Vascular endothelial growth factor-targeted therapy in patients with renal cell carcinoma pretreated with immune checkpoint inhibitors: A systematic literature review

Author:

Albiges Laurence,McGregor Bradley A.,Heng Daniel Y.C.,Procopio Giuseppe,de Velasco Guillermo,Taguieva-Pioger Naila,Martín-Couce Lidia,Tannir Nizar M.,Powles Thomas

Funder

Ipsen

Ipsen Ltd UK

Publisher

Elsevier BV

Subject

Radiology, Nuclear Medicine and imaging,Oncology,General Medicine

Reference83 articles.

1. Mechanistic overview of immune checkpoints to support the rational design of their combinations in cancer immunotherapy;Rotte;Ann Oncol,2018

2. Current insights into combination therapies with MAPK inhibitors and immune checkpoint blockade;Shin;Int J Mol Sci,2020

3. European Medicines Agency. European Medicines Agency (EMA). New treatment for advanced form of kidney cancer. February 26, 2016. Available from: https://www.ema.europa.eu/en/news/new-treatment-advanced-form-kidney-cancer (Accessed May 2022).

4. Bristol-Myers Squibb. Bristol-Myers Squibb receives FDA approval for Opdivo (nivolumab), the only treatment to deliver significant overall survival in advanced renal cell carcinoma vs. a standard of care, in patients who have received prior anti-angiogenic therapy. November 23, 2015. Available from: https://news.bms.com/news/details/2015/Bristol-Myers-Squibb-Receives-FDA-Approval-for-Opdivo-nivolumab-the-Only-Treatment-to-Deliver-Significant-Overall-Survival-in-Advanced-Renal-Cell-Carcinoma-vs-a-Standard-of-Care-in-Patients-Who-Have-Received-Prior-Anti-Angiogenic-Therapy1/default.aspx (Accessed May 2022).

5. Bristol-Myers Squibb Pharma EEIG. EMA. Summary of Product Characteristics: OPDIVO 10 mg/mL concentrate for solution for infusion. Available from: https://www.ema.europa.eu/en/documents/product-information/opdivo-epar-product-information_en.pdf (Accessed May 2022).

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