Evidence map›Paper›PMID 24572293›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2014

A phase 1 trial of oncolytic HSV-1, G207, given in combination with radiation for recurrent GBM demonstrates safety and radiographic responses.

James M Markert, Shantanu N Razdan, Hui-Chien Kuo, Alan Cantor, Anette Knoll, Matthias Karrasch, L Burt Nabors, Michael Markiewicz, Bonita S Agee, Jennifer M Coleman and 7 more

Open access · bronzeAbstract readClinical Trial, Phase I
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 207 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
207citing papers in PubMed, 1 pooled it
12.6field-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.

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

207 citing papers in PubMed, 1 synthesis or guideline pooled it, 313 citations in OpenAlex.

  1. Clinical Application of Oncolytic Viruses: A Systematic Review.International journal of molecular sciences · 2020
    Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Oncolytic H-1 Parvovirus Shows Safety and Signs of Immunogenic Activity in a First Phase I/IIa Glioblastoma Trial.Molecular therapy : the journal of the American Society of Gene Therapy · 2017
    Trial
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Oncolytic viruses: advanced strategies in cancer therapy.Signal transduction and targeted therapy · 2026
    Review
  17. Article
  18. Article
  19. Review
  20. Review

147 more citing papers are in PubMed but not listed here.

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

17 authors at 4 institutions in 2 countries.

James M Markert1] Department of Neurosurgery, University of Alabama at Birmingham, Birmingham, Alabama, USA [2] Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama, USA [3] Department of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Shantanu N RazdanSchool of Public Health, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Hui-Chien KuoDepartment of Medicine, Division of Preventative Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Alan CantorDepartment of Medicine, Division of Preventative Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Anette KnollAK Statistics, Bavaria, Germany.
Matthias KarraschInstitute of Medical Microbiology, University Hospital of Friedrich-Schiller-University, Jena, Germany.
L Burt NaborsDepartment of Neurology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Michael MarkiewiczSchool of Public Health, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Bonita S AgeeDepartment of Neurosurgery, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Jennifer M ColemanDepartment of Neurosurgery, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Alfred D LakemanDepartment of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Cheryl A PalmerDepartment of Pathology, Division of Anatomic Pathology, The University of Utah, Salt Lake City, Utah, USA.
Jacqueline N Parker1] Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama, USA [2] Department of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Richard J Whitley1] Department of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, Alabama, USA [2] Department of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Ralph R WeichselbaumDepartment of Radiation Oncology, University of Chicago, Chicago, Illinois, USA.
John B FiveashDepartment of Radiation Oncology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
G Yancey Gillespie1] Department of Neurosurgery, University of Alabama at Birmingham, Birmingham, Alabama, USA [2] Department of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, Alabama, USA [3] Department of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
University of Alabama at Birmingham · USFriedrich Schiller University Jena · DEUniversity of Chicago · USUniversity of Utah · US

Funding

Zevalin Radioimmunotherapy Using a Modified TreatmentM01RR000032 · NCRR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI RICH, ROBERT R. · 1985 to 2008
$23.6M
Virus Production CoreP01CA071933 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WEICHSELBAUM, RALPH R · 1997 to 2013
$14.5M
Viral and molecular chemotherapy of malignant CNS tumorsP50CA097247 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GILLESPIE, G. YANCEY · 2002 to 2009
$13.5M
NCI NIH HHS P01 CA071933NCI NIH HHS P01 CA71933NCI NIH HHS P50 CA097247NCRR NIH HHS M01 RR000032
6 · The paper itself

Abstract

G207, a mutant herpes simplex virus (HSV) type 1, is safe when inoculated into recurrent malignant glioma. We conducted a phase 1 trial of G207 to demonstrate the safety of stereotactic intratumoral administration when given 24 hours prior to a single 5 Gy radiation dose in patients with recurrent malignant glioma. Nine patients with progressive, recurrent malignant glioma despite standard therapy were included. Patients received one dose of G207 stereotactically inoculated into the multiple sites of the enhancing tumor margin and were then treated focally with 5 Gy radiation. Treatment was well tolerated, and no patient developed HSV encephalitis. The median interval between initial diagnosis and G207 inoculation was 18 months (mean: 23 months; range: 11-51 months). Six of the nine patients had stable disease or partial response for at least one time point. Three instances of marked radiographic response to treatment occurred. The median survival time from G207 inoculation until death was 7.5 months (95% confidence interval: 3.0-12.7). In conclusion, this study showed the safety and the potential for clinical response of single-dose oncolytic HSV therapy augmented with radiation in the treatment of malignant glioma patients. Additional studies with oncolytic HSV such as G207 in the treatment of human glioma are recommended.

Indexed as

Genetic TherapyAdultFemaleGliomaHerpesvirus 1, HumanHumansMaleMiddle AgedOncolytic VirotherapyOncolytic VirusesRadiographyVirus Replication

Identifiers

PMID24572293
PMCPMC4015243
OpenAlexW2038709470

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.