Evidence map›Paper›PMID 36074181›Full record

ReviewAnnals of hematology2022

Circulating tumor DNA in Hodgkin lymphoma.

Maria Maco, Kristyna Kupcova, Vaclav Herman, Iva Ondeckova, Tomas Kozak, Heidi Mocikova, Ondrej Havranek, Czech Hodgkin Lymphoma Study Group

Open access · hybridAbstract readReview
In one paragraph

Review in Annals of hematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Trial
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  9. Analysis by TeloViewCancers · 2024
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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

8 authors at 1 institution in 1 country.

Maria MacoDepartment of Hematology, University Hospital Kralovske Vinohrady, Third Faculty of Medicine, Charles University, Prague, Czech Republic.
Kristyna KupcovaBIOCEV, First Faculty of Medicine, Charles University, Prumyslova 595, 25250, Vestec, Czech Republic.
Vaclav HermanBIOCEV, First Faculty of Medicine, Charles University, Prumyslova 595, 25250, Vestec, Czech Republic.
Iva OndeckovaBIOCEV, First Faculty of Medicine, Charles University, Prumyslova 595, 25250, Vestec, Czech Republic.
Tomas KozakDepartment of Hematology, University Hospital Kralovske Vinohrady, Third Faculty of Medicine, Charles University, Prague, Czech Republic.
Heidi MocikovaDepartment of Hematology, University Hospital Kralovske Vinohrady, Third Faculty of Medicine, Charles University, Prague, Czech Republic.
Ondrej HavranekBIOCEV, First Faculty of Medicine, Charles University, Prumyslova 595, 25250, Vestec, Czech Republic. ondrej.havranek@lf1.cuni.cz.ORCID http://orcid.org/0000-0001-5826-3557
Czech Hodgkin Lymphoma Study Group
Charles University · CZ

Funding

Agentura Pro Zdravotnický Výzkum České Republiky NU22-03-00182Ministerstvo Zdravotnictví Ceské Republiky 00064165Ministerstvo Zdravotnictví Ceské Republiky MH CZ-DROUniverzita Karlova v Praze CooperatioUniverzita Karlova v Praze PRIMUS/17/MED/9; UNCE/MED/016; SVV260521
6 · The paper itself

Abstract

Somatic mutations of genes involved in NF-κB, PI3K/AKT, NOTCH, and JAK/STAT signaling pathways play an important role in the pathogenesis of Hodgkin lymphoma (HL). HL tumor cells form only about 5% of the tumor mass; however, it was shown that HL tumor-derived DNA could be detected in the bloodstream. This circulating tumor DNA (ctDNA) reflects the genetic profile of HL tumor cells and can be used for qualitative and quantitative analysis of tumor-specific somatic DNA mutations within the concept of liquid biopsy. Overall, the most frequently mutated gene in HL is STAT6; however, the exact spectrum of mutations differs between individual HL histological subtypes. Importantly, reduction of ctDNA plasma levels after initial treatment is highly correlated with prognosis. Therefore, ctDNA shows great promise as a novel tool for non-invasive tumor genome analysis for biomarker driven therapy as well as for superior minimal residual disease monitoring and treatment resistance detection. Here, we summarize the recent advancements of ctDNA analysis in HL with focus on ctDNA detection methodologies, genetic profiling of HL and its clonal evolution, and the emerging prognostic value of ctDNA.

Indexed as

Circulating Tumor DNAHodgkin DiseaseBiomarkers, TumorDNA, NeoplasmHumansMutationNF-kappa BPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktBiomarkers, TumorCirculating Tumor DNADNA, NeoplasmNF-kappa BPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktCirculating tumor DNActDNAGenomic profileHodgkin lymphomaRisk factors

Identifiers

PMID36074181
PMCPMC9546971
OpenAlexW4294991500

What OpenQuestion holds

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Registered trials

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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.