Evidence map›Paper›PMID 39758244›Full record

ArticleCancer diagnosis & prognosis

Current Status of Sequential Treatment for Castration-resistant Prostate Cancer: A Retrospective Analysis.

Kazuhiko Oshinomi, Toshiki Mugita, Tatsuki Inoue, Madoka Omizu, Motoki Yamagishi, Yoshihiro Nakagami, Masakazu Nagata, Hideaki Shimoyama, Michiya Ota, Jun Morita and 6 more

Abstract read
In one paragraph

Article in Cancer diagnosis & prognosis. 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

16 authors.

Kazuhiko OshinomiDepartment of Urology, Showa University School of Medicine, Tokyo, Japan.
Toshiki MugitaDepartment of Urology, Showa University School of Medicine, Tokyo, Japan.
Tatsuki InoueDepartment of Urology, Showa University School of Medicine, Tokyo, Japan.
Madoka OmizuDepartment of Urology, Showa University School of Medicine, Tokyo, Japan.
Motoki YamagishiDepartment of Urology, Showa University School of Medicine, Tokyo, Japan.
Yoshihiro NakagamiDepartment of Urology, Showa University School of Medicine, Tokyo, Japan.
Masakazu NagataDepartment of Urology, Showa University School of Medicine, Tokyo, Japan.
Hideaki ShimoyamaDepartment of Urology, Showa University Fujigaoka Hospital, Yokohama, Japan.
Michiya OtaDepartment of Urology, Showa University Fujigaoka Hospital, Yokohama, Japan.
Jun MoritaDepartment of Urology, Showa University Fujigaoka Hospital, Yokohama, Japan.
Haruaki SasakiDepartment of Urology, Showa University Fujigaoka Hospital, Yokohama, Japan.
Eiji MatsubaraDepartment of Urology, Showa University Northern Yokohama Hospital, Yokohama, Japan.
Katsuyuki SaitoDepartment of Urology, Showa University Northern Yokohama Hospital, Yokohama, Japan.
Kohzo FujiDepartment of Urology, Showa University Northern Yokohama Hospital, Yokohama, Japan.
Masashi MoritaDepartment of Urology, Showa University Koto Toyosu Hospital, Tokyo, Japan.
Takashi FukagaiDepartment of Urology, Showa University School of Medicine, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Aim: Although multiple treatments are available for metastatic castration-resistant prostate cancer, data to determine the optimal treatment sequence are limited. This study aimed to investigate the current status of drug therapy for castration-resistant prostate cancer and clarify the sequential treatment in actual clinical practice. Patients and Methods: This retrospective study included 425 patients diagnosed with castration-resistant prostate cancer at Showa University Hospital and affiliated hospitals between January 2014 and December 2021, who were treated with any of the following four drugs: novel androgen receptor signal inhibitors (abiraterone acetate and enzalutamide) and anticancer drugs (docetaxel and cabazitaxel). We investigated the actual treatment choices for castration-resistant prostate cancer, focusing on the order of administration of the four drugs. This analysis was visualized using a Sankey diagram. Results: Regarding the number of drugs administered, most patients received one type of drug, with androgen receptor signal inhibitors being the most commonly administered (total, 179; enzalutamide, 139 and abiraterone acetate, 40). Enzalutamide was the most frequently selected first-line drug (58.4%). The most common sequence for second-line treatment was androgen receptor signal inhibitor-androgen receptor signal inhibitor (n=96), followed by androgen receptor signal inhibitor-docetaxel (n=85), docetaxel-androgen receptor signal inhibitor (n=59), and docetaxel-cabazitaxel (n=6). Conclusion: Androgen receptor signal inhibitors is the most commonly used drug category for first-line treatment of castration-resistant prostate cancer, with enzalutamide being the most commonly used drug. Further investigations are required regarding patient background and prognosis.

Indexed as

Castration-resistantenzalutamideprostate cancersequencetreatment

Identifiers

PMID39758244
PMCPMC11696339

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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.