TY - JOUR
T1 - Prognostic importance of CDK4/6-specific activity as a predictive marker for recurrence in patients with endometrial cancer, with or without adjuvant chemotherapy
AU - Ikeda, Yuji
AU - Oda, Katsutoshi
AU - Ishihara, Hideki
AU - Wada-Hiraike, Osamu
AU - Miyasaka, Aki
AU - Kashiyama, Tomoko
AU - Inaba, Kanako
AU - Fukuda, Tomohiko
AU - Sone, Kenbun
AU - Matsumoto, Yoko
AU - Arimoto, Takahide
AU - Maeda, Daichi
AU - Ikemura, Masako
AU - Fukayama, Masahi
AU - Kawana, Kei
AU - Yano, Tetsu
AU - Aoki, Daisuke
AU - Osuga, Yutaka
AU - Fujii, Tomoyuki
N1 - Funding Information:
We thank Toshiyuki Sato and Hirokazu Kurata from Sysmex Co. Ltd., and Keiko Shoji, Satoko Kojima, Yuichiro Miyamoto, Kensuke Tomio, Michihiro Tanikawa, Kazunori Nagasaka, and Reiko Kurikawa from the University of Tokyo for their support and assistance. This work was supported by Sysmex Co. Ltd. and by a Grant-in-Aid for Scientific Research (C) (grant number 26462515 to KO), Grant-in-Aid for Young Scientists (B) (grant numbers 15K20128 to KS and 25861471 to TA), and Grant-in-Aid for Research Activity Start-up (grant number 25893229 to YI) from the Ministry of Education, Culture, Sports, Science and Technology of Japan. This study was also supported by a research program from the Project for Development of Innovative Research on Cancer Therapeutics (P-Direct), Ministry of Education, Culture, Sports, Science, and Technology of Japan (to TY).
Publisher Copyright:
© 2015 Cancer Research UK. All rights reserved.
PY - 2015/11/17
Y1 - 2015/11/17
N2 - Background:Pathologically low-risk endometrial cancer patients do not receive postoperative treatment; however, 10-15% of these patients show recurrence with poor prognosis. We evaluated the clinical importance of cyclin-dependent kinase 4/6 (CDK4/6) activity, and its significance as a novel biomarker for the prognosis and chemo-sensitivity of endometrioid endometrial carcinoma (EEC).Methods:Cyclin-dependent kinase 4/6 expression and enzyme activity in 109 tumour samples from patients with EEC were examined with a cell-cycle profiling (C2P) assay. CDK4/6-specific activity (CDK4/6SA) was determined, and its relationship with clinicopathological factors and expression of Ki-67 was analysed.Results:CDK4/6-specific activity was significantly correlated with Ki-67 (P=0.035), but not with any other clinicopathological characteristics. CDK4/6SA was significantly higher (P=0.002) in pathologically low-risk patients (not receiving adjuvant chemotherapy, n=74) than in intermediate- or high-risk patients (receiving adjuvant chemotherapy, n=35). In addition, patients with high CDK4/6SA (>3.0) showed significantly (P=0.024) shorter progression-free survival (PFS) than those with low CDK4/6SA (<3.0). Although Ki-67 expression itself was not a marker for prognosis, the combination of high CDK4/6SA and high Ki-67 expression (>15%) was robustly associated with shorter PFS (P=0.015), and this combination was an independent poor prognostic factor in the low-risk group. Inversely, in the intermediate-/high-risk group, patients with high CDK4/6SA had a tendency of a more favourable prognosis compared with patients with low CDK4/6SA (P=0.063).Conclusions:CDK4/6-specific activity can be used as a biomarker to predict prognosis and, possibly, chemo-sensitivity. The combination of Ki-67 expression might strengthen the clinical usefulness of CDK4/6SA as a biomarker.
AB - Background:Pathologically low-risk endometrial cancer patients do not receive postoperative treatment; however, 10-15% of these patients show recurrence with poor prognosis. We evaluated the clinical importance of cyclin-dependent kinase 4/6 (CDK4/6) activity, and its significance as a novel biomarker for the prognosis and chemo-sensitivity of endometrioid endometrial carcinoma (EEC).Methods:Cyclin-dependent kinase 4/6 expression and enzyme activity in 109 tumour samples from patients with EEC were examined with a cell-cycle profiling (C2P) assay. CDK4/6-specific activity (CDK4/6SA) was determined, and its relationship with clinicopathological factors and expression of Ki-67 was analysed.Results:CDK4/6-specific activity was significantly correlated with Ki-67 (P=0.035), but not with any other clinicopathological characteristics. CDK4/6SA was significantly higher (P=0.002) in pathologically low-risk patients (not receiving adjuvant chemotherapy, n=74) than in intermediate- or high-risk patients (receiving adjuvant chemotherapy, n=35). In addition, patients with high CDK4/6SA (>3.0) showed significantly (P=0.024) shorter progression-free survival (PFS) than those with low CDK4/6SA (<3.0). Although Ki-67 expression itself was not a marker for prognosis, the combination of high CDK4/6SA and high Ki-67 expression (>15%) was robustly associated with shorter PFS (P=0.015), and this combination was an independent poor prognostic factor in the low-risk group. Inversely, in the intermediate-/high-risk group, patients with high CDK4/6SA had a tendency of a more favourable prognosis compared with patients with low CDK4/6SA (P=0.063).Conclusions:CDK4/6-specific activity can be used as a biomarker to predict prognosis and, possibly, chemo-sensitivity. The combination of Ki-67 expression might strengthen the clinical usefulness of CDK4/6SA as a biomarker.
KW - Ki-67 expression
KW - chemo-sensitivity
KW - cyclin-dependent kinase
KW - endometrial cancer
KW - low risk
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U2 - 10.1038/bjc.2015.369
DO - 10.1038/bjc.2015.369
M3 - Article
C2 - 26554657
AN - SCOPUS:84947487062
SN - 0007-0920
VL - 113
SP - 1477
EP - 1483
JO - British Journal of Cancer
JF - British Journal of Cancer
IS - 10
ER -