Targeting hypoxia-inducible factor pathways in sporadic and Von Hippel-Lindau syndrome-related kidney cancers
Critical Reviews in Oncology/Hematology, ISSN: 1040-8428, Vol: 176, Page: 103750
2022
- 11Citations
- 12Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations11
- Citation Indexes11
- 11
- CrossRef1
- Captures12
- Readers12
- 12
Review Description
Hereditary and sporadic renal cell carcinomas (RCCs) are often associated with Von Hippel-Lindau (VHL)-gene inactivation. Patients with VHL disease have an increased risk of RCC, leading to bilateral nephrectomy and dialysis. In patients with advanced RCC, no standard second-lines are available after progression to immune checkpoint inhibitors (ICIs), and new agents are required to manage progression. HIFs have emerged as a promising target for metastatic RCC patients who have progressed to ICI-based combinations, as well as for those with RCC and VHL syndrome where the goal is to delay surgery and/or and preserve kidney function and avoid dialysis. This review describes the available evidence supporting the use of the small-molecule HIF-2 alpha inhibitor, belzutifan (MK-6482), as well as other new anti-HIF molecules that have demonstrated significant efficacy in VHL disease-related RCCs as well as for sporadic RCC that has progressed after the use of ICI-based combinations.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1040842822001743; http://dx.doi.org/10.1016/j.critrevonc.2022.103750; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85132945216&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/35728738; https://linkinghub.elsevier.com/retrieve/pii/S1040842822001743; https://dx.doi.org/10.1016/j.critrevonc.2022.103750
Elsevier BV
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