4.7 Article

Neratinib as extended adjuvant therapy in patients with copositive early breast cancer: German health technology assessment-driven analyses from the ExteNET study

Journal

EUROPEAN JOURNAL OF CANCER
Volume 150, Issue -, Pages 268-277

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.ejca.2021.03.045

Keywords

Neratinib; Extended adjuvant treatment; Breast cancer; HER2-positive; Hormone receptor-positive; Copositive; Triple-positive

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Funding

  1. Pierre Fabre Pharma GmbH, Freiburg, Germany

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Analyses from the ExteNET trial show that neratinib provides a significant disease-free survival advantage in hormone receptor-positive early breast cancer patients, supporting its use in extended adjuvant treatment.
Background: Neratinib is approved in the European Union for extended adjuvant treatment of human epidermal growth factor receptor 2-positive/hormone receptor-positive (copositive) early breast cancer <1 year of completion of prior trastuzumab-based therapy. Here, we report analyses of the hormone receptor-positive subgroup (N = 1631) from the ExteNET trial performed for the German health technology assessment (HTA). Results: With 2 years of median follow-up, HTA analyses revealed a significant advantage in disease-free survival (DFS) for neratinib vs. placebo (absolute/relative risk reduction: 4.1/ 48.2%; hazard ratio [HR] [95% confidence interval {CI}]: 0.45 [0.29; 0.69]; p = 0.0002), consistent with distant DFS (absolute/relative risk reduction: 3.1/46.3%; HR [95% CI]: 0.52 [0.32; 0.84]; p = 0.0082). The 5-year follow-up confirmed this outcome.Quality of life analyses did not show clinically relevant differences over all time points. Only at month 1, the Functional Assessment of Cancer Therapy -General total score revealed a statistically rele-vant difference to the disadvantage of neratinib classified as clinically relevant. The tolerability profile of neratinib was dominated by gastrointestinal events, mainly diarrhoea (all grades: 94.4%; grade III: 39.4%; no systematic antidiarrhoeal prophylaxis), nausea (all grades/grade III: 43.9/1.6%), vomiting (26.6/3.2%), abdominal pain (23.8/1.9%), fatigue (28.1/1.9%) and rash (14.3/0.4%). No cumulative or irreversible toxicities were observed. As shown in the CONTROL study and instituted via a risk management plan, diarrhoea management can reduce frequency, cumulative duration and severity of diarrhoea. Conclusion: Extended adjuvant neratinib provides a clinically relevant benefit with further in-cremental reduction of relapse risk in the curative setting. Accordingly, the German HTA au-thority has granted an added benefit for this new treatment option. & ordf; 2021 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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