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@ARTICLE{Fortner:132470,
author = {R. T. Fortner$^*$ and H. Schock$^*$ and C. Le Cornet$^*$
and A. Hüsing$^*$ and A. F. Vitonis and T. S. Johnson and
R. N. Fichorova and T. Fashemi and H. S. Yamamoto and A.
Tjønneland and L. Hansen and K. Overvad and M.-C.
Boutron-Ruault and M. Kvaskoff and G. Severi and H. Boeing
and A. Trichopoulou and E.-M. Papatesta and C. La Vecchia
and D. Palli and S. Sieri and R. Tumino and C. Sacerdote and
A. Mattiello and N. C. Onland-Moret and P. H. Peeters and H.
B. A. Bueno-de-Mesquita and E. Weiderpass and J. R. Quirós
and E. J. Duell and M.-J. Sánchez and C. Navarro and E.
Ardanaz and N. Larrañaga and B. Nodin and K. Jirström and
A. Idahl and E. Lundin and K.-T. Khaw and R. C. Travis and
M. Gunter and M. Johansson and L. Dossus and M. A. Merritt
and E. Riboli and K. L. Terry and D. W. Cramer and R.
Kaaks$^*$},
title = {{O}varian cancer early detection by circulating {CA}125 in
the context of anti-{CA}125 autoantibody levels: {R}esults
from the {EPIC} cohort.},
journal = {International journal of cancer},
volume = {142},
number = {7},
issn = {0020-7136},
address = {Bognor Regis},
publisher = {Wiley-Liss},
reportid = {DKFZ-2018-00158},
pages = {1355 - 1360},
year = {2018},
abstract = {CA125 is the best ovarian cancer early detection marker to
date; however, sensitivity is limited and complementary
markers are required to improve discrimination between
ovarian cancer cases and non-cases. Anti-CA125
autoantibodies are observed in circulation. Our objective
was to evaluate whether these antibodies (1) can serve as
early detection markers, providing evidence of an immune
response to a developing tumor, and (2) modify the
discriminatory capacity of CA125 by either masking CA125
levels (resulting in lower discrimination) or acting
synergistically to improve discrimination between cases and
non-cases. We investigated these objectives using a nested
case-control study within the European Prospective
Investigation into Cancer and Nutrition cohort (EPIC)
including 250 cases diagnosed within 4 years of blood
collection and up to four matched controls. Circulating
CA125 antigen and antibody levels were quantified using an
electrochemiluminescence assay. Adjusted areas under the
curve (aAUCs) by 2-year lag-time intervals were calculated
using conditional logistic regression calibrated toward the
absolute risk estimates from a pre-existing epidemiological
risk model as an offset-variable. Anti-CA125 levels alone
did not discriminate cases from controls. For cases
diagnosed <2 years after blood collection, discrimination by
CA125 antigen was suggestively higher with higher anti-CA125
levels (aAUC, highest antibody tertile: 0.84 [0.76-0.92];
lowest tertile: 0.76 [0.67-0.86]; phet = 0.06). We
provide the first evidence of potentially synergistic
discrimination effects of CA125 and anti-CA125 antibodies in
ovarian early detection. If these findings are replicated,
evaluating CA125 in the context of its antibody may improve
ovarian cancer early detection.},
cin = {C020},
ddc = {610},
cid = {I:(DE-He78)C020-20160331},
pnm = {313 - Cancer risk factors and prevention (POF3-313)},
pid = {G:(DE-HGF)POF3-313},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:29159934},
pmc = {pmc:PMC5805613},
doi = {10.1002/ijc.31164},
url = {https://inrepo02.dkfz.de/record/132470},
}