Evidence map›Paper›PMID 29911685›Full record

ArticleEuropean urology oncology2018

Docetaxel Treatment in PTEN- and ERG-aberrant Metastatic Prostate Cancers.

Pasquale Rescigno, David Lorente, David Dolling, Roberta Ferraldeschi, Daniel Nava Rodrigues, Ruth Riisnaes, Susana Miranda, Diletta Bianchini, Zafeiris Zafeiriou, Spyridon Sideris and 8 more

Open access · hybridAbstract read
In one paragraph

Article in European urology oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 3 pooled it
3.1field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 3 syntheses or guidelines pooled it, 46 citations in OpenAlex.

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  7. Phase I Trial of Ipatasertib plus Atezolizumab Enhances PI3K/AKT Pathway Immune Responses in Solid Tumors and Refractory Glioblastoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
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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

18 authors at 2 institutions in 2 countries.

Pasquale RescignoThe Institute of Cancer Research, Sutton, UK; Department of Clinical Medicine and Surgery, Department of Translational Medical Sciences, AOU Federico II, Naples, Italy.
David LorenteMedical Oncology Service, Hospital Universitario La Fe, Valencia, Spain.
David DollingThe Institute of Cancer Research, Sutton, UK.
Roberta FerraldeschiThe Institute of Cancer Research, Sutton, UK.
Daniel Nava RodriguesThe Institute of Cancer Research, Sutton, UK.
Ruth RiisnaesThe Institute of Cancer Research, Sutton, UK.
Susana MirandaThe Institute of Cancer Research, Sutton, UK.
Diletta BianchiniThe Institute of Cancer Research, Sutton, UK.
Zafeiris ZafeiriouThe Institute of Cancer Research, Sutton, UK.
Spyridon SiderisThe Institute of Cancer Research, Sutton, UK.
Ana FerreiraThe Institute of Cancer Research, Sutton, UK.
Ines FigueiredoThe Institute of Cancer Research, Sutton, UK.
Semini SumanasuriyaThe Institute of Cancer Research, Sutton, UK.
Joaquin MateoThe Institute of Cancer Research, Sutton, UK.
Raquel Perez-LopezThe Institute of Cancer Research, Sutton, UK.
Adam SharpThe Institute of Cancer Research, Sutton, UK.
Nina TunariuThe Institute of Cancer Research, Sutton, UK.
Johann S de BonoThe Institute of Cancer Research, Sutton, UK. Electronic address: Johann.de-Bono@icr.ac.uk.
Institute of Cancer Research · GBHospital Universitari i Politècnic La Fe · ES

Funding

Medical Research Council MR/M018318/1
6 · The paper itself

Abstract

backgroundLoss of PTEN is a common genomic aberration in castration-resistant prostate cancer (CRPC) and is frequently concurrent with ERG rearrangements, causing resistance to next-generation hormonal treatment (NGHT) including abiraterone. The relationship between PTEN loss and docetaxel sensitivity remains uncertain.

objectiveTo study the antitumor activity of docetaxel in metastatic CRPC in relation to PTEN and ERG aberrations. DESIGN SETTING AND

participantsSingle-centre, retrospective analysis of PTEN loss and ERG expression using a previously described immunohistochemistry (IHC) binary classification system. Patients received docetaxel between January 1, 2006 and July 31, 2016. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Response correlations were analyzed using Pearson's χ RESULTS AND LIMITATIONS: Overall, 215 patients were eligible. Established metastatic CRPC prognostic factors were well balanced between PTEN loss (39%) and normal patients (61%). PTEN loss was associated with shorter median OS (25.4 vs 34.7 mo; hazard ratio [HR] 1.66, 95% confidence interval [CI] 1.18-2.13;

conclusionsOur findings suggest that metastatic CRPC with PTEN loss might benefit more from docetaxel than from NGHT. PATIENT SUMMARY: In this study we found that metastatic prostate cancer with loss of the PTEN switch may benefit more from docetaxel than from abiraterone.

Indexed as

DocetaxelERGProstate cancerPTEN

Identifiers

PMID29911685
PMCPMC5995869
OpenAlexW2805640141

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.