Evidence map›Paper›PMID 36039059›Full record

ArticleOncology letters2022

Androgen receptor axis-targeted agents are not superior to conventional hormonal therapy for treatment of metastatic prostate cancer.

Akinori Wada, Mitsuhiro Narita, Masayuki Nagasawa, Takuto Kusaba, Shigehisa Kubota, Tetsuya Yoshida, Kazuyoshi Johnin, Akihiro Kawauchi, Susumu Kageyama

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 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
–field-weighted citation impact, top 82% 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, 0 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

9 authors at 1 institution in 1 country.

Akinori WadaDepartment of Urology, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
Mitsuhiro NaritaDepartment of Urology, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
Masayuki NagasawaDepartment of Urology, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
Takuto KusabaDepartment of Urology, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
Shigehisa KubotaDepartment of Urology, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
Tetsuya YoshidaDepartment of Urology, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
Kazuyoshi JohninDepartment of Urology, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
Akihiro KawauchiDepartment of Urology, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
Susumu KageyamaDepartment of Urology, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
Shiga University of Medical Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study aimed to use real-world Japanese data to compare the treatment outcome of conventional hormonal therapy to that of using androgen receptor axis-targeted (ARAT) agents for patients with metastatic castration-resistant prostate cancer. The overall survival between the conventional hormonal therapy group and the ARAT agent therapy group was compared using a group of 75 Japanese patients who were treated for metastatic castration-resistant prostate cancer. A subgroup analysis was carried out and the risk factors that affected overall survival (OS) were determined. The median OS from the time of prostate-specific antigen recurrence was 73.1 months in the ARAT group and 45.2 months in the conventional treatment group (P=0.414). Although OS tended to be slightly longer in the ARAT group, the difference between the groups was not significant. Subgroup analysis suggested that the therapeutic outcome of using ARAT agents tended to be less beneficial in patients who were older, and in those with a higher tumor volume or low Gleason grade. In conclusion, use of ARAT agents did not impart a significant survival benefit to patients with metastatic castration-resistant prostate cancer when compared with survival rates in response to conventional therapy. However, there was some clinical benefit when ARAT agents were used after patients developed castration-resistant prostate cancer. These findings suggest that up-front therapy using ARAT agents at the time of the initial hormone therapy can impart clinical benefit in Japanese patients with metastatic prostate cancer.

Indexed as

androgen receptor antagonistscastration-resistantestramustineOSprednisoloneprostatic neoplasm

Identifiers

PMID36039059
PMCPMC9404690
OpenAlexW4293778794

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.