Evidence map›Paper›PMID 16612595›Full record

ReviewCancer immunology, immunotherapy : CII2006

Immuno-gene therapy of cancer with tumour-mRNA transfected dendritic cells.

Jon A Kyte, Gustav Gaudernack

5 registry-linked trialsOpen access · greenAbstract readReview
In one paragraph

Review in Cancer immunology, immunotherapy : CII, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 5 registered trials, which are not on this map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.2field-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.

NCT02632006 phase1 / phase2unknown statusnot on this mapstarted 2015, after this paper: background citation

A Clinical Study of Adoptive Cellular Immunotherapy Using Pluripotent Killer T Cells Expressing Antibodies for Programmed Death 1 (PD-1) in Treating Patients With Advanced Hepatocellular Carcinoma

TypeinterventionalSponsorSecond Military Medical UniversityRan2015 to 2017Enrolled40ConditionsAdvanced Hepatocellular CarcinomaArmsPIK-PD-1 cells, DC-PMAT
NCT02632019 phase1 / phase2unknown statusnot on this mapstarted 2015, after this paper: background citation

A Clinical Study of Adoptive Cellular Immunotherapy Using Precision T Cells Specific to Personalized Neo-antigen in Treating Patients With Advanced Malignant Tumor of Biliary Tract

TypeinterventionalSponsorSecond Military Medical UniversityRan2015 to 2017Enrolled40ConditionsAdvanced Biliary Tract Malignant TumorArmsGemcitabine, Dendritic cell-precision T cell for neo-antigen combined with gemcitabine treatment
NCT02632188 phase1 / phase2unknown statusnot on this mapstarted 2015, after this paper: background citation

A Controlled Clinic Trial to Survey the Outcome of Immunotherapy Using Precision T Cells Specific to Multiple Common Tumor-Associated Antigen in Treating Patients Underwent Radical Surgery for Hepatocellular Carcinoma

TypeinterventionalSponsorSecond Military Medical UniversityRan2015 to 2017Enrolled60ConditionsLiver CancerArmsPostoperative routine treatment, DC-PMAT treatment
NCT02632201 phase1 / phase2unknown statusnot on this mapstarted 2015, after this paper: background citation

A Clinical Study of Adoptive Cellular Immunotherapy Using Pluripotent Killer T Cells Expressing Antibodies for Human Epidermal Growth Factor Receptor-2 (HER2) in Treating Patients With HER2-Positive Advanced Gastric Cancer With Liver Metastasis

TypeinterventionalSponsorSecond Military Medical UniversityRan2015 to 2017Enrolled40ConditionsLiver Metastasis, Gastric CancerArmsPIK-HER2, DC-PMAT
NCT02638857 phase1 / phase2unknown statusnot on this mapstarted 2015, after this paper: background citation

A Controlled Clinic Trial of Immunotherapy Using Precision T Cells Specific to Multiple Common Tumor-Associated Antigen in Combination With Transcatheter Arterial Chemoembolization in Treating Patients With Advanced Hepatocellular Carcinoma

TypeinterventionalSponsorSecond Military Medical UniversityRan2015 to 2017Enrolled60ConditionsRecurrence Hepatocellular Carcinoma, Advanced Hepatocellular CarcinomaArmsTACE, Dendritic Cell, lipiodol, Mitomycin (MMC), Epirubicin(EADM)
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 87 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Dendritic cells loaded with CD44Oncology letters · 2019
    Article
  7. Review
  8. The Pattern of Signatures in Gastric Cancer Prognosis.International journal of molecular sciences · 2018
    Review
  9. Review
  10. Immunotherapy in gastric cancer.World journal of gastroenterology · 2014
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Advancement and prospects of tumor gene therapy.Chinese journal of cancer · 2011
    Review
  17. Article
  18. Article
  19. Article
  20. Article
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

2 authors at 1 institution in 1 country.

Jon A KyteSection for Immunotherapy, Department of Immunology, Cancer Research Institute, The Norwegian Radium Hospital, University of Oslo, 0310 Oslo, Norway. j.a.kyte@klinmed.uio.no
Gustav Gaudernack
University of Oslo · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have developed immuno-gene therapy for malignant melanoma and prostate cancer. The therapy is based on monocyte-derived dendritic cells (DCs) that are transfected with autologous melanoma-mRNA or mRNA from three prostate cancer cell lines (DU-145, LN-CaP and PC-3). A broad spectrum of tumour-associated antigens will be included in both DC-vaccines. The use of autologous melanoma-mRNA moreover allows targeting of individual tumour antigens that are specific to each patient. Effective protocols have been established for mRNA-transfection by square wave electroporation and for the generation of clinical grade DCs. A full scale preclinical evaluation demonstrated in vitro T cell responses in 6/6 advanced melanoma patients. The responses were specific to antigens encoded by the transfected tumour-mRNA. Recently, we have conducted two phase I/II trials, in advanced malignant melanoma and androgen-resistant prostate cancer. Successful vaccine preparations were obtained for all 41 patients elected. No serious adverse effects were observed. Specific T cell responses (T cell proliferation and/or IFNgamma ELISPOT) were demonstrated in 9/19 evaluable melanoma patients and in 12/19 prostate cancer patients. The response rates were higher for patients receiving intradermal vaccination, compared to intranodal injection. Thirteen prostate cancer patients developed a decrease in log-slope PSA. The PSA-response was significantly related to the T cell response (P=0.002). We conclude that the DC-vaccine is feasible and safe, and that T cell responses are elicited in about 50% of patients.

Indexed as

Cancer VaccinesClinical Trials as TopicDendritic CellsGenetic TherapyHumansImmunotherapyMaleNeoplasmsProstatic NeoplasmsRNA, MessengerT-LymphocytesTransfectionCancer VaccinesRNA, Messenger

Identifiers

PMID16612595
PMCPMC11030124
OpenAlexW2070613265

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.