TY - JOUR
T1 - The evolving role of monoclonal antibodies in the treatment of patients with advanced renal cell carcinoma
T2 - a systematic review
AU - Di Lorenzo, Giuseppe
AU - De Placido, Sabino
AU - Pagliuca, Martina
AU - Ferro, Matteo
AU - Lucarelli, Giuseppe
AU - Rossetti, Sabrina
AU - Bosso, Davide
AU - Puglia, Livio
AU - Pignataro, Piero
AU - Ascione, Ilaria
AU - De Cobelli, Ottavio
AU - Caraglia, Michele
AU - Aieta, Michele
AU - Terracciano, Daniela
AU - Facchini, Gaetano
AU - Buonerba, Carlo
AU - Sonpavde, Guru
PY - 2016/11/1
Y1 - 2016/11/1
N2 - Introduction: While the majority of the vascular endothelial growth factor (VEGF) and mammalian target of rapamycin (mTOR) inhibitors currently used for the therapy of metastatic renal cell carcinoma (mRCC) are small molecule agents inhibiting multiple targets, monoclonal antibodies are inhibitors of specific targets, which may decrease off-target effects while preserving on-target activity. A few monoclonal antibodies have already been approved for mRCC (bevacizumab, nivolumab), while many others may play an important role in the therapeutic scenario of mRCC. Areas covered: This review describes emerging monoclonal antibodies for treating RCC. Currently, bevacizumab, a VEGF monoclonal antibody, is approved in combination with interferon for the therapy of metastatic RCC, while nivolumab, a Programmed Death (PD)-1 inhibitor, is approved following prior VEGF inhibitor treatment. Other PD-1 and PD-ligand (L)-1 inhibitors are undergoing clinical development. Expert opinion: Combinations of inhibitors of the PD1/PD-L1 axis with VEGF inhibitors or cytotoxic T-lymphocyte antigen (CTLA)-4 inhibitors have shown promising efficacy in mRCC. The development of biomarkers predictive for benefit and rational tolerable combinations are both important pillars of research to improve outcomes in RCC.
AB - Introduction: While the majority of the vascular endothelial growth factor (VEGF) and mammalian target of rapamycin (mTOR) inhibitors currently used for the therapy of metastatic renal cell carcinoma (mRCC) are small molecule agents inhibiting multiple targets, monoclonal antibodies are inhibitors of specific targets, which may decrease off-target effects while preserving on-target activity. A few monoclonal antibodies have already been approved for mRCC (bevacizumab, nivolumab), while many others may play an important role in the therapeutic scenario of mRCC. Areas covered: This review describes emerging monoclonal antibodies for treating RCC. Currently, bevacizumab, a VEGF monoclonal antibody, is approved in combination with interferon for the therapy of metastatic RCC, while nivolumab, a Programmed Death (PD)-1 inhibitor, is approved following prior VEGF inhibitor treatment. Other PD-1 and PD-ligand (L)-1 inhibitors are undergoing clinical development. Expert opinion: Combinations of inhibitors of the PD1/PD-L1 axis with VEGF inhibitors or cytotoxic T-lymphocyte antigen (CTLA)-4 inhibitors have shown promising efficacy in mRCC. The development of biomarkers predictive for benefit and rational tolerable combinations are both important pillars of research to improve outcomes in RCC.
KW - bevacizumab
KW - Kidney neoplasm
KW - monoclonal antibodies
KW - nivolumab
KW - targeted therapy
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U2 - 10.1080/14712598.2016.1216964
DO - 10.1080/14712598.2016.1216964
M3 - Review article
AN - SCOPUS:84989298043
SN - 1471-2598
VL - 16
SP - 1387
EP - 1401
JO - Expert Opinion on Biological Therapy
JF - Expert Opinion on Biological Therapy
IS - 11
ER -