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转移性融合驱动型甲状腺乳头状癌患者对再分化的持久反应

Durable Response to Redifferentiation in a Patient With Metastatic Fusion-driven Papillary Thyroid Cancer.

作者信息

Tarasova Valentina D, Chung Christine H, Agosto Salgado Sarimar

机构信息

Department of Head and Neck-Endocrine Oncology, Moffitt Cancer Center, Tampa, FL 33612, USA.

出版信息

JCEM Case Rep. 2025 May 5;3(6):luaf054. doi: 10.1210/jcemcr/luaf054. eCollection 2025 Jun.

Abstract

Redifferentiation therapy (RDT) is a promising strategy for follicular cell-derived thyroid cancer (TC) in the era of personalized oncology. Limited data are available on long-term clinical outcomes of RDT in patients with fusion-driven TC. A 22-year-old female with recurrent radioactive iodine (RAI)-refractory metastatic progressive, fusion-driven papillary TC was treated with selective inhibitor, selpercatinib, for 3 months before a therapeutic dose of RAI 146 mCi (5402 MBq). The posttherapy scan showed enhancement of RAI avidity of previously mildly avid pulmonary metastases. After RDT, the thyroglobulin levels significantly declined, and pulmonary nodules completely resolved on chest computed tomography scan. At 24 months of follow-up, the patient did not have evidence of progression. Moreover, thyroglobulin levels continued to decline. RDT with selpercatinib enhanced RAI uptake in the lungs, with a persistent structural and biochemical response sustained 24 months after RAI therapy and discontinuation of selpercatinib. Clinical trials are warranted further to investigate RDT with selective inhibitors in oncogene fusion-driven TC.

摘要

在个性化肿瘤学时代,再分化疗法(RDT)是滤泡细胞源性甲状腺癌(TC)的一种有前景的治疗策略。关于融合驱动型TC患者接受RDT的长期临床结局的数据有限。一名22岁女性,患有复发性放射性碘(RAI)难治性转移性进展性、融合驱动型乳头状TC,在给予146 mCi(5402 MBq)治疗剂量的RAI之前,先用选择性抑制剂塞尔帕替尼治疗了3个月。治疗后扫描显示,之前轻度摄取的肺转移灶的RAI摄取增加。RDT后,甲状腺球蛋白水平显著下降,胸部计算机断层扫描显示肺结节完全消失。在随访24个月时,患者没有疾病进展的证据。此外,甲状腺球蛋白水平持续下降。使用塞尔帕替尼进行RDT可增强肺部对RAI的摄取,在RAI治疗和停用塞尔帕替尼24个月后,仍持续存在结构和生化反应。有必要进一步开展临床试验,以研究在致癌基因融合驱动型TC中使用选择性抑制剂进行RDT的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccf1/12050687/9158bae3073e/luaf054f1.jpg

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