Evidence map›Paper›PMID 36353661›Full record

ArticleEuropean urology open science2022

Real-world Treatment Sequencing in Patients with Metastatic Castration-resistant Prostate Cancer: Results from the Prospective, International, Observational Prostate Cancer Registry.

Anders Bjartell, Luis Costa, Gero Kramer, Bogdan Zurawski, Luca Galli, Patrick Werbrouck, Thorsten Ecke, Omi Parikh, Mostefa Bennamoun, Camilo Garcia Freire and 7 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in European urology open science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02236637 (A Prospective Registry of Patients With a Confirmed Diagnosis of Adenocarcinoma of the Prostate Presenting With Metastatic Castrate-Resistant Prostate Cancer), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 12% 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.

NCT02236637 completednot on this map

A Prospective Registry of Patients With a Confirmed Diagnosis of Adenocarcinoma of the Prostate Presenting With Metastatic Castrate-Resistant Prostate Cancer

TypeobservationalSponsorJanssen Pharmaceutica N.V., BelgiumRan2013 to 2018Enrolled3,050ConditionsProstate Cancer
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 14 citations in OpenAlex.

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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

17 authors at 17 institutions in 13 countries.

Anders BjartellDepartment of Urology, Skåne University Hospital, Lund University, Malmö, Sweden.
Luis CostaOncology Division, Centro Hospitalar Universitário Lisboa Norte, Lisbon, Portugal.
Gero KramerDepartment of Urology, Medical University of Vienna, Vienna, Austria.
Bogdan ZurawskiCentrum Onkologii im. Prof. F. Lukaszczyka w Bydgoszczy, Dzial Onkologii Klinicznej, Ambulatorium Chemioterapii, Bydgoszcz, Poland.
Luca GalliPisana University Hospital, Pisa, Italy.
Patrick WerbrouckAZ Groeninge, Kortrijk, Belgium.
Thorsten EckeHelios Klinikum Bad Saarow, Bad Saarow, Germany.
Omi ParikhRoyal Blackburn Hospital, Blackburn, UK.
Mostefa BennamounInstitut Mutualiste Montsouris, Paris, France.
Camilo Garcia FreireHospital Clínico Universitario de Santiago, Servicio de Urología, Santiago de Compostela, Spain.
Avivit PeerRambam Medical Center, Haifa, Israel.
Börje LjungbergDepartment of Surgical and Perioperative Sciences, Urology and Andrology, Umeå University, Umeå, Sweden.
Irfan CicinTrakya University Hospital Medical Oncology Department, Edirne, Turkey.
Emma SmithJanssen-Cilag, High Wycombe, UK.
Martin LukacParexel International Czech Republic sro, on behalf of Janssen Pharmaceutica NV, Beerse, Belgium.
Robert WapenaarJanssen-Cilag BV, Breda, The Netherlands.
Simon ChowdhuryGuy's and St Thomas' NHS Foundation Trust and Sarah Cannon Research Institute, London, UK.
AZ Groeninge · BEAzienda Ospedaliera Universitaria Pisana · ITCentrum Onkologii · PLComplejo Hospitalario Universitario de Santiago · ESGuy's and St Thomas' NHS Foundation Trust · GBHelios Hospital Bad Saarow · DEInstitute Mutualiste Montsouris · FRJanssen (Belgium) · BEJanssen (Netherlands) · NLJanssen (United Kingdom) · GBLund University · SEMedical University of Vienna · ATRambam Health Care Campus · ILRoyal Blackburn Teaching Hospital · GBTrakya University · TRUmeå University · SEUniversity of Lisbon · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Prostate cancer has a multifaceted treatment pattern. Evidence is lacking for optimal treatment sequences for metastatic castration-resistant prostate cancer (mCRPC). Objective: To increase the understanding of real-world treatment pathways and outcomes in patients with mCRPC. Design setting and participants: A prospective, noninterventional, real-world analysis of 3003 patients with mCRPC in the Prostate Cancer Registry (PCR; NCT02236637) from June 14, 2013 to July 9, 2018 was conducted. Intervention: Patients received first- and second-line hormonal treatment and chemotherapy as follows: abiraterone acetate plus prednisone (abiraterone)-docetaxel (ABI-DOCE), abiraterone-enzalutamide (ABI-ENZA), abiraterone-radium-223 (ABI-RAD), docetaxel-abiraterone (DOCE-ABI), docetaxel-cabazitaxel (DOCE-CABA), docetaxel-enzalutamide (DOCE-ENZA), and enzalutamide-docetaxel (ENZA-DOCE). Outcome measurements and statistical analysis: Baseline patient characteristics, quality of life, mCRPC treatments, and efficacy outcomes (progression and survival) were presented descriptively. Results and limitations: Data from 727 patients were eligible for the analysis (ABI-DOCE Conclusions: The real-world PCR data complement clinical trial data, reflecting more highly selected patient populations than seen in routine clinical practice. Baseline characteristics play a role in mCRPC first-line treatment selection, but other factors, such as treatment availability, have an impact. Efficacy observations are limited and should be interpreted with caution. Patient summary: Baseline characteristics appear to have a role in the first-line treatment selection of metastatic castration-resistant prostate cancer in the real-world setting. First-line abiraterone acetate plus prednisone seems to be the preferred treatment option for older patients and those with lower Gleason scores, first-line docetaxel for younger patients and those with more advanced disease, and first-line enzalutamide for patients with fewer metastases and more favourable performance status. The benefit to patients from these observations remains unknown.

Indexed as

Abiraterone acetateAndrogen deprivation therapyAntiandrogenCabazitaxelCastration-resistant prostate cancerDocetaxelEnzalutamideRa-223Real-world evidence

Identifiers

PMID36353661
PMCPMC9637537
OpenAlexW4296116685

What OpenQuestion holds

Textmetadata
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.