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Comparing the impact of atezolizumab plus bevacizumab and lenvatinib on the liver function in hepatocellular carcinoma patients: A mixed‐effects regression model approach

医学 倾向得分匹配 阿替唑单抗 肝细胞癌 内科学 贝伐单抗 伦瓦提尼 肝功能 不利影响 比例危险模型 胃肠病学 肿瘤科 癌症 化疗 无容量 索拉非尼 免疫疗法
作者
Takeshi Hatanaka,Satoru Kakizaki,Atsushi Hiraoka,Toshifumi Tada,Masashi Hirooka,Kazuya Kariyama,Joji Tani,Masanori Atsukawa,Koichi Takaguchi,Ei Itobayashi,Shinya Fukunishi,Kunihiko Tsuji,Toru Ishikawa,Kazuto Tajiri,Hironori Ochi,Satoshi Yasuda,Hidenori Toyoda,Chikara Ogawa,Keisuke Yokohama,Hiroki Nishikawa,Takashi Nishimura,Noritomo Shimada,Kazuhito Kawata,Hisashi Kosaka,Atsushi Naganuma,Yutaka Yata,Hidekatsu Kuroda,Hidekatsu Kuroda,Kazunari Tanaka,Takaaki Tanaka,Fujimasa Tada,Kazuhiro Nouso,Asahiro Morishita,Akemi Tsutsui,Takuya Nagano,Norio Itokawa,Tomomi Okubo,Taeang Arai,Michitaka Imai,Yohei Koizumi,Kazuhiro Nouso,Masaki Kaibori,Hiroko Iijima,Yoichi Hiasa,Masatoshi Kudo,Takashi Kumada
出处
期刊:Cancer Medicine [Wiley]
卷期号:12 (24): 21680-21693 被引量:3
标识
DOI:10.1002/cam4.6726
摘要

Abstract Aim This retrospective study compared the impact of atezolizumab plus bevacizumab (Atez/Bev) and lenvatinib (LEN) on the liver function in patients with hepatocellular carcinoma. Methods We included 526 patients who received Atez/Bev and 731 who received LEN March 2018 and July 2022 in this study. We conducted a 1:1 propensity‐score‐matched analysis and identified 324 patients in each group for inclusion in the present analysis. Nonlinear mixed‐effects regression models were employed, allowing for the evaluation and inclusion of cases where treatment was interrupted due to disease progression, adverse events, or loss to follow‐up. These models were used to compare the ALBI score between the Atez/Bev and LEN groups. Results Following propensity score matching, the mean ALBI scores in the Atez/Bev and LEN groups were −2.41 ± 0.40 and −2.44 ± 0.42 at baseline, and −2.17 ± 0.56 and −2.19 ± 0.58 at 12 weeks, respectively. Although the ALBI score significantly worsened during treatment in both groups ( p < 0.001), there was no significant difference in the rate of ALBI score deterioration between the groups ( p = 0.06). Subgroup analyses showed that LEN‐treated patients with BCLC advanced stage ( p = 0.02) and those who initially received the full dose ( p < 0.001) had a significantly greater worsening of ALBI score compared to Atez/Bev. Conclusions Using a nonlinear mixed‐effects regression approach, which allowed for the inclusion of cases with treatment interruption, we found no significant difference in the trend of liver function deterioration between the Atez/Bev and LEN groups. Caution should be exercised for LEN‐treated patients with BCLC advanced stage or those receiving the full dose of LEN.
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