Show simple item record

Liver Graft‐Versus‐Host Disease is associated with poor survival among allogeneic hematopoietic stem cell transplant recipients

dc.contributor.authorModi, Dipenkumar
dc.contributor.authorYe, Jing Christine
dc.contributor.authorSurapaneni, Malini
dc.contributor.authorSingh, Vijendra
dc.contributor.authorChen, Wei
dc.contributor.authorJang, Hyejeong
dc.contributor.authorDeol, Abhinav
dc.contributor.authorAyash, Lois
dc.contributor.authorAlavi, Asif
dc.contributor.authorRatanatharathorn, Voravit
dc.contributor.authorUberti, Joseph P.
dc.date.accessioned2019-10-30T15:31:09Z
dc.date.availableWITHHELD_13_MONTHS
dc.date.available2019-10-30T15:31:09Z
dc.date.issued2019-10
dc.identifier.citationModi, Dipenkumar; Ye, Jing Christine; Surapaneni, Malini; Singh, Vijendra; Chen, Wei; Jang, Hyejeong; Deol, Abhinav; Ayash, Lois; Alavi, Asif; Ratanatharathorn, Voravit; Uberti, Joseph P. (2019). "Liver Graft‐Versus‐Host Disease is associated with poor survival among allogeneic hematopoietic stem cell transplant recipients." American Journal of Hematology 94(10): 1072-1080.
dc.identifier.issn0361-8609
dc.identifier.issn1096-8652
dc.identifier.urihttps://hdl.handle.net/2027.42/151888
dc.description.abstractLiver Graft‐versus‐host disease (GVHD) is common in patients with post‐transplant liver dysfunction following allogeneic hematopoietic stem cell transplantation (AHSCT). Oftentimes, the diagnosis is made clinically, and liver biopsy is deferred. Our objective was to evaluate the risk factors and clinical outcomes of liver GVHD among patients who developed post‐transplant liver dysfunction. Additionally, we evaluated the feasibility of liver biopsy in this population. We compared outcomes between liver GVHD and a “non‐liver GVHD” group, which consisted of other etiologies of post‐transplant liver dysfunction. Between January 2003 and December 2010, 249 patients developed post‐transplant liver dysfunction following AHSCT: 124 patients developed liver GVHD and 125 were in the “non‐liver GVHD” group. The incidence of acute and chronic liver GVHD at one year was 15.7% and 31.0%, respectively. The competing risk analysis revealed full intensity conditioning regimen (Hazard ratio [HR], 1.76; P = .008) and related donor (HR, 1.68; P = .004) as independent risk factors for liver GVHD. The time‐varying covariate Cox regression analysis with competing risk event, demonstrated that liver GVHD was independently associated with higher non‐relapse mortality, and adverse relapse‐free and overall survival. A total of 112 liver biopsies were performed in 100 patients. No major complications were observed. Liver biopsy confirmed prebiopsy hypotheses in 49% of cases, and led to treatment modification in 49% of patients. Our study shows that liver GVHD is associated with adverse survival. Liver biopsy is safe and often helps directing care in this setting.
dc.publisherJohn Wiley & Sons, Inc.
dc.titleLiver Graft‐Versus‐Host Disease is associated with poor survival among allogeneic hematopoietic stem cell transplant recipients
dc.typeArticle
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biology
dc.subject.hlbsecondlevelOncology and Hematology
dc.subject.hlbtoplevelHealth Sciences
dc.subject.hlbtoplevelScience
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/151888/1/ajh25575.pdf
dc.description.bitstreamurlhttps://deepblue.lib.umich.edu/bitstream/2027.42/151888/2/ajh25575_am.pdf
dc.identifier.doi10.1002/ajh.25575
dc.identifier.sourceAmerican Journal of Hematology
dc.identifier.citedreferencePidala J, Chai X, Kurland BF, et al. Analysis of gastrointestinal and hepatic chronic graft‐versus‐host [corrected] disease manifestations on major outcomes: a chronic graft‐versus‐host [corrected] disease consortium study. Biol Blood Marrow Transplant. 2013; 19 ( 5 ): 784 ‐ 791.
