Evidence map›Paper›PMID 33184050›Full record

Trial reportJournal for immunotherapy of cancer2020

Vaccination against RhoC induces long-lasting immune responses in patients with prostate cancer: results from a phase I/II clinical trial.

Juliane Schuhmacher, Sonja Heidu, Torben Balchen, Jennifer Rebecca Richardson, Camilla Schmeltz, Jesper Sonne, Jonas Schweiker, Hans-Georg Rammensee, Per Thor Straten, Martin Andreas Røder and 2 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase IClinical Trial, Phase II
In one paragraph

Trial report in Journal for immunotherapy of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03199872 (A Phase I/II Study of RV001V, a RhoC Anticancer Vaccine, Against Metastasis From Solid Tumours), which is not on this map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.7field-weighted citation impact, top 9% 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.

NCT03199872 phase1 / phase2completednot on this map

A Phase I/II Study of RV001V, a RhoC Anticancer Vaccine, Against Metastasis From Solid Tumours

TypeinterventionalSponsorRhoVac APSRan2017 to 2019Enrolled22ConditionsProstate CancerArmsRV001V
3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
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  3. Article
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  9. Bolstering CD8Biology · 2025
    Review
  10. Article
  11. Identification of AK4 and RHOC as potential oncogenes addicted by adult T cell leukemia.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Exploring treatment options in cancer: Tumor treatment strategies.Signal transduction and targeted therapy · 2024
    Review
  18. Review
  19. The role of CD4MedComm · 2023
    Review
  20. Review
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

12 authors at 5 institutions in 3 countries.

Juliane SchuhmacherDepartment of Immunology, Institute for Cell Biology, University of Tübingen, Tubingen, Germany.
Sonja HeiduDepartment of Immunology, Institute for Cell Biology, University of Tübingen, Tubingen, Germany.
Torben BalchenZelo Phase I Unit, DanTrials ApS, Copenhagen, Denmark.
Jennifer Rebecca RichardsonDepartment of Immunology, Institute for Cell Biology, University of Tübingen, Tubingen, Germany.
Camilla SchmeltzZelo Phase I Unit, DanTrials ApS, Copenhagen, Denmark.
Jesper SonneZelo Phase I Unit, DanTrials ApS, Copenhagen, Denmark.
Jonas SchweikerDepartment of Oncology, Haematology, Immunology, Rheumatology and Pulmonology, University Hospital of Tübingen, Tübingen, Germany.
Hans-Georg RammenseeDepartment of Immunology, Institute for Cell Biology, University of Tübingen, Tubingen, Germany.
Per Thor StratenDepartment of Oncology, Center for Cancer Immune Therapy (CCIT), University Hospital Herlev & Department of Immunology and Microbiology, University of Copenhagen, Copenhagen, Denmark.
Martin Andreas RøderDepartment of Urology, Copenhagen Prostate Cancer Center, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Klaus BrassoDepartment of Urology, Copenhagen Prostate Cancer Center, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Cécile GouttefangeasDepartment of Immunology, Institute for Cell Biology, University of Tübingen, Tubingen, Germany cecile.gouttefangeas@uni-tuebingen.de.ORCID 0000-0002-6410-2378
Copenhagen Business School · DKUniversity of Copenhagen · DKUniversity of Tübingen · DEGerman Cancer Research Center · DEUniversity Children's Hospital Tübingen · DE

Funding

HEPATITIS C VIRAL MUTANTS AND HUMAN T CELL FUNCTIONK01DK002970 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI WANG, HUIRU · 2001 to 2003
$265k
NIDDK NIH HHS K01 DK002970
6 · The paper itself

Abstract

backgroundPeptide-based vaccination is a rational option for immunotherapy of prostate cancer. In this first-in-man phase I/II study, we assessed the safety, tolerability and immunological impact of a synthetic long peptide vaccine targeting Ras homolog gene family member C (RhoC) in patients with prostate cancer. RhoC is a small GTPase overexpressed in advanced solid cancers, metastases and cancer stem cells.

methodsTwenty-two patients who had previously undergone radical prostatectomy received subcutaneous injections of 0.1 mg of a single RhoC-derived 20mer peptide emulsified in Montanide ISA-51 every 2 weeks for the first six times, then five times every 4 weeks for a total treatment time of 30 weeks. The drug safety and vaccine-specific immune responses were assessed during treatment and thereafter within a 13-month follow-up period. Serum level of prostate-specific antigen was measured up to 26 months postvaccination.

resultsMost patients (18 of 21 evaluable) developed a strong CD4 T cell response against the vaccine, which lasted at least 10 months following the last vaccination. Three promiscuouslypresented HLA-class II epitopes were identified. Vaccine-specific CD4 T cells were polyfunctional and effector memory T cells that stably expressed PD-1 (CD279) and OX-40 (CD134), but not LAG-3 (CD223). One CD8 T cell response was detected in addition. The vaccine was well tolerated and no treatment-related adverse events of grade ≥3 were observed.

conclusionTargeting of RhoC induced a potent and long-lasting T cell immunity in the majority of the patients. The study demonstrates an excellent safety and tolerability profile. Vaccination against RhoC could potentially delay or prevent tumor recurrence and metastasis formation. TRIAL REGISTRATION NUMBER: NCT03199872.

Indexed as

AgedCancer VaccinesHumansMaleMiddle AgedProstatic NeoplasmsrhoC GTP-Binding ProteinCancer VaccinesrhoC GTP-Binding ProteinRHOC protein, humanimmunotherapyprostatic neoplasmsT-Lymphocytestranslational medical researchvaccination

Identifiers

PMID33184050
PMCPMC7662471
OpenAlexW3102686571

What OpenQuestion holds

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LicenceCC BY-NC
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.