Real‐world effectiveness and safety with nivolumab plus ipilimumab or nivolumab alone in patients with or without melanoma brain metastasis: Results from the German noninterventional <scp>NICO</scp> study
The prospective, German NICO study (ClinicalTrials.gov identifier: NCT02990611) evaluated real-world effectiveness and safety with nivolumab plus ipilimumab or nivolumab alone (any-line) in patients with advanced melanoma with/without melanoma brain metastasis (MBM). A total of 755 patients treated with nivolumab plus ipilimumab (n = 486; median follow-up, 46.8 months) or nivolumab alone (n = 269; median follow-up, 38.7 months) were enrolled. Baseline characteristics differed between the treatment groups, with the nivolumab plus ipilimumab group being younger and having poorer prognostic factors. At baseline, 221 patients (29.3%) had MBM, among whom 15 patients had symptomatic MBM based on dexamethasone use. In patients with/without MBM receiving first-line nivolumab plus ipilimumab, objective response rates (ORRs) were 46.2% and 54.0%, respectively; 3-year overall survival (OS) rates were 34.0% and 47.0%. In patients with/without MBM receiving first-line nivolumab alone, ORRs were 61.5% and 55.1%, respectively; 3-year OS rates were 42.7% and 47.8%. In a 3-month landmark analysis, patients with MBM with a complete/partial response demonstrated 3-year OS rates of 71.9% with nivolumab plus ipilimumab and 89.6% with nivolumab alone. Three-year OS rates were 42.2% and 20.0% with asymptomatic and symptomatic MBM, respectively. There were no substantial differences in the rates of serious grade 3/4 treatment-related adverse events between patients with/without MBM. HRQoL was stable. Results from this real-world study show that a substantial proportion of patients with MBM derive long-term benefit from nivolumab plus ipilimumab or nivolumab alone, particularly those with asymptomatic MBM.
Authors
- Carsten Weishaupt (ORCID: https://orcid.org/0000-0003-1195-2106)
- Ralf Gutzmer (ORCID: https://orcid.org/0000-0001-7921-2820)
- Christoffer Gebhardt (ORCID: https://orcid.org/0000-0001-7090-9584)
- Thomas Sickmann
- Michael Weichenthal (ORCID: https://orcid.org/0000-0002-9060-4961)
- Thomas Eigentler (ORCID: https://orcid.org/0000-0003-0019-2770)
- Anca Sindrilaru (ORCID: https://orcid.org/0000-0002-1691-0047)
- P. Dücker
- Jens Ulrich
- Selma Ugurel
- Katharina C. Kähler
- Patrick Terheyden
- Sebastian Haferkamp
- Friedegund Meier
- Jochen Utikal
- Peter Mohr
- Claudia Pföhler
- Dirk Schadendorf
- Imke von Wasielewski
Institutions
- Bristol-Myers Squibb (Germany) (DE)
- Universität Hamburg (DE)
- German Cancer Research Center (DE)
- Bielefeld University (DE)
- Hochschule Bielefeld (DE)
- Heidelberg University (DE)
- Luther University (KR)
- Dorothea Dix Hospital (US)
- Medizinische Hochschule Hannover (DE)
- Humboldt-Universität zu Berlin (DE)
- Düsseldorf University Hospital (DE)
- University Hospital Münster (DE)
- University Medical Center Hamburg-Eppendorf (DE)
- National Center for Tumor Diseases (DE)
- University Hospital Schleswig-Holstein (DE)
- Essen University Hospital (DE)
- Klinikum Dortmund (DE)
- Klinikum Bielefeld (DE)
- Elbe Kliniken Stade-Buxtehude (DE)
- University Hospital Ulm (DE)
- University Medical Centre Mannheim (DE)
- University Hospital Carl Gustav Carus (DE)
- Johannes Wesling Klinikum Minden (DE)
- Heinrich Heine University Düsseldorf (DE)
- Martin Luther University Halle-Wittenberg (DE)
- Saarland University (DE)
- University of Lübeck (DE)
Publication Details
- Journal
- International Journal of Cancer
- Published
- 2026-03-15
- DOI
- https://doi.org/10.1002/ijc.70440
- Primary Topic
- Cancer Immunotherapy and Biomarkers
- Type
- article
- Field-Weighted Citation Impact
- 0.00