Evidence map›Paper›PMID 40900758›Full record

SynthesisPeerJ2025

Surgery, radiotherapy and endocrine therapy for oligometastatic prostate cancer efficacy: a systematic review and network meta-analysis.

Wenwei Ying, Zhenshan Ding, Yuhui He, Jianfeng Wang, Xing Chen, Xuesong Li, Yanqing Gong

Abstract readSystematic ReviewNetwork Meta-Analysis
In one paragraph

Synthesis in PeerJ, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. 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

7 authors.

Wenwei Ying *Department of Urology, Peking University First Hospital, Beijing, China.
Zhenshan Ding *Department of Urology, China-Japan Friendship Hospital, Beijing, China.
Yuhui HeDepartment of Urology, China-Japan Friendship Hospital, Beijing, China.
Jianfeng WangDepartment of Urology, China-Japan Friendship Hospital, Beijing, China.
Xing ChenDepartment of Urology, China-Japan Friendship Hospital, Beijing, China.
Xuesong LiDepartment of Urology, Peking University First Hospital, Beijing, China.
Yanqing GongDepartment of Urology, Peking University First Hospital, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, the treatment approach for metastatic prostate cancer has evolved, with early combination therapies increasingly being favored over androgen-deprivation therapy (ADT) alone. Despite the availability of various treatments, their relative effectiveness and safety trade-offs remain uncertain. Randomized controlled trials have explored a range of treatments for oligometastatic prostate cancer, but clear conclusions regarding their prognostic benefits and patient-centered outcomes have not been established. This network meta-analysis (NMA) aims to quantify the benefits of different treatments by analyzing data from a systematic search of Medline, EMBASE, and Cochrane databases, covering trials up to October 1, 2024. The primary outcomes evaluated in this study include overall survival (OS), progression-free survival (PFS), treatment-related adverse events (TRAEs), and quality of life (QoL). This study is registered with PROSPERO (CRD42022370203). We analyzed individual patient data from 13 eligible trials, involving a total of 2,524 patients. Our analysis revealed that ADT+ radiation therapy (RT) (hazard ratio (HR) = 0.39, 95% confidence interval (CI) [0.27-0.56]) and ADT+stereotactic body radiotherapy (SBRT) (HR = 0.35, 95% CI [0.21-0.58]) significantly improved progression-free survival (PFS) compared to ADT alone, while no treatment showed a significant overall survival (OS) benefit. Safety analysis revealed ADT monotherapy had the lowest risk of grade ≥3 adverse events (TRAEs), whereas ADT+abiraterone increased toxicity (OR = 1.54). Limited quality of life (QoL) data suggested ADT+RT may offer slight improvement (surface under the cumulative ranking curve (SUCRA) 74.3%). Most trials exhibited low bias risk, though heterogeneity and small sample sizes for some comparisons warrant cautious interpretation. These findings support ADT+RT/SBRT for PFS benefit but highlight the need for further research to optimize survival outcomes and treatment tolerability.

Indexed as

Androgen AntagonistsProstatic NeoplasmsCombined Modality TherapyHumansMaleNeoplasm MetastasisProgression-Free SurvivalQuality of LifeRadiosurgeryTreatment OutcomeAndrogen AntagonistsAdverse eventsDrug endocrine therapyEfficacyNetwork meta-analysisOligometastatic prostate cancerRadiotherapySurgery

Identifiers

PMID40900758
PMCPMC12401018

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.