Evidence map›Paper›PMID 38216554›Full record

ArticleNature communications2024

Carcinoembryonic antigen-expressing oncolytic measles virus derivative in recurrent glioblastoma: a phase 1 trial.

Evanthia Galanis, Katharine E Dooley, S Keith Anderson, Cheyne B Kurokawa, Xiomara W Carrero, Joon H Uhm, Mark J Federspiel, Alexey A Leontovich, Ileana Aderca, Kimberly B Viker and 12 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase I
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00390299 (Phase I Trial of a Measles Virus Derivative Producing CEA), which is not on this map. Cited by 53 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 2 pooled it
34.1field-weighted citation impact, top 1% 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.

NCT00390299 phase1completednot on this map

Phase I Trial of a Measles Virus Derivative Producing CEA (MV-CEA) in Patients With Recurrent Glioblastoma Multiforme (GBM)

TypeinterventionalSponsorMayo ClinicRan2006 to 2019Enrolled23ConditionsAnaplastic Astrocytoma, Anaplastic Oligodendroglioma, Mixed Glioma, Recurrent GlioblastomaArmsCarcinoembryonic Antigen-Expressing Measles Virus, Laboratory Biomarker Analysis, Therapeutic Conventional Surgery
3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 2 syntheses or guidelines pooled it, 62 citations in OpenAlex.

  1. Pooled it
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  11. Advancements in Drug Delivery Systems in Glioblastoma Therapy.International journal of molecular sciences · 2026
    Review
  12. Article
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  15. Current Status and Evolution of Immunotherapy in Glioma Management.International journal of medical sciences · 2026
    Review
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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

22 authors at 3 institutions in 1 country.

Evanthia GalanisDepartment of Oncology, Division of Medical Oncology, Mayo Clinic, Rochester, MN, USA. galanis.evanthia@mayo.edu.ORCID 0000-0001-8014-786X
Katharine E DooleyQuantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.ORCID 0000-0003-4565-5767
S Keith AndersonQuantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.ORCID 0000-0003-1542-9726
Cheyne B KurokawaDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
Xiomara W CarreroQuantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
Joon H UhmDepartment of Neurology, Division of Neuro-Oncology, Mayo Clinic, Rochester, MN, USA.
Mark J FederspielDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
Alexey A LeontovichQuantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
Ileana AdercaDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
Kimberly B VikerDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
Julie E HammackDepartment of Neurology, Division of Neuro-Oncology, Mayo Clinic, Rochester, MN, USA.
Randolph S MarksDepartment of Oncology, Division of Medical Oncology, Mayo Clinic, Rochester, MN, USA.
Steven I RobinsonDepartment of Oncology, Division of Medical Oncology, Mayo Clinic, Rochester, MN, USA.
Derek R JohnsonDepartment of Radiology, Mayo Clinic, Rochester, MN, USA.
Timothy J KaufmannDepartment of Radiology, Mayo Clinic, Rochester, MN, USA.
Jan C BucknerDepartment of Oncology, Division of Medical Oncology, Mayo Clinic, Rochester, MN, USA.
Daniel H LachanceDepartment of Neurology, Division of Neuro-Oncology, Mayo Clinic, Rochester, MN, USA.
Terry C BurnsDepartment of Neurologic Surgery, Mayo Clinic, Rochester, MN, USA.ORCID 0000-0001-7633-3045
Caterina GianniniDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.ORCID 0000-0003-2757-6782
Aditya RaghunathanDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Ianko D IankovDepartment of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
Ian F ParneyDepartment of Neurologic Surgery, Mayo Clinic, Rochester, MN, USA.
Mayo Clinic in Arizona · USMayo Clinic in Florida · USMayo Clinic · US

Funding

Targeted MV-CEA as a Potent Antitumor Agent against GBMP50CA108961 · NCI · MAYO CLINIC ROCHESTER · PI O'NEILL, BRIAN PATRICK · 2004 to 2015
$22.5M
Novel multipronged Immunovirotherapy Approach for GBM TreatmentR01CA258239 · NCI · MAYO CLINIC ROCHESTER · PI GALANIS, EVANTHIA · 2021 to 2025
$1.9M
Measles Virotherapy for Glioblastoma MultiformeR21CA123839 · NCI · MAYO CLINIC ROCHESTER · PI GALANIS, EVANTHIA · 2006 to 2007
$457k
NCI NIH HHS P50 CA108961NCI NIH HHS R01 CA258239NCI NIH HHS R21 CA123839The Ben & Catherine Ivy Foundation
6 · The paper itself

Abstract

Measles virus (MV) vaccine strains have shown significant preclinical antitumor activity against glioblastoma (GBM), the most lethal glioma histology. In this first in human trial (NCT00390299), a carcinoembryonic antigen-expressing oncolytic measles virus derivative (MV-CEA), was administered in recurrent GBM patients either at the resection cavity (Group A), or, intratumorally on day 1, followed by a second dose administered in the resection cavity after tumor resection on day 5 (Group B). A total of 22 patients received study treatment, 9 in Group A and 13 in Group B. Primary endpoint was safety and toxicity: treatment was well tolerated with no dose-limiting toxicity being observed up to the maximum feasible dose (2×10

Indexed as

GlioblastomaOncolytic VirotherapyOncolytic VirusesCarcinoembryonic AntigenHumansMeasles VaccineMeasles virusNeoplasm Recurrence, LocalTumor MicroenvironmentCarcinoembryonic AntigenMeasles Vaccine

Identifiers

PMID38216554
PMCPMC10786937
OpenAlexW4390796571

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.