Evidence map›Paper›PMID 34759042›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2022

Longitudinal Copy-Number Alteration Analysis in Plasma Cell-Free DNA of Neuroendocrine Neoplasms is a Novel Specific Biomarker for Diagnosis, Prognosis, and Follow-up.

Gitta Boons, Timon Vandamme, Laura Mariën, Willem Lybaert, Geert Roeyen, Tim Rondou, Konstantinos Papadimitriou, Katrien Janssens, Bart Op de Beeck, Marc Simoens and 5 more

Registry-linked trialOpen access · bronzeAbstract readComment
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05255133 (A Prospective, Multicentric, Proof-of-concept Study to Evaluate the Value of Circulating Tumour DNA in Follow-up of Patients With an Advanced Gastroenteropancreatic or Lung Neuroendocrine Tumour Under Everolimus +- SSA Treatment), which is not on this map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.9field-weighted citation impact, top 7% 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.

NCT05255133 nacompletednot on this map

A Prospective, Multicentric, Proof-of-concept Study to Evaluate the Value of Circulating Tumour DNA in Follow-up of Patients With an Advanced Gastroenteropancreatic or Lung Neuroendocrine Tumour Under Everolimus +- SSA Treatment

TypeinterventionalSponsorUniversiteit AntwerpenRan2017 to 2022Enrolled22ConditionsNeuroendocrine TumorsArmsLiquid biopsies, Scans (CT, gallium-68 DOTATE/TOC/NOC PET-CT)
3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 38 citations in OpenAlex.

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  19. Neuroendocrine Tumors and Peptide Receptor Radionuclide Therapy: When Is the Right Time?Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2022
    Review
  20. Circulating tumor DNA: current challenges for clinical utility.The Journal of clinical investigation · 2022
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 2 institutions in 3 countries.

Gitta BoonsCenter for Oncological Research (CORE), Integrated Personalized and Precision Oncology Network (IPPON), University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.ORCID 0000-0001-8521-8508
Timon VandammeCenter for Oncological Research (CORE), Integrated Personalized and Precision Oncology Network (IPPON), University of Antwerp and Antwerp University Hospital, Antwerp, Belgium. Timon.Vandamme@uantwerpen.be.ORCID 0000-0003-3701-5305
Laura MariënCenter for Oncological Research (CORE), Integrated Personalized and Precision Oncology Network (IPPON), University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.ORCID 0000-0001-8838-0607
Willem LybaertNETwerk, Antwerp University Hospital, Edegem, Belgium.
Geert RoeyenNETwerk, Antwerp University Hospital, Edegem, Belgium.ORCID 0000-0003-2947-1407
Tim RondouNETwerk, Antwerp University Hospital, Edegem, Belgium.ORCID 0000-0002-9569-6746
Konstantinos PapadimitriouCenter for Oncological Research (CORE), Integrated Personalized and Precision Oncology Network (IPPON), University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.
Katrien JanssensCenter of Medical Genetics, University of Antwerp and Antwerp University Hospital, Edegem, Belgium.
Bart Op de BeeckNETwerk, Antwerp University Hospital, Edegem, Belgium.
Marc SimoensNETwerk, Antwerp University Hospital, Edegem, Belgium.
Wim DemeyNETwerk, Antwerp University Hospital, Edegem, Belgium.
Isabel DeroNETwerk, Antwerp University Hospital, Edegem, Belgium.
Guy Van CampCenter for Oncological Research (CORE), Integrated Personalized and Precision Oncology Network (IPPON), University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.
Marc PeetersCenter for Oncological Research (CORE), Integrated Personalized and Precision Oncology Network (IPPON), University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.ORCID 0000-0003-4969-2303
Ken Op de BeeckCenter for Oncological Research (CORE), Integrated Personalized and Precision Oncology Network (IPPON), University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.
Antwerp University Hospital · BEAZ Klina · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAs noninvasive biomarkers are an important unmet need for neuroendocrine neoplasms (NEN), biomarker potential of genome-wide molecular profiling of plasma cell-free DNA (cfDNA) was prospectively studied in patients with NEN. EXPERIMENTAL

designLongitudinal plasma samples were collected from patients with well-differentiated, metastatic gastroenteropancreatic and lung NEN. cfDNA was subjected to shallow whole-genome sequencing to detect genome-wide copy-number alterations (CNA) and estimate circulating tumor DNA (ctDNA) fraction, and correlated to clinicopathologic and survival data. To differentiate pancreatic NENs (PNEN) from pancreatic adenocarcinomas (PAAD) using liquid biopsies, a classification model was trained using tissue-based CNAs and validated in cfDNA.

resultsOne hundred and ninety-five cfDNA samples from 43 patients with NEN were compared with healthy control cfDNA (

conclusionsSequential genome-wide profiling of plasma cfDNA is a novel, noninvasive biomarker with high specificity for diagnosis, prognosis, and follow-up in metastatic NENs.

Indexed as

Cell-Free Nucleic AcidsPancreatic NeoplasmsBiomarkers, TumorFollow-Up StudiesHumansPrognosisBiomarkers, TumorCell-Free Nucleic Acids

Identifiers

PMID34759042
PMCPMC9401546
OpenAlexW3212011634

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.