Abstract

BackgroundWe evaluated the treatment response and predictive factors for overall survival (OS) in patients with hepatocellular carcinoma (HCC) and portal vein tumour thrombosis (PVTT), who underwent stereotactic body radiotherapy (SBRT). Additionally, we developed and validated a personalised prediction model for patient survival.MethodsClinical information was retrospectively collected for 80 patients with HCC and PVTT, who were treated with SBRT at the Cancer Hospital of the University of Chinese Academy of Sciences (Zhejiang Cancer Hospital) between December 2015 and June 2019. A multivariate Cox proportional hazard regression model was used to identify the independent predictive factors for survival. Clinical factors were subsequently presented in a nomogram. The area under the receiver operating characteristic curve (AUC) and decision curve analysis (DCA) were used to evaluate the accuracy of the model and the net clinical benefit.ResultsAll patients completed the planned radiotherapy treatment, and the median follow-up duration was 10 months (range, 1–35.3 months). The median survival duration was 11.5 months, with 3-, 6-, and 12-month survival rates of 92.5, 74.5, and 47.5%, respectively. The multivariable Cox regression model indicated that the following were significant independent predictors of OS: clinical T stage (p = 0.001, hazard ratio [HR] = 3.085, 95% confidence interval [CI]: 1.514–6.286), cirrhosis (p = 0.014, HR = 2.988, 95% CI: 1.246–7.168), age (p = 0.005, HR = 1.043, 95% CI: 1.013–1.075), alpha-fetoprotein level (p = 0.022, HR = 1.000, 95% CI: 1.000–1.000), and haemoglobin level (p = 0.008, HR = 0.979, 95% CI: 0.963–0.994). A nomogram based on five independent risk factors and DCA demonstrated a favourable predictive accuracy of patient survival (AUC = 0.74, 95% CI: 0.63–0.85) and the clinical usefulness of the model.ConclusionsSBRT is an effective treatment for patients with HCC with PVTT. Notably, clinical T stage, presence of cirrhosis, age, alpha-fetoprotein levels, and haemoglobin levels are independent prognostic factors for survival. The presented nomogram can be used to predict the survival of patients with HCC and PVTT, who underwent SBRT.

Highlights

  • We evaluated the treatment response and predictive factors for overall survival (OS) in patients with hepatocellular carcinoma (HCC) and portal vein tumour thrombosis (PVTT), who underwent stereotactic body radiotherapy (SBRT)

  • The inclusion criteria were as follows: (1) patients aged between 25 and 75 years who were diagnosed with HCC complicated through PVTT by histopathological or radiological assessment; (2) patients who were ineligible for surgery or with tumours medically unsuitable for resection; (3) an Eastern Cooperative Oncology Group (ECOG) performance status score of 0–2; (4) patients with ChildPugh class A or B liver function; (5) patients without a history of liver radiotherapy; and (6) patients with a liver volume above 700 cc outside of the planning target volume (PTV)

  • Development and validation of an individualised prediction model To provide a quantitative tool for clinicians to individually predict the survival of patients, we developed a nomogram based on five independent risk factors

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Summary

Introduction

We evaluated the treatment response and predictive factors for overall survival (OS) in patients with hepatocellular carcinoma (HCC) and portal vein tumour thrombosis (PVTT), who underwent stereotactic body radiotherapy (SBRT). It is estimated to be the fourth most common cause of cancer-related deaths globally [2]. Macrovascular invasion, such as portal vein tumour thrombosis (PVTT) or inferior vena cava tumour thrombosis (IVCTT), is a common complication of advanced hepatocellular carcinoma (HCC), with an incidence rate of 10–40% at the time of initial diagnosis [3, 4]. The survival rate after comprehensive treatment for HCC has improved in recent years, patients with both HCC and PVTT still have a poor prognosis. PVTT formation is often accompanied by portal hypertension, tumour spread, and a deterioration of liver function, partially limiting the applicability of surgical resection and transarterial chemoembolisation (TACE) [7, 8]

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