Evidence map›Paper›PMID 39187338›Full record

ArticleIn vivo (Athens, Greece)

The Omission of Upfront Treatment Intensification Does Not Adversely Affect Oncological Outcomes in a Subset of Castration-Highly Sensitive Metastatic Prostate Cancer.

Naohiro Fujimoto, Yujiro Nagata, Masaki Shiota, Akinori Minato, Ikko Tomisaki, Kenichi Harada, Masatoshi Eto, Hiroshi Miyamoto

Abstract read
In one paragraph

Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Naohiro FujimotoDepartment of Urology, Local Incorporated Administrative Agency Kurate Hospital, Kurate, Japan; n-fuji@kurate-hp.com.
Yujiro NagataDepartment of Urology, University of Occupational and Environmental Health, Kitakyushu, Japan.
Masaki ShiotaDepartment of Urology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Akinori MinatoDepartment of Urology, University of Occupational and Environmental Health, Kitakyushu, Japan.
Ikko TomisakiDepartment of Urology, University of Occupational and Environmental Health, Kitakyushu, Japan.
Kenichi HaradaDepartment of Urology, University of Occupational and Environmental Health, Kitakyushu, Japan.
Masatoshi EtoDepartment of Urology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Hiroshi MiyamotoDepartments of Pathology & Laboratory Medicine and Urology, University of Rochester Medical Center, Rochester, NY, U.S.A.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimIn patients with metastatic castration-sensitive prostate cancer (mCSPC), upfront treatment intensification with the addition of new hormonal agents and/or docetaxel to androgen deprivation therapy (ADT) is recommended. However, this modality is potentially excessive in a subset of these patients. This study aimed to identify patients who may be eligible to omit upfront treatment intensification. PATIENTS AND

methodsPatients with mCSPC who underwent ADT were enrolled. The association between undetectable prostate-specific antigen (PSA) (<0.2 ng/ml) after ADT initiation and overall or castration-resistance-free survival was evaluated.

resultsNinety-seven out of the 242 enrolled patients had low-risk and/or low-volume cancer and were further analyzed. Of these, 45 (46.4%) patients achieved undetectable PSA. The median follow-up period after ADT initiation was 70 months. The median overall survival among patients with undetectable PSA was quite long, reaching 226 months and significantly longer than that among patients with detectable PSA [71 months, hazard ratio (HR)=0.27, 95% confidence interval (CI)=0.15-0.49, p<0.001]. Time to development of castration-resistance was also long and significantly longer in the undetectable PSA group than that in the detectable PSA group (median: 124 vs. 17 months, HR=0.20, 95% CI=0.12-0.34, p<0.001).

conclusionPatients with low-risk and/or low-volume mCSPC showed long-term survival when undetectable PSA was achieved during conventional ADT. In these patients, skipping upfront treatment intensification does not seem to negatively impact survival.

Indexed as

Androgen AntagonistsProstate-Specific AntigenProstatic Neoplasms, Castration-ResistantAgedAged, 80 and overDocetaxelHumansMaleMiddle AgedNeoplasm MetastasisProstatic NeoplasmsTreatment OutcomeAndrogen AntagonistsDocetaxelProstate-Specific AntigenAndrogen deprivation therapycastration-sensitive metastatic prostate cancertreatment intensificationundetectable PSA

Identifiers

PMID39187338
PMCPMC11363787

What OpenQuestion holds

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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.