Horiuchi Toshihide, Nishimura Koichi, Nakamura Kazutaka, Nemoto Yuki, Ishiyama Yudai, Katsurayama Nanaka, Toki Daisuke, Kobayashi Hirohito, Kondo Tsunenori
Department of Urology, Tokyo Women's Medical University Adachi Medical Center, 4-33-1 Kohoku, Adachi, Tokyo, 123-8558, Japan.
Department of Urology, Tokiwakai Jyoban Hospital, 57 Kaminodai, Jyoban Kamiyunagayamachi, Iwaki, Fukushima, 972-8322, Japan.
Jpn J Clin Oncol. 2025 Aug 3;55(8):947-953. doi: 10.1093/jjco/hyaf070.
The real-world incidence of hepatic dysfunction after combination therapy with cabozantinib plus nivolumab (CABO+NIVO) in Japanese patients with metastatic renal cell carcinoma remains undetermined; hence, this study aimed to determine the incidence of hepatotoxicity in these patients.
A total of 48 patients treated with CABO+NIVO were enrolled in this study. Alanine aminotransferase (ALT) levels were used to evaluate liver dysfunction because of its liver specificity.
ALT elevation of any grade was found in 30 patients (63%), and grade 3 elevation was found in eight patients (17%). No grade 4 or 5 elevations were observed. Female gender and a higher body mass index were independent predictive factors for ALT elevation. All patients were managed with dose reduction or interruption of cabozantinib and concomitant use of hepatoprotective agents without high-dose corticosteroids. Of the seven patients that underwent cabozantinib rechallenge after grade 3 ALT elevation, only two (23%) required re-interruption due to repeat grade 3 ALT elevation.
This is the first study to examine hepatic dysfunction caused by CABO+NIVO in Japanese patients. The incidence of hepatic dysfunction was higher in real-world patients than in global patients found in pivotal phase 3 trials. Cabozantinib appeared to be a major cause of hepatic dysfunction since dose reduction or interruption of cabozantinib without the use of corticosteroids resolved hepatotoxicity. In addition, additional care should be taken when treating female or obese patients with CABO+NIVO.
在日本转移性肾细胞癌患者中,卡博替尼联合纳武利尤单抗(CABO+NIVO)联合治疗后肝功能不全的真实世界发病率尚未确定;因此,本研究旨在确定这些患者肝毒性的发生率。
本研究共纳入48例接受CABO+NIVO治疗的患者。由于丙氨酸氨基转移酶(ALT)具有肝脏特异性,因此用其水平来评估肝功能不全。
30例患者(63%)出现任何级别的ALT升高,8例患者(17%)出现3级升高。未观察到4级或5级升高。女性和较高的体重指数是ALT升高的独立预测因素。所有患者均通过减少卡博替尼剂量或中断治疗,并同时使用肝保护剂,而未使用大剂量皮质类固醇进行处理。在7例3级ALT升高后接受卡博替尼重新挑战的患者中,只有2例(23%)因再次出现3级ALT升高而需要再次中断治疗。
这是第一项研究日本患者中由CABO+NIVO引起的肝功能不全的研究。真实世界患者中肝功能不全的发生率高于关键3期试验中的全球患者。卡博替尼似乎是肝功能不全的主要原因,因为在不使用皮质类固醇的情况下减少或中断卡博替尼剂量可解决肝毒性。此外,在用CABO+NIVO治疗女性或肥胖患者时应格外小心。