Neratinib as Extended Adjuvant Treatment of HER2-Positive/HR-Positive Early Breast Cancer Patients in Germany, Austria, and Switzerland: Interim Results of the Prospective, Observational ELEANOR Study

来那替尼 医学 中期分析 不利影响 观察研究 内科学 曲妥珠单抗 四分位间距 乳腺癌 佐剂 肿瘤科 癌症 临床试验
作者
Nadia Harbeck,Denise Wrobel,Matthias Zaiss,Jürgen Terhaag,Dagmar Guth,Andrea Distelrath,Mark‐Oliver Zahn,Rachel Würstlein,A. Lorenz,Rupert Bartsch,Urs Breitenstein,Michael Schwitter,Marija Balić,Christian Jackisch,Volkmar Müller,Gabriel Rinnerthaler,Marcus Schmidt,Khalil Zaman,Timo Schinköthe,Anna Resch,Roberta Valenti,Diana Lueftner
出处
期刊:Breast Care [Karger Publishers]
卷期号:: 1-8
标识
DOI:10.1159/000533657
摘要

Prognosis of patients diagnosed with HER2+ early breast cancer (eBC) has substantially improved, but distant recurrences impacting quality of life and survival still occur. One treatment option for extended adjuvant treatment of patients with HER2+/HR+ eBC is neratinib, available in Europe for patients who completed adjuvant trastuzumab-based therapy within 1 year. The ELEANOR study is investigating the real-world use of neratinib in Germany, Austria, and Switzerland. Results from an interim analysis of the first 200 patients observed for ≥3 months are reported.The primary objective of this prospective, multicenter, observational study is to assess patient adherence to neratinib (defined as the percentage of patients taking neratinib on ≥75% prescribed days). Secondary objectives are patient characteristics and treatment outcomes.At cut-off (May 2, 2022), a total of 202 patients had been observed for ≥3 months, with neratinib treatment documented for 187 patients (median age: 53.0 years; 67.9% at increased risk of disease recurrence). In total, 151 (80.7%) patients had received prior neoadjuvant treatment; of these, 82 (54.3%) patients achieved a pathologically complete response. Neratinib was initiated at a median 3.6 months after trastuzumab-based treatment, with 36.4% starting at a dose <240 mg/day. Treatment is ongoing for 46.0% of patients, with median treatment duration of 11.2 (interquartile range 0.9-12.0) months. Diarrhea was the most common adverse event (78.6% any grade, 20.3% grade ≥3); pharmacologic prophylaxis was used in 85.6% of patients.The pattern of anti-HER2 pretreatment observed reflected the current treatment for HER2+/HR+ eBC in Germany, Austria, and Switzerland. These interim results suggest that neratinib as an extended adjuvant is a feasible option after various anti-HER2 pretreatments and that its tolerability can be managed and improved with proactive diarrhea management.

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