Hepatocellular carcinoma tumour burden score to stratify prognosis after resection

Author:

Tsilimigras D I1ORCID,Moris D1,Hyer J M1,Bagante F12ORCID,Sahara K1,Moro A1,Paredes A Z1,Mehta R1,Ratti F3,Marques H P4,Silva S4,Soubrane O5,Lam V6,Poultsides G A7,Popescu I8,Alexandrescu S8,Martel G9,Workneh A9,Guglielmi A2,Hugh T10,Aldrighetti L3ORCID,Endo I11,Sasaki K12,Rodarte A I12,Aucejo F N12,Pawlik T M1ORCID

Affiliation:

1. Department of Surgery, Ohio State University Wexner Medical Center, Columbus, USA

2. Department of Surgery, University of Verona, Verona, Italy

3. Department of Surgery, Ospedale San Raffaele, Milan, Italy

4. Department of Surgery, Curry Cabral Hospital, Lisbon, Portugal

5. Department of Hepatobiliopancreatic Surgery, Assistance Publique – Hôpitaux de Paris, Beaujon Hospital, Clichy, France

6. Department of Surgery, Westmead Hospital, Sydney, New South Wales, Australia

7. Department of Digestive Disease Institute, Stanford University, Stanford, California, USA

8. Department of Surgery, Fundeni Clinical Institute, Bucharest, Romania

9. Department of Surgery, University of Ottawa, Ottawa, Ontario, Canada

10. Department of Surgery, University of Sydney, School of Medicine, Sydney, New South Wales, Australia

11. Yokohama City University School of Medicine, Yokohama, Japan

12. Department of Digestive Disease Institute, Cleveland Clinic, Cleveland, Ohio, USA

Abstract

Abstract Background Although the Barcelona Clinic Liver Cancer (BCLC) staging system has been largely adopted in clinical practice, recent studies have emphasized the need for further refinement and subclassification of this system. Methods Patients who underwent hepatectomy with curative intent for BCLC-0, -A or -B hepatocellular carcinoma (HCC) between 2000 and 2017 were identified using a multi-institutional database. The tumour burden score (TBS) was calculated, and overall survival (OS) was examined in relation to TBS and BCLC stage. Results Among 1053 patients, 63 (6·0 per cent) had BCLC-0, 826 (78·4 per cent) BCLC-A and 164 (15·6 per cent) had BCLC-B HCC. OS worsened incrementally with higher TBS (5-year OS 77·9, 61 and 39 per cent for low, medium and high TBS respectively; P < 0·001). No differences in OS were noted among patients with similar TBS, irrespective of BCLC stage (61·6 versus 58·9 per cent for BCLC-A/medium TBS versus BCLC-B/medium TBS, P = 0·930; 45 versus 13 per cent for BCLC-A/high TBS versus BCLC-B/high TBS, P = 0·175). Patients with BCLC-B HCC and a medium TBS had better OS than those with BCLC-A disease and a high TBS (58·9 versus 45 per cent; P = 0·005). On multivariable analysis, TBS remained associated with OS among patients with BCLC-A (medium TBS: hazard ratio (HR) 2·07, 95 per cent c.i. 1·42 to 3·02, P < 0·001; high TBS: HR 4·05, 2·40 to 6·82, P < 0·001) and BCLC-B (high TBS: HR 3·85, 2·03 to 7·30; P < 0·001) HCC. TBS could also stratify prognosis among patients in an external validation cohort (5-year OS 79, 51·2 and 28 per cent for low, medium and high TBS respectively; P = 0·010). Conclusion The prognosis of patients with HCC varied according to the BCLC stage but was largely dependent on the TBS.

Publisher

Oxford University Press (OUP)

Subject

Surgery

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