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Personalized surveillance for hepatocellular carcinoma in cirrhosis - using machine learning adapted to HCV status.
Audureau, Etienne; Carrat, Fabrice; Layese, Richard; Cagnot, Carole; Asselah, Tarik; Guyader, Dominique; Larrey, Dominique; De Lédinghen, Victor; Ouzan, Denis; Zoulim, Fabien; Roulot, Dominique; Tran, Albert; Bronowicki, Jean-Pierre; Zarski, Jean-Pierre; Riachi, Ghassan; Calès, Paul; Péron, Jean-Marie; Alric, Laurent; Bourlière, Marc; Mathurin, Philippe; Blanc, Jean-Frédéric; Abergel, Armand; Chazouillères, Olivier; Mallat, Ariane; Grangé, Jean-Didier; Attali, Pierre; d'Alteroche, Louis; Wartelle, Claire; Dao, Thông; Thabut, Dominique; Pilette, Christophe; Silvain, Christine; Christidis, Christos; Nguyen-Khac, Eric; Bernard-Chabert, Brigitte; Zucman, David; Di Martino, Vincent; Sutton, Angela; Pol, Stanislas; Nahon, Pierre.
Afiliação
  • Audureau E; AP-HP, Hôpital Henri Mondor, Département de Santé Publique, and Université Paris-Est, A-TVB DHU, CEpiA (Clinical Epidemiology and Ageing) Unit EA7376, UPEC, F-94000, Créteil, France.
  • Carrat F; Sorbonne Université, Inserm, Institut Pierre Louis d'Epidémiologie et de Santé Publique, Paris, France; AP-HP, Hôpital Saint-Antoine, Unité de Santé Publique, Paris, France.
  • Layese R; AP-HP, Hôpital Henri Mondor, Département de Santé Publique, and Université Paris-Est, A-TVB DHU, CEpiA (Clinical Epidemiology and Ageing) Unit EA7376, UPEC, F-94000, Créteil, France.
  • Cagnot C; Unit for Basic and Clinical research on Viral Hepatitis, ANRS (France REcherche Nord & sud Sida-HIV Hépatites-FRENSH).
  • Asselah T; AP-HP, Hôpital Beaujon, Service d'Hépatologie, Clichy.
  • Guyader D; CHU Pontchaillou, Service d'Hépatologie, Rennes.
  • Larrey D; Hôpital Saint Eloi, Service d'Hépatologie, Montpellier.
  • De Lédinghen V; Hôpital Haut-Lévêque, Service d'Hépatologie, Bordeaux.
  • Ouzan D; Institut Arnaud Tzanck, Service d'Hépatologie, St Laurent du Var.
  • Zoulim F; Hospices Civils de Lyon, Service d'Hépatologie; INSERM U1052 - CRCL; Université de Lyon, Lyon.
  • Roulot D; AP-HP, Hôpital Avicenne, Service d'Hépatologie, Bobigny.
  • Tran A; CHU de Nice, Service d'Hépatologie, F-06202, Cedex 3, Nice; Inserm U1065, C3M, Team 8, "Hepatic Complications in Obesity", F-06204, Cedex 3, Nice.
  • Bronowicki JP; Inserm 954, CHU de Nancy, Université de Lorraine, Vandoeuvre-les-Nancy.
  • Zarski JP; Hôpital Michallon, Service d'Hépatologie, Grenoble.
  • Riachi G; Hôpital Charles-Nicolle, Service d'Hépatologie, Rouen.
  • Calès P; CHU d'Angers, Service d'Hépato-Gastroentérologie, Angers.
  • Péron JM; Hôpital Purpan, Service d'Hépatologie, Toulouse.
  • Alric L; CHU Toulouse, Service de Médecine Interne-Pôle Digestif UMR 152, Toulouse.
  • Bourlière M; Hôpital Saint Joseph, Service d'Hépatologie, Marseille.
  • Mathurin P; Hôpital Claude Huriez, Service d'Hépatologie, Lille.
  • Blanc JF; Hôpital St André, Service d'Hépatologie, Bordeaux et Hôpital Haut-Lévêque, CHU Bordeaux, 33604 Pessac.
  • Abergel A; Hôpital Hôtel Dieu, Service d'Hépatologie, Clermont-Ferrand.
  • Chazouillères O; AP-HP, Hôpital Saint-Antoine, Service d'Hépatologie, and Sorbonne Université, INSERM, Centre de Recherche Saint-Antoine, Paris.
  • Mallat A; AP-HP, Hôpital Henri Mondor, Service d'Hépatologie, Créteil.
  • Grangé JD; AP-HP, Hôpital Tenon, Service d'Hépatologie, Paris.
  • Attali P; AP-HP, Hôpital Paul Brousse, Service d'Hépatologie, Villejuif.
  • d'Alteroche L; Hôpital Trousseau, Unité d'Hépatologie, CHRU de Tours.
  • Wartelle C; Hôpital d'Aix-En-Provence, Service d'Hépatologie, Aix-En-Provence.
  • Dao T; Hôpital de la Côte de Nacre, Service d'Hépatologie, Caen.
  • Thabut D; AP-HP, Groupe Hospitalier de La Pitié-Salpêtrière, Service d'Hépatologie, Paris.
  • Pilette C; CHU Le Mans, Service d'Hépatologie, Le Mans.
  • Silvain C; CHU de Poitiers, Service d'Hépatologie, Poitiers.
  • Christidis C; Institut Mutualiste Montsouris, Service d'Hépatologie, Paris.
  • Nguyen-Khac E; CHU Amiens Picardie Hôpital Sud, Service d'Hépatologie, Amiens.
  • Bernard-Chabert B; Hôpital Robert Debré, Service d'Hépatologie, Reims.
  • Zucman D; Hôpital Foch, Service de Médecine Interne, Suresnes.
  • Di Martino V; Hôpital Jean Minjoz, Service d'Hépatologie, Besançon.
  • Sutton A; CRB (liver disease biobank) Groupe Hospitalier Paris Seine-Saint-Denis BB-0033-00027; AP-HP, Hôpital Jean Verdier, Service de Biochimie, Bondy; Inserm U1148, Université Paris 13, Bobigny.
  • Pol S; AP-HP, Hôpital Cochin, Département d'Hépatologie; Inserm UMS20 et U1223, Institut Pasteur, Université Paris Descartes, Paris.
  • Nahon P; AP-HP, Hôpital Jean Verdier, Service d'Hépatologie, Bondy; Université Paris 13, Sorbonne Paris Cité, "Equipe labellisée Ligue Contre le Cancer", F-93206 Saint-Denis; Inserm, UMR-1162, "Génomique fonctionnelle des tumeur solides", F-75000, Paris, France. Electronic address: pierre.nahon@aphp.fr.
J Hepatol ; 73(6): 1434-1445, 2020 12.
Article em En | MEDLINE | ID: mdl-32615276
ABSTRACT
BACKGROUND &

