Reduction of bleeding by cabozantinib in metastatic renal cell carcinoma with hereditary hemorrhagic telangiectasia.

IF 0.5 Q4 ONCOLOGY International Cancer Conference Journal Pub Date : 2024-10-01 eCollection Date: 2025-01-01 DOI:10.1007/s13691-024-00727-w
Satoshi Kitamura, Takuto Hara, Yasuyoshi Okamura, Tomoaki Terakawa, Koji Chiba, Jun Teishima, Yuzo Nakano, Hideaki Miyake
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Abstract

Hereditary hemorrhagic telangiectasia (HHT) is a rare genetic disorder characterized by refractory recurrent epistaxis and gastrointestinal bleeding. Recent studies have reported the hemostatic effects of tyrosine kinase inhibitors on HHT-related bleeding. A 67-year-old man with HHT underwent laparoscopic radical nephrectomy for right renal cell carcinoma discovered during an investigation of anemia. Five years after surgery, pancreatic metastasis with biliary dilatation was found on computed tomography. After a biliary stent was inserted, the patient was treated with cabozantinib plus nivolumab. His hemoglobin level significantly improved from 4.8 g/dL to a maximum of 14.7 g/dL, and transfusion frequency reduced from five to one per 5 months. Despite tumor reduction after 6 months of treatment, the patient developed acute cholangitis because of biliary hemorrhage, which ultimately resulted in hepatic failure and death. This case is the first to indicate the potential of the tyrosine kinase inhibitor cabozantinib to control bleeding and tumor progression in patients with metastatic renal cell carcinoma with HHT-related bleeding.

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卡博替尼减少转移性肾细胞癌伴遗传性出血性毛细血管扩张的出血。
遗传性出血性毛细血管扩张症(HHT)是一种罕见的遗传性疾病,其特征是难治性复发性鼻出血和胃肠道出血。最近的研究报道了酪氨酸激酶抑制剂对hht相关出血的止血作用。一位67岁男性HHT患者在检查贫血时发现右肾细胞癌,接受腹腔镜根治性肾切除术。术后5年,计算机断层扫描发现胰腺转移伴胆道扩张。胆道支架置入后,患者接受卡博赞替尼加纳武单抗治疗。他的血红蛋白水平从4.8 g/dL显著改善到最高14.7 g/dL,输血频率从每5个月5次减少到1次。尽管治疗6个月后肿瘤缩小,但由于胆道出血,患者发生急性胆管炎,最终导致肝功能衰竭和死亡。该病例首次表明酪氨酸激酶抑制剂cabozantinib在转移性肾细胞癌伴hht相关出血患者中控制出血和肿瘤进展的潜力。
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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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