Pubmed-entry ::= {
pmid 22187035,
medent {
em std {
year 2012,
month 2,
day 1
},
cit {
title {
name "A pilot study to explore circulating tumour cells in pancreatic
cancer as a novel biomarker."
},
authors {
names ml {
"Khoja L",
"Backen A",
"Sloane R",
"Menasce L",
"Ryder D",
"Krebs M",
"Board R",
"Clack G",
"Hughes A",
"Blackhall F",
"Valle JW",
"Dive C"
},
affil str "Clinical and Experimental Pharmacology Group, Paterson
Institute for Cancer Research, Wilmslow Road, Manchester M20 4BX, UK."
},
from journal {
title {
iso-jta "Br. J. Cancer",
ml-jta "Br J Cancer",
issn "1532-1827",
name "British journal of cancer"
},
imp {
date std {
year 2012,
month 1,
day 31
},
volume "106",
issue "3",
pages "508-516",
language "eng",
pubstatus ppublish,
history {
{
pubstatus aheadofprint,
date std {
year 2011,
month 12,
day 20
}
},
{
pubstatus other,
date std {
year 2011,
month 12,
day 22,
hour 6,
minute 0
}
},
{
pubstatus pubmed,
date std {
year 2011,
month 12,
day 22,
hour 6,
minute 0
}
},
{
pubstatus medline,
date std {
year 2012,
month 3,
day 28,
hour 6,
minute 0
}
},
{
pubstatus other,
date std {
year 2013,
month 1,
day 31,
hour 0,
minute 0
}
}
}
}
},
ids {
pii "bjc2011545",
doi "10.1038/bjc.2011.545",
pubmed 22187035,
other {
db "pmc",
tag str "PMC3273340"
},
other {
db "ELocationID doi",
tag str "10.1038/bjc.2011.545"
}
}
},
abstract "BACKGROUND: Obtaining tissue for pancreatic carcinoma diagnosis
and biomarker assessment to aid drug development is challenging. Circulating
tumour cells (CTCs) may represent a potential biomarker to address these
unmet needs. We compared prospectively the utility of two platforms for CTC
enumeration and characterisation in pancreatic cancer patients in a pilot
exploratory study. PATIENTS AND METHODS: Blood samples were obtained
prospectively from 54 consenting patients and analysed by CellSearch and
isolation by size of epithelial tumour cells (ISET). CellSearch exploits
immunomagnetic capture of CTCs-expressing epithelial markers, whereas ISET is
a marker independent, blood filtration device. Circulating tumour cell
expression of epithelial and mesenchymal markers was assessed to explore any
discrepancy in CTC number between the two platforms. RESULTS: ISET detected
CTCs in more patients than CellSearch (93% vs 40%) and in higher numbers
(median CTCs/7.5 ml, 9 (range 0-240) vs 0 (range 0-144)). Heterogeneity
observed for epithelial cell adhesion molecule, pan-cytokeratin (CK),
E-Cadherin, Vimentin and CK 7 expression in CTCs may account for discrepancy
in CTC number between platforms. CONCLUSION: ISET detects more CTCs than
CellSearch and offers flexible CTC characterisation with potential to
investigate CTC biology and develop biomarkers for pancreatic cancer patient
management.",
mesh {
{
term "Adenocarcinoma",
qual {
{
mp TRUE,
subh "diagnosis"
},
{
subh "mortality"
},
{
subh "pathology"
}
}
},
{
term "Adult"
},
{
term "Aged"
},
{
term "Aged, 80 and over"
},
{
term "England"
},
{
term "Female"
},
{
term "Humans"
},
{
term "Male"
},
{
term "Middle Aged"
},
{
mp TRUE,
term "Neoplastic Cells, Circulating"
},
{
term "Pancreatic Neoplasms",
qual {
{
mp TRUE,
subh "diagnosis"
},
{
subh "mortality"
},
{
subh "pathology"
}
}
},
{
term "Pilot Projects"
},
{
term "Predictive Value of Tests"
},
{
term "Prospective Studies"
},
{
term "Survival Analysis"
},
{
mp TRUE,
term "Tumor Markers, Biological"
}
},
substance {
{
type nameonly,
name "Tumor Markers, Biological"
}
},
idnum {
"c147/A12328a/Cancer Research UK"
},
pmid 22187035,
pub-type {
"Evaluation Studies",
"Journal Article",
"Research Support, Non-U.S. Gov't"
},
status medline
}
}
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