| Literature DB >> 34202275 |
Ibon Gurruchaga Sotés1, Ana Nuño Alves2, Sandra Vicente Arregui3, Carmen Santander Lobera1.
Abstract
In current clinical guidelines, such as those provided by the National Comprehensive Cancer Network (NCCN), evidence for treatment is based on a small clinical trial that included patients with HLRCC. They support the use of the combination of erlotinib and bevacizumab as the first therapeutic option in this rare condition. In the present study, we report a rare case of this condition in an 18-year-old male with a family history of kidney cancer whom we successfully treated with surgery and a novel drug treatment modality based on the combination of an immune check-point inhibitor (ICPI) and a tyrosine-kinase inhibitor (TKI) with excellent and promising results.Entities:
Keywords: axitinib; hereditary leyomiomatosis; pembrolizumab; renal cell cancer
Year: 2021 PMID: 34202275 DOI: 10.3390/curroncol28040216
Source DB: PubMed Journal: Curr Oncol ISSN: 1198-0052 Impact factor: 3.677