Evidence map›Paper›PMID 10587357›Full record

Trial reportThe Journal of experimental medicine1999

Vaccination with mage-3A1 peptide-pulsed mature, monocyte-derived dendritic cells expands specific cytotoxic T cells and induces regression of some metastases in advanced stage IV melanoma.

B Thurner, I Haendle, C Röder, D Dieckmann, P Keikavoussi, H Jonuleit, A Bender, C Maczek, D Schreiner, P von den Driesch and 5 more

2 registry-linked trialsOpen access · bronzeAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in The Journal of experimental medicine, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 273 papers.

0numbers the graph read from it
0cells of the map it votes in
273citing papers in PubMed
32.7field-weighted citation impact, top 1% 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.

NCT00683670 phase1completednot on this mapstarted 2008, after this paper: background citation

Mature Dendritic Cell Vaccination Against gp100 in Patients With Advanced Melanoma

TypeinterventionalSponsorUniversity of PennsylvaniaRan2008 to 2016Enrolled17ConditionsMelanomaArmscyclophosphamide, Mature dendritic cell vaccine
NCT04212377 phase2completednot on this mapstarted 2019, after this paper: background citation

An Exploratory Study: Dendritic Cells for Immunotherapy of Metastatic Endometrial Cancer Patients

TypeinterventionalSponsorRadboud University Medical CenterRan2019 to 2021Enrolled8ConditionsEndometrial CancerArmsDendritic Cells for endometrial cancer
3 · Its place in the literature

Who cites it

273 citing papers in PubMed, 1,225 citations in OpenAlex.

  1. Trial
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  3. Immunotherapy by autologous dendritic cell vaccine in patients with advanced HCC.Journal of cancer research and clinical oncology · 2013
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  16. Article
  17. Review
  18. Cellular immunotherapy in melanoma: the next frontier in cancer treatment.Journal of experimental & clinical cancer research : CR · 2026
    Review
  19. Article
  20. Review

213 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

15 authors at 4 institutions in 2 countries.

B ThurnerDepartment of Dermatology, University of Erlangen-Nuremberg, D-91052 Erlangen, Germany.
I Haendle
C Röder
D Dieckmann
P Keikavoussi
H Jonuleit
A Bender
C Maczek
D Schreiner
P von den Driesch
E B Bröcker
R M Steinman
A Enk
E Kämpgen
G Schuler
Friedrich-Alexander-Universität Erlangen-Nürnberg · DEUniversity of Würzburg · DEJohannes Gutenberg University Mainz · DERockefeller University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DCs) are considered to be promising adjuvants for inducing immunity to cancer. We used mature, monocyte-derived DCs to elicit resistance to malignant melanoma. The DCs were pulsed with Mage-3A1 tumor peptide and a recall antigen, tetanus toxoid or tuberculin. 11 far advanced stage IV melanoma patients, who were progressive despite standard chemotherapy, received five DC vaccinations at 14-d intervals. The first three vaccinations were administered into the skin, 3 x 10(6) DCs each subcutaneously and intradermally, followed by two intravenous injections of 6 x 10(6) and 12 x 10(6) DCs, respectively. Only minor (less than or equal to grade II) side effects were observed. Immunity to the recall antigen was boosted. Significant expansions of Mage-3A1-specific CD8(+) cytotoxic T lymphocyte (CTL) precursors were induced in 8/11 patients. Curiously, these immune responses often declined after the intravenous vaccinations. Regressions of individual metastases (skin, lymph node, lung, and liver) were evident in 6/11 patients. Resolution of skin metastases in two of the patients was accompanied by erythema and CD8(+) T cell infiltration, whereas nonregressing lesions lacked CD8(+) T cells as well as Mage-3 mRNA expression. This study proves the principle that DC "vaccines" can frequently expand tumor-specific CTLs and elicit regressions even in advanced cancer and, in addition, provides evidence for an active CD8(+) CTL-tumor cell interaction in situ as well as escape by lack of tumor antigen expression.

Indexed as

Cancer VaccinesAdultAgedAntigens, NeoplasmCD8-Positive T-LymphocytesDendritic CellsFemaleHumansImmunization ScheduleLung NeoplasmsLymphocytes, Tumor-InfiltratingMaleMelanomaMiddle AgedMonocytesNeoplasm MetastasisAntigens, NeoplasmCancer VaccinesMAGEA3 protein, humanNeoplasm ProteinsTetanus ToxoidTuberculin

Identifiers

PMID10587357
PMCPMC2195739
OpenAlexW2117216774

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.