Trial reportNature communications2026
Anti-PD-1 plus nab-paclitaxel and bevacizumab for second-line treatment of cancer of unknown primary (Fudan CUP-002): a phase II trial.
Trial report in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04848597 (Phase 2, Open-label, Single Center, Prospective Study of Recombinant Humanized Anti-PD-1 Monoclonal Antibody Combined With Nab-paclitaxel and Bevacizumab in the Second-line Treatment of Patients With Cancer of Unknown Primary), which is not on this map. Cited by 1 paper.
What it found
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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.
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.
Phase 2, Open-label, Single Center, Prospective Study of Recombinant Humanized Anti-PD-1 Monoclonal Antibody Combined With Nab-paclitaxel and Bevacizumab in the Second-line Treatment of Patients With Cancer of Unknown Primary (CUP)
Who cites it
1 citing paper in PubMed.
- Cancer of unknown primary: the evolution of tissue of origin identification in the artificial intelligence era.Biomarker research · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
12 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Fudan CUP-002 study (ClinicalTrials.gov identifier: NCT04848597), an investigator-initiated prospective trial, was designed to evaluate the efficacy and safety of an anti-PD-1 antibody in combination with nab-paclitaxel and bevacizumab as a second-line treatment for cancer of unknown primary (CUP). Between June 2, 2021, and April 19, 2024, 48 eligible patients were enrolled. At data cutoff (January 10, 2025), the median follow-up was 27.1 months (95% CI, 20.2 to 37.2). The objective response rate (ORR) was 54.2% (26/48; 95% CI, 40.3% to 67.4%), and the disease control rate (DCR) was 95.8% (46/48; 95% CI, 86.0% to 98.9%). The median progression-free survival (PFS) was 13.1 months (95% CI, 8.0 to 19.6), while the median overall survival (OS) was 25.1 months (95% CI, 14.6 to 29.5). Treatment-related adverse events (TRAEs) of any grade occurred in 46 patients (95.8%). The exploratory analysis identified systemic eosinophil counts as a prognostic biomarker for treatment response and survival outcomes in second-line setting for CUP. However, current experimental systems are unable to provide the established cell lines or animal models needed to investigate therapeutic mechanisms for CUP. Our present study demonstrated that an anti-PD-1 antibody plus nab-paclitaxel and bevacizumab was effective and well-tolerated in the second-line treatment for patients with CUP.Trial registration: ClinicalTrials.gov identifier: NCT04848597.
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