Prospective evaluation of 64 serum autoantibodies as biomarkers for early detection of colorectal cancer in a true screening setting

被引:35
作者
Chen, Hongda [1 ]
Werner, Simone [1 ]
Butt, Julia [2 ]
Zoernig, Inka [3 ]
Knebel, Phillip [4 ]
Michel, Angelika [2 ]
Eichmueller, Stefan B. [5 ]
Jaeger, Dirk [3 ]
Waterboer, Tim [2 ]
Pawlita, Michael [2 ]
Brenner, Hermann [1 ,6 ,7 ,8 ]
机构
[1] German Canc Res Ctr, Div Clin Epidemiol & Aging Res, Heidelberg, Germany
[2] German Canc Res Ctr, Div Mol Diagnost Oncogen Infect, Heidelberg, Germany
[3] Heidelberg Univ, Dept Med Oncol, Natl Ctr Tumor Dis NCT, Internal Med 6, Heidelberg, Germany
[4] Heidelberg Univ, Dept Gen Visceral & Transplantat Surg, Heidelberg, Germany
[5] German Canc Res Ctr, GMP & T Cell Therapy Unit, Heidelberg, Germany
[6] German Canc Res Ctr, Div Prevent Oncol, Heidelberg, Germany
[7] Natl Ctr Tumor Dis NCT, Heidelberg, Germany
[8] German Canc Res Ctr, German Canc Consortium DKTK, Heidelberg, Germany
关键词
autoantibody; diagnosis; colorectal cancer; tumor-associated antigens; screening setting; GLUTATHIONE-S-TRANSFERASE; TUMOR-ASSOCIATED ANTIGENS; OCCULT BLOOD-TESTS; CANCER/TESTIS ANTIGENS; COLONOSCOPY; P53; PERFORMANCE; POPULATION; STATISTICS; ADENOMAS;
D O I
10.18632/oncotarget.7500
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Novel blood-based screening tests are strongly desirable for early detection of colorectal cancer (CRC). We aimed to identify and evaluate autoantibodies against tumor-associated antigens as biomarkers for early detection of CRC. 380 clinically identified CRC patients and samples of participants with selected findings from a cohort of screening colonoscopy participants in 2005-2013 (N=6826) were included in this analysis. Sixty-four serum autoantibody markers were measured by multiplex bead-based serological assays. A two-step approach with selection of biomarkers in a training set, and validation of findings in a validation set, the latter exclusively including participants from the screening setting, was applied. Anti-MAGEA4 exhibited the highest sensitivity for detecting early stage CRC and advanced adenoma. Multi-marker combinations substantially increased sensitivity at the price of a moderate loss of specificity. Anti-TP53, anti-IMPDH2, anti-MDM2 and anti-MAGEA4 were consistently included in the best-performing 4-, 5-, and 6-marker combinations. This four-marker panel yielded a sensitivity of 26% (95% CI, 13-45%) for early stage CRC at a specificity of 90% (95% CI, 83-94%) in the validation set. Notably, it also detected 20% (95% CI, 13-29%) of advanced adenomas. Taken together, the identified biomarkers could contribute to the development of a useful multi-marker blood-based test for CRC early detection.
引用
收藏
页码:16420 / 16432
页数:13
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