Identifying High Gleason Score Prostate Cancer by Prostate Fluid Metabolic Fingerprint‐Based Multi‐Modal Recognition

Author:

Peng Zehong1,Wang Yuning2ORCID,Wu Xinrui1,Yang Shouzhi2,Du Xinxing1,Xu Xiaoyu2,Hu Cong1,Liu Wanshan2,Zhu Yinjie1,Dong Baijun1,Pan Jiahua1,Bao Qingui3,Qian Kun2,Dong Liang1,Xue Wei1

Affiliation:

1. Department of Urology Ren Ji Hospital School of Medicine Shanghai Jiao Tong University 160 Pujian Road Shanghai 200127 P. R. China

2. State Key Laboratory of Systems Medicine for Cancer School of Biomedical Engineering and Institute of Medical Robotics Shanghai Jiao Tong University Shanghai 200030 P. R. China

3. Fosun Diagnostics (Shanghai) Co., Ltd. No. 830, Chengyin Road Baoshan Shanghai 200435 P. R. China

Abstract

AbstractProstate cancer (PCa) is the second most common cancer in males worldwide. The Gleason scoring system, which classifies the pathological growth pattern of cancer, is considered one of the most important prognostic factors for PCa. Compared to indolent PCa, PCa with high Gleason score (h‐GS PCa, GS ≥ 8) has greater clinical significance due to its high aggressiveness and poor prognosis. It is crucial to establish a rapid, non‐invasive diagnostic modality to decipher patients with h‐GS PCa as early as possible. In this study, ferric nanoparticle‐assisted laser desorption/ionization mass spectrometry (FeNPALDI‐MS) to extract prostate fluid metabolic fingerprint (PSF‐MF) is employed and combined with the clinical features of patients, such as prostate‐specific antigen (PSA), to establish a multi‐modal diagnosis assisted by machine learning. This approach yields an impressive area under the curve (AUC) of 0.87 to diagnose patients with h‐GS, surpassing the results of single‐modal diagnosis using only PSF‐MF or PSA, respectively. Additionally, using various screening methods, six key metabolites that exhibit greater diagnostic efficacy (AUC = 0.96) are identified. These findings also provide insights into related metabolic pathways, which may provide valuable information for further elucidation of the pathological mechanisms underlying h‐GS PCa.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Innovative Research Team of High-level Local University in Shanghai

Science and Technology Commission of Shanghai Municipality

Publisher

Wiley

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