High real-world incidence of hepatic dysfunction from cabozantinib plus nivolumab for Japanese patients with metastatic renal cell carcinoma

被引:0
作者
Horiuchi, Toshihide [1 ]
Nishimura, Koichi [1 ]
Nakamura, Kazutaka [1 ]
Nemoto, Yuki [2 ]
Ishiyama, Yudai [1 ]
Katsurayama, Nanaka [1 ]
Toki, Daisuke [1 ]
Kobayashi, Hirohito [1 ]
Kondo, Tsunenori [1 ]
机构
[1] Tokyo Womens Med Univ, Adachi Med Ctr, Dept Urol, 4-33-1 Kohoku, Adachi, Tokyo 1238558, Japan
[2] Tokiwakai Jyoban Hosp, Dept Urol, 57 Kaminodai Jyoban Kamiyunagayamachi, Iwaki, Fukushima 9728322, Japan
关键词
kidney cancer; nivolumab; cabozantinib; alanine aminotransferase; chemical and drug-induced liver injury; INDUCED HEPATOTOXICITY; LIVER; CYP3A;
D O I
10.1093/jjco/hyaf070
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective 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.Methods 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.Results 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.Conclusions 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. Higher incidence of ALT elevation was observed in Japanese real-world CABO+NIVO than that reported in Checkmate9ER. Around 71% of patients with grade 3 disease were successfully rechallenged with cabozantinib.
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