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首页> 外文期刊>Archives of Endocrinology and Metabolism >Rapid response of hypercortisolism to vandetanib treatment in a patient with advanced medullary thyroid cancer and ectopic Cushing syndrome
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Rapid response of hypercortisolism to vandetanib treatment in a patient with advanced medullary thyroid cancer and ectopic Cushing syndrome

机译:皮质醇过多症对晚期甲状腺髓样癌和异位库欣综合征患者vandetanib治疗的快速反应

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摘要

Medullary thyroid carcinoma (MTC) may rarely present with paraneoplastic syndromes. Among the most frequent ones are the appearance of diarrhea and ectopic Cushing syndrome (ECS). The ECS in the context of MTC is usually present in patients with distant metastatic disease. The use of drugs such as ketoconazole, metyrapone, somatostatin analogs and etomidate have been ineffective alternatives to control hypercortisolism in these patients. Bilateral adrenalectomy is often required to manage this situation. Recently, the use of tyrosine kinase inhibitors has been shown to be a useful tool to achieve eucortisolism in patients with metastatic MTC and ECS. We present a patient with sporadic advanced persistent and progressive MTC with lymph node and liver metastases, which after 16 years of follow-up developed an ECS. After one month of 300 mg/day vandetanib treatment, a biochemical and clinical response of the ECS was achieved but it did not result in significant reduction of tumor burden. However the patient reached criteria for stable disease according to response evaluation criteria in solid tumors (RECIST 1.1) after 8 months of follow-up.
机译:甲状腺髓样癌(MTC)很少伴有副肿瘤综合征。最常见的是腹泻和异位库欣综合征(ECS)。在MTC背景下,ECS通常存在于远处转移性疾病患者中。在这些患者中,使用酮康唑,甲吡酮,生长抑素类似物和依托咪酯等药物对控制皮质醇过多是无效的替代方法。通常需要进行双侧肾上腺切除术来处理这种情况。最近,已证明酪氨酸激酶抑制剂的使用是在转移性MTC和ECS患者中实现全皮质溶血的有用工具。我们介绍了一位零星的晚期持续性和进行性MTC患者,伴有淋巴结转移和肝转移,在经过16年的随访后发展为ECS。经过300毫克/天的vandetanib治疗一个月后,实现了ECS的生化和临床反应,但并未导致肿瘤负荷的显着降低。但是,患者在随访8个月后,根据实体瘤反应评估标准(RECIST 1.1)达到了稳定疾病的标准。

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