Urine steroid metabolomics for the differential diagnosis of adrenal incidentalomas in the EURINE-ACT study: a prospective test validation study.
Journal
The lancet. Diabetes & endocrinology
ISSN: 2213-8595
Titre abrégé: Lancet Diabetes Endocrinol
Pays: England
ID NLM: 101618821
Informations de publication
Date de publication:
09 2020
09 2020
Historique:
received:
05
03
2020
revised:
28
05
2020
accepted:
03
06
2020
pubmed:
28
7
2020
medline:
2
9
2020
entrez:
27
7
2020
Statut:
ppublish
Résumé
Cross-sectional imaging regularly results in incidental discovery of adrenal tumours, requiring exclusion of adrenocortical carcinoma (ACC). However, differentiation is hampered by poor specificity of imaging characteristics. We aimed to validate a urine steroid metabolomics approach, using steroid profiling as the diagnostic basis for ACC. We did a prospective multicentre study in adult participants (age ≥18 years) with newly diagnosed adrenal masses. We assessed the accuracy of diagnostic imaging strategies based on maximum tumour diameter (≥4 cm vs <4 cm), imaging characteristics (positive vs negative), and urine steroid metabolomics (low, medium, or high risk of ACC), separately and in combination, using a reference standard of histopathology and follow-up investigations. With respect to imaging characteristics, we also assessed the diagnostic utility of increasing the unenhanced CT tumour attenuation threshold from the recommended 10 Hounsfield units (HU) to 20 HU. Of 2169 participants recruited between Jan 17, 2011, and July 15, 2016, we included 2017 from 14 specialist centres in 11 countries in the final analysis. 98 (4·9%) had histopathologically or clinically and biochemically confirmed ACC. Tumours with diameters of 4 cm or larger were identified in 488 participants (24·2%), including 96 of the 98 with ACC (positive predictive value [PPV] 19·7%, 95% CI 16·2-23·5). For imaging characteristics, increasing the unenhanced CT tumour attenuation threshold to 20 HU from the recommended 10 HU increased specificity for ACC (80·0% [95% CI 77·9-82·0] vs 64·0% [61·4-66.4]) while maintaining sensitivity (99·0% [94·4-100·0] vs 100·0% [96·3-100·0]; PPV 19·7%, 16·3-23·5). A urine steroid metabolomics result indicating high risk of ACC had a PPV of 34·6% (95% CI 28·6-41·0). When the three tests were combined, in the order of tumour diameter, positive imaging characteristics, and urine steroid metabolomics, 106 (5·3%) participants had the result maximum tumour diameter of 4 cm or larger, positive imaging characteristics (with the 20 HU cutoff), and urine steroid metabolomics indicating high risk of ACC, for which the PPV was 76·4% (95% CI 67·2-84·1). 70 (3·5%) were classified as being at moderate risk of ACC and 1841 (91·3%) at low risk (negative predictive value 99·7%, 99·4-100·0). An unenhanced CT tumour attenuation cutoff of 20 HU should replace that of 10 HU for exclusion of ACC. A triple test strategy of tumour diameter, imaging characteristics, and urine steroid metabolomics improves detection of ACC, which could shorten time to surgery for patients with ACC and help to avoid unnecessary surgery in patients with benign tumours. European Commission, UK Medical Research Council, Wellcome Trust, and UK National Institute for Health Research, US National Institutes of Health, the Claire Khan Trust Fund at University Hospitals Birmingham Charities, and the Mayo Clinic Foundation for Medical Education and Research.
Sections du résumé
BACKGROUND
Cross-sectional imaging regularly results in incidental discovery of adrenal tumours, requiring exclusion of adrenocortical carcinoma (ACC). However, differentiation is hampered by poor specificity of imaging characteristics. We aimed to validate a urine steroid metabolomics approach, using steroid profiling as the diagnostic basis for ACC.
METHODS
We did a prospective multicentre study in adult participants (age ≥18 years) with newly diagnosed adrenal masses. We assessed the accuracy of diagnostic imaging strategies based on maximum tumour diameter (≥4 cm vs <4 cm), imaging characteristics (positive vs negative), and urine steroid metabolomics (low, medium, or high risk of ACC), separately and in combination, using a reference standard of histopathology and follow-up investigations. With respect to imaging characteristics, we also assessed the diagnostic utility of increasing the unenhanced CT tumour attenuation threshold from the recommended 10 Hounsfield units (HU) to 20 HU.
