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甲状腺髓样癌——特征综述及系统治疗更新。

Medullary Thyroid Cancer - Feature Review and Update on Systemic Treatment.

机构信息

1Department of Oncology and Nuclear Medicine, Sestre Milosrdnice University Hospital Centre, Zagreb, Croatia; 2University of Zagreb, School of Medicine; 3University of Zagreb, School of Dental Medicine.

出版信息

Acta Clin Croat. 2020 Jun;59(Suppl 1):50-59. doi: 10.20471/acc.2020.59.s1.06.

Abstract

Medullary thyroid carcinoma (MTC) is a rare malignancy that originates from parafollicular (C cells) of the thyroid and accounts for 2-4% of all thyroid malignancies. MTC may be sporadic or inherited, the latter as part of the MEN 2 syndromes. Germline mutations in the proto-oncogene (REarranged during Transfection) are driver mutations in hereditary MTC, whereas somatic mutations and, less frequently, mutations, have been described in tumor tissues of sporadic MTC. Genetic screening for germline mutations in proto-oncogene identifies gene carriers of germline mutations. That enables primary prevention (the avoidance of disease onset by total prophylactic thyroidectomy), or at least secondary prevention (early detection) of the disease. Radical surgery with complete tumor resection is still pivotal in attaining cure for MTC. Despite recent advances, the treatment of advanced, metastatic, and progressive MTC remains challenging. Metastatic MTC can have an indolent clinical course; therefore, it is necessary to assess which patient to cure and when to initiate the treatment. Multidisciplinary boards of various specialists involved in the diagnostics and therapy of the patients with MTC in highly specialized centers with a high volume of patients provide optimal patient management. Multikinase inhibitors (MKI) vandetanib and cabozantinib were approved for the treatment of progressive or symptomatic metastatic/unresectable MTC. Although these treatments have been shown to improve progression-free survival (PFS) with higher overall response rates (ORR) compared with placebo, no MKI has been shown to increase the overall survival (OS) yet, except in the subgroup of patients with -mutations on cabozantinib therapy. As these drugs are nonselective, significant off-target toxicities may occur. Recently, next-generation small-molecule tyrosine kinase inhibitors (TKIs) have been developed. These highly selective RET-inhibitors are specifically designed for highly potent and selective targeting of oncogenic RET alterations, making them promising drugs for the treatment of advanced MTC. The selective RET-inhibitor selpercatinib has been very recently registered for the treatment of -mutated thyroid cancer.

摘要

甲状腺髓样癌(MTC)是一种罕见的恶性肿瘤,起源于甲状腺的滤泡旁细胞(C 细胞),占所有甲状腺恶性肿瘤的 2-4%。MTC 可能是散发性的,也可能是遗传性的,后者是 MEN 2 综合征的一部分。原癌基因(转染过程中重排)的种系突变是遗传性 MTC 的驱动突变,而体细胞突变,以及较少见的突变,已在散发性 MTC 的肿瘤组织中被描述。原癌基因种系突变的基因筛查可识别种系突变的基因携带者。这使得能够进行原发性预防(通过全甲状腺预防性切除术避免疾病发作),或至少进行二级预防(早期发现)。根治性手术完全切除肿瘤仍然是治愈 MTC 的关键。尽管最近取得了进展,但晚期、转移性和进展性 MTC 的治疗仍然具有挑战性。转移性 MTC 可能具有惰性的临床病程;因此,有必要评估要治愈的患者以及何时开始治疗。涉及 MTC 患者诊断和治疗的各种专科的多学科委员会在高度专业化的中心,拥有大量患者,为患者提供最佳的管理。多激酶抑制剂(MKI)凡德他尼和卡博替尼被批准用于治疗进展性或有症状的转移性/不可切除的 MTC。尽管这些治疗方法已被证明与安慰剂相比,能提高无进展生存期(PFS),并提高总缓解率(ORR),但尚未有 MKI 能提高总生存期(OS),除了卡博替尼治疗组的 -突变患者亚组。由于这些药物是非选择性的,可能会发生明显的脱靶毒性。最近,开发了下一代小分子酪氨酸激酶抑制剂(TKI)。这些高度选择性的 RET 抑制剂是专门为高度有效和选择性靶向致癌性 RET 改变而设计的,使它们成为治疗晚期 MTC 的有前途的药物。选择性 RET 抑制剂塞尔帕替尼最近已被注册用于治疗 -突变型甲状腺癌。

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本文引用的文献

1
Updates on the Management of Thyroid Cancer.
Horm Metab Res. 2020 Aug;52(8):562-577. doi: 10.1055/a-1089-7870. Epub 2020 Feb 10.
2
Thyroid cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up†.
Ann Oncol. 2019 Dec 1;30(12):1856-1883. doi: 10.1093/annonc/mdz400.
3
Medullary thyroid carcinoma beyond surgery: advances, challenges, and perspectives.
Endocr Relat Cancer. 2019 Aug 1;26(9):R499-R518. doi: 10.1530/ERC-18-0574.
6
Navigating Systemic Therapy in Advanced Thyroid Carcinoma: From Standard of Care to Personalized Therapy and Beyond.
J Endocr Soc. 2018 Aug 13;2(10):1109-1130. doi: 10.1210/js.2018-00180. eCollection 2018 Oct 1.
7
Selective RET kinase inhibition for patients with RET-altered cancers.
Ann Oncol. 2018 Aug 1;29(8):1869-1876. doi: 10.1093/annonc/mdy137.
9
Precision Targeted Therapy with BLU-667 for -Driven Cancers.
Cancer Discov. 2018 Jul;8(7):836-849. doi: 10.1158/2159-8290.CD-18-0338. Epub 2018 Apr 15.
10
Genotype-specific progression of hereditary medullary thyroid cancer.
Hum Mutat. 2018 Jun;39(6):860-869. doi: 10.1002/humu.23430. Epub 2018 May 3.

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