Final Efficacy Results of Neratinib in HER2-positive Hormone Receptor-positive Early-stage Breast Cancer From the Phase III ExteNET Trial

来那替尼 危险系数 医学 内科学 乳腺癌 安慰剂 肿瘤科 临床终点 胃肠病学 置信区间 酪氨酸激酶抑制剂 曲妥珠单抗 癌症 随机对照试验 病理 替代医学
作者
Arlene Chan,Beverly Moy,Janine Mansi,Bent Ejlertsen,Frankie A. Holmes,Stephen Chia,Hiroji Iwata,Michael Gnant,Sibylle Loibl,Carlos H. Barrios,İşıl Somali,Snezhana Smichkoska,Noelia Martínez,Mirta Garcia Alonso,John S. Link,Ingrid A. Mayer,Søren Cold,Serafín Morales Murillo,Francis M. Senecal,Kentaro Inoue,Manuel Ruíz‐Borrego,Rina Hui,Neelima Denduluri,Debra Patt,Hope S. Rugo,Stephen Johnston,Richard Bryce,Bo Zhang,Feng Xu,Alvin Wong,Miguel Martín
出处
期刊:Clinical Breast Cancer [Elsevier]
卷期号:21 (1): 80-91.e7 被引量:150
标识
DOI:10.1016/j.clbc.2020.09.014
摘要

BackgroundThe ExteNET trial demonstrated improved invasive disease-free survival (iDFS) with neratinib, an irreversible pan-HER tyrosine kinase inhibitor, versus placebo in patients with human epidermal growth factor receptor 2-positive (HER2+)/hormone receptor-positive (HR+) early-stage breast cancer (eBC).Patients and MethodsExteNET was a multicenter, randomized, double-blind, phase III trial of 2840 patients with HER2+ eBC after neoadjuvant/adjuvant trastuzumab-based therapy. Patients were stratified by HR status and randomly assigned 1-year oral neratinib 240 mg/day or placebo. The primary endpoint was iDFS. Descriptive analyses were performed in patients with HR+ eBC who initiated treatment ≤ 1 year (HR+/≤ 1-year) and > 1 year (HR+/> 1-year) post-trastuzumab.ResultsHR+/≤ 1-year and HR+/> 1-year populations comprised 1334 (neratinib, n = 670; placebo, n = 664) and 297 (neratinib, n = 146; placebo, n = 151) patients, respectively. Absolute iDFS benefits at 5 years were 5.1% in HR+/≤ 1-year (hazard ratio, 0.58; 95% confidence interval [CI], 0.41-0.82) and 1.3% in HR+/>1-year (hazard ratio, 0.74; 95% CI, 0.29-1.84). In HR+/≤ 1-year, neratinib was associated with a numerical improvement in overall survival (OS) at 8 years (absolute benefit, 2.1%; hazard ratio, 0.79; 95% CI, 0.55-1.13). Of 354 patients in the HR+/≤ 1-year group who received neoadjuvant therapy, 295 had residual disease, and results showed absolute benefits of 7.4% at 5-year iDFS (hazard ratio, 0.60; 95% CI, 0.33-1.07) and 9.1% at 8-year OS (hazard ratio, 0.47; 95% CI, 0.23-0.92). There were fewer central nervous system events with neratinib. Adverse events were similar to those previously reported.ConclusionNeratinib significantly improved iDFS in the HER2+/HR+/≤ 1-year population, and a similar trend was observed in patients with residual disease following neoadjuvant treatment. Numerical improvements in central nervous system events and OS were consistent with iDFS benefits and suggest long-term benefit for neratinib in this population.
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