Evidence map›Paper›PMID 22781695›Full record

ReviewNature biotechnology2012

Oncolytic virotherapy.

Stephen J Russell, Kah-Whye Peng, John C Bell

Abstract readReview
In one paragraph

Review in Nature biotechnology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 896 papers.

0numbers the graph read from it
0cells of the map it votes in
896citing papers in PubMed
–field-weighted citation impact
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

896 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Tuning epigenetics to enhance cancer virotherapy.Acta pharmaceutica Sinica. B · 2026
    Review
  10. Review
  11. Article
  12. Fully intravenous split-dose administration of the oncolytic adenovirus TILT-123 in advanced solid tumors.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Article

836 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

3 authors.

Stephen J RussellDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA. sjr@mayo.edu
Kah-Whye Peng
John C Bell

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI AKHILESH PANDEY · 1985 to 2026
$151.3M
Use of microfluidic tumor cultures to enable clinical trials of therapies for ovarian cancerP50CA136393 · NCI · MAYO CLINIC ROCHESTER · PI ELLEN L. GOODE · 2009 to 2026
$37.0M
Radiovirotherapy for Multiple MyelomaR01CA100634 · NCI · MAYO CLINIC ROCHESTER · PI RUSSELL, STEPHEN J · 2003 to 2012
$3.2M
Antibody Neutralization of Therapeutic VirusesR01CA129966 · NCI · MAYO CLINIC ROCHESTER · PI RUSSELL, STEPHEN J · 2008 to 2012
$2.5M
Optimizing Measles Virotherapy in the Treatment of Ovarian CancerR01CA136547 · NCI · MAYO CLINIC ROCHESTER · PI GALANIS, EVANTHIA, PENG, KAH-WHYE · 2009 to 2012
$2.0M
Enhancing localization of therapeutic viruses and cells to tumor sitesR01CA129193 · NCI · MAYO CLINIC ROCHESTER · PI PENG, KAH-WHYE · 2009 to 2014
$1.8M
Measles Virotherapy for Multiple MyelomaR01CA168719 · NCI · MAYO CLINIC ROCHESTER · PI DISPENZIERI, ANGELA, RUSSELL, STEPHEN J · 2012 to 2014
$1.5M
Retargeted Oncolytic Measles Viruses Displaying Single-Chain AntibodiesR01CA118488 · NCI · MAYO CLINIC ROCHESTER · PI PENG, KAH-WHYE · 2006 to 2010
$1.3M
NCI NIH HHS CA100634NCI NIH HHS CA118488NCI NIH HHS CA129193NCI NIH HHS CA129966NCI NIH HHS CA136393NCI NIH HHS CA136547NCI NIH HHS N01 CA015083NCI NIH HHS P30 CA015083NCI NIH HHS P50 CA136393NCI NIH HHS R01 CA100634NCI NIH HHS R01 CA118488NCI NIH HHS R01 CA129193NCI NIH HHS R01 CA129966NCI NIH HHS R01 CA136547NCI NIH HHS R01 CA168719
6 · The paper itself

Abstract

Oncolytic virotherapy is an emerging treatment modality that uses replication-competent viruses to destroy cancers. Recent advances include preclinical proof of feasibility for a single-shot virotherapy cure, identification of drugs that accelerate intratumoral virus propagation, strategies to maximize the immunotherapeutic action of oncolytic viruses and clinical confirmation of a critical viremic threshold for vascular delivery and intratumoral virus replication. The primary clinical milestone has been completion of accrual in a phase 3 trial of intratumoral herpes simplex virus therapy using talimogene laherparepvec for metastatic melanoma. Key challenges for the field are to select 'winners' from a burgeoning number of oncolytic platforms and engineered derivatives, to transiently suppress but then unleash the power of the immune system to maximize both virus spread and anticancer immunity, to develop more meaningful preclinical virotherapy models and to manufacture viruses with orders-of-magnitude higher yields than is currently possible.

Indexed as

Immunity, CellularOncolytic VirotherapyAdenoviridaeClinical Trials as TopicGenetic VectorsHumansNeoplasmsOncolytic VirusesSimplexvirus

Identifiers

PMID22781695
PMCPMC3888062

What OpenQuestion holds

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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.