The emerging HER2 landscape in colorectal cancer: the key to unveil the future treatment algorithm?
- PMID: 39304034
- DOI: 10.1016/j.critrevonc.2024.104515
The emerging HER2 landscape in colorectal cancer: the key to unveil the future treatment algorithm?
Erratum in
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Corrigendum to "The emerging HER2 landscape in Colorectal Cancer: The key to unveil the future treatment algorithm?" [Crit. Rev. Oncol./Hematol. 204 (2024) 104515].Crit Rev Oncol Hematol. 2024 Dec;204:104530. doi: 10.1016/j.critrevonc.2024.104530. Epub 2024 Oct 15. Crit Rev Oncol Hematol. 2024. PMID: 39414526 No abstract available.
Abstract
Colorectal cancer (CRC) represents a global health threat, standing as the second leading cause of cancer-related death worldwide. Targeted therapies brought new hope for the metastatic stage, which historically bore a very poor prognosis. Human epidermal growth receptor 2 (HER2) overexpression concerns about 5 % of the metastatic CRC (mCRC) patients, including both gene amplifications and point mutations. Albeit its controversial prognostic role, preclinical and clinical data indicate HER2 as a negative predictive biomarker of response to anti-EGFR therapies. Tissue and plasma-based NGS testing, could permit a precise identification of this resistance mechanism both at baseline and during treatment, thus guiding decision-making. Furthermore, promising results come from completed and ongoing randomized trials, testing HER2 as an actionable target. In this review, we discuss the available evidence on HER2 targeting in advanced CRC, analyzing its possible future role in the treatment algorithm.
Keywords: HER2 amplifications; HER2 mutations; Metastatic colorectal cancer; Negative predictive biomarker; Resistance mechanism; ctDNA.
Copyright © 2024 The Authors. Published by Elsevier B.V. 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: D.R. received honoraria from Amgen, MSD and Takeda. The other authors declare no competing interests
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