Journal Article

DKFZ-2026-01359

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Intrathecal nivolumab in metastatic solid tumors with leptomeningeal disease: dose escalation part of the multicenter IT-PD1/NOA-26 phase 1 trial.

Tabatabai, G.DKFZ* ; Ramirez, I. ; Welte, B. ; Bombach, P. ; Becker, H. ; Bernhardt, D. ; Mayer-Steinacker, R. ; Meier, F.DKFZ* ; Neidert, N. ; Roelz, R. ; Mildenberger, I.DKFZ* ; Bunse, L.DKFZ* ; Platten, M.DKFZ* ; Herrlinger, U. ; Martens, U. M. ; Ernemann, U. ; Neumann, M. ; Tatagiba, M. ; Serna-Higuita, L. M. ; Martus, P. ; Renovanz, M.

2026
Nature Research London

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 ).

Note: #DKTKZFB26# / #NCTZFB26# / epub

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Contributing Institute(s):

1. DKTK Koordinierungsstelle Tübingen (TU01)
2. Koordinierungsstelle NCT Dresden (DD04)
3. KKE Neuroimmunologie und Hirntumorimmunologie (D170)
4. DKTK HD zentral (HD01)

Research Program(s):

1. 314 - Immunologie und Krebs (POF4-314) (POF4-314)

Appears in the scientific report 2026

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Database coverage:
; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Clinical Medicine ; DEAL Nature ; Essential Science Indicators ; IF >= 20 ; JCR ; National-Konsortium ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection

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