% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Lee:157423,
author = {A. W. Lee and S. Rosenzweig and A. Wiensch and S. J. Ramus
and U. Menon and A. Gentry-Maharaj and A. Ziogas and H.
Anton-Culver and A. S. Whittemore and W. Sieh and J. H.
Rothstein and V. McGuire and N. Wentzensen and E. V. Bandera
and B. Qin and K. L. Terry and D. W. Cramer and L. Titus and
J. M. Schildkraut and A. Berchuck and E. L. Goode and S. K.
Kjaer and A. Jensen and S. J. Jordan and R. B. Ness and F.
Modugno and K. Moysich and P. J. Thompson and M. T. Goodman
and M. E. Carney and J. Chang-Claude$^*$ and M. A. Rossing
and H. R. Harris and J. A. Doherty and H. A. Risch and L.
Khoja and A. Alimujiang and M. T. Phung and K. Brieger and
B. Mukherjee and P. D. P. Pharoah and A. H. Wu and M. C.
Pike and P. M. Webb and C. L. Pearce},
collaboration = {A. O. C. S. Group},
title = {{E}xpanding our understanding of ovarian cancer risk: the
role of incomplete pregnancies.},
journal = {Journal of the National Cancer Institute},
volume = {113},
number = {3},
issn = {1460-2105},
address = {Oxford},
publisher = {Oxford Univ. Press},
reportid = {DKFZ-2020-01618},
pages = {301-308},
year = {2021},
note = {2021 Mar 1;113(3):301-308},
abstract = {Parity is associated with decreased risk of invasive
ovarian cancer; however, the relationship between incomplete
pregnancies and invasive ovarian cancer risk is unclear.
This relationship was examined using 15 case-control studies
from the Ovarian Cancer Association Consortium (OCAC).
Histotype-specific associations, which have not been
examined previously with large sample sizes, were also
evaluated.A pooled analysis of 10,470 invasive epithelial
ovarian cancer cases and 16,942 controls was conducted. Odds
ratios and $95\%$ confidence intervals for the association
between incomplete pregnancies and invasive epithelial
ovarian cancer were estimated using logistic regression. All
models were conditioned on OCAC study, race/ethnicity, age,
and education level, and adjusted for number of complete
pregnancies, oral contraceptive use, and history of
breastfeeding. The same approach was used for
histotype-specific analyses.Ever having an incomplete
pregnancy was associated with a $16\%$ reduction in ovarian
cancer risk (OR = 0.84, $95\%$ CI = 0.79 to 0.89).
There was a trend of decreasing risk with increasing number
of incomplete pregnancies (two-sided Ptrend <.001). An
inverse association was observed for all major histotypes;
it was strongest for clear cell ovarian cancer.Incomplete
pregnancies are associated with a reduced risk of invasive
epithelial ovarian cancer. Pregnancy, including incomplete
pregnancy, was associated with a greater reduction in risk
of clear cell ovarian cancer, but the result was broadly
consistent across histotypes. Future work should focus on
understanding the mechanisms underlying this reduced risk.},
cin = {C020},
ddc = {610},
cid = {I:(DE-He78)C020-20160331},
pnm = {313 - Krebsrisikofaktoren und Prävention (POF4-313)},
pid = {G:(DE-HGF)POF4-313},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:32766851},
doi = {10.1093/jnci/djaa099},
url = {https://inrepo02.dkfz.de/record/157423},
}