| Literature DB >> 29396065 |
Davis G Taylor1, Adeel Ilyas2, Gautam U Mehta2, Ching-Jen Chen2, David Schiff2, Edward H Oldfield2, Ashok R Asthagiri2.
Abstract
Von Hippel-Lindau (VHL) disease is a multisystem genetic disease, the cardinal manifestations of which include central nervous system hemangioblastomas (CNS HB), renal cell carcinomas (RCC), and pheochromocytoma. Tumorigenesis in VHL of both RCC and CNS HB occurs secondary to downstream effects of a mutated or absent VHL protein. Treatment of RCCs with tyrosine kinase inhibitors (TKIs) such as Pazopanib is now first line therapy, but their effect on VHL-associated CNS HBs remains unknown. We report the use of Pazopanib in a patient with VHL disease for treatment of RCC who also harbored multiple CNS HBs. Following initiation of treatment, a large cervical and a lumbar spinal HB regressed in size while the remaining CNS HBs exhibited stable or progressive disease. These findings highlight the multiplicity of factors contributing to hemangioblastoma development, even among tumors with a common germline mutation, and the potential limitations of TKIs, but additionally this report supports the conservative management of asymptomatic VHL patients with spinal HBs whereby tumor response to TKI treatment may alleviate or postpone the need for surgery.Entities:
Keywords: Central nervous system; Hemangioblastoma; Pazopanib; Renal cell carcinoma; Spinal; Tyrosine Kinase Inhibitor (TKI); Von Hippel-Lindau (VHL)
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Year: 2018 PMID: 29396065 DOI: 10.1016/j.jocn.2018.01.040
Source DB: PubMed Journal: J Clin Neurosci ISSN: 0967-5868 Impact factor: 1.961