA2022-68
6 · The paper itself

Abstract

purposeGlutamatergic neuron-glioma synaptogenesis and peritumoral hyperexcitability promote glioma growth in a positive feedback loop. The objective of this study was to evaluate the feasibility and estimated effect sizes of the targeted AMPA receptor antagonist perampanel on peritumoral hyperexcitability. EXPERIMENTAL

designAn open-label trial was performed comparing perampanel with standard of care (SOC) in patients undergoing resection of newly diagnosed radiologic high-grade glioma. Perampanel was administered as a preoperative loading dose followed by maintenance therapy until progressive disease or up to 12 months. SOC treatment involved levetiracetam for 7 days or as clinically indicated. The primary outcome of hyperexcitability was defined by intraoperative electrocorticography high-frequency oscillation (HFO) rates. Seizure freedom and overall survival were estimated by the Kaplan-Meier method. Tissue concentrations of perampanel, levetiracetam, and correlative biomarkers were measured by mass spectrometry.

resultsHFO rates were similar between patients treated with perampanel and levetiracetam. The trial was terminated early after a planned interim analysis, and outcomes assessed in 11 patients (seven perampanel treated; four treated with SOC). Over a median 281 days of postenrollment follow-up, 27% of patients had seizures, including 14% maintained on perampanel and 50% treated with SOC. Overall survival in perampanel-treated patients was similar to that in a glioblastoma reference cohort. Glutamate concentrations in surface biopsies were positively correlated with HFO rates in adjacent electrode contacts and were not significantly associated with treatment assignment or drug concentrations.

conclusionsGlioma peritumoral glutamate concentrations correlated with high-gamma oscillation rates. Targeting glutamatergic activity with perampanel achieved similar electrocorticographic hyperexcitability levels as in levetiracetam-treated patients.

Indexed as

Brain NeoplasmsGliomaNitrilesPyridonesAdultAgedAnticonvulsantsElectrocorticographyFemaleHumansLevetiracetamMaleMiddle AgedNeoplasm GradingPilot ProjectsReceptors, AMPAAnticonvulsantsLevetiracetamNitrilesperampanelPyridonesReceptors, AMPA

Identifiers

PMID39499201
PMCPMC11611619

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.