Evidence map›Paper›PMID 25985882›Full record

ArticleEuropean urology2015

Impact of bone-targeted therapies in chemotherapy-naïve metastatic castration-resistant prostate cancer patients treated with abiraterone acetate: post hoc analysis of study COU-AA-302.

Fred Saad, Neal Shore, Hendrik Van Poppel, Dana E Rathkopf, Matthew R Smith, Johann S de Bono, Christopher J Logothetis, Paul de Souza, Karim Fizazi, Peter F A Mulders and 13 more

2 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in European urology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
6.7field-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.

NCT00887198 phase3completednot on this map

A Phase 3, Randomized, Double-blind, Placebo-Controlled Study of Abiraterone Acetate (CB7630) Plus Prednisone in Asymptomatic or Mildly Symptomatic Patients With Metastatic Castration-Resistant Prostate Cancer

TypeinterventionalSponsorJanssen Research & Development, LLCRan2009 to 2017Enrolled1,088ConditionsProstate CancerArmsAbiraterone acetate, Placebo, Prednisone
NCT03336983 phase2completednot on this mapstarted 2017, after this paper: background citation

Bone Response After Luteinizing Hormone-releasing Hormone Analogue and Enzalutamide +/- Zoledronic Acid in Prostate Cancer Patients With Hormone Sensitive Metastatic Bone Disease: a Prospective, Phase II, Randomized, Multicenter Study

TypeinterventionalSponsorAzienda Socio Sanitaria Territoriale degli Spedali Civili di BresciaRan2017 to 2023Enrolled126ConditionsProstate Cancer, Bone MetastasesArmsZoledronic Acid, Enzalutamide
3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 62 citations in OpenAlex.

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  11. Prognosis by cancer type and incidence of zoledronic acid-related osteonecrosis of the jaw: a single-center retrospective study.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 17 institutions in 7 countries.

Fred SaadUniversity of Montréal, Montréal, Québec, Canada. Electronic address: fredsaad@videotron.ca.
Neal ShoreCarolina Urologic Research Center, Atlantic Urology Clinics, Myrtle Beach, SC, USA.
Hendrik Van PoppelUniversity Hospital Leuven, Leuven, Belgium.
Dana E RathkopfMemorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY, USA.
Matthew R SmithHarvard Medical School and Massachusetts General Hospital, Boston, MA, USA.
Johann S de BonoInstitute of Cancer Research and Royal Marsden Hospital, Sutton, UK.
Christopher J LogothetisMD Anderson Cancer Center, Houston, TX, USA.
Paul de SouzaUniversity of Western Sydney School of Medicine, Ingham Institute, Liverpool, Australia.
Karim FizaziInstitut Gustave Roussy, University of Paris Sud, Villejuif, France.
Peter F A MuldersRadboud University Medical Centre, Nijmegen, The Netherlands.
Paul MainwaringHematology and Oncology Clinics of Australia, Brisbane, Australia.
John D HainsworthSarah Cannon Research Institute, Nashville, TN, USA.
Tomasz M BeerOregon Health & Science University Knight Cancer Institute, Portland, OR, USA.
Scott NorthCross Cancer Institute, Edmonton, Alberta, Canada.
Yves FradetLaval University, Québec City, Québec, Canada.
Thomas A GriffinJanssen Research & Development, Los Angeles, CA, USA.
Peter De PorreJanssen Research & Development, Beerse, Belgium.
Anil LondheJanssen Research & Development, Raritan, NJ, USA.
Thian KheohJanssen Research & Development, San Diego, CA, USA.
Eric J SmallHelen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, CA, USA.
Howard I ScherMemorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY, USA.
Arturo MolinaJanssen Research & Development, Menlo Park, CA, USA.
Charles J RyanHelen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, CA, USA.
Janssen (United States) · USJanssen (Belgium) · BEMemorial Sloan Kettering Cancer Center · USUniversity of California, San Francisco · USAlberta Cancer Foundation · CACarolina Urologic Research Center · USIngham Institute · AUInstitute of Cancer Research · GBKU Leuven · BEMassachusetts General Hospital · USOregon Health & Science University · USRadboud University Nijmegen · NLSarah Cannon · USThe University of Texas MD Anderson Cancer Center · USUniversité de Montréal · CAUniversité Laval · CAUniversité Paris-Sud · FR

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundMetastatic castration-resistant prostate cancer (mCRPC) often involves bone, and bone-targeted therapy (BTT) has become part of the overall treatment strategy.

objectiveInvestigation of outcomes for concomitant BTT in a post hoc analysis of the COU-AA-302 trial, which demonstrated an overall clinical benefit of abiraterone acetate (AA) plus prednisone over placebo plus prednisone in asymptomatic or mildly symptomatic chemotherapy-naïve mCRPC patients. DESIGN, SETTING, AND

participantsThis report describes the third interim analysis (prespecified at 55% overall survival [OS] events) for the COU-AA-302 trial.

interventionPatients were grouped by concomitant BTT use or no BTT use. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Radiographic progression-free survival and OS were coprimary end points. This report describes the third interim analysis (prespecified at 55% OS events) and involves patients treated with or without concomitant BTT during the COU-AA-302 study. Median follow-up for OS was 27.1 mo. Median time-to-event variables with 95% confidence intervals (CIs) were estimated using the Kaplan-Meier method. Adjusted hazard ratios (HRs), 95% CIs, and p values for concomitant BTT versus no BTT were obtained via Cox models. RESULTS AND LIMITATIONS: While the post hoc nature of the analysis is a limitation, superiority of AA and prednisone versus prednisone alone was demonstrated for clinical outcomes with or without BTT use. Compared with no BTT use, concomitant BTT significantly improved OS (HR 0.75; p=0.01) and increased the time to ECOG deterioration (HR 0.75; p<0.001) and time to opiate use for cancer-related pain (HR 0.80; p=0.036). The safety profile of concomitant BTT with AA was similar to that reported for AA in the overall intent-to-treat population. Osteonecrosis of the jaw (all grade 1/2) with concomitant BTT use was reported in <3% of patients.

conclusionsAA with concomitant BTT was safe and well tolerated in men with chemotherapy-naïve mCRPC. The benefits of AA on clinical outcomes were increased with concomitant BTT. PATIENT SUMMARY: Treatment of advanced prostate cancer often includes bone-targeted therapy. This post hoc analysis showed that in patients with advanced prostate cancer who were treated with abiraterone acetate and prednisone in combination with bone-targeted therapy, there was a continued trend in prolongation of life when compared with patients treated with prednisone alone.

trial registrationClinicalTrials.gov NCT00887198.

Indexed as

Abiraterone AcetateAgedAntineoplastic Agents, HormonalAntineoplastic Combined Chemotherapy ProtocolsBisphosphonate-Associated Osteonecrosis of the JawBone Density Conservation AgentsBone NeoplasmsClinical Trials, Phase III as TopicDisease-Free SurvivalHumansKaplan-Meier EstimateMaleMiddle AgedMulticenter Studies as TopicOdds RatioPrednisoneAbiraterone AcetateAntineoplastic Agents, HormonalBone Density Conservation AgentsPrednisoneSteroid Synthesis InhibitorsAbiraterone acetateBone-targeted therapyChemotherapy-naïveMetastatic castration-resistant prostate cancer

Identifiers

PMID25985882
PMCPMC5056561
OpenAlexW1549522748

What OpenQuestion holds

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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.