TY - JOUR
T1 - Prediction of peritoneal metastasis in advanced gastric cancer by gene expression profiling of the primary site
AU - Motoori, Masaaki
AU - Takemasa, Ichiro
AU - Doki, Yuichiro
AU - Saito, Sakae
AU - Miyata, Hiroshi
AU - Takiguchi, Shuji
AU - Fujiwara, Yoshiyuki
AU - Yasuda, Takushi
AU - Yano, Masahiko
AU - Kurokawa, Yukinori
AU - Komori, Takamichi
AU - Yamasaki, Makoto
AU - Ueno, Noriko
AU - Oba, Shigeyuki
AU - Ishii, Shin
AU - Monden, Morito
AU - Kato, Kikuya
PY - 2006/8
Y1 - 2006/8
N2 - Peritoneal metastasis is the most common cause of tumour progression in advanced gastric cancer. Clinicopathological findings including cytologic examination of peritoneal lavage have been applied to assess the risk of peritoneal metastasis, but are sometimes inadequate for predicting peritoneal metastasis in individuals. Hence, we tried to construct a new prediction system for peritoneal metastasis by using a PCR-based high throughput array with 2304 genes. The prediction system, constructed from the learning set comprised of 30 patients with the most informative 18 genes, classified each case into a 'good signature group' or 'poor signature group'. Then, we confirmed the predictive performance in an additional validation set comprised of 24 patients, and the prediction accuracy for peritoneal metastasis was 75%. Kaplan-Meier analysis with peritoneal metastasis revealed significant difference between these two groups (P = 0.0225). By combining our system with conventional clinicopathological factors, we can identify high risk cases for peritoneal metastasis more accurately.
AB - Peritoneal metastasis is the most common cause of tumour progression in advanced gastric cancer. Clinicopathological findings including cytologic examination of peritoneal lavage have been applied to assess the risk of peritoneal metastasis, but are sometimes inadequate for predicting peritoneal metastasis in individuals. Hence, we tried to construct a new prediction system for peritoneal metastasis by using a PCR-based high throughput array with 2304 genes. The prediction system, constructed from the learning set comprised of 30 patients with the most informative 18 genes, classified each case into a 'good signature group' or 'poor signature group'. Then, we confirmed the predictive performance in an additional validation set comprised of 24 patients, and the prediction accuracy for peritoneal metastasis was 75%. Kaplan-Meier analysis with peritoneal metastasis revealed significant difference between these two groups (P = 0.0225). By combining our system with conventional clinicopathological factors, we can identify high risk cases for peritoneal metastasis more accurately.
KW - ATAC-PCR
KW - Gastric cancer
KW - Gene expression profiling
KW - Peritoneal metastasis
UR - http://www.scopus.com/inward/record.url?scp=33746592549&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33746592549&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2006.04.007
DO - 10.1016/j.ejca.2006.04.007
M3 - Article
C2 - 16831544
AN - SCOPUS:33746592549
SN - 0959-8049
VL - 42
SP - 1897
EP - 1903
JO - European Journal of Cancer
JF - European Journal of Cancer
IS - 12
ER -