Evidence map›Paper›PMID 42192575›Full record

SynthesisRadiation oncology (London, England)2026

Efficacy and safety of metastasis-directed therapy for oligometastatic cancer: a systematic review and meta-analysis of randomized controlled trials.

David Chen, Ealia Khoshkish, Jane Jomy, Kristen Arnold, Joshua Yi, David Palma, Mitchell Liu, Xiang Y Ye, Zhihui Liu, Gabriel Boldt and 2 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Radiation oncology (London, England), 2026. 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

12 authors.

David ChenPrincess Margaret Hospital Cancer Centre, Radiation Medicine Program, Toronto, Ontario, Canada.
Ealia KhoshkishTemerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Jane Jomy *Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Kristen Arnold *Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Joshua YiTemerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
David PalmaDivision of Radiation Oncology, Western University, London, Ontario, Canada.
Mitchell LiuDepartment of Radiation Oncology, BC Cancer Vancouver, Vancouver, British Columbia, Canada.
Xiang Y YeDepartment of Biostatistics, Princess Margaret Cancer Centre, University Health Network, Toronto, Canada.
Zhihui LiuDepartment of Biostatistics, Princess Margaret Cancer Centre, University Health Network, Toronto, Canada.
Gabriel BoldtLibrary Services, Verspeeten Family Cancer Centre, London, Ontario, Canada.
Philip WongDepartment of Radiation Oncology, Princess Margaret Cancer Centre, University of Toronto, Toronto, Canada.
Srinivas RamanDepartment of Radiation Oncology, BC Cancer Vancouver, Vancouver, British Columbia, Canada. Srinivas.Raman@bccancer.bc.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetastasis-directed therapy (MDT) is a promising therapeutic strategy in oligometastatic cancer, but its safety and efficacy remains uncertain. This systematic review and meta-analysis aims to evaluate the efficacy and safety of MDT interventions in randomized controlled trials (RCT) of oligometastatic cancer.

methodsThis study was prospectively registered in PROSPERO (CRD420251075947). A literature search of MEDLINE, Embase, and Cochrane CENTRAL was conducted from inception to June 9, 2025. Eligible RCTs compared MDT interventions with standard of care in patients with oligometastatic cancer (≤5 lesions). Hazard ratios (HRs) for overall survival (OS) and progression-free survival (PFS), and adverse event (AE) rates were pooled using random-effects meta-analysis.

resultsThirty seven records representing 3,500 participants were included. Subgroup analyses showed upfront MDT improved both PFS (HR = 0.45, 95% CI 0.32-0.64) and OS (HR = 0.49, 95% CI 0.38-0.64), while consolidation MDT improved PFS only (HR = 0.56, 95% CI 0.40-0.78). In de novo oligometastatic disease, MDT improved PFS (HR = 0.50, 95% CI 0.32-0.78) but not OS, while recurrent oligometastatic disease benefited in both PFS (HR = 0.57, 95% CI 0.42-0.78) and OS (HR = 0.70, 95% CI 0.52-0.93). MDT was associated with an increased odds of Grade ≥ 2 adverse events (OR = 1.77, 95% CI [1.30-2.41]).

conclusionThe addition of MDT to standard of care improves OS and PFS in oligometastatic cancer patients, with a moderate increase in adverse events. MDT is a valuable component of multimodal therapy for oligometastatic disease, warranting further study of optimal timing, patient selection, and long-term outcomes.

Indexed as

NeoplasmsHumansNeoplasm MetastasisRandomized Controlled Trials as Topic

Identifiers

PMID42192575
PMCPMC13386770

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.