Ramucirumab: preclinical research and clinical development

Abstract

Ramucirumab (IMC-1121B, LY3009806), a fully humanized monoclonal antibody directed against the extracellular domain of vascular endothelial growth factor receptor 2 (VEGFR-2), is a new therapeutic option that selectively inhibits the human VEGFR-2 with a much greater affinity than its natural ligands. Based on the promising results of both preclinical and early clinical studies, ramucirumab has been tested in different tumor types either alone or in combination with chemotherapy. While it has recently been granted its first US Food and Drug Administration approval for use as a single agent in patients with advanced or metastatic gastric cancer or gastroesophageal junction carcinoma, its role for metastatic breast cancer or advanced non-small-cell lung cancer is still debated. The aims of this review are to recall and discuss the most significant preclinical and clinical studies that led to the development of ramucirumab and to present the results of the randomized clinical trials that have tested its efficacy in different malignancies, including gastric and lung cancer.

Keywords: antiangiogenic; breast cancer; gastric cancer; lung cancer; ramucirumab.

Figure 1

A graphical representation of the effect of ramucirumab when blocking VEGFR-2. VEGF ligands and their receptors are represented. A: VEGF-A, B: VEGF-B, C: VEGF-C, D: VEGF-D, E: VEGF-E. Abbreviations: VEGFR-2, vascular endothelial growth factor receptor 2; VEGF, vascular endothelial growth factor; PIGF, placental growth factor.