Real-world efficacy of zanidatamab in patients with HER2 positive advanced biliary tract cancers
- PMID: 40319675
- DOI: 10.1016/j.ejca.2025.115432
Real-world efficacy of zanidatamab in patients with HER2 positive advanced biliary tract cancers
Abstract
Introduction: In the HERIZON BTC 01 trial for patients with HER2-positive biliary tract cancer (BTC) previously treated with systemic therapy, zanidatamab improved the objective response rate, disease control rate (DCR), progression-free survival (PFS), and overall survival (OS). However, real-world data are needed to assess its efficacy and safety outside clinical trials.
Patients & methods: We conducted an investigator initiated national multicenter retrospective study of most patients with BTC treated with zanidatamab in France as part of a compassionate access. The primary endpoint was PFS.
Results: Our study included 20 patients with metastatic BTC enrolled between September 2022 and November 2024. The median age at diagnosis was 61.5 (interquartile range: 55-69) years and the majority of patients had gallbladder cancer (n = 12, 60 %). After a median follow-up of 8.5 (95 % confidence interval [CI]: 3.3-11.8) months, the median PFS was 6.7 (95 % CI 1.3-11.8) months, with an estimated OS at 1 year of 79.1 % (95 % CI: 53.2-91.6 %). The DCR was 65 %, with 40 % confirmed partial responses and a median duration of response of 7.3 (95 % CI: 2.06-16) months. Patients with immunohistochemistry (IHC) 3 + HER2 scores had a better PFS [8 (95 % CI: 1.5-18.4) months] than those with 2 + HER2 scores obtained by IHC followed by fluorescence in situ hybridization amplification or next-generation sequencing [1.4 (95 % CI: 1.1-6.8) months] (P = 0.02). No statistical difference in 1-year estimated OS rates was observed (P = 0.39). There were no grade 3 or 4 treatment-related adverse events or cardiac toxicities.
Conclusion: The benefits of in patients with HER2-positive BTC were confirmed. Zanidatamab should be considered for patients with this condition.
Keywords: Cholangiocarcinoma; HER amplification; Targetable treatment.
Copyright © 2025 Elsevier Ltd. All rights reserved.
Conflict of interest statement
Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Declaration of interest related to the manuscript: none. Other declaration of interest. MD: Roche, Servier. JFB: Bayer, Eisai, Ipsen, Roche, Astra-Zeneca, Bms. SC: Abbvie, Astellas, Merck, Servier, Pierre Farbe, Bms, Gsk, Roche, Boeringer Ingelhem. M.D: Merck, Roche, Bohringer, Amgen, Novartis, Sanofi, Roche, Pfizer, Sandoz, Servier. A.H:, Incyte, EISAI; Basilea, Tahio, Relay Therapeutics, QED Therapeutics, Debiopharm, MSD, Boehringer Ingelheim; AstraZeneca; AbbVie; Roche; Merus; Seagen; Tahio; Mirati; Adaptimmune; Sanofi; Pfizer; Relay Therapeutics; Celgene/BMS; Loxo-IDH AstraZeneca; Sotio; Gilead; Boehringer Ingelheim. A.B: none. M.V: none. AL: none. EK, VJM: none.
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