Evaluating Prognostic Factors for Liver Transplantation Among United States Patients With Hereditary Transthyretin-Mediated (hATTR) Amyloidosis Using National Registry Data

被引:0
作者
Brandman, Danielle [1 ]
Lin, Hollis [2 ]
McManus, Anastasia [2 ]
Agarwal, Sonalee [2 ]
Gache, Larry M. [3 ]
Irish, William [4 ]
Gollob, Jared [5 ]
Zivkovic, Sasa A. [6 ]
机构
[1] Univ Calif San Francisco, Dept Med, Div Gastroenterol, 513 Parnassus Ave,S357,Box 0538, San Francisco, CA 94143 USA
[2] Alnylam Pharmaceut, Cambridge, MA USA
[3] CTI Clin Trial & Consulting Serv, Covington, KY USA
[4] East Carolina Univ, Dept Surg, Greenville, NC USA
[5] Kymera Therapeut, Cambridge, MA USA
[6] Univ Pittsburgh, Med Ctr, Dept Neurol, Pittsburgh, PA USA
关键词
liver transplant recipient; population characteristics; heart transplant recipient; other transplant recipient; transplant donor; anonymous; POLYNEUROPATHY; SURVIVAL; EXPERIENCE; OUTCOMES; PROGRESSION; MUTATIONS; PHENOTYPE; THAOS;
D O I
10.1177/1526924819853832
中图分类号
R61 [外科手术学];
学科分类号
摘要
Introduction: Orthotopic liver transplantation has been used as a treatment for hereditary transthyretin-mediated (hATTR) amyloidosis, a rare, progressive, and multisystem disease. Research Question: The objective is to evaluate survival outcomes post-liver transplantation in patients with hATTR amyloidosis in the United States and assess whether previously published prognostic factors of patient survival in hATTR amyloidosis are generalizable to the US population. Design: This cohort study examined patients with hATTR amyloidosis undergoing liver transplant in the United States (N = 168) between March 2002 and March 2016 using data reported to the Organ Procurement and Transplantation Network (UNOS)/United Network for Organ Sharing (OPTN). Results: A multivariable Cox hazards regression model showed among all factors tested, only modified body mass index (kg/m(2) x g/L) at the time of transplant was significantly associated with survival. Higher modified BMI was associated with lower risk of death relative to a reference population (<600) with historically poor post-transplant outcomes. Patients with modified BMI 1000 to <1200 (hazard ratio [HR] = 0.27; 95% confidence interval [CI] = 0.10-0.73), 1200 to <1400 (HR = 0.20; 95% CI = 0.06-0.75), and >= 1400 (HR = 0.15; 95% CI = 0.04-0.61) exhibited improved adjusted 5-year post-transplant survival of 74%, 80%, and 85%, respectively, versus 33% in the reference population. Discussion: The association between a higher modified BMI threshold at the time of transplant and improved post-transplant survival suggests that the previously published patient selection criterion for modified BMI may not be applicable to the US population.
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页码:213 / 219
页数:7
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共 30 条
[1]   The course and prognostic factors of familial amyloid polyneuropathy after liver transplantation [J].
Adams, D ;
Samuel, D ;
Goulon-Goeau, C ;
Nakazato, M ;
Costa, PMP ;
Feray, C ;
Planté, V ;
Ducot, B ;
Ichai, P ;
Lacroix, C ;
Metral, S ;
Bismuth, H ;
Said, G .
BRAIN, 2000, 123 :1495-1504
[2]   Trial design and rationale for APOLLO, a Phase 3, placebo-controlled study of patisiran in patients with hereditary ATTR amyloidosis with polyneuropathy [J].
Adams, David ;
Suhr, Ole B. ;
Dyck, Peter J. ;
Litchy, William J. ;
Leahy, Raina G. ;
Chen, Jihong ;
Gollob, Jared ;
Coelho, Teresa .
BMC NEUROLOGY, 2017, 17
[3]   Rapid progression of familial amyloidotic polyneuropathy A multinational natural history study [J].
Adams, David ;
Coelho, Teresa ;
Obici, Laura ;
Merlini, Giampaolo ;
Mincheva, Zoia ;
Suanprasert, Narupat ;
Bettencourt, Brian R. ;
Gollob, Jared A. ;
Gandhi, Pritesh J. ;
Litchy, William J. ;
Dyck, Peter J. .
NEUROLOGY, 2015, 85 (08) :675-682
[4]   Recent advances in the treatment of familial amyloid polyneuropathy [J].
Adams, David .
THERAPEUTIC ADVANCES IN NEUROLOGICAL DISORDERS, 2013, 6 (02) :129-139
[5]   Guideline of transthyretin-related hereditary amyloidosis for clinicians [J].
Ando, Yukio ;
Coelho, Teresa ;
Berk, John L. ;
Cruz, Marcia Waddington ;
Ericzon, Bo-Goran ;
Ikeda, Shu-ichi ;
Lewis, W. David ;
Obici, Laura ;
Plante-Bordeneuve, Violaine ;
Rapezzi, Claudio ;
Said, Gerard ;
Salvi, Fabrizio .
ORPHANET JOURNAL OF RARE DISEASES, 2013, 8
[6]   Outcomes of Patients With Familial Transthyretin Amyloidosis After Liver Transplantation [J].
Banerjee, Dipti ;
Roeker, Lindsey E. ;
Grogan, Martha ;
Swiecicki, Paul ;
Poterucha, John ;
Heimbach, Julie ;
Zeldenrust, Steve ;
Gertz, Morie ;
Edwards, Brooks ;
Daly, Richard ;
Klarich, Kyle W. ;
Dispenzieri, Angela .
PROGRESS IN TRANSPLANTATION, 2017, 27 (03) :246-250
[7]   Results of liver transplantation for familial amyloid polyneuropathy type I in Brazil [J].
Bittencourt, PL ;
Couto, CA ;
Farias, AQ ;
Marchiori, P ;
Massarollo, PCB ;
Mies, S .
LIVER TRANSPLANTATION, 2002, 8 (01) :34-39
[8]   Liver Transplantation in Transthyretin Amyloidosis: Issues and Challenges [J].
Carvalho, Andreia ;
Rocha, Ana ;
Lobato, Luisa .
LIVER TRANSPLANTATION, 2015, 21 (03) :282-292
[9]   THAOS - The Transthyretin Amyloidosis Outcomes Survey: initial report on clinical manifestations in patients with hereditary and wild-type transthyretin amyloidosis [J].
Coelho, Teresa ;
Maurer, Mathew S. ;
Suhr, Ole B. .
CURRENT MEDICAL RESEARCH AND OPINION, 2013, 29 (01) :63-76
[10]   "Red-flag" symptom clusters in transthyretin familial amyloid polyneuropathy [J].
Conceicao, Isabel ;
Gonzalez-Duarte, Alejandra ;
Obici, Laura ;
Schmidt, Hartmut H. -J. ;
Simoneau, Damien ;
Ong, Moh-Lim ;
Amass, Leslie .
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2016, 21 (01) :5-9