医学
阿替唑单抗
内科学
伦瓦提尼
肝细胞癌
肿瘤科
贝伐单抗
置信区间
队列
胃肠病学
癌症
无容量
化疗
免疫疗法
索拉非尼
作者
Toshifumi Tada,Takashi Kumada,Atsushi Hiraoka,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,Takashi Nishimura,Takeshi Hatanaka,Satoru Kakizaki
摘要
Abstract Background & Aims The study goal was to compare the outcomes of patients with intermediate‐stage (Barcelona Clinic Liver Cancer [BCLC]‐B) hepatocellular carcinoma (HCC) who received atezolizumab plus bevacizumab (Atezo/Bev) or lenvatinib (LEN) as first‐line systemic therapy. Methods A total of 358 patients with BCLC‐B HCC treated with Atezo/Bev ( n = 177) or LEN ( n = 181) as first‐line systemic therapy were included. Results The median progression‐free survival (PFS) times in the Atezo/Bev and LEN groups were 10.8 months (95% confidence interval [CI], 7.8–12.6) and 7.3 months (95% CI, 6.3–8.5), respectively ( p = .019). In the propensity score‐matched cohort, the median PFS times in the Atezo/Bev ( n = 151) and LEN ( n = 151) groups were 10.2 months (95% CI, 7.0–12.3) and 6.9 months (95% CI, 5.9–8.1), respectively ( p = .020). Restricted mean survival times of PFS were significantly higher in the Atezo/Bev group than in the LEN group at landmarks of 12 and 18 months ( p = .031 and .012, respectively). In a subgroup analysis of patients with HCC beyond the up‐to‐seven criteria, the median PFS times in the Atezo/Bev ( n = 134) and LEN ( n = 117) groups were 10.5 months (95% CI, 7.0–11.8) and 6.3 months (95% CI, 5.5–7.3), respectively ( p = .044). Conclusions The use of Atezo/Bev as first‐line systemic therapy in patients with BCLC‐B HCC is expected to result in good PFS.
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