Evidence map›Paper›PMID 15627214›Full record

Trial reportCancer immunology, immunotherapy : CII2005

A phase I vaccination study with tyrosinase in patients with stage II melanoma using recombinant modified vaccinia virus Ankara (MVA-hTyr).

Ralf G Meyer, Cedrik M Britten, Ulrike Siepmann, Barbara Petzold, Tolga A Sagban, Hans A Lehr, Bernd Weigle, Marc Schmitz, Luis Mateo, Burkhard Schmidt and 14 more

Open access · greenAbstract readClinical TrialClinical Trial, Phase I
In one paragraph

Trial report in Cancer immunology, immunotherapy : CII, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 65 citations in OpenAlex.

  1. Trial
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  7. p53MVA therapy in patients with refractory gastrointestinal malignancies elevates p53-specific CD8+ T-cell responses.Clinical cancer research : an official journal of the American Association for Cancer Research · 2014
    Article
  8. Article
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  10. Modified vaccinia virus Ankara delivers a robust surrogate marker for immune monitoring to sarcoma cells even if cells are being exposed to chemotherapy and heat treatment.International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group · 2012
    Article
  11. Article
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  14. Review
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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

24 authors at 6 institutions in 1 country.

Ralf G MeyerIII. Medizinische Klinik, Johannes Gutenberg-Universitaet, Langenbeckstrasse 1, 55116 Mainz, Germany.
Cedrik M Britten
Ulrike Siepmann
Barbara Petzold
Tolga A Sagban
Hans A Lehr
Bernd Weigle
Marc Schmitz
Luis Mateo
Burkhard Schmidt
Helga Bernhard
Thilo Jakob
Rüdiger Hein
Gerold Schuler
Beatrice Schuler-Thurner
Stephan N Wagner
Ingo Drexler
Gerd Sutter
Nathaly Arndtz
Paul Chaplin
Jost Metz
Alexander Enk
Christoph Huber
Thomas Wölfel
Johannes Gutenberg University Mainz · DEBavarian Nordic (Germany) · DETU Dresden · DEUniversitätsklinikum Erlangen · DEEssen University Hospital · DEFresenius (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A significant percentage of patients with stage II melanomas suffer a relapse after surgery and therefore need the development of adjuvant therapies. In the study reported here, safety and immunological response were analyzed after vaccination in an adjuvant setting with recombinant modified vaccinia virus Ankara carrying the cDNA for human tyrosinase (MVA-hTyr). A total of 20 patients were included and vaccinated three times at 4-week intervals with 5x10(8) IU of MVA-hTyr each time. The responses to the viral vector, to known HLA class I-restricted tyrosinase peptides, and to dendritic cells transfected with tyrosinase mRNA, were investigated by ELISpot assay on both ex vivo T cells and on T cells stimulated in vitro prior to testing. The delivery of MVA-hTyr was safe and did not cause any side effects above grade 2. A strong response to the viral vector was achieved, indicated by an increase in the frequency of MVA-specific CD4+ and CD8+ T cells and an increase in virus-specific antibody titers. However, no tyrosinase-specific T-cell or antibody response was observed with MVA-hTyr in any of the vaccinated patients. Although MVA-hTyr provides a safe and effective antigen-delivery system, it does not elicit a measurable immune response to its transgene product in patients with stage II melanoma after repeated combined intradermal and subcutaneous vaccination. We presume that modification of the antigen and/or prime-boost vaccination applying different approaches to antigen delivery may be required to induce an effective tyrosinase-specific immune response.

Indexed as

AdultAgedAntibodiesAntibody FormationCancer VaccinesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesDendritic CellsDNA, ComplementaryGenetic VectorsHLA-A AntigensHumansMaleMelanomaMiddle AgedMonophenol MonooxygenaseAntibodiesCancer VaccinesDNA, ComplementaryHLA-A AntigensMonophenol MonooxygenaseRNA, Messenger

Identifiers

PMID15627214
PMCPMC11033008
OpenAlexW2109011613

What OpenQuestion holds

Textmetadata
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.