Dynamic changes of the inflammation‐based index predict mortality following chemoembolisation for hepatocellular carcinoma: a prospective study. Issue 11 (18th October 2014)

• Record Type: Journal Article
• Authors: Pinato, D. J.; Karamanakos, G.; Arizumi, T.; Adjogatse, D.; Kim, Y. W.; Stebbing, J.; Kudo, M.; Jang, J. W.; Sharma, R.
• Is Part Of: Alimentary pharmacology & therapeutics. Volume 40:Issue 11/12(2014)
• Page Start: 1270
• Page End: 1281
• Publication Date: 2014-10-18
• Subjects: Digestive organs -- Diseases -- Treatment -- Periodicals; Digestive organs -- Effect of drugs on -- Periodicals; Gastrointestinal system -- Diseases -- Treatment -- Periodicals; Gastrointestinal system -- Effect of drugs on -- Periodicals; 615.73
• DOI: 10.1111/apt.12992
• Languages: English
• ISSNs: 0269-2813

Abstract

Summary: Background: Transarterial chemoembolisation (TACE) is a standard treatment for unresectable, intermediate stage hepatocellular carcinoma (HCC). Survival after TACE, however, can be highly variable, with no suitable biomarker predicting therapeutic outcome. The inflammation‐based index (IBI) has previously been shown to independently predict overall survival (OS) in all stages of HCC. Aim: To explore the prognostic ability of IBI as a predictor of survival after TACE. Methods: Baseline staging, biochemical and clinicopathological features including IBI were studied in a derivation set of 64 patients undergoing TACE for intermediate stage HCC. Dynamic changes in IBI before and after TACE were studied as predictors of survival using both a univariate and multivariate Cox regression model and further validated in two independent patient cohorts from Korea ( n = 76) and Japan ( n = 577). Results: Pre‐treatment IBI predicted for OS in the derivation set ( P = 0.001). Other univariate predictors of OS included radiological response to TACE ( P < 0.001), pre‐TACE CLIP score ( P < 0.01), tumour diameter >5 cm ( P = 0.05) and AFP ≥400 ( P < 0.001). Normalisation of IBI post‐TACE was associated with radiological response by mRECIST criteria and improved OS ( P < 0.001). Normalisation of IBI remained a significant multivariate predictor of OS in both the derivation and validation sets ( P < 0.001). Conclusions: Normalisation of IBI after TACE is shown to be an independent predictor of survival and may be integrated into the retreatment criteria for repeat TACE in intermediate stage HCC. IBI and its dynamic changes after treatment are validated as a biomarker allowing the stratification of patients with a significant survival advantage following initial TACE.