Evidence map›Paper›PMID 22361632›Full record

ArticleBritish journal of cancer2012

Prognostic value of a cell cycle progression signature for prostate cancer death in a conservatively managed needle biopsy cohort.

J Cuzick, D M Berney, G Fisher, D Mesher, H Møller, J E Reid, M Perry, J Park, A Younus, A Gutin and 5 more

Registry-linked trialAbstract read
In one paragraph

Article in British journal of cancer, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03912883 (Prognostic Factors in Prostate Cancer for Patients Treated by Watchful Waiting), which is not on this map. Cited by 177 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
177citing papers in PubMed, 5 pooled it
–field-weighted citation impact
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.

NCT03912883 active not recruitingnot on this map

Prognostic Factors in Prostate Cancer for Patients Treated by Watchful Waiting

TypeobservationalSponsorQueen Mary University of LondonRan1999 to 2030Enrolled3,350ConditionsProstate Cancer
3 · Its place in the literature

Who cites it

177 citing papers in PubMed, 5 syntheses or guidelines pooled it.

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  6. Copy number alteration burden predicts prostate cancer relapse.Proceedings of the National Academy of Sciences of the United States of America · 2014
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117 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

15 authors.

J CuzickCentre for Cancer Prevention, Wolfson Institute of Preventive Medicine, Queen Mary, University of London, Charterhouse Square, London EC1 M 6BQ, UK. j.cuzick@qmul.ac.uk
D M Berney
G Fisher
D Mesher
H Møller
J E Reid
M Perry
J Park
A Younus
A Gutin
C S Foster
P Scardino
J S Lanchbury
S Stone
Transatlantic Prostate Group

Funding

Cancer Research UK
6 · The paper itself

Abstract

backgroundThe natural history of prostate cancer is highly variable and it is difficult to predict. We showed previously that a cell cycle progression (CCP) score was a robust predictor of outcome in a conservatively managed cohort diagnosed by transurethral resection of the prostate. A greater need is to predict outcome in patients diagnosed by needle biopsy.

methodsTotal RNA was extracted from paraffin specimens. A CCP score was calculated from expression levels of 31 genes. Clinical variables consisted of centrally re-reviewed Gleason score, baseline prostate-specific antigen level, age, clinical stage, and extent of disease. The primary endpoint was death from prostate cancer.

resultsIn univariate analysis (n=349), the hazard ratio (HR) for death from prostate cancer was 2.02 (95% CI (1.62, 2.53), P<10(-9)) for a one-unit increase in CCP score. The CCP score was only weakly correlated with standard prognostic factors and in a multivariate analysis, CCP score dominated (HR for one-unit increase=1.65, 95% CI (1.31, 2.09), P=3 × 10(-5)), with Gleason score (P=5 × 10(-4)) and prostate-specific antigen (PSA) (P=0.017) providing significant additional contributions.

conclusionFor conservatively managed patients, the CCP score is the strongest independent predictor of cancer death outcome yet described and may prove valuable in managing clinically localised prostate cancer.

Indexed as

Cell CycleAdenocarcinomaAgedBiopsy, NeedleCohort StudiesHumansKaplan-Meier EstimateMaleMultivariate AnalysisNeoplasm GradingNeoplasm StagingProportional Hazards ModelsProstate-Specific AntigenProstatic NeoplasmsTransurethral Resection of ProstateProstate-Specific Antigen

Identifiers

PMID22361632
PMCPMC3304411

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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.