病例报告:一名患有 NRAS 突变转移性肝内胆管癌的年轻女性对曲美替尼、羟氯喹和贝伐单抗的反应。

Q3 Medicine
Exploration of targeted anti-tumor therapy Pub Date : 2024-01-01 Epub Date: 2024-06-28 DOI:10.37349/etat.2024.00246
Aram A Musaelyan, Ekaterina M Anokhina, Alina I Turdubaeva, Natalia V Mitiushkina, Anastasia N Ershova, Anna D Shestakova, Aigul R Venina, Evgeny N Imyanitov, Sergey V Orlov
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引用次数: 0

摘要

全身化疗是晚期肝内胆管癌(iCCA)患者的主要治疗选择,但其疗效有限。在此,我们报告了一名患有NRAS突变的化疗耐药转移性iCCA的年轻患者,该患者接受了曲美替尼(MEK1/2抑制剂)、羟氯喹(自噬抑制剂)和贝伐珠单抗(血管生成抑制剂)联合疗法的二线治疗。治疗期间取得了明显的反应,治疗 2 个月后肿瘤病灶缩小了 25%,患者的病情也得到了改善。这种反应持续了 4 个月,但患者在开始这种三联疗法 10 个月后死亡。通过本病例报告和对其他现有研究的分析,我们有理由进一步研究在RAS突变肿瘤中联合使用MEK和自噬抑制剂的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Response to trametinib, hydroxychloroquine, and bevacizumab in a young woman with NRAS-mutated metastatic intrahepatic cholangiocarcinoma: a case report.

Systemic chemotherapy is the main treatment option for patients with advanced intrahepatic cholangiocarcinoma (iCCA), however, its efficacy is limited. Herein, we report a young patient with NRAS-mutated chemoresistant metastatic iCCA, who received second-line therapy with a combination of trametinib (MEK1/2 inhibitor), hydroxychloroquine (autophagy inhibitor), and bevacizumab (angiogenesis inhibitor). A significant response was achieved during therapy, resulting in a 25% decrease in the size of tumor lesions after 2 months of treatment and an improvement in the patient's condition. The duration of this response was 4 months, but the patient died 10 months after the initiation of this triple therapy. This case report and the analysis of other available studies warrant further investigations on combined MEK and autophagy inhibition in RAS-mutated tumors.

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CiteScore
2.80
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