Evidence map›Paper›PMID 41882599›Full record

ArticleBMC cancer2026

Metastasis-directed SBRT for oligometastatic hormone sensitive prostate cancer (METRO): protocol for a prospective randomised phase III trial, NCT04983095.

Karin Söderkvist, Maira Zia, Adalsteinn Gunnlaugsson, Andreas Josefsson, Bjørg Aksnessæther, Chunde Li, Camilla Thellenberg-Karlsson, Daniel Alm, David Kudrén, Erik Lundin and 12 more

Registry-linked trialAbstract readClinical Trial Protocol
In one paragraph

Article in BMC cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04983095 (Metastasis Directed Stereotactic Body Radiotherapy for Oligo Metastatic Hormone Sensitive Prostate Cancer), which is not on this 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.

NCT04983095 narecruitingnot on this map

Metastasis Directed Stereotactic Body Radiotherapy for Oligo Metastatic Hormone Sensitive Prostate Cancer

TypeinterventionalSponsorKarin SoderkvistRan2021 to 2033Enrolled118ConditionsProstate Cancer Metastatic, Radiation Therapy, Positron-Emission TomographyArmsstereotactic body radiotherapy, androgen deprivation therapy, Radiotherapy
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

22 authors.

Karin SöderkvistDepartment of Diagnostics and Intervention, Umeå University, Umeå, Sweden. karin.soderkvist@umu.se.
Maira ZiaDepartment of Diagnostics and Intervention, Umeå University, Umeå, Sweden.
Adalsteinn GunnlaugssonHematology, Oncology and Radiation Physics, Skåne University Hospital, Lund University, Lund, Sweden.
Andreas JosefssonDepartment of Diagnostics and Intervention, Umeå University, Umeå, Sweden.
Bjørg AksnessætherDepartment for Cancer and Rehabilitation, Ålesund Hospitalt, Helse Møre and Romsdal Hospital Trust, Ålesund, Norway.
Chunde LiClinical Science and Education, Karolinska Institutet, Stockholm, Sweden.
Camilla Thellenberg-KarlssonDepartment of Diagnostics and Intervention, Umeå University, Umeå, Sweden.
Daniel AlmRadiation Oncology, Karolinska University Hospital, Stockholm, Sweden.
David KudrénClinical Science and Education, Karolinska Institutet, Stockholm, Sweden.
Erik LundinOncology, Örebro University Hospital, Örebro, Sweden.
Gabriel MoiseOncology, County Hospital Ryhov, Jönköping, Sweden.
Jenny Kahlmeter BrandellOncology, Örebro University Hospital, Örebro, Sweden.
Jon KindblomOncology, Clinical Sciences, Sahlgrenska Academy at Gothenburg University, Gothenburg, Sweden.
Kirsten BjörnlingerOncology, County Hospital Ryhov, Jönköping, Sweden.
Kristin KarlssonRadiotherapy Physics and Engineering, Karolinska University Hospital, Stockholm, Sweden.
Katrine RiklundDepartment of Diagnostics and Intervention, Umeå University, Umeå, Sweden.
Martina WestinOncologyCapio Saint Göran's Hospital, Stockholm, Sweden.
Mattias HedmanRadiation Oncology, Karolinska University Hospital, Stockholm, Sweden.
Natalie SkorveDepartment for Clinical and Molecular Medicin, NTNU, St Olavs Hospital, Trondheim, Norway.
Pernilla WikströmDepartment of Medical Biosciences, Umeå University, Umeå, Sweden.
Sara StrandbergDepartment of Diagnostics and Intervention, Umeå University, Umeå, Sweden.
Joakim JonssonDepartment of Diagnostics and Intervention, Umeå University, Umeå, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetastasis-directed stereotactic body radiotherapy (MD-SBRT) has shown promise in retrospective and phase II studies for oligometastatic hormone-sensitive prostate cancer. However, prospective randomized phase III data-particularly in newly diagnosed cases and in combination with androgen deprivation therapy and next-generation androgen receptor pathway inhibitors-are limited. The METRO trial investigates the addition of MD-SBRT to standard of care in patients with prostate-specific membrane antigen (PSMA) PET/CT-detected oligometastatic disease.

methodsMETRO is a multicentre, double arm, open-label, phase III randomized trial comparing MD-SBRT plus standard of care versus standard of care alone in patients with one to three PSMA PET/CT-detected distant metastases. The PSMA-RADS scale is used to support inclusion, and only patients with PSMA-RADS 4 or 5 lesions in bone or non-regional lymph nodes are eligible. Standard of care includes time-limited androgen deprivation therapy and/or androgen receptor pathway inhibitor, as well as local radiotherapy to the prostate or prostate bed. Patients are stratified by disease type (synchronous or metachronous) and metastasis location (lymph node/bone). The primary endpoint is biochemical progression-free survival; secondary endpoints include time to castration-resistant prostate cancer, adverse events, and health-related quality of life. The intervention is prescribed either 30 Gy in 3 fractions or 40 Gy in 5 fractions and delivered by stereotactic treatment principles. DISCUSSION: The METRO trial investigates the added value of combining MD-SBRT with time-limited intensified hormonal therapy in both synchronous and metachronous oligometastatic hormone-sensitive prostate cancer staged by PSMA‑PET/CT. The use of the PSMA-RADS scale for inclusion ensures a standardized and reproducible approach for patient selection.

trial registrationClinicalTrials.gov Identifier: NCT04983095.

Indexed as

Prostatic NeoplasmsRadiosurgeryAndrogen AntagonistsAntigens, SurfaceClinical Trials, Phase III as TopicHumansMaleMulticenter Studies as TopicNeoplasm MetastasisPositron Emission Tomography Computed TomographyProspective StudiesQuality of LifeRandomized Controlled Trials as TopicAndrogen AntagonistsAntigens, SurfaceHormone sensitive prostate cancerOligo-metastaticPhase III randomised controlled trialStereotactic body radiotherapyStudy protocol

Identifiers

PMID41882599
PMCPMC13063559

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Registered trials

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.