Evidence map›Paper›PMID 39127809›Full record

ArticleNature communications2024

A real-world observation of patients with glioblastoma treated with a personalized peptide vaccine.

Pauline Latzer, Henning Zelba, Florian Battke, Annekathrin Reinhardt, Borong Shao, Oliver Bartsch, Armin Rabsteyn, Johannes Harter, Martin Schulze, Thomas Okech and 40 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
–field-weighted citation impact
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

51 citing papers in PubMed.

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  10. Automating neoantigen selection for personalized cancer vaccine design.medRxiv : the preprint server for health sciences · 2026
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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

50 authors.

Pauline LatzerZentrum für Humangenetik Tübingen, Tübingen, Germany.ORCID 0000-0003-0479-084X
Henning ZelbaZentrum für Humangenetik Tübingen, Tübingen, Germany.
Florian BattkeCeGaT GmbH, Tübingen, Germany.ORCID 0000-0001-6021-5837
Annekathrin ReinhardtZentrum für Humangenetik Tübingen, Tübingen, Germany.
Borong ShaoZentrum für Humangenetik Tübingen, Tübingen, Germany.
Oliver BartschZentrum für Humangenetik Tübingen, Tübingen, Germany.
Armin RabsteynZentrum für Humangenetik Tübingen, Tübingen, Germany.
Johannes HarterCeGaT GmbH, Tübingen, Germany.
Martin SchulzeZentrum für Humangenetik Tübingen, Tübingen, Germany.
Thomas OkechMVZ Zentrum für ambulante Onkologie GmbH, Tübingen, Germany.
Alexander GolfMVZ Zentrum für ambulante Onkologie GmbH, Tübingen, Germany.
Christina Kyzirakos-FegerZentrum für Humangenetik Tübingen, Tübingen, Germany.
Simone KayserZentrum für Humangenetik Tübingen, Tübingen, Germany.
Natalia PieperZentrum für Humangenetik Tübingen, Tübingen, Germany.
Magdalena FeldhahnCeGaT GmbH, Tübingen, Germany.
Julian WünscheZentrum für Humangenetik Tübingen, Tübingen, Germany.
Christian SeitzUniversitätsklinikum Heidelberg, KiTZ, Hopp Children's Cancer Center, Heidelberg, Germany.
Dirk HadaschikCeCaVa GmbH, Tübingen, Germany.
Claus GarbeDepartment of Dermatology, University Hospital Tübingen, Tübingen, Germany.
Till-Karsten HauserDepartment für Radiologie, Universitätsklinikum Tübingen, Tübingen, Germany.ORCID 0000-0001-7604-3419
Christian la FougèreNuklearmedizin und Klinische Molekulare Bildgebung, Universitätsklinikum Tübingen, Tübingen, Germany.ORCID 0000-0001-7519-0417
Dirk BiskupCeGaT GmbH, Tübingen, Germany.
Dawn BrookeProvenance Precision Medicine Foundation, Wilmette, IL, USA.
David ParkerPHM, Los Angeles, CA, USA.
Uwe M MartensDepartment of Hematology and Oncology, Cancer Center Heilbronn-Franken, SLK Kliniken GmbH, Heilbronn, Germany.ORCID 0000-0001-7999-4359
Gerald IllerhausKlinikum Stuttgart, Stuttgart, Germany.
Deborah T BlumenthalTel-Aviv Sourasky Medical Center, Tel-Aviv University, Tel Aviv, Israel.ORCID 0000-0002-8868-0148
Ryan MerrellVanderbilt University Medical Center, Nashville, TN, USA.
Luisa Sánchez LorenzoClínica Universidad de Navarra, Madrid, Spain.
Máté HidvégiJewish Theological Seminary-University of Jewish Studies (OR-ZSE), Budapest, Hungary.ORCID 0000-0003-1616-0829
Paula de RoblesDepartment of Clinical Neurosciences, University of Calgary, Calgary, AB, Canada.
Sied KebirUniversitätsklinikum Essen, Essen, Germany.
William W LiAngiogenesis Foundation, Cambridge, MA, USA.
Vincent W LiAngiogenesis Foundation, Cambridge, MA, USA.
Matthew WilliamsNHS London, London, UK.
Alexandra M MillerBrain and Spine Tumor Center, NYU Langone Health's Perlmutter Cancer Center, New York, NY, USA.
Santosh KesariPacific Neuroscience Institute, Saint John's Cancer Institute, Providence Saint John's Health Center, Santa Monica, CA, USA.ORCID 0000-0003-3772-6000
Michael CastroCellworks Group Inc, South San Francisco, CA, USA.
Annick DesjardinsDepartment of Neurosurgery, Duke University Medical Center, Durham, NC, USA.ORCID 0000-0003-3869-8283
David M AshleyDepartment of Neurosurgery, Duke University Medical Center, Durham, NC, USA.ORCID 0000-0002-4754-5900
Henry S FriedmanDepartment of Neurosurgery, Duke University Medical Center, Durham, NC, USA.ORCID 0000-0001-7588-032X
Patrick Y WenCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Elisabeth C NeilDepartment of Neurology, University of Minnesota Health, Minneapolis, MN, USA.
Fabio M IwamotoColumbia University Medical Center, New York, NY, USA.
Bence SiposBAG für Pathologie und Molekularpathologie Stuttgart, Molekularpathologie Baden-Württemberg GbR, Stuttgart, Germany.ORCID 0000-0002-7311-3343
Karsten GeletnekyKlinikum Darmstadt GmbH, Darmstadt, Germany.
Lars ZenderUniversity Hospital Tübingen, Internal Medicine VIII, Tübingen, Germany.ORCID 0000-0001-7626-2849
Martin GlasDivision of Clinical Neurooncology, Department of Neurology, Universitätsklinikum Essen Klinik für Neurologie, Essen, Germany.
David A ReardonCenter for Neuro-Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.ORCID 0000-0001-6674-0157
Saskia BiskupZentrum für Humangenetik Tübingen, Tübingen, Germany. Saskia.Biskup@humangenetik-tuebingen.de.ORCID 0000-0002-1573-861X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current treatment outcome of patients with glioblastoma (GBM) remains poor. Following standard therapy, recurrence is universal with limited survival. Tumors from 173 GBM patients are analysed for somatic mutations to generate a personalized peptide vaccine targeting tumor-specific neoantigens. All patients were treated within the scope of an individual healing attempt. Among all vaccinated patients, including 70 treated prior to progression (primary) and 103 treated after progression (recurrent), the median overall survival from first diagnosis is 31.9 months (95% CI: 25.0-36.5). Adverse events are infrequent and are predominantly grade 1 or 2. A vaccine-induced immune response to at least one of the vaccinated peptides is detected in blood samples of 87 of 97 (90%) monitored patients. Vaccine-specific T-cell responses are durable in most patients. Significantly prolonged survival is observed for patients with multiple vaccine-induced T-cell responses (53 months) compared to those with no/low induced responses (27 months; P = 0.03). Altogether, our results highlight that the application of personalized neoantigen-targeting peptide vaccine is feasible and represents a promising potential treatment option for GBM patients.

Indexed as

Brain NeoplasmsCancer VaccinesGlioblastomaPrecision MedicineProtein Subunit VaccinesAdultAgedAntigens, NeoplasmFemaleHumansMaleMiddle AgedT-LymphocytesTreatment OutcomeAntigens, NeoplasmCancer VaccinesProtein Subunit Vaccines

Identifiers

PMID39127809
PMCPMC11316744

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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.