FINDINGS
Of 2169 participants recruited between Jan 17, 2011, and July 15, 2016, we included 2017 from 14 specialist centres in 11 countries in the final analysis. 98 (4·9%) had histopathologically or clinically and biochemically confirmed ACC. Tumours with diameters of 4 cm or larger were identified in 488 participants (24·2%), including 96 of the 98 with ACC (positive predictive value [PPV] 19·7%, 95% CI 16·2-23·5). For imaging characteristics, increasing the unenhanced CT tumour attenuation threshold to 20 HU from the recommended 10 HU increased specificity for ACC (80·0% [95% CI 77·9-82·0] vs 64·0% [61·4-66.4]) while maintaining sensitivity (99·0% [94·4-100·0] vs 100·0% [96·3-100·0]; PPV 19·7%, 16·3-23·5). A urine steroid metabolomics result indicating high risk of ACC had a PPV of 34·6% (95% CI 28·6-41·0). When the three tests were combined, in the order of tumour diameter, positive imaging characteristics, and urine steroid metabolomics, 106 (5·3%) participants had the result maximum tumour diameter of 4 cm or larger, positive imaging characteristics (with the 20 HU cutoff), and urine steroid metabolomics indicating high risk of ACC, for which the PPV was 76·4% (95% CI 67·2-84·1). 70 (3·5%) were classified as being at moderate risk of ACC and 1841 (91·3%) at low risk (negative predictive value 99·7%, 99·4-100·0).
INTERPRETATION
An unenhanced CT tumour attenuation cutoff of 20 HU should replace that of 10 HU for exclusion of ACC. A triple test strategy of tumour diameter, imaging characteristics, and urine steroid metabolomics improves detection of ACC, which could shorten time to surgery for patients with ACC and help to avoid unnecessary surgery in patients with benign tumours.
FUNDING
European Commission, UK Medical Research Council, Wellcome Trust, and UK National Institute for Health Research, US National Institutes of Health, the Claire Khan Trust Fund at University Hospitals Birmingham Charities, and the Mayo Clinic Foundation for Medical Education and Research.
Identifiants
pubmed: 32711725
pii: S2213-8587(20)30218-7
doi: 10.1016/S2213-8587(20)30218-7
pmc: PMC7447976
pii:
doi:
Substances chimiques
Steroids
0
Types de publication
Journal Article
Multicenter Study
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Validation Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
773-781Subventions
Organisme : Medical Research Council
ID : G0801473
Pays : United Kingdom
Organisme : NIDDK NIH HHS
ID : K23 DK121888
Pays : United States
Organisme : Wellcome Trust
ID : WT101671
Pays : United Kingdom
Investigateurs
Stephan Glöckner
(S)
Richard O Sinnott
(RO)
Anthony Stell
(A)
Maria C Fragoso
(MC)
Darko Kastelan
(D)
Ivana D Pupovac
(ID)
Bojana Simunov
(B)
Sarah Cazenave
(S)
Magalie Haissaguerre
(M)
Antoine Tabarin
(A)
Jérôme Bertherat
(J)
Rossella Libé
(R)
Tina Kienitz
(T)
Marcus Quinkler
(M)
Katharina Langton
(K)
Graeme Eisenhofer
(G)
Felix Beuschlein
(F)
Christina Brugger
(C)
Martin Reincke
(M)
Anna Riester
(A)
Ariadni Spyroglou
(A)
