Evidence map›Paper›PMID 31807475›Full record

ArticleSouth Asian journal of cancer

Droplet digital polymerase chain reaction offers an improvisation over conventional immunohistochemistry and fluorescent

Moushumi Suryavanshi, Jiten Jaipuria, Anurag Mehta, Dushyant Kumar, Manoj Kumar Panigrahi, Haristuti Verma, Mumtaz Saifi, Sanjeev Sharma, Simran Tandon, Dinesh Chandra Doval and 1 more

Open access · diamondAbstract read
In one paragraph

Article in South Asian journal of cancer. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 42% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 2 institutions in 1 country.

Moushumi SuryavanshiRajiv Gandhi Cancer Institute and Research Centre, New Delhi, India.
Jiten JaipuriaDepartment of Urogynaeoncology, Rajiv Gandhi Cancer Institute and Research Centre, New Delhi, India.
Anurag MehtaRajiv Gandhi Cancer Institute and Research Centre, New Delhi, India.
Dushyant KumarRajiv Gandhi Cancer Institute and Research Centre, New Delhi, India.
Manoj Kumar PanigrahiRajiv Gandhi Cancer Institute and Research Centre, New Delhi, India.
Haristuti VermaRajiv Gandhi Cancer Institute and Research Centre, New Delhi, India.
Mumtaz SaifiRajiv Gandhi Cancer Institute and Research Centre, New Delhi, India.
Sanjeev SharmaRajiv Gandhi Cancer Institute and Research Centre, New Delhi, India.
Simran TandonAmity Institute of Molecular Medicine and Stem Cell Research, Amity University, Noida, Uttar Pradesh, India.
Dinesh Chandra DovalRajiv Gandhi Cancer Institute and Research Centre, New Delhi, India.
Bhudev C DasAmity Institute of Molecular Medicine and Stem Cell Research, Amity University, Noida, Uttar Pradesh, India.
Rajiv Gandhi Cancer Institute and Research Centre · INInstitute of Molecular Medicine · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDroplet digital polymerase chain reaction (DDPCR) is a recent modality for detecting Her2 expression which is quantitative, cheaper, easier to standardize, and free from interobserver variation. PURPOSE: The purpose of this study is to incorporate DDPCR in the current diagnostic paradigm with clinical benefit. MATERIALS AND

methodsFifty-four consecutive patients were tested by immunohistochemistry (IHC), fluorescent

resultsClinical benefit of DDPCR as an initial test in the test cohort was 57%, while it was 65% if used as a second-line test among those with an initial inconclusive IHC result. Sensitivity analysis in the simulation cohort revealed that if DDPCR cost was ≤0.6 times the cost of IHC, then a three-step pathway with DDPCR upfront would near certainly prove most cost beneficial. If DDPCR cost was >0.6 but ≤2 times the cost of IHC, then a three-step pathway with DDPCR as second-line test had a higher probability to prove most cost beneficial. If DDPCR cost was >2 times the cost of IHC, then conventional pathway had a higher probability to prove most cost-effective.

conclusionIncorporating DDPCR in the current clinical diagnostic paradigm has the potential to improve its cost-effectiveness and benefit.

Indexed as

Breast cancerdroplet digital polymerase chain reactionfluorescent in situ hybridizationformalin fixed paraffin embeddedHer2immunohistochemistryRNA

Identifiers

PMID31807475
PMCPMC6852626
OpenAlexW2982099890

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.