Evidence map›Paper›PMID 16710345›Full record

Trial reportCancer gene therapy2006

Phase I/II trial of melanoma therapy with dendritic cells transfected with autologous tumor-mRNA.

J A Kyte, L Mu, S Aamdal, G Kvalheim, S Dueland, M Hauser, H P Gullestad, T Ryder, K Lislerud, H Hammerstad and 1 more

Registry-linked trialAbstract readClinical Trial, Phase IClinical Trial, Phase II
PubMed Publisher
In one paragraph

Trial report in Cancer gene therapy, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01278940 (Phase I/II Trial of Vaccine Therapy With mRNA- Transfected Dendritic Cells in Patients With Advanced Malignant Melanoma), which is not on this map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
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.

NCT01278940 phase1 / phase2completednot on this map

Phase I/II Trial of Vaccine Therapy With mRNA- Transfected Dendritic Cells in Patients With Advanced Malignant Melanoma

TypeinterventionalSponsorOslo University HospitalRan2002 to 2015Enrolled31ConditionsMalignant MelanomaArmsDendritic Cells (DC) malignant melanoma, IL-2
3 · Its place in the literature

Who cites it

77 citing papers in PubMed, 207 citations in OpenAlex.

  1. Trial
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  7. National science review · 2026
    Article
  8. Review
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  12. Review
  13. mRNA vaccines and their delivery strategies: A journey from infectious diseases to cancer.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Review
  14. Review
  15. mRNA vaccines in disease prevention and treatment.Signal transduction and targeted therapy · 2023
    Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Review

17 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

11 authors at 2 institutions in 1 country.

J A KyteSection for Immunotherapy, Department of Immunology, Cancer Research Institute, The Norwegian Radium Hospital, University of Oslo, Oslo, Norway. j.a.kyte@klinmed.uio.no
L Mu
S Aamdal
G Kvalheim
S Dueland
M Hauser
H P Gullestad
T Ryder
K Lislerud
H Hammerstad
G Gaudernack
Norwegian Cancer Society · NOUniversity of Oslo · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have developed an individualized melanoma vaccine based on transfection of autologous dendritic cells (DCs) with autologous tumor-mRNA. Dendritic cells loaded with complete tumor-mRNA may generate an immune response against a broad repertoire of antigens, including unique patient-specific antigens. The purpose of the present phase I/II trial was to evaluate the feasibility and safety of the vaccine, and the ability of the DCs to elicit T-cell responses in melanoma patients. Further, we compared intradermal (i.d.) and intranodal (i.n.) vaccine administration. Twenty-two patients with advanced malignant melanoma were included, each receiving four weekly vaccines. Monocyte-derived DCs were transfected with tumor-mRNA by electroporation, matured and cryopreserved. We obtained successful vaccine production for all patients elected. No serious adverse effects were observed. A vaccine-specific immune response was demonstrated in 9/19 patients evaluable by T-cell assays (T-cell proliferation/interferon-gamma ELISPOT) and in 8/18 patients evaluable by delayed-type hypersensitivity (DTH) reaction. The response was demonstrated in 7/10 patients vaccinated intradermally and in 3/12 patients vaccinated intranodally. We conclude that immuno-gene-therapy with the described DC-vaccine is feasible and safe, and that the vaccine can elicit in vivo T-cell responses against antigens encoded by the transfected tumor-mRNA. The response rates do not suggest an advantage in applying i.n. vaccination.

Indexed as

Cell TransplantationDendritic CellsTransfectionAdultAgedAnimalsCancer VaccinesDogsElectroporationEnzyme-Linked Immunosorbent AssayHumansHypersensitivity, DelayedImmunity, CellularMelanomaMiddle AgedRNA, MessengerCancer VaccinesRNA, Messenger

Identifiers

PMID16710345
OpenAlexW2001740055

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.