Evidence map›Paper›PMID 31874108›Full record

Trial reportThe Journal of clinical investigation2020

Genomics of lethal prostate cancer at diagnosis and castration resistance.

Joaquin Mateo, George Seed, Claudia Bertan, Pasquale Rescigno, David Dolling, Ines Figueiredo, Susana Miranda, Daniel Nava Rodrigues, Bora Gurel, Matthew Clarke and 25 more

Open access · hybridAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in The Journal of clinical investigation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 183 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
183citing papers in PubMed, 5 pooled it
24.4field-weighted citation impact, top 1% 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

183 citing papers in PubMed, 5 syntheses or guidelines pooled it, 295 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Trial
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  13. A Randomized Phase II Study of Androgen Deprivation Therapy with or without Palbociclib in RB-positive Metastatic Hormone-Sensitive Prostate Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Trial
  14. Review
  15. Review
  16. Article
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  18. Article
  19. Circulating Tumor DNA Genomic Profiling inJournal of nuclear medicine : official publication, Society of Nuclear Medicine · 2026
    Observational
  20. Review

123 more citing papers are in PubMed but not listed here.

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

35 authors at 10 institutions in 4 countries.

Joaquin MateoVall d'Hebron Institute of Oncology (VHIO) and Vall d'Hebron University Hospital, Barcelona, Spain.
George SeedThe Institute of Cancer Research, London, United Kingdom.
Claudia BertanThe Institute of Cancer Research, London, United Kingdom.
Pasquale RescignoThe Institute of Cancer Research, London, United Kingdom.
David DollingThe Institute of Cancer Research, London, United Kingdom.
Ines FigueiredoThe Institute of Cancer Research, London, United Kingdom.
Susana MirandaThe Institute of Cancer Research, London, United Kingdom.
Daniel Nava RodriguesThe Institute of Cancer Research, London, United Kingdom.
Bora GurelThe Institute of Cancer Research, London, United Kingdom.
Matthew ClarkeThe Institute of Cancer Research, London, United Kingdom.
Mark AtkinThe Institute of Cancer Research, London, United Kingdom.
Rob ChandlerThe Institute of Cancer Research, London, United Kingdom.
Carlo MessinaThe Institute of Cancer Research, London, United Kingdom.
Semini SumanasuriyaThe Institute of Cancer Research, London, United Kingdom.
Diletta BianchiniThe Institute of Cancer Research, London, United Kingdom.
Maialen BarreroThe Institute of Cancer Research, London, United Kingdom.
Antonella PetermoloThe Institute of Cancer Research, London, United Kingdom.
Zafeiris ZafeiriouThe Institute of Cancer Research, London, United Kingdom.
Mariane FontesThe Institute of Cancer Research, London, United Kingdom.
Raquel Perez-LopezVall d'Hebron Institute of Oncology (VHIO) and Vall d'Hebron University Hospital, Barcelona, Spain.
Nina TunariuThe Institute of Cancer Research, London, United Kingdom.
Ben FultonThe Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom.
Robert JonesThe Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom.
Ursula McGovernUniversity College Hospital, London, United Kingdom.
Christy RalphSt James's University Hospital, Leeds, United Kingdom.
Mohini VarugheseMusgrove Park Hospital, Taunton, United Kingdom.
Omi ParikhRoyal Blackburn Hospital, Blackburn, United Kingdom.
Suneil JainBelfast City Hospital, Belfast, United Kingdom.
Tony ElliottThe Christie Hospital, Manchester, United Kingdom.
Shahneen SandhuPeter McCallum Cancer Center, Melbourne, Australia.
Nuria PortaThe Institute of Cancer Research, London, United Kingdom.
Emma HallThe Institute of Cancer Research, London, United Kingdom.
Wei YuanThe Institute of Cancer Research, London, United Kingdom.
Suzanne CarreiraThe Institute of Cancer Research, London, United Kingdom.
Johann S de BonoThe Institute of Cancer Research, London, United Kingdom.
Institute of Cancer Research · GBRoyal Marsden NHS Foundation Trust · GBBeatson West of Scotland Cancer Centre · GBMusgrove Park Hospital · GBPeter MacCallum Cancer Centre · AURoyal Blackburn Teaching Hospital · GBSt James's University Hospital · GBThe Christie Hospital · GBUniversity College Hospital · GBUniversity of Ulster · GB

Funding

Cancer Research UK 12829Cancer Research UK 20447Cancer Research UK 25351Cancer Research UK C12540/A13230Cancer Research UK C12540/A20447Cancer Research UK CRUK/11/029Department of HealthMedical Research Council MR/M003272/1
6 · The paper itself

Abstract

The genomics of primary prostate cancer differ from those of metastatic castration-resistant prostate cancer (mCRPC). We studied genomic aberrations in primary prostate cancer biopsies from patients who developed mCRPC, also studying matching, same-patient, diagnostic, and mCRPC biopsies following treatment. We profiled 470 treatment-naive prostate cancer diagnostic biopsies and, for 61 cases, mCRPC biopsies, using targeted and low-pass whole-genome sequencing (n = 52). Descriptive statistics were used to summarize mutation and copy number profile. Prevalence was compared using Fisher's exact test. Survival correlations were studied using log-rank test. TP53 (27%) and PTEN (12%) and DDR gene defects (BRCA2 7%; CDK12 5%; ATM 4%) were commonly detected. TP53, BRCA2, and CDK12 mutations were markedly more common than described in the TCGA cohort. Patients with RB1 loss in the primary tumor had a worse prognosis. Among 61 men with matched hormone-naive and mCRPC biopsies, differences were identified in AR, TP53, RB1, and PI3K/AKT mutational status between same-patient samples. In conclusion, the genomics of diagnostic prostatic biopsies acquired from men who develop mCRPC differ from those of the nonlethal primary prostatic cancers. RB1/TP53/AR aberrations are enriched in later stages, but the prevalence of DDR defects in diagnostic samples is similar to mCRPC.

Indexed as

Gene Expression ProfilingGene Expression Regulation, NeoplasticGenomicsNeoplasm ProteinsProstatic Neoplasms, Castration-ResistantBiopsyDisease-Free SurvivalHumansMaleSurvival RateNeoplasm ProteinsCancerCell BiologyMolecular biologyOncologyProstate cancer

Identifiers

PMID31874108
PMCPMC7108902
OpenAlexW2997243361

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.