Transarterial chemoembolization for hepatocellular carcinoma: development and external validation of the Munich-TACE score. Issue 1 (January 2018)

• Record Type: Journal Article
• Authors: op den Winkel, Mark; Nagel, Dorothea; op den Winkel, Philip; Trojan, Jörg; Paprottka, Philipp M.; Steib, Christian J.; Schmidt, Laura; Göller, Markus; Stieber, Petra; Göhring, Peter; Herbst, Andreas; Rentsch, Markus; De Toni, Enrico N.; Göke, Burkhard; Gerbes, Alexander L.; Kolligs, Frank T.
• Is Part Of: European journal of gastroenterology & hepatology. Volume 30:Issue 1(2018:Jan.)
• Publication Date: 2018-01
• Subjects: Barcelona Clinic Liver Cancer -- Cancer of the Liver Italian Program -- Hepatoma Arterial embolization Prognostic -- hepatocellular carcinoma staging systems -- Selection for Transarterial Chemoembolization Treatment; Digestive organs -- Diseases -- Periodicals; Liver -- Diseases -- Periodicals; Digestive organs -- Diseases; Liver -- Diseases; Periodicals; 616.33
• DOI: 10.1097/MEG.0000000000001005
• Languages: English
• ISSNs: 0954-691X

Abstract

Abstract : Background: Allocation of patients with hepatocellular carcinoma (HCC) to the adequate therapy is determined by both tumor burden and liver function. The Barcelona Clinic Liver Cancer (BCLC) staging system and therapeutic algorithm recommends transarterial chemoembolization (TACE) based on the best evidence available to patients with intermediate-stage HCC (BCLC-B). However, many centers also treat subgroups of patients outside these recommendations and with more advanced disease by TACE. The purpose of this study was to identify prognostic factors in a TACE cohort, including BCLC-B patients, as well as patients treated outside of BCLC-B, to test the prognostic capabilities of published staging systems and to optimize prognostication for TACE patients. Patients and methods: A cohort of 186 first-line TACE patients was analyzed. Independent prognostic factors were identified and used to construct the Munich-TACE score (M-TACE). M-TACE was tested against established staging systems (including BCLC and two recently published TACE-specific scores) and a ranking using concordance index and Akaike Information Criterion was performed. Finally, an external validation in an independent TACE cohort ( n =71) was conducted. Results: Bilirubin, Quick/international normalized ratio, C-reactive protein, creatinine, α-feto protein, and tumor extension were identified as independent prognostic factors and used to construct M-TACE. M-TACE identifies three distinct subgroups ( P <0.0001) with median survival times of 35.2, 16.9, and 8.6 months, respectively. Compared with established staging systems, M-TACE showed the best prognostic capabilities in both cohorts of patients (cohort 1: c -index, 0.71; Akaike Information Criterion: 1276; cohort 2: c -index, 0.754). Conclusion: We identified independent risk factors for patients treated with TACE. The newly constructed M-TACE score is superior to established staging systems and might prove helpful to identify patients who are most suitable for TACE. Abstract : Supplemental Digital Content is available in the text.