Evidence map›Paper›PMID 31727154›Full record

Trial reportJournal for immunotherapy of cancer2019

Blood-derived dendritic cell vaccinations induce immune responses that correlate with clinical outcome in patients with chemo-naive castration-resistant prostate cancer.

Harm Westdorp, Jeroen H A Creemers, Inge M van Oort, Gerty Schreibelt, Mark A J Gorris, Niven Mehra, Michiel Simons, Anna L de Goede, Michelle M van Rossum, Alexandra J Croockewit and 10 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Journal for immunotherapy of cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02692976 (A Randomized Phase IIa Study), which is not on this map. Cited by 73 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 2 pooled it
4.4field-weighted citation impact, top 5% 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.

NCT02692976 phase2completednot on this map

A Randomized Phase IIa Study: Natural Dendritic Cells for Immunotherapy of Chemo-naive Metastatic Castration-resistant Prostate Cancer Patients

TypeinterventionalSponsorRadboud University Medical CenterRan2015 to 2019Enrolled21ConditionsProstatic Neoplasms, Immunotherapy, Dendritic Cells, VaccinesArmsmDC vaccination, pDC vaccination, mDC and pDC vaccination
3 · Its place in the literature

Who cites it

73 citing papers in PubMed, 2 syntheses or guidelines pooled it, 110 citations in OpenAlex.

  1. Pooled it
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  12. Role of cDC2 in priming CD8Journal for immunotherapy of cancer · 2025
    Review
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  15. Article
  16. Review
  17. Research progress of MUC1 in genitourinary cancers.Cellular & molecular biology letters · 2024
    Review
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  19. NY-ESO-1 antigen: A promising frontier in cancer immunotherapy.Clinical and translational medicine · 2024
    Review
  20. Review

13 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

20 authors at 2 institutions in 2 countries.

Harm WestdorpDepartment of Tumor Immunology and Medical Oncology, Radboud Institute for Molecular Life Sciences, Radboudumc, Geert Grooteplein 26, 6525 GA, Nijmegen, The Netherlands.ORCID 0000-0002-3336-4164
Jeroen H A CreemersDepartment of Tumor Immunology and Medical Oncology, Radboud Institute for Molecular Life Sciences, Radboudumc, Geert Grooteplein 26, 6525 GA, Nijmegen, The Netherlands.
Inge M van OortDepartment of Urology, Radboudumc, Nijmegen, The Netherlands.
Gerty SchreibeltDepartment of Tumor Immunology and Medical Oncology, Radboud Institute for Molecular Life Sciences, Radboudumc, Geert Grooteplein 26, 6525 GA, Nijmegen, The Netherlands.
Mark A J GorrisDepartment of Tumor Immunology and Medical Oncology, Radboud Institute for Molecular Life Sciences, Radboudumc, Geert Grooteplein 26, 6525 GA, Nijmegen, The Netherlands.
Niven MehraDepartment of Tumor Immunology and Medical Oncology, Radboud Institute for Molecular Life Sciences, Radboudumc, Geert Grooteplein 26, 6525 GA, Nijmegen, The Netherlands.
Michiel SimonsDepartment of Pathology, Radboudumc, Nijmegen, The Netherlands.
Anna L de GoedeDepartment of Pharmacy, Radboudumc, Nijmegen, The Netherlands.
Michelle M van RossumDepartment of Dermatology, Radboudumc, Nijmegen, The Netherlands.
Alexandra J CroockewitDepartment of Hematology, Radboudumc, Nijmegen, The Netherlands.
Carl G FigdorDepartment of Tumor Immunology and Medical Oncology, Radboud Institute for Molecular Life Sciences, Radboudumc, Geert Grooteplein 26, 6525 GA, Nijmegen, The Netherlands.
J Alfred WitjesDepartment of Urology, Radboudumc, Nijmegen, The Netherlands.
Erik H J G AarntzenDepartment of Radiology and Nuclear Medicine, Radboudumc, Nijmegen, The Netherlands.
Roel D M MusDepartment of Radiology and Nuclear Medicine, Radboudumc, Nijmegen, The Netherlands.
Mareke BrüningMiltenyi Biotec GmbH, Bergisch Gladbach, Germany.
Katja PetryMiltenyi Biotec GmbH, Bergisch Gladbach, Germany.
Martin GotthardtDepartment of Radiology and Nuclear Medicine, Radboudumc, Nijmegen, The Netherlands.
Jelle O BarentszDepartment of Radiology and Nuclear Medicine, Radboudumc, Nijmegen, The Netherlands.
I Jolanda M de VriesDepartment of Tumor Immunology and Medical Oncology, Radboud Institute for Molecular Life Sciences, Radboudumc, Geert Grooteplein 26, 6525 GA, Nijmegen, The Netherlands. Jolanda.deVries@radboudumc.nl.
Winald R GerritsenDepartment of Tumor Immunology and Medical Oncology, Radboud Institute for Molecular Life Sciences, Radboudumc, Geert Grooteplein 26, 6525 GA, Nijmegen, The Netherlands.
Radboud University Nijmegen · NLMiltenyi Biotec (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClinical benefit of cellular immunotherapy has been shown in patients with castration-resistant prostate cancer (CRPC). We investigated the immunological response and clinical outcome of vaccination with blood-derived CD1c

methodsIn this randomized phase IIa trial, 21 chemo-naive CRPC patients received maximally 9 vaccinations with mature mDCs, pDCs or a combination of mDCs plus pDCs. DCs were stimulated with protamine/mRNA and loaded with tumor-associated antigens NY-ESO-1, MAGE-C2 and MUC1. Primary endpoint was the immunological response after DC vaccination, which was monitored in peripheral blood and in T cell cultures of biopsies of post-treatment delayed-type hypersensitivity-skin tests. Main secondary endpoints were safety, feasibility, radiological PFS (rPFS) and overall survival. Radiological responses were assessed by MRIs and contrast-enhanced

resultsBoth tetramer/dextramer-positive (dm

conclusionsImmunotherapy with blood-derived DC subsets was feasible and safe and induced functional antigen-specific T cells. The presence of functional antigen-specific T cells correlated with an improved clinical outcome.

trial registrationClinicalTrials.gov identifier NCT02692976, registered 26 February 2016, retrospectively registered.

Indexed as

Cancer VaccinesAgedAntigens, NeoplasmDendritic CellsHumansKaplan-Meier EstimateMaleMembrane ProteinsMiddle AgedMucin-1Neoplasm ProteinsProstatic Neoplasms, Castration-ResistantSkinT-LymphocytesTreatment OutcomeVaccinationAntigens, NeoplasmCancer VaccinesCTAG1B protein, humanMAGEC2 protein, humanMembrane ProteinsMUC1 protein, humanMucin-1Neoplasm ProteinsCastration-resistant prostate cancerDendritic cell vaccinationImmunotherapy

Identifiers

PMID31727154
PMCPMC6854814
OpenAlexW2986470936

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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.