Evidence map›Paper›PMID 24154719›Full record

ArticleCancer prevention research (Philadelphia, Pa.)2013

A multiantigen vaccine targeting neu, IGFBP-2, and IGF-IR prevents tumor progression in mice with preinvasive breast disease.

Mary L Disis, Ekram Gad, Daniel R Herendeen, Vy Phan- Lai, Kyong Hwa Park, Denise L Cecil, Megan M O'Meara, Piper M Treuting, Ronald A Lubet

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Cancer prevention research (Philadelphia, Pa.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02780401 (A Phase I Trial of the Safety and Immunogenicity of a DNA Plasmid Based Vaccine), which is not on this map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 6% 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.

NCT02780401 phase1completednot on this mapstarted 2016, after this paper: background citation

A Phase I Trial of the Safety and Immunogenicity of a DNA Plasmid Based Vaccine (WOKVAC) Encoding Epitopes Derived From Three Breast Cancer Antigens (IGFBP-2, HER2, and IGF-1R) in Patients With Breast Cancer

TypeinterventionalSponsorUniversity of WashingtonRan2016 to 2022Enrolled32ConditionsHER2/Neu Negative, No Evidence of Disease, One or More Positive Axillary Nodes, Stage IB Breast CancerArmsLaboratory Biomarker Analysis, pUMVC3-IGFBP2-HER2-IGF1R Plasmid DNA Vaccine, Sargramostim
3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 70 citations in OpenAlex.

  1. Pooled it
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  13. Emerging Therapeutic Agents for Colorectal Cancer.Molecules (Basel, Switzerland) · 2021
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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 2 countries.

Mary L DisisTumor Vaccine Group, Center for Translational Medicine in Women's Health, 850 Republican Street, Box 358050, University of Washington, Seattle, WA 98109. ndisis@uw.edu.
Ekram Gad
Daniel R Herendeen
Vy Phan- Lai
Kyong Hwa Park
Denise L Cecil
Megan M O'Meara
Piper M Treuting
Ronald A Lubet
University of Washington · USNational Cancer Institute · US

Funding

Vaccinating against IGFBP-2 to prevent ovarian cancer relapseP50CA083636 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI DRESCHER, CHARLES, URBAN, NICOLE DENISE · 1999 to 2015
$35.1M
Immune diagnostics and vaccine targets: breast cancer antigens from mice to womenU01CA141539 · NCI · UNIVERSITY OF WASHINGTON · PI DISIS, MARY L. · 2009 to 2013
$3.7M
NCI NIH HHS N01 CN053300NCI NIH HHS N01-CN-53300NCI NIH HHS P50 CA083636NCI NIH HHS U01 CA141539
6 · The paper itself

Abstract

A multiantigen multipeptide vaccine, targeting proteins expressed in preinvasive breast lesions, can stimulate type I CD4(+) T cells which have been shown to be deficient in both patients with breast cancer and mice that develop mammary tumors. Transgenic mice (TgMMTV-neu) were immunized with a multiantigen peptide vaccine specific for neu, insulin-like growth factor-binding protein 2 and insulin-like growth factor receptor-I at a time when some of the animals already had preinvasive lesions (18 weeks of age). Although immunization with each individual antigen was partially effective in inhibiting tumor growth, immunization with the multiantigen vaccine was highly effective, blocking development of palpable lesions in 65% of mice and slowing tumor growth in the infrequent palpable tumors, which did arise. Protection was mediated by CD4(+) T cells, and the few slow-growing tumors that did develop demonstrated a significant increase in intratumoral CD8(+) T cells as compared with controls (P = 0.0007). We also combined the vaccine with agents that were, by themselves, partially effective inhibitors of tumor progression in this model; lapatinib and the RXR agonist bexarotene. Although the combination of lapatinib and vaccination performed similarly to vaccination alone (P = 0.735), bexarotene and vaccination significantly enhanced disease-free survival (P < 0.0001), and approximately 90% of the mice showed no pathologic evidence of carcinomas at one year. The vaccine also demonstrated significant clinical efficacy in an additional transgenic model of breast cancer (TgC3(I)-Tag). Chemoimmunoprevention combinations may be an effective approach to breast cancer prevention even when the vaccine is administered in the presence of subclinical disease.

Indexed as

Adoptive TransferAnimalsAntineoplastic Combined Chemotherapy ProtocolsBexaroteneErb-b2 Receptor Tyrosine KinasesFemaleInsulin-Like Growth Factor Binding Protein 2LapatinibLymphocytes, Tumor-InfiltratingMammary Neoplasms, AnimalMiceMice, TransgenicNeoplasm InvasivenessPrecancerous ConditionsQuinazolinesReceptor, IGF Type 1BexaroteneERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesIGFBP2 protein, humanInsulin-Like Growth Factor Binding Protein 2LapatinibQuinazolinesReceptor, IGF Type 1TetrahydronaphthalenesVaccines, Subunit

Identifiers

PMID24154719
PMCPMC3864759
OpenAlexW2143450041

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.