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

Authors :
Hiroaki Iwamoto
Kouji Izumi
Ryunosuke Nakagawa
Ren Toriumi
Shuhei Aoyama
Takafumi Shimada
Hiroshi Kano
Tomoyuki Makino
Suguru Kadomoto
Hiroshi Yaegashi
Shohei Kawaguchi
Takahiro Nohara
Kazuyoshi Shigehara
Yoshifumi Kadono
Atsushi Mizokami
Source :
Japanese Journal of Clinical Oncology.
Publication Year :
2022
Publisher :
Oxford University Press (OUP), 2022.

Abstract

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 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.

Details

ISSN :
14653621
Database :
OpenAIRE
Journal :
Japanese Journal of Clinical Oncology
Accession number :
edsair.doi.dedup.....b0cd60d3e7c799440e0a6d2d61db75b4