Evidence map›Paper›PMID 40126447›Full record

ArticleFuture oncology (London, England)2025

Treatment intensification in metastatic castration-sensitive prostate cancer: a real-world study in Alberta, Canada.

Steven M Yip, Winson Y Cheung, Armen Aprikian, Matthias Stoelzel, Kelvin Wong, Alessandra Pranzo, Thomas McLean, Dylan E O'Sullivan, Andrew Chilelli

Abstract read
In one paragraph

Article in Future oncology (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Steven M YipDepartment of Oncology, Tom Baker Cancer Centre, University of Calgary, Calgary, Alberta, Canada.
Winson Y CheungDepartment of Oncology, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-3679-4290
Armen AprikianDepartment of Oncology, McGill University, Montreal, Quebec, Canada.
Matthias StoelzelRWE, Astellas Pharma GmbH, Leiden, Germany.ORCID 0000-0002-2058-7385
Kelvin WongMedical Affairs, Astellas Pharma, British Columbia, Canada.
Alessandra PranzoMedical Affairs Oncology, Astellas Pharma Europe Ltd, Surrey, UK.
Thomas McLeanHEOR Oncology, Astellas Pharma Europe Ltd, Surrey, UK.
Dylan E O'SullivanDepartment of Oncology, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-2562-0017
Andrew ChilelliHEOR Oncology, Astellas Pharma Europe Ltd, Surrey, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo assess the current status of and factors associated with treatment intensification (TI) (with androgen receptor pathway inhibitors [ARPIs] and/or docetaxel) for metastatic castration-sensitive prostate cancer (mCSPC) in Canada. MATERIALS &

methodsRetrospective analysis of data for 431 patients with mCSPC from the Alberta Prostate Cancer Research Initiative database (July 2014-March 2022). The primary objective was to assess the patient proportion receiving TI, time to TI, and associated factors. The secondary and exploratory objectives were evaluating TI patterns and factors associated with choice of therapy, respectively.

resultsOverall, 42% of patients received TI; most (65%) within 3 months post-index. TI was likely to occur within 3 months post-index in de novo mCSPC, but occurred later for recurrent mCSPC. Patients with recurrent mCSPC (HR [95% CI]: 0.52 [0.38-0.72]) and those aged ≥ 75 years (0.57 [0.36-0.93]) were less likely to receive TI. Patients with multiple metastatic sites and bone metastasis had a 2-3-fold higher likelihood of receiving TI. An ARPI was predominantly used (75%) for TI (median duration: 16.0 months).

conclusionTI rates for mCSPC are suboptimal in Canada especially for older patients and those with recurrent mCSPC. TI prioritization in such groups may improve patient outcomes.

Indexed as

Androgen Receptor AntagonistsAntineoplastic Combined Chemotherapy ProtocolsProstatic Neoplasms, Castration-ResistantAgedAged, 80 and overAlbertaDocetaxelHumansMaleMiddle AgedNeoplasm MetastasisNeoplasm Recurrence, LocalRetrospective StudiesTreatment OutcomeAndrogen Receptor AntagonistsDocetaxelCanadade novo mCSPCMetastatic castration-sensitive prostate cancerreal-worldrecurrent mCSPCtreatment intensification

Identifiers

PMID40126447
PMCPMC11988207

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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.