Evidence map›Paper›PMID 38263486›Full record

ArticleJournal of neuro-oncology2024

Phase I study targeting newly diagnosed grade 4 astrocytoma with bispecific antibody armed T cells (EGFR BATs) in combination with radiation and temozolomide.

Camilo E Fadul, Archana Thakur, Jungeun Kim, Jessica Kassay-McAllister, Dana Schalk, M Beatriz Lopes, Joseph Donahue, Benjamin Purow, Patrick Dillon, Tri Le and 3 more

2 registry-linked trialsOpen access · hybridAbstract readClinical Trial, Phase I
In one paragraph

Article in Journal of neuro-oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.5field-weighted citation impact, top 9% of its field
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.

NCT03344250 phase1completednot on this map

A Phase I Study Targeting Newly Diagnosed Glioblastoma With Anti-CD3 × Anti-EGFR Bispecific Antibody Armed T Cells (EGFR BATs) in Combination With Radiation and Temozolomide

TypeinterventionalSponsorUniversity of VirginiaRan2018 to 2023Enrolled16ConditionsGlioblastoma, Glioblastoma MultiformeArmsEGFR BATs with TMZ following SOC RT/TMZ, Weekly EGFR BATs following SOC RT/TMZ
NCT07343986 phase1recruitingnot on this mapstarted 2026, after this paper: background citation

Phase I Clinical Trial of Anti-CD3 × Anti-EGFR Bispecific-armed T Cells (EGFR BATs) and Low-Intensity Focused Ultrasound (LIFU) Blood-brain Barrier Opening in Patients With MGMT Unmethylated Glioblastoma (GBM)

TypeinterventionalSponsorUniversity of VirginiaRan2026 to 2028Enrolled12ConditionsGlioblastoma (GBM)Armsanti-EGFR bispecific-armed T cells, Low-Intensity Focused Ultrasound
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 10 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 1 country.

Camilo E Fadul *Department of Neurology, Division of Neuro-Oncology, University of Virginia Health System, P.O. Box 800394, Charlottesville, VA, 22908, USA. cef3w@uvahealth.org.
Archana Thakur *Bone Marrow Transplant Program, Division Hematology/Oncology, Department of Medicine, University of Virginia Cancer Center, Charlottesville, VA, USA.
Jungeun KimOffice of Clinical Research, School of Medicine, University of Virginia Cancer Center, Charlottesville, VA, USA.
Jessica Kassay-McAllisterBone Marrow Transplant Program, Division Hematology/Oncology, Department of Medicine, University of Virginia Cancer Center, Charlottesville, VA, USA.
Dana SchalkBone Marrow Transplant Program, Division Hematology/Oncology, Department of Medicine, University of Virginia Cancer Center, Charlottesville, VA, USA.
M Beatriz LopesDepartment of Pathology, Divisions of Neuropathology, University of Virginia Health System, Charlottesville, VA, USA.
Joseph DonahueDepartment of Radiology and Medical Imaging, Division of Neuroradiology, University of Virginia Health System, Charlottesville, VA, USA.
Benjamin PurowDepartment of Neurology, Division of Neuro-Oncology, University of Virginia Health System, P.O. Box 800394, Charlottesville, VA, 22908, USA.
Patrick DillonDivision Hematology/Oncology, Department of Medicine, University of Virginia Cancer Center, Charlottesville, VA, USA.
Tri LeDivision Hematology/Oncology, Department of Medicine, University of Virginia Cancer Center, Charlottesville, VA, USA.
David SchiffDepartment of Neurology, Division of Neuro-Oncology, University of Virginia Health System, P.O. Box 800394, Charlottesville, VA, 22908, USA.
Qin LiuBiostatistics Unit, Molecular & Cellular Oncogenesis Program, The Wistar Institute, Philadelphia, PA, USA.
Lawrence G LumBone Marrow Transplant Program, Division Hematology/Oncology, Department of Medicine, University of Virginia Cancer Center, Charlottesville, VA, USA.
University of Virginia Health System · USUniversity of Virginia Cancer CenterUniversity of Virginia · USThe Wistar Institute · US

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Jay William FOX · 1987 to 2026
$72.1M
Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI Julie Lynn Boerner · 1985 to 2026
$68.4M
Targeting Neuroblastoma with armed T cellsR01CA182526 · NCI · WAYNE STATE UNIVERSITY · PI CHEUNG, NAI-KONG V, LUM, LAWRENCE G · 2014 to 2019
$3.9M
NCI NIH HHS P30 CA010815NCI NIH HHS P30 CA022453NCI NIH HHS P30CA022453NCI NIH HHS P30 CA044579NCI NIH HHS R01 CA182526
6 · The paper itself

Abstract

purposeThe purpose of this study was to determine the safety, feasibility, and immunologic responses of treating grade 4 astrocytomas with multiple infusions of anti-CD3 x anti-EGFR bispecific antibody (EGFRBi) armed T cells (EGFR BATs) in combination with radiation and chemotherapy.

methodsThis phase I study used a 3 + 3 dose escalation design to test the safety and feasibility of intravenously infused EGFR BATs in combination with radiation and temozolomide (TMZ) in patients with newly diagnosed grade 4 astrocytomas (AG4). After finding the feasible dose, an expansion cohort with unmethylated O

resultsThe highest feasible dose was 80 × 10

conclusionTargeting AG4 with EGFR BATs at the maximum feasible dose of 80 × 10 CLINICALTRIALS: gov Identifier: NCT03344250.

Indexed as

Brain NeoplasmsGlioblastomaAntineoplastic Agents, AlkylatingErbB ReceptorsHumansLeukocytes, MononuclearTemozolomideT-LymphocytesAntineoplastic Agents, AlkylatingEGFR protein, humanErbB ReceptorsTemozolomideBispecific antibodiesEGFRGlioblastomaImmune therapyPhase I

Identifiers

PMID38263486
PMCPMC10834565
OpenAlexW4391130728

What OpenQuestion holds

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Registered trials

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 OpenQuestion graph.