Stephanie Burger-Stritt
(S)
Timo Deutschbein
(T)
Martin Fassnacht
(M)
Stefanie Hahner
(S)
Matthias Kroiss
(M)
Cristina L Ronchi
(CL)
Sotiria Palimeri
(S)
Stylianos Tsagarakis
(S)
Ioanna Tsirou
(I)
Dimitra A Vassiliadi
(DA)
Vittoria Basile
(V)
Elisa Ingargiola
(E)
Giuseppe Reimondo
(G)
Massimo Terzolo
(M)
Letizia Canu
(L)
Massimo Mannelli
(M)
Hester Ettaieb
(H)
Harm R Haak
(HR)
Thomas M Kerkhofs
(TM)
Michael Biehl
(M)
Richard A Feelders
(RA)
Johannes Hofland
(J)
Leo J Hofland
(LJ)
Marianne A Grytaas
(MA)
Eystein S Husebye
(ES)
Grethe A Ueland
(GA)
Urszula Ambroziak
(U)
Tomasz Bednarczuk
(T)
Agnieszka Kondracka
(A)
Magdalena Macech
(M)
Malgorzata Zawierucha
(M)
Isabel Paiva
(I)
M Conall Dennedy
(MC)
Ahmed Sajwani
(A)
Mark Sherlock
(M)
Rachel K Crowley
(RK)
Miomira Ivovic
(M)
Ljiljana Marina
(L)
Jonathan J Deeks
(JJ)
Alice J Sitch
(AJ)
Wiebke Arlt
(W)
Irina Bancos
(I)
Vasileios Chortis
(V)
Lorna C Giligan
(LC)
Beverly A Hughes
(BA)
Katharina Lang
(K)
Hannah E Ivison
(HE)
Carl Jenkinson
(C)
Konstantinos Manolopoulos
(K)
Donna M O'Neil
(DM)
Michael W O'Reilly
(MW)
Thomas G Papathomas
(TG)
Alessandro Prete
(A)
Cedric H L Shackleton
(CHL)
Angela E Taylor
(AE)
Miriam Asia
(M)
Robert P Sutcliffe
(RP)
Peter Guest
(P)
Kassiani Skordilis
(K)
Cristian Bancos
(C)
Alice Chang
(A)
Caroline J Davidge-Pitts
(CJ)
Danae A Delivanis
(DA)
Dana Erickson
(D)
Neena Natt
(N)
Todd B Nippoldt
(TB)
Melinda Thomas
(M)
William F Young
(WF)
Commentaires et corrections
Type : CommentIn
Type : CommentIn
Informations de copyright
Copyright © 2020 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.
Références
J Clin Endocrinol Metab. 2005 Feb;90(2):871-7
pubmed: 15572420
J Clin Endocrinol Metab. 2008 May;93(5):1526-40
pubmed: 18334580
J Clin Endocrinol Metab. 2011 Dec;96(12):3775-84
pubmed: 21917861
Endocr Rev. 2004 Apr;25(2):309-40
pubmed: 15082524
Endocr Rev. 2014 Apr;35(2):282-326
pubmed: 24423978
J Clin Endocrinol Metab. 2008 Sep;93(9):3266-81
pubmed: 18552288
AJR Am J Roentgenol. 2008 May;190(5):1163-8
pubmed: 18430826
Endocr Rev. 1995 Aug;16(4):460-84
pubmed: 8521790
Horm Cancer. 2016 Dec;7(5-6):327-335
pubmed: 27370636
Mayo Clin Proc Innov Qual Outcomes. 2017 Dec 21;2(1):30-39
pubmed: 30225430
J Endocrinol Invest. 2006 Apr;29(4):298-302
pubmed: 16699294
Eur J Endocrinol. 2016 Aug;175(2):R65-80
pubmed: 27257146
Eur J Endocrinol. 2011 Jun;164(6):851-70
pubmed: 21471169
Eur J Endocrinol. 2016 Aug;175(2):R51-64
pubmed: 27257145
N Engl J Med. 2007 Feb 8;356(6):601-10
pubmed: 17287480
J Clin Endocrinol Metab. 2010 Sep;95(9):4106-13
pubmed: 20823463
J Clin Endocrinol Metab. 2000 Feb;85(2):637-44
pubmed: 10690869
Eur J Endocrinol. 2016 Aug;175(2):G1-G34
pubmed: 27390021
Horm Cancer. 2015 Aug;6(4):168-75
pubmed: 25985881
J Clin Endocrinol Metab. 2014 Jun;99(6):1915-42
pubmed: 24893135
Curr Opin Endocrinol Diabetes Obes. 2017 Jun;24(3):200-207
pubmed: 28234802
Eur J Endocrinol. 2018 Oct 01;179(4):G1-G46
pubmed: 30299884
Clin Chem. 2017 Dec;63(12):1824-1835
pubmed: 28814383