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Title: | Dual HER2 inhibition strategies in the management of treatment-refractory metastatic colorectal cancer: History and status |
Authors: | Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Onkoloji Anabilim Dalı. 0000-0003-1591-3323 0000-0001-6973-6540 0000-0001-8306-4349 Kanat, Özkan Ertaş, Hülya Caner, Burcu HJH-6371-2023 AAE-8549-2022 55881548500 57195326915 57193498477 |
Keywords: | General & internal medicine Epidermal growth factor receptor Cetuximab Panitumumab Human epidermal growth factor receptor 2 Anti-epidermal growth factor receptor resistance Trastuzumab Dual inhibition Plus cetuximab Ras mutations Phase-ii Overexpression Therapy Erbb2 Resistance Predictor Receptors Benefit |
Issue Date: | 8-Jun-2018 |
Publisher: | Baishideng Publishing Group |
Citation: | Kanat, Ö. vd. (2018). ''Dual HER2 inhibition strategies in the management of treatment-refractory metastatic colorectal cancer: History and status''. World Journal of Clinical Cases, 6(11), 418-425. |
Abstract: | Human epidermal growth factor receptor 2 (HER2) signaling pathway activation has been identified as a contributor to de novo or acquired resistance to epidermal growth factor receptor (EGFR) inhibitors in a small subset of patients with metastatic colorectal cancer (mCRC). Dual anti-HER2-targeted treatment exhibits strong antitumor activity in preclinical models of HER2-positive mCRC, supporting its testing in clinical trials. The HERACLES trial at four Italian academic cancer centers has confirmed the effectiveness of dual blockage of HER2 with trastuzumab plus lapatinib in patients with heavily pretreated HER2-positive mCRC, refractory to the anti-EGFR antibodies cetuximab or panitumumab. Here, we reviewed the preclinical studies exploring the role of HER2 signaling in the development of anti-EGFR therapy resistance and discussed the status of clinical trials assessing the activity of HER2 inhibitors in this setting. |
URI: | https://doi.org/10.12998/wjcc.v6.i11.418 https://www.wjgnet.com/2307-8960/full/v6/i11/418.htm http://hdl.handle.net/11452/34475 |
ISSN: | 2307-8960 |
Appears in Collections: | Scopus Web of Science |
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