Evidence mapPaperPMID 37240717Full record

ArticleLife (Basel, Switzerland)2023

Efficacy and Safety of Neoadjuvant Luteinizing Hormone-Releasing Hormone Antagonist and Tegafur-Uracil Chemohormonal Therapy for High-Risk Prostate Cancer.

Fumiya Sugino, Keita Nakane, Makoto Kawase, Shota Ueda, Masayuki Tomioka, Yasumichi Takeuchi, Risa Tomioka-Inagawa, Toyohiro Yamada, Sanae Namiki, Naotaka Kumada and 7 more

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2023. 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
1.0field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 4 citations in OpenAlex.

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

17 authors at 4 institutions in 1 country.

Fumiya SuginoDepartment of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
Keita NakaneDepartment of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.ORCID 0000-0002-2589-1722
Makoto KawaseDepartment of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.ORCID 0000-0001-7269-2462
Shota UedaDepartment of Urology, Japanese Red Cross Takayama Hospital, Takayama 5068550, Japan.
Masayuki TomiokaDepartment of Urology, Chuno Kosei Hospital, Seki 5013802, Japan.
Yasumichi TakeuchiDepartment of Urology, Japanese Red Cross Gifu Hospital, Gifu 5028511, Japan.
Risa Tomioka-InagawaDepartment of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
Toyohiro YamadaDepartment of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
Sanae NamikiDepartment of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
Naotaka KumadaDepartment of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
Shinichi TakeuchiDepartment of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
Kota KawaseDepartment of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
Daiki KatoDepartment of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.ORCID 0000-0003-4932-0497
Manabu TakaiDepartment of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
Koji IinumaDepartment of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
Yuki TobisawaDepartment of Urology, Hirosaki University Graduate School of Medicine, Hirosaki 0358562, Japan.
Takuya KoieDepartment of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.ORCID 0000-0002-2980-127X
Gifu University · JPGifu Red Cross Hospital · JPHirosaki University · JPTakayama Red Cross Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis retrospective single-center cohort study evaluated the efficacy and safety of a combination of neoadjuvant luteinizing hormone-releasing hormone (LHRH) antagonist and tegafur-uracil (UFT) therapy (NCHT) and investigated the medical records of patients with high-risk PCa who underwent robot-assisted radical prostatectomy (RARP). The therapy was followed by RARP for high-risk PCa. MATERIALS AND

methodsThe enrolled patients were divided into two groups: low-intermediate-risk PCa patients who underwent RARP without neoadjuvant therapy (non-high-risk) and those who underwent NCHT followed by RARP (high-risk group). This study enrolled 227 patients (126: non-high-risk and 101: high-risk group). Patients in the high-risk-group had high-grade cancer compared to those in the non-high-risk-group.

resultsAt the median follow-up period of 12.0 months, there were no PCa deaths; two patients (0.9%) died of other causes. Twenty patients developed biochemical recurrence (BCR); the median time until BCR was 9.9 months after surgery. The 2-year biochemical recurrence-free survival rates were 94.2% and 91.1% in the non-high-risk and high-risk-group, respectively (

conclusionsThis study indicates that combining neoadjuvant LHRH antagonists and UFT followed by RARP may improve oncological outcomes in patients with high-risk PCa.

Indexed as

high-risk prostate cancerluteinizing hormone-releasing hormone antagonistneoadjuvant chemohormonal therapyrobot-assisted radical prostatectomytegafur-uracil

Identifiers

PMID37240717
PMCPMC10223720
OpenAlexW4366827438

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.