Outcomes of Patients with Child-Pugh B and Unresectable Hepatocellular Carcinoma Undergoing First-Line Systemic Treatment with Sorafenib, Lenvatinib, or Atezolizumab Plus Bevacizumab.

IF 2.5 3区 医学 Q3 ONCOLOGY
Oncology Pub Date : 2024-01-01 Epub Date: 2023-09-20 DOI:10.1159/000533859
Chihiro Kikugawa, Shinsuke Uchikawa, Tomokazu Kawaoka, Takahiro Kinami, Shigeki Yano, Kei Amioka, Kensuke Naruto, Yuwa Ando, Kenji Yamaoka, Masataka Tsuge, Yumi Kosaka, Kazuki Ohya, Nami Mori, Shintaro Takaki, Keiji Tsuji, Hirotaka Kouno, Hiroshi Kohno, Kei Morio, Takashi Moriya, Michihiro Nonaka, Yasuyuki Aisaka, Keiichi Masaki, Yohji Honda, Noriaki Naeshiro, Akira Hiramatsu, Hiroshi Aikata, Shiro Oka
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引用次数: 0

Abstract

Introduction: Systemic therapy is recommended for patients with Child-Pugh A in hepatocellular carcinoma (HCC). We analyzed the outcomes of a cohort of patients with HCC who received either sorafenib (Sor), lenvatinib (Len) or atezolizumab plus bevacizumab (Atezo + Bev) as first-line systemic therapy for HCC, with the aim of identifying prognostic factors for survival.

Methods: A total of 825 patients with advanced HCC and Child-Pugh A or B received either Sor, Len or Atezo + Bev as first-line systemic therapy. Liver function was assessed according to the Child-Pugh score and the modified albumin-bilirubin (mALBI) grade.

Results: Prognosis was analyzed according to liver function such as Child-Pugh classifications, scores, and mALBI grades that worsened with a decline in liver function (p <0.001 for all). A Child-Pugh score of 7 was a factor significantly associated with OS. In patients with a Child-Pugh score of 7, an mALBI grade of 3 was an independent predictor of OS. In Child-Pugh B patients with HCC, receiving Atezo + Bev was identified as a factor associated with PFS.

Conclusion: Determining the hepatic reserve of patients with unresectable HCC might be useful for identifying patents suitable for systemic treatment for HCC. Atezo + Bev might prolong the PFS of patients with a Child-Pugh score of 7.

接受索拉非尼、乐伐替尼或atezolizumab联合贝伐单抗一线全身治疗的Child-Pugh B和不可切除肝细胞癌患者的结果。
背景:建议对肝细胞癌(HCC)中的Child-Pugh A患者进行系统治疗。我们分析了一组HCC患者的结果,这些患者接受索拉非尼(Sor)、乐伐替尼(Len)或atezolizumab加贝伐单抗(Atezo+Bev)作为HCC的一线系统治疗,目的是确定生存的预后因素。方法:共有825例晚期HCC和Child-Pugh A或B患者接受Sor、Len或Atezo+Bev作为一线系统治疗。根据Child-Pugh评分和改良白蛋白-胆红素(mALBI)分级评估肝功能。结果:当根据肝功能(如Child-Pugh分类、评分和mALBI分级)分析预后时,预后随着肝功能的下降而恶化(所有患者均<0.001)。Child-Pugh评分为7是一个与OS显著相关的因素。在Child-Pugh评分为7的患者中,mALBI评分为3是OS的独立预测因素。在Child-Pugh B型HCC患者中,接受Atezo+Bev被确定为与PFS相关的因素。结论:确定不可切除HCC患者的肝脏储备可能有助于确定适合全身治疗HCC的专利。Atezo+Bev可能延长Child-Pugh评分为7的患者的PFS。
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来源期刊
Oncology
Oncology 医学-肿瘤学
CiteScore
6.00
自引率
2.90%
发文量
76
审稿时长
6-12 weeks
期刊介绍: Although laboratory and clinical cancer research need to be closely linked, observations at the basic level often remain removed from medical applications. This journal works to accelerate the translation of experimental results into the clinic, and back again into the laboratory for further investigation. The fundamental purpose of this effort is to advance clinically-relevant knowledge of cancer, and improve the outcome of prevention, diagnosis and treatment of malignant disease. The journal publishes significant clinical studies from cancer programs around the world, along with important translational laboratory findings, mini-reviews (invited and submitted) and in-depth discussions of evolving and controversial topics in the oncology arena. A unique feature of the journal is a new section which focuses on rapid peer-review and subsequent publication of short reports of phase 1 and phase 2 clinical cancer trials, with a goal of insuring that high-quality clinical cancer research quickly enters the public domain, regardless of the trial’s ultimate conclusions regarding efficacy or toxicity.
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