Serum Mesothelin for Early Detection of Asbestos-Induced Cancer Malignant Mesothelioma

被引:59
作者
Creaney, Jenette [1 ,4 ]
Olsen, Nola J. [2 ,3 ]
Brims, Fraser [2 ]
Dick, Ian M. [1 ,4 ]
Musk, Arthur W. [2 ,3 ,4 ]
de Klerk, Nicholas H. [3 ,4 ,5 ]
Skates, Steven J. [6 ]
Robinson, Bruce W. S. [1 ,2 ,4 ]
机构
[1] Univ Western Australia, Sch Med & Pharmacol, QEII Med Ctr, Nedlands, WA 6009, Australia
[2] Sir Charles Gairdner Hosp, Dept Resp Med, Nedlands, WA 6009, Australia
[3] Univ Western Australia, Sch Populat Hlth, Nedlands, WA 6009, Australia
[4] Sir Charles Gairdner Hosp, Natl Res Ctr Asbestos Related Dis, Nedlands, WA 6009, Australia
[5] Telethon Inst Child Hlth Res, Biostat & Epidemiol Unit, Subiaco, WA, Australia
[6] Massachusetts Gen Hosp, Ctr Biostat, Boston, MA 02114 USA
基金
英国医学研究理事会;
关键词
SOLUBLE MESOTHELIN; PLEURAL MESOTHELIOMA; BLUE ASBESTOS; VITAMIN-A; WITTENOOM; PREVENTION; MORTALITY; DIAGNOSIS; PROGRESS; PROTEIN;
D O I
10.1158/1055-9965.EPI-10-0346
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Malignant mesothelioma is an aggressive, almost uniformly fatal tumor, primarily caused by exposure to asbestos. Since the recent discovery that serum mesothelin is a sensitive and highly specific biomarker for mesothelioma, one of the key issues raised is whether mesothelin levels represent a useful screening test for asbestos-exposed at-risk individuals. In this study, soluble mesothelin was determined in sequential serum samples collected from asbestos-exposed individuals before the development of mesothelioma. Methods: Archival serum samples from 106 individuals who developed mesothelioma, 99 asbestos-exposed individuals from the Wittenoom Cancer Surveillance Program, and 109 non-asbestos-exposed individuals from the Busselton Health Survey were identified. Serum mesothelin concentrations were determined using the MESOMARK assay. Results: Longitudinal mesothelin levels determined in healthy asbestos-exposed individuals over a period of 4 years were stable (Pearson's r = 0.96; P < 0.0001). There was no correlation between mesothelin concentration and cumulative asbestos exposure. Mesothelin concentrations were greater than the threshold value of 2.5 nmol/L in the penultimate serum sample before the diagnosis of mesothelioma in 17 of 106 people. Using an increase above the 95% confidence interval of the mean of a given individual's longitudinal mesothelin results, 33 of 82 individuals had increasing mesothelin levels before diagnosis. Conclusion: In a population with a high pretest probability of developing mesothelioma, the serum biomarker mesothelin is elevated in absolute terms in 15% and in relative terms in 40% of the group. Impact: Future studies examining a combination of biomarkers could improve sensitivity of screening. Cancer Epidemiol Biomarkers Prev; 19(9); 2238-46. (C) 2010 AACR.
引用
收藏
页码:2238 / 2246
页数:9
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