| Literature DB >> 30858035 |
Matthew K Labriola1, Kristen A Batich1, Jason Zhu1, Megan A McNamara1, Michael R Harrison1, Andrew J Armstrong1, Daniel J George1, Tian Zhang2.
Abstract
The incidence of renal-cell carcinoma has been increasing each year, with nearly one third of new cases diagnosed at advanced or metastatic stage. The advent of targeted therapies for metastatic renal-cell carcinoma (mRCC) has underscored the need to subtype tumors according to tumor-immune expression profiles that may more reliably predict treatment outcomes. Over the past 2 decades, several vascular endothelial growth factor (VEGF) and tyrosine kinase inhibitors have been the mainstay for first- and second-line treatment of mRCC. Very recently, immunotherapy checkpoint inhibitors have significantly changed the treatment landscape for patients with mRCC, particularly for first-line treatment of intermediate to poor risk mRCC patients. Now, combination immunotherapy as well as combinations of immunotherapy with targeted agents can significantly alter disease outcomes. The field of immuno-oncology for mRCC has unveiled a deeper understanding of the immunoreactivity inherent to these tumors, and as a result combination therapy is evolving as a first-line modality. This review provides a timeline of advances and controversies in first-line treatment of mRCC, describes recent advances in understanding the immunoreactivity of these tumors, and addresses the future of combination anti-VEGF and immunotherapeutic platforms.Entities:
Keywords: Immune checkpoint inhibitors; Metastatic renal-cell carcioma; Targeted therapies; VEGF therapies; VEGF-immunotherapy combinations
Mesh:
Year: 2019 PMID: 30858035 PMCID: PMC7004481 DOI: 10.1016/j.clgc.2019.01.017
Source DB: PubMed Journal: Clin Genitourin Cancer ISSN: 1558-7673 Impact factor: 2.872