Successful treatment of paraganglioma with sorafenib: a case report and brief review of the literature

Onco Targets Ther. 2013 Nov 5:6:1559-62. doi: 10.2147/OTT.S53813. eCollection 2013.

Abstract

Introduction: To date, no effective systemic therapies have been made available for paraganglioma. However, multiple mutations in susceptibility genes have been identified that are potential targets for sorafenib, an oral multitargeted tyrosine-kinase inhibitor.

Case presentation: We report the case of a 69-year-old Chinese man with mediastinal paraganglioma that had metastasized to the bone. The paraganglioma responded to sorafenib, a novel multi-tyrosine kinase inhibitor that targets angiogenesis, the Raf-kinase pathway, the platelet-derived growth factor Ret, and c-Kit. The patient was diagnosed as having paraganglioma after biopsy of the mediastinal mass. We first treated the patient with radiotherapy. Then he tolerated an etoposide-and-cisplatin chemotherapy regimen. Subsequently, he received 6 months of maintenance treatment with sorafenib (400 mg twice daily). A dramatic reduction in tumor volume was observed. At present, the patient has achieved a partial response, and his clinical status remains unchanged.

Conclusion: We suggest that sorafenib should be further investigated in the management of patients with paraganglioma.

Keywords: molecular-targeted drug; paraganglioma; sorafenib.

Publication types

  • Case Reports