Evidence map›Paper›PMID 32448171›Full record

Trial reportBMC cancer2020

Metastasis-directed therapy in castration-refractory prostate cancer (MEDCARE): a non-randomized phase 2 trial.

Charlien Berghen, Steven Joniau, Kato Rans, Gaëtan Devos, Kenneth Poels, Koen Slabbaert, Herlinde Dumez, Maarten Albersen, Karolien Goffin, Karin Haustermans and 1 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in BMC cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04222634 (Metastasis-directed Therapy in Castration-refractory Prostate Cancer MEDCARE), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 20% 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.

NCT04222634 naactive not recruitingnot on this map

Metastasis-directed Therapy in Castration-refractory Prostate Cancer MEDCARE : a Non-randomized Phase 2 Trial

TypeinterventionalSponsorUniversitaire Ziekenhuizen KU LeuvenRan2019 to 2030Enrolled18ConditionsCastration-resistant Prostate CancerArmsRadiotherapy (SBRT) and/or surgery (metastasectomy)
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Annals of nuclear medicine · 2021
    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

11 authors at 1 institution in 1 country.

Charlien BerghenDepartment of Radiation Oncology, University Hospitals Leuven, Leuven, Belgium. charlien.berghen@uzleuven.be.
Steven JoniauDepartment of Urology, University Hospitals Leuven, Leuven, Belgium.
Kato RansDepartment of Radiation Oncology, University Hospitals Leuven, Leuven, Belgium.
Gaëtan DevosDepartment of Urology, University Hospitals Leuven, Leuven, Belgium.
Kenneth PoelsDepartment of Radiation Oncology, University Hospitals Leuven, Leuven, Belgium.
Koen SlabbaertDepartment of Urology, RZ Tienen, Tienen, Belgium.
Herlinde DumezDepartment of Medical Oncology, University Hospitals Leuven, Leuven, Belgium.
Maarten AlbersenDepartment of Urology, University Hospitals Leuven, Leuven, Belgium.
Karolien GoffinDepartment of Nuclear Medicine and Molecular Imaging, University Hospitals Leuven, Leuven, Belgium.
Karin HaustermansDepartment of Radiation Oncology, University Hospitals Leuven, Leuven, Belgium.
Gert De MeerleerDepartment of Radiation Oncology, University Hospitals Leuven, Leuven, Belgium.
KU Leuven · BE

Funding

Stichting Tegen Kanker FAF-C/2018/1309
6 · The paper itself

Abstract

backgroundPatients diagnosed with metastatic castration-refractory prostate cancer (mCRPC) rely on a limited number of therapeutic agents resulting in a median survival of 2-3 years. A subgroup of those patients with mCRPC presents with oligoprogressive disease, with a limited number of progressive lesions while other metastases are still controlled by ongoing systemic treatment.

methodsIn this single arm prospective phase II trial, we aim to include 18 patients with oligoprogressive mCRPC (1-3 metastases and/or local recurrence) who will be treated with metastasis-directed therapy to all visible progressive lesions. Progression is based on conventional imaging, as the use of PSMA PET-CT is considered investigational. However all patients will undergo PSMA PET-CT and the images will be blinded until progression. Primary endpoint is the postponement of the start of next-line systemic treatment (NEST) and the additional clinical value of PSMA PET-CT. Recruitment of patients for this trial started in January 2020 and will be completed approximately by December 2020. DISCUSSION: In this phase 2 trial on oligoprogressive mCRPC, we will investigate the benefit of progression-directed therapy while continuing ongoing systemic treatment. We hypothesize that progression-directed therapy (PDT) with surgery or stereotactic body radiation therapy for these oligoprogressive lesions will postpone the start of next-line systemic treatment and therefore serve as a new or add-on therapy in the spectrum of treatments available for mCRPC. The results of this trial will serve as guidance for a later randomized phase 3 trial. All participants are given an information sheet and are required to give written informed consent. Results will be published in a peer-reviewed journal.

trial registrationThis study is registered at ClinicalTrials.gov: NCT04222634 (December 18th 2019).

Indexed as

AdolescentAdultAgedAged, 80 and overCombined Modality TherapyFollow-Up StudiesHumansMaleMetastasectomyMiddle AgedNeoplasm MetastasisNeoplasm Recurrence, LocalNon-Randomized Controlled Trials as TopicPrognosisProspective StudiesProstatic Neoplasms, Castration-ResistantCastration-refractory prostate cancerLymph node dissectionMetastasectomyNext-line systemic treatmentOligoprogressionProstate cancerPSMA PET-CTStereotactic body radiotherapy

Identifiers

PMID32448171
PMCPMC7245754
OpenAlexW3027625748

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.