Evidence map›Paper›PMID 40143736›Full record

ArticleInternational journal of surgery (London, England)2025

Development and validation of a machine learning-based risk model for metastatic disease in nmCRPC patients: a tumor marker prognostic study.

Xudong Ni, Ziyun Wang, Xiaomeng Li, Jixinnan Sui, Weiwei Ma, Jian Pan, Dingwei Ye, Yao Zhu

2 registry-linked trialsAbstract readValidation Study
In one paragraph

Article in International journal of surgery (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01946204 phase3active not recruitingnot on this map

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase III Study of ARN-509 in Men With Non-Metastatic (M0) Castration-Resistant Prostate Cancer

TypeinterventionalSponsorAragon Pharmaceuticals, Inc.Ran2013 to 2027Enrolled1,207ConditionsProstatic NeoplasmsArmsApalutamide, Placebo
NCT02200614 phase3completednot on this map

A Multinational, Randomised, Double-blind, Placebo-controlled, Phase III Efficacy and Safety Study of Darolutamide (ODM-201) in Men With High-risk Non-metastatic Castration-resistant Prostate Cancer

TypeinterventionalSponsorBayerRan2014 to 2021Enrolled1,509ConditionsProstate Cancer Non-Metastatic, Castration-ResistantArmsDarolutamide (Nubeqa, BAY1841788), Placebo
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Article
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  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Xudong NiDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Ziyun WangDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Xiaomeng LiDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Jixinnan SuiDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Weiwei MaDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Jian PanDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Dingwei YeDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Yao ZhuDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.ORCID 0000-0001-7950-6669

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNonmetastatic castration-resistant prostate cancer (nmCRPC) is a clinical challenge due to the high progression rate to metastasis and mortality. To date, no prognostic model has been developed to predict the metastatic probability for nmCRPC patients. In this study, we developed and externally validated a machine-learning model capable of calculating risk scores and predicting the likelihood of metastasis in nmCRPC patients. PATIENTS AND

methodsA total of 2716 nmCRPC patients were included in this study. The training and testing datasets were derived from SPARTAN (NCT01946204) and ARAMIS (NCT02200614), respectively. Regarding metastasis-free survival as the endpoint, we subjected 13 clinical features to 10 machine-learning models and their combinations to predict metastasis. Model performance was assessed through accuracy (AUC), calibration (slope and intercept), and clinical utility (DCA). The risk score calculated by the model and risk factors based on eight identified variates were used for metastatic risk stratification.

resultsThe final prognostic model included eight prognostic factors, including novel hormone therapy application, Gleason score, previous treatments received (both surgery and radiotherapy, or neither), Race (White), PSA doubling time (PSADT), hemoglobin (HGB), and lgPSA. The prognostic model resulted in a C-index of 0.724 (95% CI 0.700-0.747) in internal validation and relatively good performance through tAUC (>0.70 at 3-month intervals between 6 and 39 months) in external validation. In the risk score stratifying strategy, compared with the low-risk group, the metastasis HRs for medium- and high-risk groups were 1.72 (95% CI 1.39-2.12) and 4.43 (95% CI 3.66-5.38); as for risk factor count, the HRs are 1.98 (95% CI 1.50-2.61) and 4.17 (95% CI 3.16-5.52), respectively.

conclusionsIn this study, we developed and validated a machine learning prognostic model to predict the risk of metastasis in nmCRPC patients. This model can assist in the risk stratification of nmCRPC patients, guide follow-up strategies, and aid in selecting personalized treatment intensities.

Indexed as

Machine LearningProstatic Neoplasms, Castration-ResistantAgedBiomarkers, TumorHumansMaleMiddle AgedNeoplasm MetastasisPrognosisRisk AssessmentRisk FactorsBiomarkers, Tumormachine learningmetastasis-free survivalnonmetastatic castration-resistant prostate cancerprognostic modelprostate cancer

Identifiers

PMID40143736
PMCPMC12165472

What OpenQuestion holds

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LicenceCC BY
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.