Refractory Hypercalcemia Secondary to Metastatic Parathyroid Carcinoma Treated With Immunotherapy.

JCEM case reports Pub Date : 2024-07-15 eCollection Date: 2024-07-01 DOI:10.1210/jcemcr/luae127
Brenda Ta, Michael James Bennett
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Abstract

Parathyroid carcinoma (PC) is a rare endocrine malignancy and an uncommon cause of primary hyperparathyroidism. Metastatic disease confers a guarded prognosis with limited systemic treatment options available. We describe a case of a 64-year-old woman with primary hyperparathyroidism secondary to PC. Despite initial surgical resection, the patient relapsed within 6 months with widespread cerebral and skeletal metastatic disease. She developed worsening parathyroid hormone-mediated hypercalcemia that was refractory to escalating doses of cinacalcet and antiresorptive therapy. Molecular genomics identified high tumor mutation burden within the malignant tissue and single-agent nivolumab immunotherapy was administered. After one dose, there was resolution of her refractory hypercalcemia and primary hyperparathyroidism. The patient has tolerated ongoing treatment with 3 weekly cycles of nivolumab. She remains in biochemical remission as of June 2024, which is now 12 months after commencement of nivolumab.

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用免疫疗法治疗转移性甲状旁腺癌继发的难治性高钙血症
甲状旁腺癌(PC)是一种罕见的内分泌恶性肿瘤,也是原发性甲状旁腺功能亢进症的一种罕见病因。转移性疾病的预后较差,可供选择的全身治疗方案有限。我们描述了一例由PC继发原发性甲状旁腺功能亢进的64岁女性病例。尽管最初进行了手术切除,但患者在6个月内复发,并伴有广泛的脑和骨骼转移性疾病。她患上了甲状旁腺激素介导的高钙血症,且病情恶化,升级剂量的西那卡西酮和抗骨吸收治疗均无效。分子基因组学发现恶性肿瘤组织中存在大量肿瘤突变,于是对她进行了单药 nivolumab 免疫治疗。一个疗程后,患者的难治性高钙血症和原发性甲状旁腺功能亢进症得到缓解。患者能够耐受每周 3 个周期的 nivolumab 治疗。截至 2024 年 6 月,即开始使用尼妥珠单抗 12 个月后,她的生化指标仍处于缓解状态。
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