Granberg Dan, Juhlin Carl Christofer, Falhammar Henrik
Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Department of Breast, Endocrine Tumors and Sarcoma, Karolinska University Hospital, Stockholm, Sweden.
J Clin Endocrinol Metab. 2021 Apr 23;106(5):e1937-e1952. doi: 10.1210/clinem/dgaa982.
Pheochromocytomas and paragangliomas (PPGLs) are believed to harbor malignant potential; about 10% to 15% of pheochromocytomas and up to 50% of abdominal paragangliomas will exhibit metastatic behavior.
Extensive searches in the PubMed database with various combinations of the key words pheochromocytoma, paraganglioma, metastatic, malignant, diagnosis, pathology, genetic, and treatment were the basis for the present review.
To pinpoint metastatic potential in PPGLs is difficult, but nevertheless crucial for the individual patient to receive tailor-made follow-up and adjuvant treatment following primary surgery. A combination of histological workup and molecular predictive markers can possibly aid the clinicians in this aspect. Most patients with PPGLs have localized disease and may be cured by surgery. Plasma metanephrines are the main biochemical tests. Genetic testing is important, both for counseling and prognostic estimation. Apart from computed tomography and magnetic resonance imaging, molecular imaging using 68Ga-DOTATOC/DOTATATE should be performed. 123I-MIBG scintigraphy may be performed to determine whether 131I-MIBG therapy is a possible option. As first-line treatment in patients with metastatic disease, 177Lu-DOTATATE or 131I-MIBG is recommended, depending on which shows best expression. In patients with very low proliferative activity, watch-and-wait or primary treatment with long-acting somatostatin analogues may be considered. As second-line treatment, or first-line in patients with high proliferative rate, chemotherapy with temozolomide or cyclophosphamide + vincristine + dacarbazine is the therapy of choice. Other therapies, including sunitinib, cabozantinib, everolimus, and PD-1/PDL-1 inhibitors, have shown modest effect.
Metastatic PPGLs need individualized management and should always be discussed in specialized and interdisciplinary tumor boards. Further studies and newer treatment modalities are urgently needed.
嗜铬细胞瘤和副神经节瘤(PPGLs)被认为具有恶性潜能;约10%至15%的嗜铬细胞瘤以及高达50%的腹部副神经节瘤会表现出转移行为。
在PubMed数据库中使用嗜铬细胞瘤、副神经节瘤、转移、恶性、诊断、病理学、遗传学和治疗等关键词的各种组合进行广泛检索,是本综述的基础。
确定PPGLs的转移潜能很困难,但对于个体患者在初次手术后接受量身定制的随访和辅助治疗而言至关重要。组织学检查和分子预测标志物的联合应用可能在这方面帮助临床医生。大多数PPGLs患者的疾病局限,手术可能治愈。血浆甲氧基肾上腺素是主要的生化检查。基因检测对于咨询和预后评估都很重要。除计算机断层扫描和磁共振成像外,应进行使用68Ga - DOTATOC/DOTATATE的分子成像。可进行123I - MIBG闪烁显像以确定131I - MIBG治疗是否为一种可行选择。对于转移性疾病患者,根据哪种表现最佳,推荐使用177Lu - DOTATATE或131I - MIBG作为一线治疗。对于增殖活性非常低的患者,可考虑观察等待或用长效生长抑素类似物进行初始治疗。作为二线治疗,或对于增殖率高的患者作为一线治疗,替莫唑胺或环磷酰胺 + 长春新碱 + 达卡巴嗪化疗是首选治疗方法。其他治疗方法,包括舒尼替尼、卡博替尼、依维莫司和PD - 1/PDL - 1抑制剂,已显示出一定疗效。
转移性PPGLs需要个体化管理,应始终在专业的多学科肿瘤委员会中进行讨论。迫切需要进一步研究和更新的治疗方式。