Evidence map›Paper›PMID 9038759›Full record

ArticleJournal of clinical pathology1996

Ki-67 expression in early prostate cancer and associated pathological lesions.

M R Feneley, M P Young, C Chinyama, R S Kirby, M C Parkinson

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Journal of clinical pathology, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 73 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Inflammation and preneoplastic lesions in benign prostate as risk factors for prostate cancer.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2012
    Article
  7. Article
  8. Article
  9. Inflammation in prostate carcinogenesis.Nature reviews. Cancer · 2007
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Does screening for prostate cancer identify clinically important disease?Annals of the Royal College of Surgeons of England · 1999
    Article
  15. 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

5 authors at 1 institution in 1 country.

M R FeneleyDepartment of Urology, St Bartholomew's Hospital, London.
M P Young
C Chinyama
R S Kirby
M C Parkinson
St Bartholomew's Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo assess cell proliferation in early prostate cancer and associated pathological lesions.

methodsUsing the Ki-67 antibody, the cell proliferation index was measured in early stage prostatic carcinoma in 37 incidental tumours diagnosed at transurethral prostatectomy (TURP) and in 20 low volume cancers treated by radical prostatectomy. Proliferation indexes have also been measured in areas of normal peripheral zone, transition zone hyperplasia, atrophic appearing lobules, and high grade prostatic intraepithelial neoplasia in the radical prostatectomy cases.

resultsIn the TURP series the proliferation index correlated with grade and stage. Logistic regression analysis, however, showed that Gleason grade was the most reliable predictor of biopsy proven residual disease and clinical progression. In the radical series transition zone carcinoma the proliferation index was half that of peripheral zone carcinoma. The atrophic lobules also showed a high proliferation index of the same order as seen in the peripheral zone carcinoma. Normal peripheral zone showed the lowest proliferation index and in hyperplastic transition zone it was also less than the other areas.

conclusionsThere is only limited support for the correlation of proliferation index with grade in early stage prostatic carcinoma. The findings do not suggest that proliferation index adds to the prognostic information given by grade and stage in pT1 disease. The significant difference in proliferation index in transition zone and peripheral zone carcinomas supports the morphological distinction of these tumour types and is consistent with differences in biological behaviour. The high proliferation index in lobules considered morphologically atrophic is reminiscent of previous observations in which carcinoma was spatially associated with atrophy.

Indexed as

AdenocarcinomaAgedAged, 80 and overCell DivisionHumansImmunohistochemistryKi-67 AntigenLogistic ModelsMaleMiddle AgedPredictive Value of TestsProstatectomyProstatic NeoplasmsKi-67 Antigen

Identifiers

PMID9038759
PMCPMC500724
OpenAlexW2033286028

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.