Evidence map›Paper›PMID 34679548›Full record

ArticleDiagnostics (Basel, Switzerland)2021

Personalized First-Line Treatment of Metastatic Pancreatic Neuroendocrine Carcinoma Facilitated by Liquid Biopsy and Computational Decision Support.

Judita Szkukalek, Róbert Dóczi, Anna Dirner, Ákos Boldizsár, Ágnes Varga, Júlia Déri, Dóra Lakatos, Dóra Tihanyi, Barbara Vodicska, Richárd Schwáb and 6 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2021. 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
–field-weighted citation impact, top 83% 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

16 authors at 2 institutions in 2 countries.

Judita SzkukalekDepartment of Clinical Oncology, St. Imre Hospital, 1115 Budapest, Hungary.
Róbert DócziOncompass Medicine Hungary Ltd., 1024 Budapest, Hungary.ORCID 0000-0001-5305-8036
Anna DirnerOncompass Medicine Hungary Ltd., 1024 Budapest, Hungary.
Ákos BoldizsárOncompass Medicine Hungary Ltd., 1024 Budapest, Hungary.ORCID 0000-0002-0729-9944
Ágnes VargaOncompass Medicine Hungary Ltd., 1024 Budapest, Hungary.
Júlia DériOncompass Medicine Hungary Ltd., 1024 Budapest, Hungary.
Dóra LakatosOncompass Medicine Hungary Ltd., 1024 Budapest, Hungary.ORCID 0000-0002-6461-5800
Dóra TihanyiOncompass Medicine Hungary Ltd., 1024 Budapest, Hungary.
Barbara VodicskaOncompass Medicine Hungary Ltd., 1024 Budapest, Hungary.ORCID 0000-0003-1191-234X
Richárd SchwábOncompass Medicine Hungary Ltd., 1024 Budapest, Hungary.
Gábor PajkosOncompass Medicine Hungary Ltd., 1024 Budapest, Hungary.
Edit VárkondiOncompass Medicine Hungary Ltd., 1024 Budapest, Hungary.
István Vályi-NagyCentrum Hospital of Southern Pest, National Hematology and Infectology Institute, 1097 Budapest, Hungary.
Dorottya ValtinyiDepartment of Clinical Oncology, St. Imre Hospital, 1115 Budapest, Hungary.
Zsuzsanna NagyDepartment of Clinical Oncology, St. Imre Hospital, 1115 Budapest, Hungary.
István PetákOncompass Medicine Hungary Ltd., 1024 Budapest, Hungary.ORCID 0000-0003-0422-9286
Szent Imre Egyetemi Oktatókórház · HUSemmelweis University · HU

Funding

National Research, Development and Innovation Office 2019-1.1.1-PIACI-KFI-2019-00367
6 · The paper itself

Abstract

backgroundWe present the case of a 50-year-old female whose metastatic pancreatic neuroendocrine tumor (pNET) diagnosis was delayed by the COVID-19 pandemic. The patient was in critical condition at the time of diagnosis due to the extensive tumor burden and failing liver functions. The clinical dilemma was to choose between two registered first-line molecularly-targeted agents (MTAs), sunitinib or everolimus, or to use chemotherapy to quickly reduce tumor burden.

methodsCell-free DNA (cfDNA) from liquid biopsy was analyzed by next generation sequencing (NGS) using a comprehensive 591-gene panel. Next, a computational method, digital drug-assignment (DDA) was deployed for rapid clinical decision support.

resultsNGS analysis identified 38 genetic alterations. DDA identified 6 potential drivers, 24 targets, and 79 MTAs. Everolimus was chosen for first-line therapy based on supporting molecular evidence and the highest DDA ranking among therapies registered in this tumor type. The patient's general condition and liver functions rapidly improved, and CT control revealed partial response in the lymph nodes and stable disease elsewhere.

conclusionDeployment of precision oncology using liquid biopsy, comprehensive molecular profiling, and DDA make personalized first-line therapy of advanced pNET feasible in clinical settings.

Indexed as

cfDNAclinical decision support systemeverolimuslarge panel sequencingliquid biopsymolecular diagnosticspancreatic neuroendocrine tumorpersonalized oncology

Identifiers

PMID34679548
PMCPMC8534772
OpenAlexW3202180262

What OpenQuestion holds

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LicenceCC BY
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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.