Evidence map›Paper›PMID 30501041›Full record

ArticleDiagnostics (Basel, Switzerland)2018

A Pilot Study to Non-Invasively Track PIK3CA Mutation in Head and Neck Cancer.

Henri Schmidt, Arutha Kulasinghe, Richard J N Allcock, Lit Yeen Tan, Elisa Mokany, Liz Kenny, Chamindie Punyadeera

Open access · goldAbstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2018. 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
0.9field-weighted citation impact, top 31% 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, 26 citations in OpenAlex.

  1. Detection ofBiomolecules · 2021
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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

7 authors at 3 institutions in 2 countries.

Henri SchmidtThe School of Biomedical Sciences, Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove 4059, Queensland, Australia. henri.schmidt@connect.qut.edu.au.
Arutha KulasingheThe School of Biomedical Sciences, Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove 4059, Queensland, Australia. arutha.kulasinghe@qut.edu.au.ORCID 0000-0003-3224-7350
Richard J N AllcockSchool of Biomedical sciences, The University of Western Australia, Nedlands 6009, Western Australia, Australia. richard.allcock@uwa.edu.au.
Lit Yeen TanSpeeDx Pty. Ltd., National Innovation Centre, Australian Technology Park, Eveleigh Sydney 2015, New South Wales, Australia. littyt@speedx.com.au.
Elisa MokanySpeeDx Pty. Ltd., National Innovation Centre, Australian Technology Park, Eveleigh Sydney 2015, New South Wales, Australia. elisam@speedx.com.au.
Liz KennyCentral Integrated Regional Cancer Service, Royal Brisbane and Women's Hospital, Herston 4029, Queensland, Australia. lizkenny@bigpond.net.au.
Chamindie PunyadeeraThe School of Biomedical Sciences, Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove 4059, Queensland, Australia. chamindie.punyadeera@qut.edu.au.
Translational Research Institute · AURoyal Brisbane and Women's Hospital · AUThe University of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPIK3CA pathways are the most frequently mutated oncogenic pathway in head and neck squamous cell carcinoma (HNSCC), including virally driven HNCs. PIK3CA is involved in the PI3K-PTEN-mTOR signalling pathway. PIK3CA has been implicated in HNSCC progression and PIK3CA mutations may serve as predictive biomarkers for therapy selection. Circulating tumour DNA (ctDNA) derived from necrotic and apoptotic tumour cells are thought to harbour tumour-specific genetic alterations. As such, the detection of PIK3CA alterations detected by ctDNA holds promise as a potential biomarker in HNSCC.

methodsBlood samples from treatment naïve HNSCC patients (

resultsIn this pilot, cross sectional study, PIK3CA E545K mutation was detected in the plasma samples of 9/29 HNSCC patients using the Plex-PCR

conclusionThe results of this pilot study support the notion of using allele-specific technologies for cost-effective testing of ctDNA, and further assert the potential utility of ctDNA in HNSCC.

Indexed as

circulating tumour (ctDNA), liquid biopsiesdiagnosishead and neck cancershead and neck squamous cell carcinomamonitoring

Identifiers

PMID30501041
PMCPMC6315660
OpenAlexW2902959182

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.