Evidence map›Paper›PMID 33343995›Full record

ArticleJournal of pathology informatics2020

Computerized Image Analysis of Tumor Cell Nuclear Morphology Can Improve Patient Selection for Clinical Trials in Localized Clear Cell Renal Cell Carcinoma.

In Hwa Um, Lindesay Scott-Hayward, Monique Mackenzie, Puay Hoon Tan, Ravindran Kanesvaran, Yukti Choudhury, Peter D Caie, Min-Han Tan, Marie O'Donnell, Steve Leung and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of pathology informatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Trial
  2. 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

12 authors at 6 institutions in 2 countries.

In Hwa UmSchool of Medicine, University of St Andrews, St Andrews, Scotland.
Lindesay Scott-HaywardSchool of Mathematics and Statistics, University of St Andrews, St Andrews, Scotland.
Monique MackenzieSchool of Mathematics and Statistics, University of St Andrews, St Andrews, Scotland.
Puay Hoon TanDepartment of Pathology, Singapore General Hospital, Singapore.
Ravindran KanesvaranDivision of Medical Oncology, National Cancer Centre, Singapore.
Yukti ChoudhuryInstitute of Bioengineering and Nanotechnology, Singapore.
Peter D CaieSchool of Medicine, University of St Andrews, St Andrews, Scotland.
Min-Han TanLucence Diagnostics Pte Ltd, Singapore.
Marie O'DonnellDepartment of Pathology, Western General Hospital, Edinburgh, Scotland.
Steve LeungDepartment of Urology, Western General Hospital, Edinburgh, Scotland.
Grant D StewartDepartment of Surgery, University of Cambridge, Cambridge, England.
David J HarrisonSchool of Medicine, University of St Andrews and Lothian NHS University Hospitals, St Andrews, Scotland.
University of St Andrews · GBWestern General Hospital · GBInstitute of Bioengineering and Nanotechnology · SGNational Cancer Centre Singapore · SGSingapore General Hospital · SGUniversity of Cambridge · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClinicopathological scores are used to predict the likelihood of recurrence-free survival for patients with clear cell renal cell carcinoma (ccRCC) after surgery. These are fallible, particularly in the middle range. This inevitably means that a significant proportion of ccRCC patients who will not develop recurrent disease enroll into clinical trials. As an exemplar of using digital pathology, we sought to improve the predictive power of "recurrence free" designation in localized ccRCC patients, by precise measurement of ccRCC nuclear morphological features using computational image analysis, thereby replacing manual nuclear grade assessment. MATERIALS AND

methodsTNM 8 UICC pathological stage pT1-pT3 ccRCC cases were recruited in Scotland and in Singapore. A Leibovich score (LS) was calculated. Definiens Tissue studio® (Definiens GmbH, Munich) image analysis platform was used to measure tumor nuclear morphological features in digitized hematoxylin and eosin (H&E) images.

resultsReplacing human-defined nuclear grade with computer-defined mean perimeter generated a modified Leibovich algorithm, improved overall specificity 0.86 from 0.76 in the training cohort. The greatest increase in specificity was seen in LS 5 and 6, which went from 0 to 0.57 and 0.40, respectively. The modified Leibovich algorithm increased the specificity from 0.84 to 0.94 in the validation cohort.

conclusionsCcRCC nuclear mean perimeter, measured by computational image analysis, together with tumor stage and size, node status and necrosis improved the accuracy of predicting recurrence-free in the localized ccRCC patients. This finding was validated in an ethnically different Singaporean cohort, despite the different H and E staining protocol and scanner used. This may be a useful patient selection tool for recruitment to multicenter studies, preventing some patients from receiving unnecessary additional treatment while reducing the number of patients required to achieve adequate power within neoadjuvant and adjuvant clinical studies.

Indexed as

Clear cell renal cell carcinomacomputational image analysisLeibovich score

Identifiers

PMID33343995
PMCPMC7737492
OpenAlexW3097481303

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.