4.2 Article

Usefulness of serum CCL2 as prognostic biomarker in prostate cancer: a long-term follow-up study

期刊

JAPANESE JOURNAL OF CLINICAL ONCOLOGY
卷 52, 期 11, 页码 1337-1344

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OXFORD UNIV PRESS
DOI: 10.1093/jjco/hyac102

关键词

CCL2; biomarker; prostate cancer; risk classification; chemokine

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资金

  1. JSPS KAKENHI [25861413]
  2. Grants-in-Aid for Scientific Research [25861413] Funding Source: KAKEN

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Serum chemokine (CC motif) ligand 2 has been shown to be a valuable biomarker for long-term prognosis of prostate cancer. A novel risk classification system based on the combination of chemokine (CC motif) ligand 2, prostate-specific antigen, and Gleason score may serve as a useful prognostic tool for predicting overall survival in prostate cancer patients.
Serum chemokine (CC motif) ligand 2 were shown to be a useful biomarker for long-term prognosis of prostate cancer. Novel risk classification based on combination of chemokine (CC motif) ligand 2, prostate-specific antigen and Gleason score may be a useful prognostic tool. Objective Prostate-specific antigen is considered the most useful biomarker for prostate cancer, but not in all cases. In a previous study, we have shown that a risk classification combining prostate-specific antigen >= 100 ng/mL and chemokine (CC motif) ligand 2 >= 320 pg/mL can predict survivals. We investigated the long-term usefulness of serum chemokine (CC motif) ligand 2 as a complementary biomarker to prostate-specific antigen and developed a novel risk classification system. Methods Serum samples were collected from 379 patients who underwent prostate biopsy at Kanazawa University Hospital between 2007 and 2013, and 255 patients with histologically diagnosed prostate cancer were included in this study. We retrospectively examined the efficacy of serum chemokine (CC motif) ligand 2 as a prognostic biomarker. Results Patients with chemokine (CC motif) ligand 2 >= 320 pg/mL exhibited a significantly shorter overall survival, prostate cancer-specific survival and castration-resistant prostate cancer-free survival than those with chemokine (CC motif) ligand 2 < 320 pg/mL. Multivariate analysis was performed to determine whether chemokine (CC motif) ligand 2 was a useful prognostic factor. Independent significant predictors of worse overall survival were prostate-specific antigen >= 100 ng/mL, Gleason score >= 8 and chemokine (CC motif) ligand 2 >= 320 pg/dL. Prognostic predictors of prostate cancer-specific survival or cancer-free survival in multivariate analysis were prostate-specific antigen >= 100 ng/mL and Gleason score >= 8. A novel risk classification system was created to predict overall survival in patients based on the number of risk factors present (chemokine (CC motif) ligand 2 >= 320 pg/mL, prostate-specific antigen >= 100 ng/mL, Gleason score >= 8). Scores 2 or 3, 1 and 0 indicated Poor, Intermediate and Good risk groups, respectively. Conclusions This study demonstrated the utility of serum chemokine (CC motif) ligand 2 level as a predictive biomarker of long-term overall survival in prostate cancer. A novel risk classification system that predicts long-term overall survival based on the combined indications of chemokine (CC motif) ligand 2 level, prostate-specific antigen level and Gleason score may be a useful prognostic tool for prostate cancer.

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