Evidence map›Paper›PMID 42243276›Full record

ArticleNature cancer2026

Intrathecal nivolumab in metastatic solid tumors with leptomeningeal disease: dose escalation part of the multicenter IT-PD1/NOA-26 phase 1 trial.

Ghazaleh Tabatabai, Isabel Ramirez, Beatrix Welte, Paula Bombach, Hannes Becker, Denise Bernhardt, Regine Mayer-Steinacker, Friedegund Meier, Nicolas Neidert, Roland Roelz and 11 more

Registry-linked trialAbstract readMulticenter StudyClinical Trial, Phase I
In one paragraph

Article in Nature cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05112549 (Intrathecal Application of PD1 Antibody in Metastatic Solid Tumors With Leptomeningeal Disease), which is not on this map. Not yet cited in PubMed.

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

NCT05112549 phase1recruitingnot on this map

Intrathecal Application of PD1 Antibody in Metastatic Solid Tumors With Leptomeningeal Disease (IT-PD1/ NOA 26)

TypeinterventionalSponsorUniversity Hospital TuebingenRan2021 to 2027Enrolled46ConditionsLeptomeningeal DiseaseArmsNivolumab [Opdivo]
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

21 authors.

Ghazaleh TabatabaiDepartment of Neurology & Interdisciplinary Neuro-Oncology, Hertie Institute for Clinical Brain Research, University Hospital Tübingen, Eberhard Karls University Tübingen, Tübingen, Germany. ghazaleh.tabatabai@med.uni-tuebingen.de.ORCID http://orcid.org/0000-0002-3542-8782
Isabel RamirezCenter for Clinical Trials, University Hospital Tübingen, Eberhard Karls University Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0003-2477-664X
Beatrix WelteCenter for Clinical Trials, University Hospital Tübingen, Eberhard Karls University Tübingen, Tübingen, Germany.
Paula BombachDepartment of Neurology & Interdisciplinary Neuro-Oncology, Hertie Institute for Clinical Brain Research, University Hospital Tübingen, Eberhard Karls University Tübingen, Tübingen, Germany.
Hannes BeckerDepartment of Neurology & Interdisciplinary Neuro-Oncology, Hertie Institute for Clinical Brain Research, University Hospital Tübingen, Eberhard Karls University Tübingen, Tübingen, Germany.
Denise BernhardtDepartment of Radiation Oncology, University Hospital of the Technical University Munich, Munich, Germany.
Regine Mayer-SteinackerDepartment of Medical Oncology and Hematology, University Hospital Ulm, Ulm, Germany.
Friedegund MeierDepartment of Dermatology, Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0003-4340-9706
Nicolas NeidertDepartment of Neurosurgery, University Hospital Freiburg, Breisgau, Germany.ORCID http://orcid.org/0000-0003-0299-1138
Roland RoelzDepartment of Neurosurgery, University Hospital Freiburg, Breisgau, Germany.
Iris MildenbergerDepartment of Neurology, Medical Faculty Mannheim, MCTN, University of Heidelberg, Mannheim, Germany.ORCID http://orcid.org/0009-0008-8825-4908
Lukas BunseDepartment of Neurology, Medical Faculty Mannheim, MCTN, University of Heidelberg, Mannheim, Germany.ORCID http://orcid.org/0000-0002-4490-7574
Michael PlattenDepartment of Neurology, Medical Faculty Mannheim, MCTN, University of Heidelberg, Mannheim, Germany.ORCID http://orcid.org/0000-0002-4746-887X
Ulrich HerrlingerDepartment of Neurooncology, Center for Neurology, University Hospital Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0002-4011-9327
Uwe M MartensDepartment of Medical Oncology and Hematology, SLK-Clinics Heilbronn GmbH, Heilbronn, Germany.ORCID http://orcid.org/0000-0001-7999-4359
Ulrike ErnemannCenter for Neuro-Oncology, Comprehensive Cancer Center, University Hospital Tübingen, Eberhard Karls University Tübingen, Tübingen, Germany.
Manuela NeumannCenter for Neuro-Oncology, Comprehensive Cancer Center, University Hospital Tübingen, Eberhard Karls University Tübingen, Tübingen, Germany.
Marcos TatagibaCenter for Neuro-Oncology, Comprehensive Cancer Center, University Hospital Tübingen, Eberhard Karls University Tübingen, Tübingen, Germany.
Lina Maria Serna-HiguitaDepartment of Clinical Epidemiology and Applied Biostatistics, University Hospital Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0001-5182-8295
Peter MartusDepartment of Clinical Epidemiology and Applied Biostatistics, University Hospital Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0002-5386-5732
Mirjam RenovanzDepartment of Neurology & Interdisciplinary Neuro-Oncology, Hertie Institute for Clinical Brain Research, University Hospital Tübingen, Eberhard Karls University Tübingen, Tübingen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leptomeningeal metastatic disease (LMD) of solid tumors represents a cancer stage with high unmet therapeutic need. Here we report results from the dose escalation part of a multicenter phase 1 trial investigating intraventricular nivolumab, now continuing in the expansion part. Eligible participants had LMD from tumors with an approval for intraveneous PD1/PDL1 therapy or high tumor mutational burden. The primary endpoint was safety across four dose levels (20, 30, 40 and 50 mg) with each cohort reviewed by an independent data safety monitoring board before escalation. The secondary endpoint was overall survival. Exploratory endpoints included participant-reported outcome measures. Of 30 enrolled participants, 24 received at least one dose (intention-to-treat population) and 18 completed predefined safety evaluations (per-protocol population). One dose-limiting toxicity occurred at 40 mg. The primary endpoint was met and the recommended fixed dose for the ongoing expansion part is 50 mg. Median overall survival (OS) was 6.6 months. The 6-month, 12-month and 18-month OS rates were 55.0% (95% confidence interval (CI): 37.5-80.6%), 33.3% (95% CI: 17.8-62.4%) and 16.7% (95% CI 6.03-46.1%), respectively. Participant-reported quality of life remained stable. Intraventricular nivolumab has demonstrated safety and feasibility (ClinicalTrials.gov: NCT05112549 ).

Indexed as

Immune Checkpoint InhibitorsMeningeal CarcinomatosisNeoplasmsNivolumabAdultAgedAged, 80 and overDose-Response Relationship, DrugFemaleHumansInjections, SpinalMaleMiddle AgedTreatment OutcomeImmune Checkpoint InhibitorsNivolumab

Identifiers

PMID42243276
PMCPMC13400297

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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.