dc.identifier.citedreferenceTomas JF, Pinilla I, Garcia‐Buey ML, et al. Long‐term liver dysfunction after allogeneic bone marrow transplantation: clinical features and course in 61 patients. Bone Marrow Transplant. 2000; 26 ( 6 ): 649 ‐ 655.
dc.identifier.citedreferenceKim BK, Chung KW, Sun HS, et al. Liver disease during the first post‐transplant year in bone marrow transplantation recipients: retrospective study. Bone Marrow Transplant. 2000; 26 ( 2 ): 193 ‐ 197.
dc.identifier.citedreferenceStrasser SI, Sullivan KM, Myerson D, et al. Cirrhosis of the liver in long‐term marrow transplant survivors. Blood. 1999; 93 ( 10 ): 3259 ‐ 3266.
dc.identifier.citedreferenceEl‐Sayed MH, El‐Haddad A, Fahmy OA, Salama II, Mahmoud HK. Liver disease is a major cause of mortality following allogeneic bone‐marrow transplantation. Eur J Gastroenterol Hepatol. 2004; 16 ( 12 ): 1347 ‐ 1354.
dc.identifier.citedreferenceKusumi E, Kami M, Kanda Y, et al. Hepatic injury following reduced intensity unrelated cord blood transplantation for adult patients with hematological diseases. Biol Blood Marrow Transplant. 2006; 12 ( 12 ): 1302 ‐ 1309.
dc.identifier.citedreferenceOzdogan O, Ratip S, Ahdab YA, et al. Causes and risk factors for liver injury following bone marrow transplantation. J Clin Gastroenterol. 2003; 36 ( 5 ): 421 ‐ 426.
dc.identifier.citedreferenceSnover DC, Weisdorf SA, Ramsay NK, McGlave P, Kersey JH. Hepatic graft versus host disease: a study of the predictive value of liver biopsy in diagnosis. Hepatology. 1984; 4 ( 1 ): 123 ‐ 130.
dc.identifier.citedreferenceGlucksberg H, Storb R, Fefer A, et al. Clinical manifestations of graft‐versus‐host disease in human recipients of marrow from HL‐A‐matched sibling donors. Transplantation. 1974; 18 ( 4 ): 295 ‐ 304.
dc.identifier.citedreferenceAkpek G, Boitnott JK, Lee LA, et al. Hepatitic variant of graft‐versus‐host disease after donor lymphocyte infusion. Blood. 2002; 100 ( 12 ): 3903 ‐ 3907.
dc.identifier.citedreferenceArai Y, Kanda J, Nakasone H, et al. Risk factors and prognosis of hepatic acute GvHD after allogeneic hematopoietic cell transplantation. Bone Marrow Transplant. 2016; 51 ( 1 ): 96 ‐ 102.
dc.identifier.citedreferenceChen CT, Liu CY, Yu YB, et al. Characteristics and risk of chronic graft‐versus‐host disease of liver in allogeneic hematopoietic stem cell transplant recipients. PLoS One. 2017; 12 ( 9 ): e0185210.
dc.identifier.citedreferenceChahal P, Levy C, Litzow MR, Lindor KD. Utility of liver biopsy in bone marrow transplant patients. J Gastroenterol Hepatol. 2008; 23 ( 2 ): 222 ‐ 225.
dc.identifier.citedreferenceOshrine B, Lehmann LE, Duncan CN. Safety and utility of liver biopsy after pediatric hematopoietic stem cell transplantation. J Pediatr Hematol Oncol. 2011; 33 ( 3 ): e92 ‐ e97.
dc.identifier.citedreferenceShulman HM, Gooley T, Dudley MD, et al. Utility of transvenous liver biopsies and wedged hepatic venous pressure measurements in sixty marrow transplant recipients. Transplantation. 1995; 59 ( 7 ): 1015 ‐ 1022.
