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晚期甲状腺髓样癌患者对塞尔帕替尼的原发耐药。

Primary resistance to selpercatinib in a patient with advanced medullary thyroid cancer.

机构信息

Division of Endocrinology, Hospital de Clínicas, University of Buenos Aires, Buenos Aires, Argentina.

Servizio di Endocrinologia e Diabetologia, Ente Ospedaliero Cantonale (EOC), Lugano, Switzerland.

出版信息

Endocrine. 2024 Oct;86(1):109-113. doi: 10.1007/s12020-024-03890-5. Epub 2024 May 27.

Abstract

Selpercatinib, a selective RET kinase inhibitor, has demonstrated remarkable efficacy in treating patients with advanced medullary (MTC) and differentiated thyroid cancer with RET alterations. Primary resistance to selpercatinib is a very uncommon situation, and its underlying mechanisms are poorly understood. We report the case of a 42-year-old female with advanced MTC harboring a somatic M918T RET mutation who exhibited a primary resistance to selpercatinib. Despite prompt treatment initiation after the diagnosis of progressive disease, the patient continued experiencing rapid spread of disease, characterized by the appearance of new metastatic lesions and increased tumor burden. Genomic analysis revealed no additional mutations associated with on-target or off-target resistance. This case highlights a rare clinical scenario of primary resistance to selpercatinib in advanced MTC. While secondary resistance mechanisms have been well-documented, primary resistance remains poorly understood. Possible explanations include tumor heterogeneity and activation of alternative signaling pathways that stills need to be elucidated. Emerging therapies targeting resistance mechanisms and next-generation RET inhibitors offer promising avenues for further investigation.

摘要

塞尔帕替尼是一种选择性 RET 激酶抑制剂,已被证明在治疗晚期甲状腺髓样癌(MTC)和存在 RET 改变的分化型甲状腺癌患者中具有显著疗效。对塞尔帕替尼的原发性耐药是一种非常罕见的情况,其潜在机制尚未被充分了解。我们报告了一例 42 岁的女性晚期 MTC 患者,携带体细胞 M918T RET 突变,对塞尔帕替尼表现出原发性耐药。尽管在诊断为疾病进展后立即开始治疗,但患者的疾病仍迅速扩散,表现为新的转移病灶出现和肿瘤负荷增加。基因组分析未发现与靶内或靶外耐药相关的其他突变。该病例突出了晚期 MTC 中塞尔帕替尼原发性耐药的罕见临床情况。虽然已经很好地记录了继发性耐药机制,但对原发性耐药仍了解甚少。可能的解释包括肿瘤异质性和尚未阐明的替代信号通路的激活。针对耐药机制的新兴疗法和下一代 RET 抑制剂为进一步研究提供了有希望的途径。

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