Publication

A randomized trial of eribulin monotherapy versus eribulin plus anlotinib in patients with locally recurrent or metastatic breast cancer

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Last modified
  • 06/25/2025
Type of Material
Authors
    B Liu, Central South UniversityL Liu, Central South UniversityJ Ran, Emory UniversityN Xie, Central South UniversityJ Li, Central South UniversityH Xiao, Central South UniversityX Yang, Central South UniversityC Tian, Central South UniversityH Wu, Central South UniversityJ Lu, Central South UniversityJ Gao, Central South UniversityX Hu, Central South UniversityM Cao, Central South UniversityZ Shui, Central South UniversityZ-Y Hu, Central South UniversityQ Ouyang, Central South University
Language
  • English
Date
  • 2023-06-01
Publisher
  • ELSEVIER
Publication Version
Copyright Statement
  • © 2023 The Authors
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 8
Issue
  • 3
Start Page
  • 101563
End Page
  • 101563
Grant/Funding Information
  • This work was supported by the Hunan Provincial Natural Science Foundation of China [grant numbers 2023JJ60464], Hunan Provincial Science and Technology Department Project [grant numbers 2018SSK2120, 2018SK2124, 2019SK2032, and 2019JJ50360], the Health and Family Planning Commission of Hunan Province [grant numbers C2019070 and B2019089], the Changsha Science and Technology Project [grant numbers kq1901076, kq2004125 and kq2004137], the Chinese Anti-Cancer Association HER2 target Chinese Research Fund [grant number CORP-239-S5], and Climb Plan of Hunan Cancer Hospital [grant number ZX2021005].
Supplemental Material (URL)
Abstract
  • Background: Eribulin mesylate is a novel, nontaxane, microtubule dynamics inhibitor. In this study, we assessed the efficacy and safety of eribulin versus eribulin plus the oral small-molecule tyrosine kinase inhibitor anlotinib in patients with locally recurrent or metastatic breast cancer. Patients and methods: In this single-center, open-label, phase II clinical study (NCT05206656) conducted in a Chinese hospital, patients with human epidermal growth factor receptor 2 (HER2)-negative, locally recurrent or metastatic breast cancer previously treated with anthracycline- or taxane-based chemotherapy were randomized (1 : 1) to receive eribulin alone or in combination with anlotinib. The primary efficacy endpoint was investigator-assessed progression-free survival (PFS). Results: From June 2020 to April 2022, a total of 80 patients were randomly assigned to either eribulin monotherapy or eribulin plus anlotinib combination therapy, with 40 patients in each group. The data cut-off was 10 August 2022. The median PFS was 3.5 months [95% confidence interval (CI) 2.8-5.5 months] for eribulin and 5.1 months (95% CI 4.5-6.9 months) for eribulin plus anlotinib (hazard ratio = 0.56, 95% CI 0.32-0.98; P = 0.04). The objective response rates were 32.5% versus 52.5% (P = 0.07), respectively, and disease control rates were 67.5% versus 92.5% (P = 0.01), respectively. Patients <50 years of age, with an Eastern Cooperative Oncology Group performance status score of 0, visceral metastasis, number of treatment lines of four or more, hormone receptor negative (triple-negative), and HER2 low expression appeared to benefit more from combined treatment. The most common adverse events in both groups were leukopenia (n = 28, 70.0%, patients in the eribulin monotherapy group versus n = 35, 87.5%, patients in the combination therapy group), aspartate aminotransferase elevations (n = 28, 70.0%, versus n = 35, 87.5%), neutropenia (n = 25, 62.5%, versus n = 31, 77.5%), and alanine aminotransferase elevations (n = 25, 62.5%, versus n = 30, 75.0%). Conclusion: Eribulin plus anlotinib can be considered an alternative treatment option for HER2-negative locally advanced or metastatic breast cancer.
Author Notes
  • Prof. Quchang Ouyang and Prof. Zhe-Yu Hu, Department of Breast Cancer Medical Oncology, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Number 283, Tongzipo Road, Yuelu District, Changsha, Hunan 410000, P.R. China. Tel: +86-073189762161. Email: oyqc1969@126.com
Keywords
Research Categories
  • Health Sciences, Oncology

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