Evidence map›Paper›PMID 35105718›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2022

Immune Activity and Response Differences of Oncolytic Viral Therapy in Recurrent Glioblastoma: Gene Expression Analyses of a Phase IB Study.

Katherine E Miller, Kevin A Cassady, Justin C Roth, Jennifer Clements, Kathleen M Schieffer, Kristen Leraas, Anthony R Miller, Nripesh Prasad, Jianmei W Leavenworth, Inmaculada B Aban and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

32 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Oncolytic HSV and cancer drug interactions: Current clinical status and future directions.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Review
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

14 authors at 3 institutions in 1 country.

Katherine E Miller *The Steve and Cindy Rasmussen Institute for Genomic Medicine, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Kevin A Cassady *Department of Pediatrics, The Ohio State University College of Medicine, Columbus, Ohio.
Justin C RothDivision of Pediatric Infectious Diseases, Department of Pediatrics, Heersink School of Medicine, The University of Alabama at Birmingham, Birmingham, Alabama.
Jennifer ClementsDepartment of Neurosurgery, Heersink School of Medicine, The University of Alabama at Birmingham, Birmingham, Alabama.
Kathleen M SchiefferThe Steve and Cindy Rasmussen Institute for Genomic Medicine, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, Ohio.ORCID 0000-0002-2688-8680
Kristen LeraasThe Steve and Cindy Rasmussen Institute for Genomic Medicine, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, Ohio.ORCID 0000-0002-3799-8594
Anthony R MillerThe Steve and Cindy Rasmussen Institute for Genomic Medicine, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Nripesh PrasadHudsonAlpha Institute for Biotechnology, Heersink School of Medicine, Huntsville, Alabama.
Jianmei W LeavenworthDepartment of Neurosurgery, Heersink School of Medicine, The University of Alabama at Birmingham, Birmingham, Alabama.ORCID 0000-0002-4100-9883
Inmaculada B AbanDepartment of Biostatistics, School of Public Health, The University of Alabama at Birmingham, Birmingham, Alabama.ORCID 0000-0002-0563-1691
Richard J WhitleyDivision of Pediatric Infectious Diseases, Department of Pediatrics, Heersink School of Medicine, The University of Alabama at Birmingham, Birmingham, Alabama.
G Yancey GillespieDepartment of Neurosurgery, Heersink School of Medicine, The University of Alabama at Birmingham, Birmingham, Alabama.ORCID 0000-0001-6436-9542
Elaine R MardisThe Steve and Cindy Rasmussen Institute for Genomic Medicine, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, Ohio.ORCID 0000-0002-5892-1553
James M MarkertDepartment of Neurosurgery, Heersink School of Medicine, The University of Alabama at Birmingham, Birmingham, Alabama. jmarkert@uabmc.edu.ORCID 0000-0001-7457-7329
University of Alabama at Birmingham · USNationwide Children's Hospital · USHudsonAlpha Institute for Biotechnology · 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
Project 4:Targeting M2-like Macrophages and MDSC with Myelolytic-VirotherapyU54CA232561 · NCI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI CAIRO, MITCHELL S., CRIPE, TIMOTHY P · 2019 to 2023
$12.1M
Oncolytic Immunotherapy using Chimeric HSV C134: A Phase I Trial and Establishment of Response Indicators in Recurrent Glioma PatientsR01CA222903 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CASSADY, KEVIN A, MARKERT, JAMES M · 2018 to 2020
$1.7M
A Phase 1 Study of M032, a Genetically Engineered HSV-1 Expressing IL-12, in Patients with Recurrent/Progressive Glioblastoma Multiforme, Anaplastic Astrocytoma, or Gliosarcoma.R01CA217179 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GILLESPIE, G. YANCEY, MARKERT, JAMES M · 2017 to 2019
$1.6M
NCI NIH HHS P01 CA071933NCI NIH HHS R01 CA217179NCI NIH HHS R01 CA222903NCI NIH HHS U54 CA232561NCRR NIH HHS M01 RR000032
6 · The paper itself

Abstract

purposePreviously, clinical trials of experimental virotherapy for recurrent glioblastoma multiforme (GBM) demonstrated that inoculation with a conditionally replication-competent Δγ PATIENTS AND

methodsHere, we analyzed tumor RNA sequencing (RNA-seq) data obtained from pre- and posttreatment (collected 2 or 5 days after G207 injection) biopsies from the phase Ib study patients.

resultsUsing a Spearman rank-order correlation analysis, we identified approximately 500 genes whose expression pattern correlated with survival duration. Many of these genes were enriched for the intrinsic IFN-mediated antiviral and adaptive immune functional responses, including immune cell chemotaxis and antigen presentation to T-cells. Furthermore, we show that the expression of several T-cell-related genes was highest in the patient with the longest survival after G207 inoculation.

conclusionsOur data support that the oHSV-induced type I IFN production and the subsequent recruitment of an adaptive immune response differed between enrolled patients and showed association with survival duration in patients with recurrent malignant glioma after treatment with an early generation oHSV.

Indexed as

Clinical Trials, Phase I as TopicOncolytic VirusesSimplexvirusAdultAgedBrain NeoplasmsFemaleGene Expression ProfilingGlioblastomaHumansMaleMiddle AgedNeoplasm Recurrence, LocalOncolytic VirotherapyRNA, NeoplasmSurvival RateRNA, Neoplasm

Identifiers

PMID35105718
PMCPMC8846434
OpenAlexW4210275679

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.