Evidence map›Paper›PMID 30081947›Full record

ReviewJournal for immunotherapy of cancer2018

White paper on microbial anti-cancer therapy and prevention.

Neil S Forbes, Robert S Coffin, Liang Deng, Laura Evgin, Steve Fiering, Matthew Giacalone, Claudia Gravekamp, James L Gulley, Hal Gunn, Robert M Hoffman and 13 more

Abstract readReviewConsensus Statement
In one paragraph

Review in Journal for immunotherapy of cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing 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

80 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. AttenuatedFrontiers in immunology · 2026
    Review
  10. Review
  11. Review
  12. Mathematical Modeling ofBioengineering (Basel, Switzerland) · 2025
    Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Frontiers in immunology · 2025
    Article
  18. Review
  19. Review
  20. Article

20 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

23 authors.

Neil S Forbesgrid.266683.f0000 0001 2184 9220Department of Chemical EngineeringUniversity of Massachusetts 159 Goessmann Hall 01003 Amherst MA USA forbes@umass.edu.ORCID http://orcid.org/0000-0002-4745-753X
Robert S CoffinReplimune Abingdon UK.
Liang Deng0000 0001 2171 9952grid.51462.34Department of Medicine, Memorial Sloan Kettering Cancer Center 10065 New York NY USA.
Laura Evgin0000 0004 0459 167Xgrid.66875.3aMayo Clinic Rochester USA.
Steve Fiering0000 0001 2179 2404grid.254880.3Geisel School of Medicine at Dartmouth Hanover USA.
Matthew Giacalonegrid.431045.7Vaxiion Therapeutics San Diego USA.
Claudia Gravekamp0000000121791997grid.251993.5Albert Einstein College of Medicine Bronx USA.
James L Gulley0000 0004 1936 8075grid.48336.3aNational Cancer Institute, National Institutes of Health Bethesda USA.
Hal GunnQu Biologics Burnaby Canada.
Robert M Hoffman0000 0001 2107 4242grid.266100.3UC, San Diego San Diego USA.
Balveen Kaur0000000121548364grid.55460.32University of Texas Austin USA.
Ke Liu0000 0001 2243 3366grid.417587.8Center for Biologics Evaluation and ResearchUS Food and Drug Administration Silver Spring USA.
Herbert Kim Lyerly0000 0004 1936 7961grid.26009.3dDuke University Durham USA.
Ariel E Marciscano0000 0004 1936 8075grid.48336.3aNational Cancer Institute, National Institutes of Health Bethesda USA.
Eddie MoradianSalspera, LLC Oakdale USA.
Sheryl Ruppel0000 0004 4665 8158grid.419407.fLeidos Biomedical Research, Inc. Frederick USA.
Daniel A Saltzman0000000419368657grid.17635.36University of Minnesota Minneapolis USA.
Peter J Tattersall0000000419368710grid.47100.32Yale University New Haven USA.
Steve Thorne0000 0004 1936 9000grid.21925.3dUniversity of Pittsburgh Pittsburgh USA.
Richard G Vile0000 0004 0459 167Xgrid.66875.3aMayo Clinic Rochester USA.
Halle Huihong ZhangBioMed Valley Discoveries, Inc. Kansas City USA.
Shibin Zhou0000 0001 2171 9311grid.21107.35Johns Hopkins University Baltimore USA.
Grant McFadden0000 0001 2151 2636grid.215654.1Center for Immunotherapy, Vaccines and Virotherapy , Biodesign InstituteArizona State University 727 E Tyler Street, Room A330E 85281 Tempe AZ USA grantmcf@asu.edu.

Funding

Cancer Therapy Clinical Trials Using Novel Recombinant VaccinesZIABC010666 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GULLEY, JAMES L. · 2009 to 2025
$22.4M
MOLECULAR BASIS OF PARVOVIRUS TARGET CELL SPECIFICITYR01CA029303 · NCI · YALE UNIVERSITY · PI TATTERSALL, PETER J. · 1985 to 2016
$7.5M
Enhancing Viral Oncolysis with Vasculostatin Gene DeliveryR01CA150153 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KAUR, BALVEEN · 2011 to 2020
$4.0M
Targeting epigenetic regulators using bacterial macromolecule deliveryR01CA188382 · NCI · UNIVERSITY OF MASSACHUSETTS AMHERST · PI FORBES, NEIL S. · 2014 to 2018
$1.6M
NCI NIH HHS R01 CA029303NCI NIH HHS R01 CA150153NCI NIH HHS R01 CA188382
6 · The paper itself

Abstract

In this White Paper, we discuss the current state of microbial cancer therapy. This paper resulted from a meeting ('Microbial Based Cancer Therapy') at the US National Cancer Institute in the summer of 2017. Here, we define 'Microbial Therapy' to include both oncolytic viral therapy and bacterial anticancer therapy. Both of these fields exploit tumor-specific infectious microbes to treat cancer, have similar mechanisms of action, and are facing similar challenges to commercialization. We designed this paper to nucleate this growing field of microbial therapeutics and increase interactions between researchers in it and related fields. The authors of this paper include many primary researchers in this field. In this paper, we discuss the potential, status and opportunities for microbial therapy as well as strategies attempted to date and important questions that need to be addressed. The main areas that we think will have the greatest impact are immune stimulation, control of efficacy, control of delivery, and safety. There is much excitement about the potential of this field to treat currently intractable cancer. Much of the potential exists because these therapies utilize unique mechanisms of action, difficult to achieve with other biological or small molecule drugs. By better understanding and controlling these mechanisms, we will create new therapies that will become integral components of cancer care.

Indexed as

BacteriaGenetic VectorsVirusesAnimalsBiological TherapyCancer VaccinesClinical Studies as TopicCombined Modality TherapyDrug Evaluation, PreclinicalGenetic EngineeringHumansNeoplasmsOncolytic VirotherapyTreatment OutcomeCancer Vaccines

Identifiers

PMID30081947
PMCPMC6091193

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.