AIMS:

Refining hepatocellular carcinoma (HCC) surveillance programs requires improved individual risk prediction. Thus, we aimed to develop algorithms based on machine learning approaches to predict the risk of HCC more accurately in patients with HCV-related cirrhosis, according to their virological status.

METHODS:

Patients with compensated biopsy-proven HCV-related cirrhosis from the French ANRS CO12 CirVir cohort were included in a semi-annual HCC surveillance program. Three prognostic models for HCC occurrence were built, using (i) Fine-Gray regression as a benchmark, (ii) single decision tree (DT), and (iii) random survival forest for competing risks survival (RSF). Model performance was evaluated from C-indexes validated externally in the ANRS CO22 Hepather cohort (n = 668 enrolled between 08/2012-01/2014).

RESULTS:

Out of 836 patients analyzed, 156 (19%) developed HCC and 434 (52%) achieved sustained virological response (SVR) (median follow-up 63 months). Fine-Gray regression models identified 6 independent predictors of HCC occurrence in patients before SVR (past excessive alcohol intake, genotype 1, elevated AFP and GGT, low platelet count and albuminemia) and 3 in patients after SVR (elevated AST, low platelet count and shorter prothrombin time). DT analysis confirmed these associations but revealed more complex interactions, yielding 8 patient groups with varying cancer risks and predictors depending on SVR achievement. On RSF analysis, the most important predictors of HCC varied by SVR status (non-SVR platelet count, GGT, AFP and albuminemia; SVR prothrombin time, ALT, age and platelet count). Externally validated C-indexes before/after SVR were 0.64/0.64 [Fine-Gray], 0.60/62 [DT] and 0.71/0.70 [RSF].

CONCLUSIONS:

Risk factors for hepatocarcinogenesis differ according to SVR status. Machine learning algorithms can refine HCC risk assessment by revealing complex interactions between cancer predictors. Such approaches could be used to develop more cost-effective tailored surveillance programs. LAY

SUMMARY:

Patients with HCV-related cirrhosis must be included in liver cancer surveillance programs, which rely on ultrasound examination every 6 months. Hepatocellular carcinoma (HCC) screening is hampered by sensitivity issues, leading to late cancer diagnoses in a substantial number of patients. Refining surveillance periodicity and modality using more sophisticated imaging techniques such as MRI may only be cost-effective in patients with the highest HCC incidence. Herein, we demonstrate how machine learning algorithms (i.e. data-driven mathematical models to make predictions or decisions), can refine individualized risk prediction.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hepatite C / Carcinoma Hepatocelular / Regras de Decisão Clínica / Cirrose Hepática / Neoplasias Hepáticas Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: J Hepatol Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hepatite C / Carcinoma Hepatocelular / Regras de Decisão Clínica / Cirrose Hepática / Neoplasias Hepáticas Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: J Hepatol Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: França