Evidence map›Paper›PMID 39657665›Full record

Observational studyCell reports. Medicine2024

Development and validation of the utLIFE-PC algorithm for noninvasive detection of prostate cancer in urine: A prospective, observational study.

Sujun Han, Mingshuai Wang, Yong Wang, Junlong Wu, Zhaoxia Guo, Huina Wang, Ranlu Liu, Xiaofu Qiu, Linjun Hu, Jianbin Bi and 17 more

Abstract readObservational StudyValidation Study
In one paragraph

Observational study in Cell reports. Medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
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

27 authors.

Sujun HanDepartment of Urology and State Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Mingshuai WangDepartment of Urology and State Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Yong WangDepartment of Urology, The Second Affiliated Hospital of Tianjin Medical University, Tianjin, China.
Junlong WuDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Zhaoxia GuoDepartment of Research and Development, Acornmed Biotechnology Co., Ltd., Beijing, China.
Huina WangDepartment of Research and Development, Acornmed Biotechnology Co., Ltd., Beijing, China.
Ranlu LiuDepartment of Urology, The Second Affiliated Hospital of Tianjin Medical University, Tianjin, China.
Xiaofu QiuDepartment of Urology, Guangdong Second Provincial General Hospital, Guangzhou, China.
Linjun HuDepartment of Urology, Cancer Hospital of HuanXing, Chaoyang District Beijing, Beijing, China.
Jianbin BiDepartment of Urology, China Medical University, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Weigang YanDepartment of Urology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Hengqing AnDepartment of Urology, The First Affiliated Hospital, Xinjiang Medical University, Urumqi, China.
Gejun ZhangDepartment of Urology, China Medical University, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Yi ZhiDepartment of Urology, The Third Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Zhiyuan ChenDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, China.
Libin ChenDepartment of Research and Development, Acornmed Biotechnology Co., Ltd., Beijing, China.
Lei LiuDepartment of Research and Development, Acornmed Biotechnology Co., Ltd., Beijing, China.
Huanqing ChengDepartment of Research and Development, Acornmed Biotechnology Co., Ltd., Beijing, China.
Shuaipeng ZhuDepartment of Research and Development, Acornmed Biotechnology Co., Ltd., Beijing, China.
Meng WangDepartment of Research and Development, Acornmed Biotechnology Co., Ltd., Beijing, China.
Yanrui ZhangDepartment of Research and Development, Acornmed Biotechnology Co., Ltd., Beijing, China.
Xiao LiuDepartment of Research and Development, Acornmed Biotechnology Co., Ltd., Beijing, China.
Feng LouDepartment of Research and Development, Acornmed Biotechnology Co., Ltd., Beijing, China. Electronic address: fenglou@acornmed.com.
Shanbo CaoDepartment of Research and Development, Acornmed Biotechnology Co., Ltd., Beijing, China. Electronic address: shanbocao@acornmed.com.
Dingwei YeDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China. Electronic address: dwyeli@163.com.
Yuanjie NiuDepartment of Urology, The Second Affiliated Hospital of Tianjin Medical University, Tianjin, China. Electronic address: niuyuanjie9317@163.com.
Nianzeng XingDepartment of Urology and State Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China; Department of Urology, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, China. Electronic address: nianzeng2006@vip.sina.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overbiopsy is a serious health issue in prostate cancer (PCa) diagnostics. We have developed a urine tumor DNA multidimensional bioinformatic algorithm, utLIFE, to avoid unnecessary biopsy. The objective is to recognize all or clinically significant PCa. Of the 801 participants recruited in our study, 630 are selected for subsequent analysis. In the training cohort (n = 237), utLIFE-PC gets an area under the receiver operating characteristic curve (AUC) of 0.967 and a sensitivity of 85.57% at 95% specificity. In the independent prospective validation cohort (n = 343), utLIFE-PC has an AUC of 0.929, sensitivity of 84.24%, and specificity of 93.26%. Notably, in patients with ≥grade group (GG)2 and ≥GG3, the assay's sensitivity is still excellent (85.33% and 87.10%, respectively). The model shows better performance than prostate-specific antigen (PSA) (p < 0.001) or the single-dimensional biomarkers (methylation, p < 0.001; copy-number variations [CNVs], p < 0.001; mutation, p < 0.001). The utLIFE-PC model can potentially optimize the PCa diagnostic process and avoid unnecessary biopsies. This study was registered at Chinese Clinical Trial Registry: ChiCTR2300071837.

Indexed as

AlgorithmsBiomarkers, TumorProstatic NeoplasmsAgedHumansMaleMiddle AgedProspective StudiesProstate-Specific AntigenROC CurveBiomarkers, TumorProstate-Specific Antigen

Identifiers

PMID39657665
PMCPMC11722088

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.