A New Approach to the Treatment of Metastatic Paraganglioma: Sorafenib
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Paragangliomas are relatively rare chromaffin cell tumors which may be cured throughresection. Patients with paragangliomas may develop metastatic diseases. There isno consensus regarding refractory chemotherapy for treatment of metastatic disease. In this report, we presented a case of a 43-year-old woman who was admitted to thehospital with a history of episodic headaches, diaphoresis, and weakness. Elevatedplasma catecholamine levels and a right paraaortic mass were observed on computedtomography. The mass was excised, and a diagnosis of paraganglioma was confirmed. After 20 months of follow-up, local recurrence and metastases were detected in thethorax, abdomen, and skeletal system. Plasma and urinary catecholamine levels werehigh. Chemotherapy was administered, and no improvement was observed. Therefore,following this palliative conventional chemotherapy, sorafenib was administered forthree months, and, finally, positron emission tomography showed that the patient’slesions had completely regressed.
Abstract
Paragangliomas are relatively rare chromaffin cell tumors which may be cured throughresection. Patients with paragangliomas may develop metastatic diseases. There isno consensus regarding refractory chemotherapy for treatment of metastatic disease. In this report, we presented a case of a 43-year-old woman who was admitted to thehospital with a history of episodic headaches, diaphoresis, and weakness. Elevatedplasma catecholamine levels and a right paraaortic mass were observed on computedtomography. The mass was excised, and a diagnosis of paraganglioma was confirmed. After 20 months of follow-up, local recurrence and metastases were detected in thethorax, abdomen, and skeletal system. Plasma and urinary catecholamine levels werehigh. Chemotherapy was administered, and no improvement was observed. Therefore,following this palliative conventional chemotherapy, sorafenib was administered forthree months, and, finally, positron emission tomography showed that the patient’slesions had completely regressed.
참고문헌 (13)
- Frankel F, "Ein Fall von doppelseitigem, vollig latent verlaufenen Nebennierentumor und gleichzeitiger Nephritis mit Veranderungen am Circulationsapparat und Retinitis", Virchows Arch, 103, pp.244~263 (1886)
- Fliedner SM, "Metastatic paraganglioma", Semin Oncol, 37, pp.627~637 (2010)
- Krawczyk A, "Germinal mutations of RET, SDHB, SDHD, and VHL genes in patients with apparently sporadic pheochromocytomas and paragangliomas", Endokrynol Pol, 61, pp.43~48 (2010)
- O'Riordain DS, "Clinical spectrum and outcome of functional extraadrenal paraganglioma", World J Surg, 20, pp.916~921 (1996)
- Lehnert H, "Malignant pheochromocytoma", Front Horm Res, 31, pp.155~162 (2004)
- Zografos GN, "Laparoscopic surgery for malignant adrenal tumors", JSLS, 13, pp.196~202 (2009)
- Kulke MH, "Phase II study of temozolomide and thalidomide in patients with metastatic neuroendocrine tumors", J Clin Oncol, 24, pp.401~406 (2006)
- Joshua AM, "Rationale and evidence for sunitinib in the treatment of malignant paraganglioma", pheochromocytoma, 2009, pp.94, 5~9
- Jimenez C, "Use of the tyrosine kinase inhibitor sunitinib in a patient with von Hippel-Lindau disease: targeting angiogenic factors in pheochromocytoma and other von Hippel-Lindau disease-related tumors", J Clin Endocrinol Metab, 94, pp.386~391 (2009)
- Park KS, "Sunitinib, a novel therapy for anthracycline- and cisplatinrefractory malignant pheochromocytoma", Jpn J Clin Oncol, 39, pp.327~331 (2009)
- Cirillo F, "Metastatic paraganglioma and treatment with sunitinib: a case report", Tumori, 96, pp.1022~1027 (2010)
- Druce MR, "Novel and evolving therapies in the treatment of malignant phaeochromocytoma: experience with the mTOR inhibitor everolimus (RAD001)", Horm Metab Res, 41, pp.697~702 (2009)
- Gross DJ, "The role of imatinib mesylate (Glivec) for treatment of patients with malignant endocrine tumors positive for c-kit or PDGF-R", Endocr Relat Cancer, 13, pp.535~540 (2006)