dc.identifier.citedreferenceJagasia MH, Greinix HT, Arora M, et al. National Institutes of Health Consensus Development Project on Criteria for Clinical Trials in Chronic Graft‐versus‐Host Disease: I. The 2014 Diagnosis and Staging Working Group Report. Biol Blood Marrow Transplant. 2015; 21 ( 3 ): 389 ‐ 401 e381.
dc.identifier.citedreferenceAl‐Kadhimi Z, Gul Z, Chen W, et al. High incidence of severe acute graft‐versus‐host disease with tacrolimus and mycophenolate mofetil in a large cohort of related and unrelated allogeneic transplantation patients. Biol Blood Marrow Transplant. 2014; 20 ( 7 ): 979 ‐ 985.
dc.identifier.citedreferenceMa SY, Au WY, Lie AK, et al. Liver graft‐versus‐host disease after donor lymphocyte infusion for relapses of hematologic malignancies post allogeneic hematopoietic stem cell transplantation. Bone Marrow Transplant. 2004; 34 ( 1 ): 57 ‐ 61.
dc.identifier.citedreferenceRingden O, Remberger M, Ruutu T, et al. Increased risk of chronic graft‐versus‐host disease, obstructive bronchiolitis, and alopecia with busulfan versus total body irradiation: long‐term results of a randomized trial in allogeneic marrow recipients with leukemia Nordic Bone Marrow Transplantation Group. Blood. 1999; 93 ( 7 ): 2196 ‐ 2201.
dc.identifier.citedreferenceCouriel DR, Saliba RM, Giralt S, et al. Acute and chronic graft‐versus‐host disease after ablative and nonmyeloablative conditioning for allogeneic hematopoietic transplantation. Biol Blood Marrow Transplant. 2004; 10 ( 3 ): 178 ‐ 185.
dc.identifier.citedreferenceRobin M, Porcher R, de Castro R, et al. Initial liver involvement in acute GVHD is predictive for nonrelapse mortality. Transplantation. 2009; 88 ( 9 ): 1131 ‐ 1136.
dc.identifier.citedreferenceRuggiu M, Bedossa P, Rautou PE, et al. Utility and safety of liver biopsy in patients with undetermined liver blood test anomalies after allogeneic hematopoietic stem cell transplantation: a monocentric retrospective cohort study. Biol Blood Marrow Transplant. 2018; 24 ( 12 ): 2523 ‐ 2531.
dc.identifier.citedreferenceCarreras E, Granena A, Navasa M, et al. Transjugular liver biopsy in BMT. Bone Marrow Transplant. 1993; 11 ( 1 ): 21 ‐ 26.
dc.identifier.citedreferenceMcAfee JH, Keeffe EB, Lee RG, Rosch J. Transjugular liver biopsy. Hepatology. 1992; 15 ( 4 ): 726 ‐ 732.
dc.identifier.citedreferencePiccinino F, Sagnelli E, Pasquale G, Giusti G. Complications following percutaneous liver biopsy. A multicentre retrospective study on 68,276 biopsies. J Hepatol. 1986; 2 ( 2 ): 165 ‐ 173.
dc.identifier.citedreferenceDohan A, Guerrache Y, Boudiaf M, Gavini JP, Kaci R, Soyer P. Transjugular liver biopsy: indications, technique and results. Diagn Interv Imaging. 2014; 95 ( 1 ): 11 ‐ 15.
dc.identifier.citedreferenceMaximova N, Gregori M, Barbieri F, Pizzol A, Sonzogni A. Safety and utility of percutaneous liver biopsy in hematopoietic stem cell transplant pediatric recipients: a retrospective study. BMC Cancer. 2016; 16: 590.
dc.identifier.citedreferenceHo GT, Parker A, MacKenzie JF, Morris AJ, Stanley AJ. Abnormal liver function tests following bone marrow transplantation: aetiology and role of liver biopsy. Eur J Gastroenterol Hepatol. 2004; 16 ( 2 ): 157 ‐ 162.
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.