Advances in treatment of metastatic renal cell carcinoma

dc.contributor.authorGong, Jun
dc.contributor.authorGerendash, Benjamin
dc.contributor.authorDizman, Nazli
dc.contributor.authorKhan, Abrar
dc.contributor.authorPal, Sumanta K.
dc.date.accessioned2025-05-10T19:39:03Z
dc.date.issued2016
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractPurpose of review Multiple agents, including vascular endothelial growth factor (VEGF) inhibitors and mammalian target of rapamycin inhibitors have been approved over the past decade for the treatment of metastatic renal cell carcinoma (mRCC). Here, we focus on nivolumab, cabozantinib, and lenvatinib plus everolimus, agents that have recently emerged with positive clinical data leading to 'Food and Drug Administration approval or pending approval in mRCC. We also review the development of novel agents of interest showing promise in mRCC as part of combination therapy'. Recent findings Nivolumab and cabozantinib both offer improved survival over everolimus in the second-line treatment of mRCC. Lenvatinib plus everolimus has similarly shown encouraging survival benefits in a phase II trial for the second-line setting. Novel combinations in mRCC, including dual immune checkpoint blockade, VEGF and programmed death 1 inhibition, VEGF and vaccine therapy, dual angiogenic blockade, and VEGF-directed therapy with nanoparticle-containing camptothecin have shown promising activity in early-phase trials. Summary Multiple promising agents are available in the treatment of mRCC. The appropriate sequencing of agents in the treatment of mRCC may become further elucidated by future studies that prospectively analyze potential biomarkers to identify patients who will derive the greatest benefit from VEGF, mammalian target of rapamycin, or checkpoint inhibitors.
dc.identifier.doi10.1097/MOU.0000000000000319
dc.identifier.endpage446
dc.identifier.issn0963-0643
dc.identifier.issn1473-6586
dc.identifier.issue5
dc.identifier.pmid27467136
dc.identifier.scopus2-s2.0-84982867279
dc.identifier.scopusqualityQ1
dc.identifier.startpage439
dc.identifier.urihttps://doi.org/10.1097/MOU.0000000000000319
dc.identifier.urihttps://hdl.handle.net/20.500.14730/9554
dc.identifier.volume26
dc.identifier.wosWOS:000380751100009
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherLippincott Williams & Wilkins
dc.relation.ispartofCurrent Opinion in Urology
dc.relation.publicationcategoryDiğer
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250302
dc.subjectbiomarkers
dc.subjectimmunotherapy
dc.subjectmetastatic renal cell carcinoma
dc.subjectmammalian target of rapamycin
dc.subjectvascular endothelial growth factor
dc.titleAdvances in treatment of metastatic renal cell carcinoma
dc.typeReview

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