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Sequential therapies after atezolizumab plus bevacizumab or lenvatinib first-line treatments in hepatocellular carcinoma patients

伦瓦提尼 阿替唑单抗 医学 贝伐单抗 索拉非尼 内科学 肝细胞癌 肿瘤科 危险系数 胃肠病学 无容量 癌症 化疗 置信区间 免疫疗法
作者
Mara Persano,Margherita Rimini,Toshifumi Tada,Goki Suda,Shigeo Shimose,Masatoshi Kudo,Jaekyung Cheon,Fabian Finkelmeier,Ho Yeong Lim,José Presa,Gianluca Masi,Changhoon Yoo,Sara Lonardi,Francesco Tovoli,Takashi Kumada,Naoya Sakamoto,Hideki Iwamoto,Tomoko Aoki,Hong Jae Chon,Vera Himmelsbach,Takashi Niizeki,Margarida Montes,Caterina Vivaldi,Caterina Soldà,Bernardo Stefanini,Atsushi Hiraoka,Takuya Sho,Naoshi Nishida,Christoph Steup,Massimo Iavarone,Giovanni Di Costanzo,Fabio Marra,Emiliano Tamburini,Giuseppe Cabibbo,Francesco Giuseppe Foschi,Marianna Silletta,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,Noritomo Shimada,Kazuhito Kawata,Fujimasa Tada,Hideko Ohama,Kazuhiro Nouso,Asahiro Morishita,Akemi Tsutsui,Takuya Nagano,Norio Itokawa,Tomomi Okubo,Taeang Arai,Michitaka Imai,Hisashi Kosaka,Atsushi Naganuma,Yohei Koizumi,Shinichiro Nakamura,Masaki Kaibori,Hiroko Iijima,Yoichi Hiasa,Claudia Campani,Elisabeth Amadeo,Federico Rossari,Valentina Burgio,Stefano Cascinu,Mario Scartozzi,Andrea Casadei‐Gardini
出处
期刊:European Journal of Cancer [Elsevier BV]
卷期号:189: 112933-112933 被引量:31
标识
DOI:10.1016/j.ejca.2023.05.021
摘要

The aim of this retrospective proof-of-concept study was to compare different second-line treatments for patients with hepatocellular carcinoma and progressive disease (PD) after first-line lenvatinib or atezolizumab plus bevacizumab.A total of 1381 patients had PD at first-line therapy. 917 patients received lenvatinib as first-line treatment, and 464 patients atezolizumab plus bevacizumab as first-line.49.6% of PD patients received a second-line therapy without any statistical difference in overall survival (OS) between lenvatinib (20.6months) and atezolizumab plus bevacizumab first-line (15.7months; p = 0.12; hazard ratio [HR]= 0.80). After lenvatinib first-line, there wasn't any statistical difference between second-line therapy subgroups (p = 0.27; sorafenib HR: 1; immunotherapy HR: 0.69; other therapies HR: 0.85). Patients who underwent trans-arterial chemo-embolization (TACE) had a significative longer OS than patients who received sorafenib (24.7 versus 15.8months, p < 0.01; HR=0.64). After atezolizumab plus bevacizumab first-line, there was a statistical difference between second-line therapy subgroups (p < 0.01; sorafenib HR: 1; lenvatinib HR: 0.50; cabozantinib HR: 1.29; other therapies HR: 0.54). Patients who received lenvatinib (17.0months) and those who underwent TACE (15.9months) had a significative longer OS than patients treated with sorafenib (14.2months; respectively, p = 0.01; HR=0.45, and p < 0.05; HR=0.46).Approximately half of patients receiving first-line lenvatinib or atezolizumab plus bevacizumab access second-line treatment. Our data suggest that in patients progressed to atezolizumab plus bevacizumab, the systemic therapy able to achieve the longest survival is lenvatinib, while in patients progressed to lenvatinib, the systemic therapy able to achieve the longest survival is immunotherapy.
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