BALAD血清学模型在肝细胞癌全身治疗中的预后意义:预测生存获益的个性化方法。

IF 3.3 Q2 ONCOLOGY
JCO Clinical Cancer Informatics Pub Date : 2025-05-01 Epub Date: 2025-05-12 DOI:10.1200/CCI-24-00175
Hidenori Toyoda, Atsushi Hiraoka, Hironori Ochi, Kunihiko Tsuji, Kazuto Tajiri, Joji Tani, Toshifumi Tada, Tomomi Okubo, Masanori Atsukawa, Masashi Hirooka, Ei Itobayashi, Takeshi Hatanaka, Kazuya Kariyama, Toru Ishikawa, Hidekatsu Kuroda, Koichi Takaguchi, Hisashi Kosaka, Kazuhito Kawada, Satoru Kakizaki, Yutaka Yada, Chikara Ogawa, Takashi Nishimura, Satoshi Yasuda, Akihiro Deguchi, Asahiro Morishita, Norio Itokawa, Taeang Arai, Akemi Tsutsui, Atsushi Naganuma, Hirayuki Enomoto, Masaki Kaibori, Kazuhiro Nouso, Yoichi Hiasa, Takashi Kumada, Tomoyuki Akita, Junko Tanaka, Philip J Johnson
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引用次数: 0

摘要

目的:BALAD模型是一种肝细胞癌(HCC)分期评分系统,基于五种血清标志物:胆红素、白蛋白、鸡眼凝集素反应性甲胎蛋白(AFP)、甲胎蛋白(AFP)和去γ -羧基凝血酶原。它已经显示出良好的预测HCC患者生存的能力,无论分期和治疗,高BALAD值与不良预后相关。然而,在接受全身治疗的晚期不可切除HCC (uHCC)患者中,其预后意义尚不清楚。我们评估了BALAD在该亚群中的预后能力。方法:在1510名接受一线全身治疗的晚期uHCC患者的多中心队列中,根据预处理血清水平计算基线BALAD评分。计算总生存期(OS)、无进展生存期(PFS)、总缓解率(ORR)和疾病控制率(DCR),并与BALAD评分相关。结果:总共有502例患者接受索拉非尼治疗,435例接受lenvatinib治疗,573例接受atezolizumab +贝伐单抗治疗。无论何种治疗方案,OS、PFS、ORR和DCR均与BALAD评分呈独立负相关。根据BALAD评分,特定全身治疗方案的有益效果有所不同。结论:BALAD评分在预测接受全身治疗的晚期肝癌患者的OS和PFS方面具有良好的预后能力,并与治疗反应相关。BALAD评分的应用提高了个体患者和HCC患者特定亚组预后预测的准确性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic Significance of the BALAD Serological Model in Systemic Therapies for Hepatocellular Carcinoma: A Personalized Approach to the Prediction of Survival Benefit.

Purpose: The BALAD model, a scoring system for staging hepatocellular carcinoma (HCC), is based on five serum markers: bilirubin, albumin, lens culinaris agglutinin-reactive alpha-fetoprotein [AFP], AFP, and des-gamma-carboxy prothrombin. It has shown good ability to predict survival in patients with HCC irrespective of stage and treatment, a high BALAD value being associated with a poor prognosis. However, its prognostic significance is unclear in patients with advanced unresectable HCC (uHCC) who undergo systemic therapies. We assessed the prognostic ability of BALAD in this subpopulation.

Methods: In a multicenter cohort of 1,510 patients with advanced uHCC treated with first-line systemic therapies, the baseline BALAD score was calculated on the basis of pretreatment serum levels. Overall survival (OS), progression-free survival (PFS), overall response rate (ORR), and disease control rate (DCR) were calculated and related to the BALAD score.

Results: In all, 502 patients were treated with sorafenib, 435 with lenvatinib, and 573 with atezolizumab plus bevacizumab. Irrespective of treatment regimen, OS, PFS, ORR, and DCR were all independently negatively correlated with the BALAD score. The beneficial effects of specific systemic therapy regimens differed according to the BALAD score.

Conclusion: The BALAD score had good prognostic ability for predicting OS and PFS in patients with advanced uHCC who underwent systemic therapies and was associated with treatment response. Application of the BALAD score offers increased precision in the prediction of outcome both for individual patients and for specific subgroups of patients with HCC.

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来源期刊
CiteScore
6.20
自引率
4.80%
发文量
190
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