Evidence map›Paper›PMID 30642291›Full record

ArticleBMC cancer2019

Abiraterone acetate plus prednisone for the Management of Metastatic Castration-Resistant Prostate Cancer (mCRPC) without prior use of chemotherapy: report from a large, international, real-world retrospective cohort study.

Martin Boegemann, Sara Khaksar, Guillaume Bera, Alison Birtle, Catherine Dopchie, Louis-Marie Dourthe, Els Everaert, Martin Hatzinger, Dirko Hercher, Werner Hilgers and 7 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in BMC cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 3% 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.

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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 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 14 institutions in 5 countries.

Martin BoegemannDepartment of Urology, University of Muenster Medical Center, Albert-Schweitzer-Campus 1, GB A1, D-48149, Muenster, Germany. Martin.Boegemann@ukmuenster.de.ORCID http://orcid.org/0000-0002-2569-4446
Sara KhaksarSt Luke's Cancer Centre, The Royal Surrey County Hospital, Guildford, UK.
Guillaume BeraGroupe Hospitalier Bretagne Sud, Hôpital du Scorff, Lorient, France.
Alison BirtleRosemere Cancer Centre, Royal Preston Hospital & University of Manchester, Manchester, UK.
Catherine DopchieCHWapi site IMC, Tournai, Belgium.
Louis-Marie DourtheClinique Saint Anne, Strasbourg, France.
Els EveraertAZ Nikolaas, Sint Niklaas, Belgium.
Martin HatzingerAgaplesion Markus Hospital, Frankfurt, Germany.
Dirko HercherRefrath Urological Center, Bergisch Gladbach, Germany.
Werner HilgersInstitut Sainte Catherine, Avignon, France.
Geoffrey MatusCHC Cliniques Saint Joseph, Liège, Belgium.
Laura Garcia AlvarezIQVIA, Barcelona, Spain.
Laurent AntoniJanssen Pharmaceutica NV, Beerse, Belgium.
Martin LukacPAREXEL International, Prague, Czech Republic.
Geneviève PissartJanssen Pharmaceutica NV, Beerse, Belgium.
Paul RobinsonJanssen EMEA, London, High Wycombe, UK.
Tony ElliottThe Christie Hospital, Manchester, UK.
Janssen (Belgium) · BEAgaplesion Markus Hospital · DECentre Hospitalier de Bretagne Sud · FRCentre Hospitalier de Wallonie Picarde · BEClinique Saint-Joseph · BEFederal Highway and Transport Research Institute · DEInstituto Químico Biológico · ESInstitut Sainte Catherine · FRJanssen (United Kingdom) · GBRoyal Surrey County Hospital · GBThe Christie Hospital · GBUniversity Hospital Münster · DEUniversity of Manchester · GBVlaamse Vereniging voor Obstetrie en Gynaecolo · BE

Funding

Janssen Pharmaceutica NV n/a
6 · The paper itself

Abstract

backgroundWith the recent introduction of novel treatment options, real-world data from patients with metastatic castration-resistant prostate cancer (mCRPC) are required to better understand the impact on routine clinical practice. This study primarily aimed to describe the time to treatment failure (TTF) of mCRPC patients treated with abiraterone acetate plus prednisone or the corticosteroid of choice (AAP) in the pre-chemotherapy setting. Other relevant outcomes, clinical and treatment characteristics of these patients were also evaluated.

methodsThis retrospective, observational study collected data from chemotherapy-naïve mCRPC patients treated with AAP from four European countries. Kaplan-Meier curves were used to estimate TTF, progression-free survival (PFS), and time to first skeletal-related event. The impact of baseline characteristics on TTF and PFS was explored using univariate and multivariate Cox proportional hazard models. Log-rank test was used to assess the potential role of duration of response to ADT in predicting response to AAP treatment.

resultsData from 481 eligible patients (Belgium: 68; France: 61; Germany: 150; UK: 202) were analysed. At AAP initiation, the median age of patients was 75.0 years (interquartile range [IQR]: 69.0-81.0), and the median PSA was 56.2 ng/mL (IQR: 22.2-133.1), with over 50% of patients presenting an ECOG score of 0 or 1. Visceral metastases were present in 7.5% of patients; an exclusion criterion in the COU-AA-302 clinical trial. The median TTF with AAP was 10.0 months (95%CI: 9.2-11.1) and the median PFS was 10.8 months (95%CI: 9.6-11.8). Shorter TTF was significantly associated with higher ALP (> 119 units/L), higher PSA (> 56.2 ng/mL), or poorer ECOG PS scores at AAP initiation (p < 0.05). Patients with longer duration of response to ADT (≥12 months) presented longer TTF and longer time to progression (p < 0.0001).

conclusionsThis European real-world study provides valuable insights into the characteristics, treatment, and outcomes of chemotherapy-naïve patients with mCRPC who received AAP in routine clinical practice. Treatment effectiveness of AAP in the real-world is maintained despite patients having poorer clinical features at initiation than those observed in the COU-AA-302 trial population.

Indexed as

Abiraterone AcetateAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsComorbidityHumansKaplan-Meier EstimateMaleMiddle AgedNeoplasm GradingNeoplasm StagingPrednisoneProportional Hazards ModelsProstatic Neoplasms, Castration-ResistantRetrospective StudiesTreatment OutcomeAbiraterone AcetatePrednisoneAbiraterone acetateMetastatic castration-resistant prostate cancerReal-world evidenceTime to treatment failure

Identifiers

PMID30642291
PMCPMC6332550
OpenAlexW2913905665

What OpenQuestion holds

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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.