Evidence map›Paper›PMID 33175656›Full record

Trial reportHuman vaccines & immunotherapeutics2021

Durability of response to VGX-3100 treatment of HPV16/18 positive cervical HSIL.

Prakash K Bhuyan, Michael Dallas, Kim Kraynyak, Timothy Herring, Matthew Morrow, Jean Boyer, Susan Duff, Joseph Kim, David B Weiner

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Human vaccines & immunotherapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 8% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Signaling pathways and targeted interventions for precancers.Signal transduction and targeted therapy · 2026
    Review
  7. Review
  8. Personalizing DNA Cancer Vaccines.Journal of personalized medicine · 2025
    Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Advances in nucleic acid-based cancer vaccines.Journal of biomedical science · 2025
    Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Review
  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

9 authors at 2 institutions in 1 country.

Prakash K BhuyanInovio Pharmaceuticals, Inc., Plymouth Meeting, PA, USA.ORCID 0000-0003-1937-9658
Michael DallasInovio Pharmaceuticals, Inc., Plymouth Meeting, PA, USA.
Kim KraynyakInovio Pharmaceuticals, Inc., Plymouth Meeting, PA, USA.
Timothy HerringInovio Pharmaceuticals, Inc., Plymouth Meeting, PA, USA.ORCID 0000-0002-3475-8616
Matthew MorrowInovio Pharmaceuticals, Inc., Plymouth Meeting, PA, USA.
Jean BoyerInovio Pharmaceuticals, Inc., Plymouth Meeting, PA, USA.
Susan DuffInovio Pharmaceuticals, Inc., Plymouth Meeting, PA, USA.
Joseph KimInovio Pharmaceuticals, Inc., Plymouth Meeting, PA, USA.
David B WeinerWistar Institute, Philadelphia, PA, USA.
ECRI Institute · USThe Wistar Institute · US

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
NCI NIH HHS P30 CA010815
6 · The paper itself

Abstract

VGX-3100 is an investigational DNA-based immunotherapy being developed as an alternative to surgery and ablation for cervical High-Grade Squamous Intraepithelial Lesion (HSIL) with the aim of preserving reproductive health while treating precancerous disease. Response durability up to 1.5 y following dosing is now reported.Histologic regression and HPV16 and/or HPV 18 (HPV16/18) clearance were previously demonstrated in a randomized, placebo-controlled, double-blind trial and reported for 6 months after the last dose of VGX-3100 or placebo. The presence of HPV16/18, Pap smear diagnoses, and immunogenicity longer-term responses were assessed at 18 months after the last dose.91% (32/35) VGX-3100-treated women, whose cervical HSIL regressed and avoided excision at 6 months following study treatment completion, had no detectable HPV16/18 at 18 months following treatment completion. These results were comparable to those for women who received placebo and then later underwent surgery. For VGX-3100 recipients who regressed at 6 months following study treatment completion and avoided excision during the trial, Pap testing showed no HSIL recurrence at 18 months following VGX-3100 treatment. VGX-3100-induced cellular immune responses specific for HPV 16/18 E6/E7 remained higher than for placebo control recipients at 18 months.In women with cervical HSIL who responded to VGX-3100 and were able to avoid surgery, clinical outcomes were comparable to the placebo control group which underwent conventional surgical treatment. These findings extend the understanding of the durability of the treatment effect of VGX-3100 up to 1.5 y and support that VGX-3100 could be used as an alternative to surgery.

Indexed as

Papillomavirus InfectionsSquamous Intraepithelial LesionsUterine Cervical NeoplasmsFemaleHuman papillomavirus 16Human papillomavirus 18HumansNeoplasm Recurrence, LocalPapillomaviridaePapillomavirus VaccinesVaccines, DNAPapillomavirus VaccinesVaccines, DNAVGX-3100cancercervicalDNAdurabilityHPVimmunotherapy

Identifiers

PMID33175656
PMCPMC8078703
OpenAlexW3101789168

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.