Evidence map›Paper›PMID 10845725›Full record

Trial reportGene therapy2000

Conditionally replicating herpes simplex virus mutant, G207 for the treatment of malignant glioma: results of a phase I trial.

J M Markert, M D Medlock, S D Rabkin, G Y Gillespie, T Todo, W D Hunter, C A Palmer, F Feigenbaum, C Tornatore, F Tufaro and 1 more

Registry-linked trialAbstract readClinical TrialClinical Trial, Phase I
PubMed Publisher
In one paragraph

Trial report in Gene therapy, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00028158 (An Open-Label Phase Ib/II Study of the Safety, Tolerability and Efficacy of G207, a Genetically Engineered Herpes Simplex Type-1 Virus, Administered Intracerebrally to Patients With Recurrent Malignant Glioma), which is not on this map. Cited by 436 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
436citing papers in PubMed, 1 pooled it
36.7field-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.

NCT00028158 phase1 / phase2completednot on this mapstarted 2001, after this paper: background citation

An Open-Label Phase Ib/II Study of the Safety, Tolerability and Efficacy of G207, a Genetically Engineered Herpes Simplex Type-1 Virus, Administered Intracerebrally to Patients With Recurrent Malignant Glioma

TypeinterventionalSponsorMediGeneRan2001 to 2003Enrolled65ConditionsGlioma, Astrocytoma, GlioblastomaArmsG207, an oncolytic virus
3 · Its place in the literature

Who cites it

436 citing papers in PubMed, 1 synthesis or guideline pooled it, 974 citations in OpenAlex.

  1. 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. Trial
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Polio virotherapy provokes MDA5 signaling and CD4Microbiology and molecular biology reviews : MMBR · 2025
    Review
  16. Article
  17. Virus Against Cancer: Paradigm-Shifting Biological Concepts.Current neurology and neuroscience reports · 2025
    Review
  18. Review
  19. Review
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

J M MarkertUniversity of Alabama at Birmingham: Department of Surgery, USA.
M D Medlock
S D Rabkin
G Y Gillespie
T Todo
W D Hunter
C A Palmer
F Feigenbaum
C Tornatore
F Tufaro
R L Martuza
Georgetown University Medical Center · USUniversity of Alabama at Birmingham · USGeorgetown University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G207 is a conditionally replicating derivative of herpes simplex virus (HSV) type-1 strain F engineered with deletions of both gamma(1)34.5 loci and a lacZ insertion disabling the UL39 gene. We have demonstrated the efficacy of G207 in treating malignant glial tumors in athymic mice, as well as the safety of intracerebral G207 inoculation in mice and in Aotus nancymai. We sought to determine the safety of G207 inoculation into cerebral malignant glial tumors in humans. Criteria for inclusion into this dose-escalation study were the diagnosis of histologically proven malignant glioma, Karnofsky score > or = 70, recurrence despite surgery and radiation therapy, and an enhancing lesion greater than 1 cm in diameter. Serial magnetic resonance images were obtained for volumetric analysis. The trial commenced at a dose of 10(6) plaque forming units (p.f.u.) inoculated at a single enhancing site and was completed when the 21st patient was inoculated with 3x10(9) p.f.u. at five sites. While adverse events were noted in some patients, no toxicity or serious adverse events could unequivocally be ascribed to G207. No patient developed HSV encephalitis. We found radiographic and neuropathologic evidence suggestive of anti-tumor activity and long-term presence of viral DNA in some cases.

Indexed as

Virus ReplicationAdultAgedAntibodies, ViralBrain NeoplasmsDisease ProgressionFemaleFollow-Up StudiesGenetic TherapyGlioblastomaHerpesvirus 1, HumanHumansMagnetic Resonance ImagingMaleMiddle AgedNeoplasm Recurrence, LocalAntibodies, Viral

Identifiers

PMID10845725
OpenAlexW2057382033

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.