不依赖治疗的肝细胞癌生存预测评分的开发和验证

Terence J.Y. Tan, Liang Shen, Saur Hajiev, Lung-Yi Mak, Rohini Sharma, George B.B. Goh, Pik-Eu Chang, Man-Fung Yuen, David J. Pinato, Chee-Kiat Tan
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引用次数: 2

摘要

背景,目的肝细胞癌(HCC)患者的生存与多种因素相关。我们的目的是开发和验证HCC生存预测评分(HCC- sps),该评分基于常见的临床参数,不包括随后接受的治疗,能够在诊断时预测所有HCC患者。方法回顾性分析1988年1月以来我科收治的1270例肝癌患者。对已知的HCC预后参数进行单因素分析。参数带P <.1的单因素分析,然后纳入Cox回归与逆向模型选择。采用Cox回归法对各参数进行系数估计,得到HCC-SPS。然后用来自英国的220名患者和来自香港的90名患者的2个独立国际队列验证了衍生的HCC-SPS。对ALBI分级、AFP水平、门静脉侵犯、ECOG状态、TNM分期进行评分。结果总评分将患者分为低、中、高风险3个不同的生存风险类别,中位生存期(周)分别为249 (95% CI 195 ~ 303)、45 (95% CI 38 ~ 52)和9 (95% CI 8 ~ 10)。来自英国和香港的队列验证了评分系统。我们已经制定了一个HCC生存预测评分,使用现成的临床参数,将所有HCC患者在HCC诊断时分为不同的生存类别,而不管随后接受了什么治疗。该评分通过其他独立的国际患者队列进行验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Development and validation of a therapy-independent hepatocellular carcinoma survival prediction score

Development and validation of a therapy-independent hepatocellular carcinoma survival prediction score

Background & Aims

Survival in hepatocellular carcinoma (HCC) is associated with several factors. Our aim was to develop and validate an HCC survival prediction score (HCC-SPS) based on common clinical parameters and excluding the subsequent therapy received, which would be able to prognosticate all patients with HCC at the time of diagnosis.

Methods

The development cohort comprised 1270 patients with HCC seen in our department since January 1988. Univariate analysis was performed for known HCC prognostic parameters. Parameters with P < .1 on univariate analysis were then included in a Cox regression with backward model selection. The HCC-SPS was derived based on the coefficients estimated by Cox regression with selected parameters. The derived HCC-SPS was then validated with 2 independent international cohorts of 220 patients from the United Kingdom and 90 patients from Hong Kong (HK). Points were allocated to the following variables: ALBI grade, AFP level, portal vein invasion, ECOG status and TNM stage.

Results

The total score classified a patient into 3 distinct survival risk categories of low, medium and high risk with median survival (weeks) of 249 (95% CI 195–303), 45 (95% CI 38–52) and 9 (95% CI 8–10) respectively. The scoring system was validated by the cohorts from United Kingdom and HK.

Conclusions

We have formulated an HCC survival prediction score using readily available clinical parameters to risk stratify all HCC patients into distinct survival categories at the time of HCC diagnosis regardless of subsequent treatment received. The score was validated with other independent international cohorts of patients.

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