Literature DB >> 28712098

Precision Medicine in Metastatic Colorectal Cancer: Relevant Carcinogenic Pathways and Targets-PART 1: Biologic Therapies Targeting the Epidermal Growth Factor Receptor and Vascular Endothelial Growth Factor.

Benjamin A Weinberg, Marion L Hartley, Mohamed E Salem.   

Abstract

The survival of patients with metastatic colorectal cancer has improved dramatically in recent years, with overall survival exceeding 3 years in large randomized clinical trials. There are now several treatment options for patients with metastatic colorectal cancer. In addition to chemotherapy backbones utilizing fluoropyrimidine, oxaliplatin, and irinotecan combinations, biologic agents that target specific oncogenic pathways have contributed to the improved survival observed in this patient population. This class of medications includes epidermal growth factor receptor (EGFR)-targeted drugs (cetuximab and panitumumab) and vascular endothelial growth factor (VEGF)-targeted therapies (bevacizumab, ramucirumab, ziv-aflibercept, and regorafenib). Bevacizumab remains the only VEGF-targeted agent approved by the US Food and Drug Administration in the first-line metastatic setting. EGFR-directed treatment should be restricted to patients with extended RAS and BRAF wild-type tumors. Tumor sidedness may be a more powerful prognostic and predictive biomarker than tumor mutational profile. Patients with left-sided primary tumors derive greater benefit from EGFR-targeted therapies whereas patients with right-sided primary tumors benefit more from bevacizumab. Herein we review drugs that target the EGFR and VEGF pathways, focusing on patient selection, drug toxicities, and how to choose agents for first-line therapy.

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Year:  2017        PMID: 28712098

Source DB:  PubMed          Journal:  Oncology (Williston Park)        ISSN: 0890-9091            Impact factor:   2.990


  2 in total

1.  Combined targeting of HER-2 and HER-3 represents a promising therapeutic strategy in colorectal cancer.

Authors:  Lena-Christin Conradi; Melanie Spitzner; Anna-Lena Metzger; Merle Kisly; Peter Middel; Hanibal Bohnenberger; Jochen Gaedcke; Michael B Ghadimi; Torsten Liersch; Joseph Rüschoff; Tim Beißbarth; Alexander König; Marian Grade
Journal:  BMC Cancer       Date:  2019-09-05       Impact factor: 4.430

2.  Inhibition of MEIS3 Generates Cetuximab Resistance through c-Met and Akt.

Authors:  Ping Cai; Yangyang Xie; Mingjun Dong; Qiaoqiao Zhu
Journal:  Biomed Res Int       Date:  2020-12-08       Impact factor: 3.411

  2 in total

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