A new model based on preoperative AFP, albumin, and tumor burden score for predicting microvascular invasion in early-stage HCC.

IF 3.6 3区 医学 Q2 ONCOLOGY
American journal of cancer research Pub Date : 2024-10-15 eCollection Date: 2024-01-01 DOI:10.62347/ZGRJ7827
Yuan-Sheng Chang, Mu-Jung Tsai, Chieh-Jui Tsai, Chih-Chi Wang, Chih-Che Lin, Yi-Hao Yen, Chao-Hung Hung, Yuan-Hung Kuo, Ding-Sen Huang, Wei-Chen Tai, Tsung-Hui Hu, Ming-Chao Tsai
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Abstract

Microscopic vascular invasion (MVI) has been demonstrated as a strong risk factor associated with tumor recurrence and poor overall survival among hepatocellular carcinoma (HCC) patients after resection, but the preoperative prediction of MVI is still challenging. We aimed to build and validate a novel model to predict MVI in the preoperative setting. We retrospectively collected 857 patients with Barcelona Clinic Liver Cancer (BCLC) stage 0 or A HCC who underwent primary resection at Kaohsiung Chang Gung Hospital between January 2001 and June 2016. The patients were randomized into derivation (n = 648) and validation groups (n = 209). Logistic regression analysis was used to screen out independent risk factors for MVI and further constructed a predictive model for MVI. Prediction performance was compared by the area under the receiver operating characteristic curve (AUC). The multivariable logistic regression analysis of the training cohort found that alpha-fetoprotein (AFP) ≥ 20 ng/mL (OR = 1.96, 95% CI: 1.41-2.73, P < 0.001), albumin < 3.5 g/dL (OR = 1.48, 95% CI: 1.06-2.05, P = 0.019) and tumor burden score (TBS) ≥ 8.6 (OR = 2.54, 95% CI: 1.49-4.35, P = 0.001) to be independent risk factors for MVI. The three factors were chosen to build a model for prediction of MVI. The AUC for the training and validation group was 0.619 (95% CI: 0.575-0.663) and 0.642 (95% CI: 0.562-0.722), respectively, and the calibration plot showed good performance of the prediction model, with a low mean absolute error at 0.01. In conclusion, the new model comprised AFP, albumin, and TBS that can predict risk of MVI for early-stage HCC.

基于术前甲胎蛋白、白蛋白和肿瘤负荷评分的新模型,用于预测早期 HCC 的微血管侵犯。
显微血管侵犯(MVI)已被证实是肝细胞癌(HCC)患者切除术后肿瘤复发和总生存率低的一个重要风险因素,但术前预测MVI仍具有挑战性。我们的目的是建立并验证一个新的模型来预测术前MVI。我们回顾性地收集了2001年1月至2016年6月期间在高雄长庚医院接受初治切除术的857例巴塞罗那临床肝癌(BCLC)0期或A期HCC患者。患者被随机分为衍生组(648人)和验证组(209人)。采用逻辑回归分析筛选出MVI的独立风险因素,并进一步构建了MVI的预测模型。预测效果通过接收者操作特征曲线下面积(AUC)进行比较。对训练队列的多变量逻辑回归分析发现,甲胎蛋白(AFP)≥ 20 ng/mL(OR = 1.96,95% CI:1.41-2.73,P < 0.001)、白蛋白 < 3.5 g/dL (OR = 1.48, 95% CI: 1.06-2.05, P = 0.019) 和肿瘤负荷评分 (TBS) ≥ 8.6 (OR = 2.54, 95% CI: 1.49-4.35, P = 0.001) 是 MVI 的独立危险因素。选择这三个因素建立了一个 MVI 预测模型。训练组和验证组的AUC分别为0.619(95% CI:0.575-0.663)和0.642(95% CI:0.562-0.722),校准图显示预测模型性能良好,平均绝对误差低至0.01。总之,由 AFP、白蛋白和 TBS 组成的新模型可以预测早期 HCC 的 MVI 风险。
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来源期刊
自引率
3.80%
发文量
263
期刊介绍: The American Journal of Cancer Research (AJCR) (ISSN 2156-6976), is an independent open access, online only journal to facilitate rapid dissemination of novel discoveries in basic science and treatment of cancer. It was founded by a group of scientists for cancer research and clinical academic oncologists from around the world, who are devoted to the promotion and advancement of our understanding of the cancer and its treatment. The scope of AJCR is intended to encompass that of multi-disciplinary researchers from any scientific discipline where the primary focus of the research is to increase and integrate knowledge about etiology and molecular mechanisms of carcinogenesis with the ultimate aim of advancing the cure and prevention of this increasingly devastating disease. To achieve these aims AJCR will publish review articles, original articles and new techniques in cancer research and therapy. It will also publish hypothesis, case reports and letter to the editor. Unlike most other open access online journals, AJCR will keep most of the traditional features of paper print that we are all familiar with, such as continuous volume, issue numbers, as well as continuous page numbers to retain our comfortable familiarity towards an academic journal.
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