一例赛帕替尼治疗甲状腺无节细胞癌导致脓肿形成的病例。

IF 0.5 Q4 ONCOLOGY International Cancer Conference Journal Pub Date : 2024-06-27 eCollection Date: 2024-10-01 DOI:10.1007/s13691-024-00694-2
Ryo Kuboki, Fuminori Nomura, Satoshi Yagihashi, Takahiro Asakage
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引用次数: 0

摘要

转染过程中重排(RET)基因异常是导致甲状腺癌的驱动基因突变,舍帕替尼已被证明可用于治疗RET基因异常的甲状腺癌。无性甲状腺癌是一种预后极差的疾病,目前尚无标准的治疗方法,只有一例报道称舍佩卡替尼对RET融合基因阳性的无性甲状腺癌有疗效。我们在此报告了我们使用赛帕替尼治疗一名患有不可切除性甲状腺无节细胞癌的日本老年妇女的经验。最初曾尝试进行手术切除,但由于颈总动脉粘连而未能如愿。术后基因检测发现RET融合基因呈阳性,于是开始服用赛乐替尼。然而,由于第14天形成脓肿,第17天形成咽瘘,不得不停止用药,此后肿瘤迅速生长,患者于第65天死亡。据报道,尽管赛帕替尼的安全性较高,不良反应较少,但这一病例表明,在治疗侵犯重要器官的无性甲状腺癌时应慎重。
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A case of selpercatinib treatment for anaplastic thyroid carcinoma resulting in abscess formation.

Rearranged during transfection (RET) gene abnormality is a driver gene mutation that causes thyroid cancer, and selpercatinib has been shown to be useful for treating thyroid cancer with RET gene abnormalities. Anaplastic thyroid cancer is a disease with an extremely poor prognosis with no standard treatment established, and there are only one case reports of the efficacy of selpercatinib for RET fusion gene-positive anaplastic thyroid cancer. We herein report our experience treating an old Japanese woman with unresectable anaplastic thyroid cancer with selpercatinib. Surgical resection was initially attempted but was not possible due to adhesion to the common carotid artery. Postoperative genetic testing was positive for the RET fusion gene, and selpercatinib was administered. However, the administration had to be stopped due to the formation of an abscess on day 14 and a pharyngeal fistula on day 17, after which the tumor grew rapidly, and the patient died on day 65. Although selpercatinib has been reported to have a high safety profile with few adverse events, this case suggests that caution should be exercised when treating anaplastic thyroid cancer with invasion to vital organs.

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来源期刊
自引率
14.30%
发文量
57
期刊介绍: This online-only journal publishes original case reports on all types of cancer. In particular, we welcome not only case reports of educational value in the diagnosis and treatment of cancers, but also reports on molecularly analyzed cancer cases, including gene mutations, gene fusions, gene expression, and changes in copy number, regardless of their known clinical significance. Assessing the molecular analysis of a tumor usually requires a “cancer conference” in which experts from various fields discuss it. Even if the authors and their respective “cancer conference” were unable to determine the clinical significance of molecular changes at the time of submission and publication, their data may provide evidence that will help the scientific community develop precision medicine solutions in the future. We welcome case reports with reviews of the literature on similar cases, as they are more useful and valuable to readers than are reports of rare cases. International Cancer Conference Journal is the official publication of the Japan Society of Clinical Oncology (JSCO). - Presents an online-only collection of original case reports on all types of cancer - In particular, welcomes molecularly analyzed cancer cases - The Official Publication of the Japan Society of Clinical Oncology (JSCO)
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