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@ARTICLE{Gibbon:3496,
author = {Gibbon, P. and Masek, M. and Teubner, U. and Lu, W. and
Nicoul, M. and Shymanovich, A. and Tarasevitch, A. and Zhou,
P. and Sokolowski-Tinten, K. and von der Linde, D.},
title = {{M}odelling and optimisation of femtosecond laser-produced
{K}-alpha sources},
journal = {Applied physics / A},
volume = {96},
issn = {0947-8396},
address = {Berlin},
publisher = {Springer},
reportid = {PreJuSER-3496},
pages = {23 - 31},
year = {2009},
note = {This work was supported by the Deutsche
Forschungsgemeinschaft (DFG grant-nos. GI 300/3-1, TE
190/6-1 and So 408/6-3) and the FLASH network.},
abstract = {The most reliable prognostic factor in colon cancer is the
TNM classification. The objective of this study was to
assess and compare the prognostic role of tumor-infiltrating
lymphocytes (TILs) in stage II colon
cancer.Immunohistochemistry was used to assess the density
of TILs that were positive for cluster of differentiation 3
(CD3) (T-cell coreceptor), CD45 isoform RO (CD45RO) (protein
tyrosine phosphatase), nuclear transcription factor forkhead
box P3 (FOXP3), and CD25 (a type I transmembrane protein)
according to tumor site (intraepithelial and stromal) in
samples from 87 patients who had stage II colon cancer.
These variables were evaluated for their association with
histopathologic features along with overall survival (OS)
and disease-free survival (DFS).Intraepithelial
CD3-posititve (CD3+), CD45RO+, CD25+, and FOXP3+ TILs were
associated significantly with better DFS (P = .049, P =
.009, P = .013, and P = .001, respectively). The estimated
5-year OS rates for patients who had high-density CD45RO+
and FOXP3+ expression was $100\%$ for both compared with
$79.2\%$ and $78.8\%$ for patients who had low-density
CD45RO+ and FOXP3+ expression (P = .017 and P = .040,
respectively). A significant prognostic factor for both OS
and DFS was high-density stromal CD45RO+ lymphocytic
infiltration (OS: P = .031; relative risk [RR], 0.134;
$95\%$ confidence interval [CI], 0.015-1.164; DFS: P = .013;
RR, 0.198; $95\%$ CI, 0.055-0.710); whereas intraepithelial
FOXP3+ expression was an independent prognostic factor for
DFS (P = .032; RR, 0.108; $95\%$ CI, 0.014-0.821).FOXP3+ and
CD45RO+ TILs demonstrated independent prognostic
significance for survival in the current investigation.
These results may help to improve the prognostication of
early stage colon cancer. Cancer 2010.},
keywords = {Adult / Aged / Colonic Neoplasms: immunology / Colonic
Neoplasms: pathology / Disease-Free Survival / Female /
Humans / Immunohistochemistry / Lymphocytes,
Tumor-Infiltrating: immunology / Male / Middle Aged /
Neoplasm Invasiveness / Prognosis / J (WoSType)},
cin = {JSC},
ddc = {530},
cid = {I:(DE-Juel1)JSC-20090406},
pnm = {Scientific Computing},
pid = {G:(DE-Juel1)FUEK411},
shelfmark = {Materials Science, Multidisciplinary / Physics, Applied},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:20665489},
UT = {WOS:000266372100005},
doi = {10.1007/s00339-009-5188-0},
url = {https://juser.fz-juelich.de/record/3496},
}