Evidence map›Paper›PMID 32884090›Full record

Trial reportProstate cancer and prostatic diseases2021

Bone targeted therapy and skeletal related events in the era of enzalutamide and abiraterone acetate for castration resistant prostate cancer with bone metastases.

Bradley McGregor, Li Zhang, Kathryn P Gray, Grace Shaw, Carolyn Evan, Edoardo Francini, Christopher Sweeney

Open access · greenAbstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Prostate cancer and prostatic diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
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.

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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Review
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  6. Review
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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

7 authors at 2 institutions in 2 countries.

Bradley McGregorLank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, MA, USA. bradley_mcgregor@dfci.harvard.edu.ORCID http://orcid.org/0000-0002-8298-0289
Li ZhangNorthwest Medical Specialties, Gig Harbor, WA, USA.
Kathryn P GrayLank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Grace ShawLank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Carolyn EvanLank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Edoardo FranciniLank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID http://orcid.org/0000-0003-4270-7023
Christopher SweeneyLank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Dana-Farber Cancer Institute · USNorthwest Medical Specialties · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn an era of multiple life-prolonging therapies for metastatic castration resistant prostate cancer (mCRPC), the optimal timing of initiation and duration of antiresorptive bone targeted therapy (BTT) to prevent skeletal related events (SREs) is unknown.

methodsTo assess practice patterns of BTT use and its associations with clinical outcomes in a high-volume center in the modern era of metastatic CRPC management, a retrospective cohort of patients treated for mCRPC with BM between 2007 and 2017 was identified from a single institutions clinical research database. Study endpoints included time from the diagnosis of CRPC to the onset of SRE or OS. Cox proportional hazards model assessed association of BTT use with time to first SRE and OS.

resultsIn total, 249 patients were identified; median follow-up was 7.7 (95%CI: 5.7-10.2) years. On multivariable analysis, patients with 4 or more BM at diagnosis of mCRPC who received BTT with abiraterone acetate or enzalutamide as first line therapy had a 42% reduced risk of developing an SRE (HR 0.58; 95%CI: 0.36-0.95) compared to those who never received BTT or received it in second line. No such effect was observed in patients with 1-3 BM. No OS difference was noted in patients who received BTT, whether with first line therapy or without. This study is limited by retrospective nature at a single institution.

conclusionsOur hospital registry data indicate a potential benefit in terms of SRE prevention for early use of antiresorptive BTT in combination with life prolonging CRPC therapies for patients with CRPC and at least 4 BM.

Indexed as

Abiraterone AcetateAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsBenzamidesBone Density Conservation AgentsBone DiseasesFollow-Up StudiesHumansMaleMiddle AgedNitrilesPhenylthiohydantoinPractice Patterns, Physicians'PrognosisProstatic Neoplasms, Castration-ResistantAbiraterone AcetateBenzamidesBone Density Conservation AgentsenzalutamideNitrilesPhenylthiohydantoin

Identifiers

PMID32884090
OpenAlexW3082857820

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.