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晚期肝细胞癌的二线治疗:是时候有更多个体化治疗方案了吗?

Second-line treatment of advanced hepatocellular carcinoma: Time for more individualized treatment options?

作者信息

Rajappa Senthil, Rau Kun-Ming, Dattatreya Palanki Satya, Ramaswamy Anant, Fernandes Philana, Pruthi Aarohan, Cheng Rebecca, Lukanowski Mariusz, Huang Yi-Hsiang

机构信息

Department of Medical Oncology, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad 500034, Telangana, India.

College of Medicine, I-Shou University, Kaohsiung 822, Taiwan.

出版信息

World J Hepatol. 2022 Jun 27;14(6):1074-1086. doi: 10.4254/wjh.v14.i6.1074.

Abstract

Hepatocellular carcinoma (HCC) is the most frequently diagnosed primary tumor of the liver and is usually detected as advanced disease. It is an aggressive disease that often progresses rapidly when it fails to respond to treatment. As such, patients have limited opportunities to try different subsequent-line treatment regimens. In the last 5 years, the number of agents and/or regimens available for the treatment of advanced HCC has significantly increased, which has made treatment choices for this patient population increasingly complex. In the second-line setting, several phase III trials of regorafenib (RESORCE), ramucirumab (REACH/REACH-2), and cabozantinib (CELESTIAL) have demonstrated clinically meaningful survival benefits in patients with the disease. However, the median overall survival of patients with advanced HCC remains unchanged at approximately 12 mo from the start of systemic second-line therapy, with a limited duration of response. Evidence from the REACH/REACH-2 trials demonstrated for the first time that baseline alpha-fetoprotein (AFP) levels can be used as an identification factor to select those who are likely to benefit the most from ramucirumab treatment. Ramucirumab is both well tolerated and efficacious and has a clinically acceptable safety profile. Therefore, it should be considered an option for patients with AFP levels ≥ 400 ng/mL.

摘要

肝细胞癌(HCC)是最常被诊断出的原发性肝癌,通常在疾病进展至晚期时才被发现。它是一种侵袭性疾病,若对治疗无反应,往往进展迅速。因此,患者尝试不同后续治疗方案的机会有限。在过去5年中,可用于治疗晚期HCC的药物和/或方案数量显著增加,这使得该患者群体的治疗选择日益复杂。在二线治疗中,瑞戈非尼(RESORCE)、雷莫西尤单抗(REACH/REACH-2)和卡博替尼(CELESTIAL)的多项III期试验已证明对该疾病患者具有临床意义的生存获益。然而,晚期HCC患者从开始全身二线治疗起的中位总生存期仍约为12个月,无变化,缓解持续时间有限。REACH/REACH-2试验的证据首次表明,基线甲胎蛋白(AFP)水平可作为一个识别因素,用于选择那些可能从雷莫西尤单抗治疗中获益最大的患者。雷莫西尤单抗耐受性良好且有效,具有临床上可接受的安全性。因此,对于AFP水平≥400 ng/mL的患者,应将其视为一种治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8895/9258252/812d33adfae4/WJH-14-1074-g001.jpg

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