Evidence map›Paper›PMID 36547161›Full record

SynthesisCurrent oncology (Toronto, Ont.)2022

Addition of New Androgen Receptor Pathway Inhibitors to Docetaxel and Androgen Deprivation Therapy in Metastatic Hormone-Sensitive Prostate Cancer: A Systematic Review and Metanalysis.

Francesco Fiorica, Consuelo Buttigliero, Daniela Grigolato, Marco Muraro, Fabio Turco, Fernando Munoz, Marcello Tucci

Open access · goldAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Current oncology (Toronto, Ont.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Human Kallikrein 2: A Novel Lineage-Specific Surface Target in Prostate Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  3. Is [Cancers · 2025
    Review
  4. Review
  5. Observational
  6. Article
  7. Review
  8. 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

7 authors at 4 institutions in 1 country.

Francesco FioricaDepartment of Radiation Oncology and Nuclear Medicine, AULSS 9 Scaligera, 37045 Verona, Italy.ORCID 0000-0002-9404-3655
Consuelo ButtiglieroDepartment of Oncology, University of Turin, San Luigi Gonzaga Hospital, 10093 Torino, Italy.ORCID 0000-0002-2877-2518
Daniela GrigolatoDepartment of Radiation Oncology and Nuclear Medicine, AULSS 9 Scaligera, 37045 Verona, Italy.
Marco MuraroDepartment of Radiation Oncology and Nuclear Medicine, AULSS 9 Scaligera, 37045 Verona, Italy.
Fabio TurcoDepartment of Oncology, University of Turin, San Luigi Gonzaga Hospital, 10093 Torino, Italy.
Fernando MunozRadiation Oncology TomoTherapy Center, Hospital of Aosta, 11000 Aosta, Italy.
Marcello TucciDepartment of Medical Oncology, Cardinal Massaia Hospital, 14100 Asti, Italy.
University of Verona · ITUniversity of Turin · ITAzienda Sanitaria Locale di Asti · ITAzienda USL della Valle d’Aosta · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, significant changes have occurred in metastatic hormone-sensitive prostate cancer (mHSPC) management, where docetaxel and new androgen receptor pathway inhibitors (ARPI) have been shown to improve overall survival (OS) compared to androgen deprivation therapy (ADT). Recent data could once again radically change mHSPC treatment. PEACE-1 and ARASENS trials demonstrated a survival benefit of the addition of ARPI to docetaxel and ADT combination (triplet therapy), compared to docetaxel and ADT. With multiple options to choose from, it is crucial to identify the patients who would benefit most from triplet therapy. In this meta-analysis, we evaluated the activity of the triplet therapy versus docetaxel plus ADT in mHSPC. A systematic review of PubMed/Medline, Embase, and the proceedings of major international meetings was performed. Five RCTs fulfilled the inclusion criteria. PEACE-1 and ARASENS studies reported disease-free survival (DFS) and OS. Post hoc analysis of three other trials evaluated the combination of ARPI, docetaxel and ADT. Globally, 2538 patients were included (1270 triplet therapy; 1268 docetaxel + ADT). Triplet therapy was associated with improved OS (hazard ratio (HR) 0.74; 95% confidence interval (CI), 0.66-0.83,

Indexed as

Androgen Receptor AntagonistsAntineoplastic Combined Chemotherapy ProtocolsDocetaxelProstatic NeoplasmsAndrogensHumansMaleAndrogen Receptor AntagonistsAndrogensDocetaxelde novo metastatic diseasehigh volume metastatic diseasehormone-sensitive prostate cancermetanalysissystematic reviewtriplet therapy

Identifiers

PMID36547161
PMCPMC9776703
OpenAlexW4312072123

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.