Final clinical analysis of pre-operative ipilimumab and nivolumab in locally advanced urothelial cancer and exploration of tumor-draining lymph node composition

The NABUCCO trial

Journal Article (2025)
Author(s)

Chantal F. Stockem (Netherlands Cancer Institute)

Jeroen van Dorp (Netherlands Cancer Institute)

Nick van Dijk (Netherlands Cancer Institute)

Daniel J. Vis (Netherlands Cancer Institute, Oncode Institute)

Rolf Harkes (Netherlands Cancer Institute)

Bram van den Broek (Netherlands Cancer Institute)

Maartje Alkemade (Netherlands Cancer Institute)

Annegien Broeks (Netherlands Cancer Institute)

Kees Hendricksen (Netherlands Cancer Institute)

Lodewyk F.A. Wessels (Netherlands Cancer Institute, TU Delft - Pattern Recognition and Bioinformatics, Oncode Institute)

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Research Group
Pattern Recognition and Bioinformatics
DOI related publication
https://doi.org/10.1016/j.ejca.2025.115731
More Info
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Publication Year
2025
Language
English
Research Group
Pattern Recognition and Bioinformatics
Bibliographical Note
Green Open Access added to TU Delft Institutional Repository as part of the Taverne amendment. More information about this copyright law amendment can be found at https://www.openaccess.nl. Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public.
Journal title
European Journal of Cancer
Volume number
229
Article number
115731
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Abstract

Background: Pre-operative immune checkpoint blockade (ICB) with ipilimumab and nivolumab has shown encouraging pathological complete response (pCR) rates in stage III urothelial cancer (UC). A previous analysis of NABUCCO suggested that ipilimumab 3 mg/kg is more effective than ipilimumab 1 mg/kg. However, long-term progression-free and overall survival (PFS, OS) following pre-operative combination ICB are unknown. Methods: In NABUCCO, 54 patients received pre-operative ipilimumab plus nivolumab in different dosing regimens. PFS and OS were determined for the entire NABUCCO population and various clinically relevant subgroups. We explored ICB effects on the cellular composition of tumor-draining lymph nodes (tdLN) from ICB-treated patients (n = 5) and untreated or chemotherapy-treated patients (n = 5) using multiplex immunofluorescence for the PhenoCycler Fusion (Akoya). Results: With a median follow-up of 70 months, PFS and OS at 60 months were 67 % and 70 %, respectively, for the entire study. PFS and OS at 60 months were similar for patients with residual non-muscle invasive UC (NMIBC) and patients with a pCR. The presence of a nodal micrometastasis (<2 mm) after ICB, the development of grade ≥ 3 immune-related adverse events (irAE) and corticosteroids or antibiotics did not negatively impact survival. We observed smaller distances from CD20+ cells to CD14+ cells in tdLN following ICB compared to tdLN from untreated or chemotherapy-treated patients. Conclusions: Our data demonstrate a 5-year PFS of 67 % and OS of 70 % after pre-operative ICB in stage III UC. Survival was not impaired for patients with residual NMIBC, a nodal micrometastasis at resection, grade ≥ 3 irAE or corticosteroid use.

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