医学
内科学
阿替唑单抗
贝伐单抗
比例危险模型
倾向得分匹配
胃肠病学
肝细胞癌
体质指数
混淆
回顾性队列研究
肿瘤科
癌
癌症
化疗
无容量
免疫疗法
作者
Khanh Van Nguyen,Kosuke Matsui,Hisashi Kosaka,Hideyuki Matsushima,Hidekazu Yamamoto,Tung Thanh Lai,Kyoko Inoue,Masahiko Takada,Fujimasa Tada,Atsushi Hiraoka,Takeshi Hatanaka,Toshifumi Tada,Takashi Kumada,H Kato,Kengo Yoshii,Takashi Yamaguchi,Shinji Shimoda,Makoto Naganuma,Masaki Kaibori
出处
期刊:Oncology
[Karger Publishers]
日期:2025-03-28
卷期号:: 1-21
摘要
Background and Aim: We investigated the association between the pretreatment cachexia index (CXI) and survival outcomes in patients with unresectable hepatocellular carcinoma (u-HCC) receiving atezolizumab plus bevacizumab (Atez/Bev). Methods: We conducted a retrospective analysis of 195 patients with u-HCC treated with Atez/Bev from September 2020 to December 2023. The skeletal muscle mass index (SMI) was calculated by normalizing the psoas muscle area by the square of the height (cm²/m²). The CXI was defined as the SMI × serum albumin level (g/dL)/neutrophil-to-lymphocyte ratio. Propensity score matching (PSM) was applied to minimize the effect of potential confounders. Associations between CXI, overall survival (OS), and progression-free survival (PFS) were assessed. Results: From the initial cohort, CXI cutoffs of 7.23 for males and 4.99 for females were established. PSM matched 60 pairs of patients with low and high CXI, showing no significant differences in confounding factors between groups. Kaplan-Meier analysis indicated that the low-CXI group had shorter median OS (12.5 versus 26.1 months, p = 0.009) and PFS (6.1 versus 11.1 months, p = 0.045) compared with the high-CXI group. No significant differences existed between groups in overall response rate (p = 0.994) and disease control rate (p = 0.090). Multivariate Cox proportional hazards analysis identified low CXI as an independent prognostic factor for OS (HR: 1.89, 95% CI: 1.11–3.22, p = 0.019) and PFS (HR: 1.53, 95% CI: 1.01–2.34, p = 0.047). Conclusions: The CXI may be a valuable prognostic tool for predicting survival outcomes in patients with u-HCC receiving Atez/Bev
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