Evidence map›Paper›PMID 29705200›Full record

ArticleBiochimica et biophysica acta. General subjects2018

Thermal liquid biopsy for monitoring melanoma patients under surveillance during treatment: A pilot study.

Adrian Velazquez-Campoy, Sonia Vega, Oscar Sanchez-Gracia, Angel Lanas, Alberto Rodrigo, Alagammai Kaliappan, Melissa Barousse Hall, Taylor Q Nguyen, Guy N Brock, Jason A Chesney and 2 more

Abstract read
In one paragraph

Article in Biochimica et biophysica acta. General subjects, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 30 citations in OpenAlex.

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  13. Liquid biopsy: early and accurate diagnosis of brain tumor.Journal of cancer research and clinical oncology · 2022
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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

12 authors at 4 institutions in 2 countries.

Adrian Velazquez-CampoyInstitute of Biocomputation and Physics of Complex Systems (BIFI), Joint Units IQFR-CSIC-BIFI, and GBsC-CSIC-BIFI, Universidad de Zaragoza, Zaragoza 50018, Spain; Department of Biochemistry and Molecular and Cell Biology, Universidad de Zaragoza, Zaragoza 50009, Spain; Aragon Institute for Health Research (IIS Aragon), Zaragoza, 50009, Spain; Centro de Investigación Biomédica en Red en el Área Temática de Enfermedades Hepáticas y Digestivas (CIBERehd), Madrid, Spain; Fundacion ARAID, Government of Aragon, Zaragoza 50018, Spain. Electronic address: adrianvc@unizar.es.
Sonia VegaInstitute of Biocomputation and Physics of Complex Systems (BIFI), Joint Units IQFR-CSIC-BIFI, and GBsC-CSIC-BIFI, Universidad de Zaragoza, Zaragoza 50018, Spain.
Oscar Sanchez-GraciaEnrique Val, Zaragoza 50011, Spain.
Angel LanasAragon Institute for Health Research (IIS Aragon), Zaragoza, 50009, Spain; Centro de Investigación Biomédica en Red en el Área Temática de Enfermedades Hepáticas y Digestivas (CIBERehd), Madrid, Spain; Servicio de Aparato Digestivo, Hospital Clínico Universitario Lozano Blesa, Zaragoza, 50009, Spain; Department of Medicine, University of Zaragoza, Spain.
Alberto RodrigoDepartment of Medicine, University of Zaragoza, Spain.
Alagammai KaliappanJames Graham Brown Cancer Center, Department of Medicine, University of Louisville, Louisville, KY 40202, USA.
Melissa Barousse HallJames Graham Brown Cancer Center, Department of Medicine, University of Louisville, Louisville, KY 40202, USA.
Taylor Q NguyenJames Graham Brown Cancer Center, Department of Medicine, University of Louisville, Louisville, KY 40202, USA.
Guy N BrockDepartment of Biomedical Informatics, College of Medicine, The Ohio State University, Columbus, OH 43210, USA.
Jason A ChesneyJames Graham Brown Cancer Center, Department of Medicine, University of Louisville, Louisville, KY 40202, USA.
Nichola C GarbettJames Graham Brown Cancer Center, Department of Medicine, University of Louisville, Louisville, KY 40202, USA. Electronic address: nichola.garbett@louisville.edu.
Olga AbianInstitute of Biocomputation and Physics of Complex Systems (BIFI), Joint Units IQFR-CSIC-BIFI, and GBsC-CSIC-BIFI, Universidad de Zaragoza, Zaragoza 50018, Spain; Department of Biochemistry and Molecular and Cell Biology, Universidad de Zaragoza, Zaragoza 50009, Spain; Aragon Institute for Health Research (IIS Aragon), Zaragoza, 50009, Spain; Centro de Investigación Biomédica en Red en el Área Temática de Enfermedades Hepáticas y Digestivas (CIBERehd), Madrid, Spain; Instituto Aragonés de Ciencias de la Salud (IACS), Zaragoza 50009, Spain. Electronic address: oabifra@unizar.es.
University of Louisville · USUniversidad de Zaragoza · ESInstituto de Investigación Sanitaria Aragón · ESThe Ohio State University · US

Funding

Enhanced diagnostic assessment in lupus using differential scanning calorimetryR01AI129959 · NIAID · UNIVERSITY OF LOUISVILLE · PI GARBETT, NICHOLA C. · 2017 to 2021
$1.8M
Plasma DSC for early detection of disease and therapeutic efficacy in melanomaR21CA187345 · NCI · UNIVERSITY OF LOUISVILLE · PI GARBETT, NICHOLA C. · 2014 to 2015
$359k
NCI NIH HHS R21 CA187345NIAID NIH HHS R01 AI129959
6 · The paper itself

Abstract

backgroundDifferential Scanning Calorimetry (DSC) is a technique traditionally used to study thermally induced macromolecular transitions, and it has recently been proposed as a novel approach for diagnosis and monitoring of several diseases. We report a pilot study applying Thermal Liquid Biopsy (TLB, DSC thermograms of plasma samples) as a new clinical approach for diagnostic assessment of melanoma patients.

methodsMultiparametric analysis of DSC thermograms of patient plasma samples collected during treatment and surveillance (63 samples from 10 patients) were compared with clinical and diagnostic imaging assessment to determine the utility of thermograms for diagnostic assessment in melanoma. Nine of the ten patients were stage 2 or 3 melanoma subjects receiving adjuvant therapy after surgical resection of their melanomas. The other patient had unresectable stage 4 melanoma and was treated with immunotherapy. Two reference groups were used: (A) 36 healthy subjects and (B) 13 samples from 8 melanoma patients who had completed successful surgical management of their disease and were determined by continued clinical assessment to have no evidence of disease.

resultsPlasma thermogram analysis applied to melanoma patients generally agrees with clinical evaluation determined by physical assessment or diagnostic imaging (~80% agreement). No false negatives were obtained from DSC thermograms. Importantly, this methodology was able to detect changes in disease status before it was identified clinically.

conclusionsThermal Liquid Biopsy could be used in combination with current clinical assessment for the earlier detection of melanoma recurrence and metastasis. GENERAL SIGNIFICANCE: TLB offers advantages over current diagnostic techniques (PET/CT imaging), limited in frequency by radiation burden and expense, in providing a minimally-invasive, low-risk, low-cost clinical test for more frequent personalized patient monitoring to assess recurrence and facilitate clinical decision-making.

Indexed as

AdultCalorimetry, Differential ScanningCase-Control StudiesDifferential Thermal AnalysisFemaleHumansLiquid BiopsyMaleMelanomaMiddle AgedMonitoring, PhysiologicNeoplasm Recurrence, LocalPilot ProjectsDifferential scanning calorimetry (DSC)Early diagnostic and prognosticMelanomaNon-invasive testPatient surveillance

Identifiers

PMID29705200
PMCPMC6483604
OpenAlexW2801623920

What Socratic holds

Textmetadata
LicenceTDM
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.