Evidence map›Paper›PMID 41815370›Full record

ArticleAsian journal of urology2026

Risk of second primary malignancies in prostate cancer patients: A Surveillance, Epidemiology, and End Results population-based study.

Jiafeng Shou, Qijun Wo

Abstract read
In one paragraph

Article in Asian journal of urology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Jiafeng ShouUrology & Nephrology Center, Department of Urology, Zhejiang Provincial People's Hospital (Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, China.
Qijun WoUrology & Nephrology Center, Department of Urology, Zhejiang Provincial People's Hospital (Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Second primary malignancy (SPM) is becoming a challenge in clinical practice. However, limited studies have focused on this issue in patients with prostate cancer (PCa). We sought to explore the potential risk of SPMs in patients with a prior diagnosis of PCa and construct a model to predict the risk of developing SPMs. Methods: We retrospectively extracted data on PCa patients from the Surveillance, Epidemiology, and End Results database between 2000 and 2018. A competing-risk model was established to explore the risk factors for developing SPMs and to predict the probability of developing SPMs for PCa patients after the initial diagnosis. The calibration curve, concordance index, and decision curve analysis were used to assess the validity of the model. Results: A total of 284 738 eligible PCa patients were included, 14 845 (5.2%) of whom developed SPMs after the initial diagnosis. The results showed that age at the initial diagnosis, race, histological grade, pathological tumor stage, radiotherapy, and surgery were independent risk factors for developing SPMs. The concordance index of the model was 0.685 (95% confidence interval 0.684-0.686), and the calibration plots showed an excellent agreement between the nomogram prediction and the actual observation. Furthermore, the decision curve analysis indicated a positive benefit with the threshold risk range of 2%-12%. Conclusion: The nomogram is sufficiently accurate to predict the risk of SPMs for PCa survivors and to help surgeons identify patients who are at a high risk of developing SPMs and contribute to further management of SPMs.

Indexed as

Competing-risk modelNomogramProstate cancerSecond primary malignancySurveillance, Epidemiology, and End Results

Identifiers

PMID41815370
PMCPMC12974156

What OpenQuestion holds

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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.