Evidence map›Paper›PMID 22894670›Full record

ReviewFuture oncology (London, England)2012

Peptide vaccines and targeting HER and VEGF proteins may offer a potentially new paradigm in cancer immunotherapy.

Pravin T P Kaumaya, Kevin Chu Foy

Abstract readReview
In one paragraph

Review in Future oncology (London, England), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 pooled it
2.3field-weighted citation impact, top 12% 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

23 citing papers in PubMed, 2 syntheses or guidelines pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. A systematic review of vascular endothelial growth factor expression as a biomarker of prognosis in patients with osteosarcoma.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2013
    Pooled it
  3. Article
  4. Review
  5. VEGF signaling: Role in angiogenesis and beyond.Biochimica et biophysica acta. Reviews on cancer · 2024
    Review
  6. Review
  7. Recent Applications of Retro-Inverso Peptides.International journal of molecular sciences · 2021
    Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Clinical applications of mouse models for breast cancer engaging HER2/neu.Integrative cancer science and therapeutics · 2016
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article
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

2 authors at 1 institution in 1 country.

Pravin T P KaumayaDepartments of Obstetrics & Gynecology, OSU Wexner Medical Center, James Cancer Hospital & Solove Research Institute & the Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210, USA. pravin.kaumaya@osumc.edu
Kevin Chu Foy
The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · US

Funding

CHIMERIC AND MULTIVALENT HER 2 CANCER VACCINE STRATEGIESR01CA084356 · NCI · OHIO STATE UNIVERSITY · PI KAUMAYA, PRAVIN T.P · 2000 to 2003
$920k
Phase 1b Active Immunotherapy with HER-2 Multi-epitope vR21CA094555 · NCI · OHIO STATE UNIVERSITY · PI KAUMAYA, PRAVIN T.P · 2002 to 2003
$656k
STRUCTURE/CONFORMATION ASPECTS IN PEPTIDE VACCINESR01AI040302 · NIAID · OHIO STATE UNIVERSITY · PI KAUMAYA, PRAVIN TP · 1997 to 2001
$428k
NCI NIH HHS R01 CA084356NCI NIH HHS R21 CA094555NIAID NIH HHS R01 AI040302
6 · The paper itself

Abstract

The ErbB family (HER-1, HER-2, HER-3 and HER-4) of receptor tyrosine kinases has been the focus of cancer immunotherapeutic strategies while antiangiogenic therapies have focused on VEGF and its receptors VEGFR-1 and VEGFR-2. Agents targeting receptor tyrosine kinases in oncology include therapeutic antibodies to receptor tyrosine kinase ligands or the receptors themselves, and small-molecule inhibitors. Many of the US FDA-approved therapies targeting HER-2 and VEGF exhibit unacceptable toxicities, and show problems of efficacy, development of resistance and unacceptable safety profiles that continue to hamper their clinical progress. The combination of different peptide vaccines and peptidomimetics targeting specific molecular pathways that are dysregulated in tumors may potentiate anticancer immune responses, bypass immune tolerance and circumvent resistance mechanisms. The focus of this review is to discuss efforts in our laboratory spanning two decades of rationally developing peptide vaccines and therapeutics for breast cancer. This review highlights the prospective benefit of a new, untapped category of therapies biologically targeted to EGF receptor (HER-1), HER-2 and VEGF with potential peptide 'blockbusters' that could lay the foundation of a new paradigm in cancer immunotherapy by creating clinical breakthroughs for safe and efficacious cancer cures.

Indexed as

Angiogenesis InhibitorsAnimalsCancer VaccinesDisease Models, AnimalEpitopes, B-LymphocyteErb-b2 Receptor Tyrosine KinasesErbB ReceptorsHumansImmunotherapyMolecular MimicryMolecular Targeted TherapyNeoplasmsNeovascularization, PathologicReceptors, Vascular Endothelial Growth FactorSignal TransductionVaccines, SubunitAngiogenesis InhibitorsCancer VaccinesEpitopes, B-LymphocyteErb-b2 Receptor Tyrosine KinasesErbB ReceptorsReceptors, Vascular Endothelial Growth FactorVaccines, SubunitVascular Endothelial Growth Factors

Identifiers

PMID22894670
PMCPMC4591923
OpenAlexW2047568265

What OpenQuestion holds

Textmetadata
LicenceTDM
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.