Risk factors of de novo malignancies after liver transplantation: a French national study on 11004 adult patients

被引:14
作者
Altieri, Mario [1 ,2 ]
Seree, Olivier [3 ]
Lobbedez, Thierry [4 ]
Segol, Philippe [5 ]
Abergel, Armand [6 ]
Blaizot, Xavier [3 ]
Boillot, Olivier [7 ,8 ]
Boudjema, Karim [9 ]
Coilly, Audrey [10 ]
Conti, Filomena [11 ]
Chazouilleres, Olivier [12 ]
Debette-Gratien, Maryline [13 ]
Dharancy, Sebastien [14 ]
Durand, Francois [15 ]
Duvoux, Christophe [16 ]
Francoz, Claire [15 ]
Gugenheim, Jean [17 ]
Hardwigsen, Jean [18 ]
Houssel-Debry, Pauline [9 ]
Kamar, Nassim [19 ]
Latournerie, Marianne [20 ]
Lebray, Pascal [20 ]
Leroy, Vincent [21 ]
Neau-Cransac, Martine [22 ]
Pageaux, Georges-Philippe [23 ]
Radenne, Sylvie [24 ]
Salame, Ephrem [25 ]
Saliba, Faouzi [10 ]
Samuel, Didier [10 ]
Vanlemmens, Claire [26 ]
Besch, Camille [27 ]
Launoy, Guy [2 ]
Dumortier, Jerome [7 ,8 ]
机构
[1] Hop Cote Nacre, Serv Hepatogastroenterol Nutr & Oncol Digest, Caen, France
[2] UFR Sante Caen France U1086 INSERM ANTICIPE, Caen, France
[3] Reseau Reg Cancerol OncoBasseNormandie, Caen, France
[4] Normandie Univ, RDPLF, Unicaen UFR Med, Hop Cote Nacre,Nephrol,CUMR CAEN, Caen, France
[5] Hop Cote Nacre, Serv Chirurg Digest & Gen, Caen, France
[6] CHU Estaing, Inst Pascal, Med Digest, UMR 6602 UCA CNRS SIGMA, Clermont Ferrand, France
[7] Hop Edouard Herriot, Hosp Civils Lyon, Unite Transplantat Hepat, Lyon, France
[8] Univ Claude Bernard Lyon 1, Lyon, France
[9] Hop Univ Pontchaillou, Serv Hepatol & Transplantat Hepat, Rennes, France
[10] Hop Paul Brousse, AP HP, INSERM, Ctr Hepatobiliaire,Unite 1193, Villejuif, France
[11] Hop La Pitie Salpetriere, AP HP, Serv Hepatol & Transplantat Hepat, Paris, France
[12] Univ Paris 06, AP HP,CDR St Antoine,UMR S 938, Hop St Antoine,Filiere FILFOIE,Serv Hepatol,INSER, Ctr Reference Malad Inflammatoire Voies Biliaires, Paris, France
[13] Univ Limoges, Serv Hepatogastroenterol, CHU Limoges, INSERM U850, Limoges, France
[14] CHRU Lille, Hop Claude Huriez, Serv Hepatol, Lille, France
[15] Univ Paris Diderot, Hop Beaujon, AP HP, Serv Hepatol & Transplantat Hepat,INSERM U1149, Clichy, France
[16] Hop Henri Mondor, AP HP, Serv Hepatol, Creteil, France
[17] Univ Nice Sophia Antipolis, Serv Chirurg Digest & Transplantat Hepat, Hop Univ Nice, Nice, France
[18] Hop La Timone, AP HM, Serv Chirurg Gen & Transplantat Hepat Marseille, Marseille, France
[19] CHU Rangueil, Dept Nephrol & Transplantat Organes, Toulouse, France
[20] Univ Bourgogne Franche Comte, Serv Hepatogastroenterol & Oncol Digest, CHU Dijon, Inserm EPICAD LNC,UMR1231, Dijon, France
[21] CHU Grenoble Alpes, Serv Hepatogastroenterol, La Tronche, France
[22] CHU Bordeaux, Hop Haut Leveque, Serv Chirurg Hepatobiliaire & Transplantat Hepat, Bordeaux, France
[23] CHU St Eloi, Dept Hepatol & Transplantat Hepat, Montpellier, France
[24] Hop Croix Rousse, Serv Hepatogastroenterol, Hosp Civils Lyon, Lyon, France
[25] CHU Tours, Transplantat Hepat, Hop Trousseau Serv Chirurg Digest Oncol & Endocri, Tours, France
[26] Hop Jean Minjoz, Serv Hepatol & Soins Intensifs Digestifs, Besancon, France
[27] CHRU Hautepierre, Serv Chirurg Hepatobiliopancreat & Transplantat H, Strasbourg, France
关键词
Liver transplantationde novomalignancies; Competing risk; SINGLE-CENTER; CANCER-RISK; SKIN-CANCER; MORTALITY; EVOLUTION; HAZARDS; DISEASE;
D O I
10.1016/j.clinre.2020.07.019
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: After liver transplantation (LT),de novo malignancies are one of the leading causes of late mortality. The aim of the present retrospective study was to identify the risk factors of de novo malignancies in a large cohort of LT recipients in France, using Fine and Gray competing risks regression analysis. Methods: The study population consisted in 11004 adults transplanted between 2000 and 2013, who had no history of pre-transplant malignancy, except primary liver tumor. A Cox model adapted to the identification of prognostic factors (competitive risks) was used. Results: From the entire cohort, one (or more)de novo malignancy was reported in 1480 L T recipients (13.45%). The probability to develop a de novo malignancy after LT was 2.07% at 1 year, 13.30% at 5 years, and 28.01% at 10 years. Of the known reported malignancies, the most common malignancies were hematological malignancy (22.36%), non-melanoma skin cancer (19.53%) and lung cancer (12.36%). According to Fine and Gray competing risks regression multivariate analysis, were significant risk factors for post-LT de novo malignancy: recipient age (Subdistribution Hazard Ratio (SHR) = 1.03 95%CI 1.03 & minus;1.04), male gender (SHR = 1.45 95%CI 1.27 & minus;1.67), non-living donor (SHR = 1.67 95%CI 1.14 & minus;2.38), a first LT (SHR = 1.35 95%CI 1.09 & minus;1.69) and the type of initial liver disease (alcohol-related liver disease (SHR = 1.63 95%CI 1.22 & minus;2.17), primary sclerosing cholangitis (SHR = 1.98 95%CI 1.34 & minus;2.91), and primary liver tumor (SHR = 1.88 95%CI 1.41 & minus;2.54)). Initial immunosuppressive regimen had no significant impact. Conclusion: The present study confirms that LT recipient characteristics are associated with the risk ofde novo malignancy and this underlines the need for personalized screening in order to improve survival. (c) 2020 Elsevier Masson SAS. All rights reserved.
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页数:9
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