Evidence map›Paper›PMID 31719296›Full record

ArticleThe Indian journal of medical research2019

Diagnostic ability of real-time quantitative polymerase chain reaction versus immunohistochemistry for Ki-67 assessment in breast cancer: An Indian perspective.

Anurag Mehta, Dushyant Kumar, Prerna Chadha, Malini Goswami, Gayatri Vishwakarma, Manoj Panigrahi, Moushumi Suryavanshi, Ajit Panaych

Abstract readComparative Study
In one paragraph

Article in The Indian journal of medical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

1 citing paper in PubMed.

  1. Ki-67, an elusive marker in the prognosis of breast cancer.The Indian journal of medical research · 2019
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Anurag MehtaDepartment of Laboratory & Transfusion Services; Department of Research; Department of Molecular Diagnostics & Cell Biology, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, India.
Dushyant KumarDepartment of Molecular Diagnostics & Cell Biology, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, India.
Prerna ChadhaDepartment of Laboratory & Transfusion Services, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, India.
Malini GoswamiDepartment of Laboratory & Transfusion Services, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, India.
Gayatri VishwakarmaDepartment of Research, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, India.
Manoj PanigrahiDepartment of Molecular Diagnostics & Cell Biology, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, India.
Moushumi SuryavanshiDepartment of Molecular Diagnostics & Cell Biology, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, India.
Ajit PanaychDepartment of Laboratory & Transfusion Services, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & objectives: Breast cancer is the most common cancer of women. Inferior prognosis in some patients has been attributed to the higher proliferative capability of the tumour. Immunohistochemistry (IHC) for Ki-67, despite being a simple and cost-effective method, has not become a valid tool to evaluate this biomarker. This is ascribed to variation in pre-analytical and analytical techniques, variable expression, hotspot distribution and inter-and intra-observer inconsistency. This study was aimed at defining the analytical and clinical validity of real-time quantitative polymerase chain reaction (RT-qPCR) as an alternative to IHC evaluation. Methods: This study included a total of 109 patients with invasive breast cancers. Ki-67 IHC visual assessment was compared with the mRNA value determined by RT-qPCR. Concordance between both the methods was assessed. Receiver operating characteristic (ROC) curve analysis and Cohen's kappa value with intraclass correlation were performed. Results: The threshold value for Ki-67 by RT-qPCR obtained by ROC curve was 22.23 per cent, which was used to divide breast cancer cases into high proliferative and low proliferative groups. A significant correlation was observed between both the breast cancer groups formed using RT-qPCR threshold as well as median laboratory value of Ki-67 labelling index by IHC. Interpretation & conclusions: The study results showed a significant correlation between the two methods. While IHC is subject to technical and interpretative variability, RT-qPCR may offer a more objective alternative.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorBiopsyBreast NeoplasmsFemaleHumansImmunohistochemistryIndiaKi-67 AntigenMiddle AgedNeoplasm InvasivenessProspective StudiesReal-Time Polymerase Chain ReactionReproducibility of ResultsBiomarkers, TumorKi-67 AntigenRNA, MessengerBreast cancer - immunohistochemistry - Ki-67 - real-time quantitative polymerase chain reaction

Identifiers

PMID31719296
PMCPMC6886141

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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.