Evidence map›Paper›PMID 36092845›Full record

ArticleTranslational andrology and urology2022

The clinical efficacy and limitations of dutasteride-regulated abiraterone metabolism in abiraterone-resistant patients: a prospective single-arm clinical trial in Chinese patients.

Ying Liu, Tao Yang, Chengdang Xu, Xi Chen, Yongnan Chi, Weidong Zhou, Wei Le, Cuidong Bian, Zhenfei Li, Shengsong Huang and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Translational andrology and urology, 2022. 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
0.2field-weighted citation impact, top 49% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

11 authors at 2 institutions in 1 country.

Ying Liu *Department of Urology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Tao Yang *Department of Urology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Chengdang Xu *Department of Urology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Xi ChenDepartment of Urology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Yongnan ChiDepartment of Urology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Weidong ZhouDepartment of Urology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Wei LeDepartment of Urology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Cuidong BianDepartment of Urology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Zhenfei LiDepartment of Urology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Shengsong HuangDepartment of Urology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Denglong WuDepartment of Urology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Tongji University · CNTongji Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The steroidal metabolism of abiraterone has been proposed to be involved in abiraterone resistance and limited approaches are available for abiraterone-resistant patients. Dutasteride regulates abiraterone metabolism in patients and might enhance the clinical efficacy of abiraterone. However, the function of dutasteride to overcome abiraterone resistance has not been investigated in clinic. Here we investigated the clinical efficacy and limitations of dutasteride in patients with abiraterone-resistant prostate cancer. Methods: Abiraterone-resistant patients with metastatic castration-resistant prostate cancer (mCRPC) were enrolled in this single-arm, open-label study, patients were treated with dutasteride (0.5 mg/day), abiraterone (1,000 mg/day), and prednisone (5 mg twice daily), prostate-specific antigen (PSA) was tested monthly. The primary objective was PSA response, and the secondary objectives were to assess symptom relief and safety. Kaplan-Meier analysis was used to assess the PSA progression free survival (PSA-PFS) of patients. Results: Twenty-two patients (median age: 75 years) were enrolled, and 19 patients completed the treatment. After a median treatment of 4.0 months, 7 (37%) patients showed a slight PSA reduction (-2% to -32%), and the median PSA-PFS was 2.0 months (1-7 months). No significant improvement was observed in Eastern Cooperative Oncology Group (ECOG) performance status. Bone pain was relieved in 6 patients after 1 month of treatment, but the improvement was not significant. No grade 3 or grade 4 adverse events were observed. Conclusions: The combination of dutasteride and abiraterone showed a mild effect in patients with abiraterone-resistant. The small sample size was the limitation of this study.

Indexed as

abirateroneabiraterone resistanceDutasterideprostate cancer

Identifiers

PMID36092845
PMCPMC9459540
OpenAlexW4293199533

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.