Evidence map›Paper›PMID 35102615›Full record

ArticleInternational journal of urology : official journal of the Japanese Urological Association2022

Presence of CD133-positive circulating tumor cells predicts worse progression-free survival in patients with metastatic castration-sensitive prostate cancer.

Yunjie Yang, Zheng Liu, Qifeng Wang, Kun Chang, Junyu Zhang, Dingwei Ye, Yunyi Kong, Bo Dai

Open access · hybridAbstract read
In one paragraph

Article in International journal of urology : official journal of the Japanese Urological Association, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 12% of its field
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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
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  7. PD-L1Journal of translational medicine · 2025
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  12. Reproductive medicine and biology
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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 at 1 institution in 1 country.

Yunjie YangDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Zheng LiuDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Qifeng WangDepartment of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
Kun ChangDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Junyu ZhangDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Dingwei YeDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Yunyi KongDepartment of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
Bo DaiDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.ORCID 0000-0003-1383-3864
Shanghai Medical College of Fudan University · CN

Funding

AoXiang Project of the Shanghai Anti-Cancer Association SACA-AX201908AoXiang Project of the Shanghai Anti-Cancer Association SACA-AX202005Medical Innovation Research Project of the Science and Technology Commission of Shanghai Municipality 20Y11905000National Key R&D Program of China 2017YFC0114303Natural Science Foundation of Science and Technology Commission of Shanghai Municipality
6 · The paper itself

Abstract

objectiveTo investigate the clinical significance of the expression of the stemness marker CD133 in circulating tumor cells of newly diagnosed metastatic castration-sensitive prostate cancer patients.

methodsFor this study, 104 metastatic castration-sensitive prostate cancer patients treated at the Fudan University Shanghai Cancer Center from September 2015 to February 2017 were considered. After enrollment, the patients received androgen deprivation therapy (bicalutamide + goserelin). Circulating tumor cells were isolated and identified using the CanPatrol system, which can identify not only traditional epithelial markers but also mesenchymal markers in cells that have undergone epithelial mesenchymal transition. CD133 was used to characterize the circulating tumor cells. The primary endpoint of this research was to evaluate progression to castration resistance.

resultsAmong the 104 patients enrolled, 89 patients were circulating tumor cell positive at baseline, and the median circulating tumor cell count was four. The median follow-up was 24 months, and at the end of follow-up, the proportion of patients who progressed to castration-resistant prostate cancer in the CTC+CD133+ group was 93.3%, which was significantly higher than that of the circulating tumor cell negative group (73.3%) and the CTC+CD133- group (75.0%), with P = 0.043. After follow-up, progression-free survival for CTC+CD133+, CTC+CD133-, and circulating tumor cell patients was 10.0, 13.0, and 14.0 months, respectively, with P = 0.022. Univariate and multivariate analyses also confirmed that the characterization of circulating tumor cells using CD133 can independently predict progression-free survival in metastatic castration-sensitive prostate cancer patients after receiving androgen deprivation therapy (P = 0.042; hazard ratio 1.396).

conclusionBaseline CTC+CD133+ was a poor independent prognostic factor for metastatic castration-sensitive prostate cancer patients to progress to castration-resistant prostate cancer after receiving androgen deprivation therapy.

Indexed as

Neoplastic Cells, CirculatingProstatic Neoplasms, Castration-ResistantAndrogen AntagonistsAndrogensBiomarkers, TumorCastrationChinaHumansMalePrognosisProgression-Free SurvivalAndrogen AntagonistsAndrogensBiomarkers, TumorCD133circulating tumor cellsprogression-free survivalprostate cancertime to castration resistance

Identifiers

PMID35102615
PMCPMC9305754
OpenAlexW4210482587

What OpenQuestion holds

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Registered trials

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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.