Evidence map›Paper›PMID 14985857›Full record

Trial reportCancer immunology, immunotherapy : CII2004

Vaccination with p53-peptide-pulsed dendritic cells, of patients with advanced breast cancer: report from a phase I study.

Inge Marie Svane, Anders E Pedersen, Hans E Johnsen, Dorte Nielsen, Claus Kamby, Eva Gaarsdal, Kirsten Nikolajsen, Søren Buus, Mogens H Claesson

4 registry-linked trialsOpen access · greenAbstract readClinical TrialClinical Trial, Phase I
In one paragraph

Trial report in Cancer immunology, immunotherapy : CII, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
3.7field-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.

NCT00197860 phase1 / phase2completednot on this map

Vaccination With Autologous Dendritic Cells Pulsed With Tumor Antigens for Treatment of Patients With Renal Cell Carcinoma.A Phase I/II Study.

TypeinterventionalSponsorInge Marie SvaneRan2004 to 2010Enrolled40ConditionsAdvanced Renal Cell CarcinomaArmstumor antigen loaded autologous dendritic cells
NCT00197912 phase1 / phase2completednot on this map

Vaccination With Autologous Dendritic Cells Pulsed With Tumor Antigens for Treatment of Patients With Malignant Melanoma. Phase I/II Study

TypeinterventionalSponsorHerlev HospitalRan2004 to 2010Enrolled25ConditionsAdvanced MelanomaArmstumor antigen loaded autologous dendritic cells
NCT00197925 phase1 / phase2terminatednot on this map

Vaccination With Autologous Dendritic Cells Pulsed With Onco-Peptides for Treatment of Patients With Metastatic Breast Cancer.A Phase I/II Study

TypeinterventionalSponsorHerlev HospitalRan2004Enrolled40ConditionsMetastatic Breast CancerArmsOnco-peptide loaded autologous dendritic cells
NCT00935558 phase2withdrawnnot on this mapstarted 2009, after this paper: background citation

Evaluation of p53peptide-pulsed Dendritic Cells in Combination With an Aromatase Inhibitor as a Treatment for Patients With Breast Cancer With Disease Recurrence After Adjuvant or First Line Endocrine Therapy.

TypeinterventionalSponsorInge Marie SvaneRan2009Enrolled0ConditionsBreast CancerArmsDC vaccine, aromatase inhibitor
3 · Its place in the literature

Who cites it

48 citing papers in PubMed, 112 citations in OpenAlex.

  1. Trial
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  12. Dendritic Cell-Based Immunotherapy in Hot and Cold Tumors.International journal of molecular sciences · 2022
    Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Clinical and Immunological Effects of p53-Targeting Vaccines.Frontiers in cell and developmental biology · 2021
    Review
  18. Review
  19. Article
  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.

Inge Marie SvaneDepartment of Oncology, Herlev University Hospital, Herlev, Denmark. inge.m.svane@dadlnet.dk
Anders E Pedersen
Hans E Johnsen
Dorte Nielsen
Claus Kamby
Eva Gaarsdal
Kirsten Nikolajsen
Søren Buus
Mogens H Claesson
Herlev Hospital · DKUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peptides derived from over-expressed p53 protein are presented by class I MHC molecules and may act as tumour-associated epitopes. Due to the diversity of p53 mutations, immunogenic peptides representing wild-type sequences are preferable as a basis for a broad-spectrum p53-targeting cancer vaccine. Our preclinical studies have shown that wild-type p53-derived HLA-A2-binding peptides are able to activate human T cells and that the generated effector T cells are cytotoxic to human HLA-A2+, p53+ tumour cells. In this phase I pilot study, the toxicity and efficacy of autologous dendritic cells (DCs) loaded with a cocktail of three wild-type and three modified p53 peptides are being analysed in six HLA-A2+ patients with progressive advanced breast cancer. Vaccinations were well tolerated and no toxicity was observed. Disease stabilisation was seen in two of six patients, one patient had a transient regression of a single lymph node and one had a mixed response. ELISpot analyses showed that the p53-peptide-loaded DCs were able to induce specific T-cell responses against modified and unmodified p53 peptides in three patients, including two of the patients with a possible clinical benefit from the treatment. In conclusion, the strategy for p53-DC vaccination seems safe and without toxicity. Furthermore, indications of both immunologic and clinical effect were found in heavily pretreated patients with advanced breast cancer. An independent clinical effect of repeated administration of DCs and IL-2 can not of course be excluded; further studies are necessary to answer these questions.

Indexed as

VaccinationAdultAgedBreast NeoplasmsCancer VaccinesDendritic CellsEpitopes, T-LymphocyteFemaleHLA-A2 AntigenHumansInterferon-gammaLymphatic MetastasisMiddle AgedPeptide FragmentsPilot ProjectsTumor Suppressor Protein p53Cancer VaccinesEpitopes, T-LymphocyteHLA-A2 AntigenInterferon-gammaPeptide FragmentsTumor Suppressor Protein p53

Identifiers

PMID14985857
PMCPMC11032806
OpenAlexW2107884772

What OpenQuestion holds

Textmetadata
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.