Evidence map›Paper›PMID 27479820›Full record

ArticleHaematologica2016

Detection and prognostic value of recurrent exportin 1 mutations in tumor and cell-free circulating DNA of patients with classical Hodgkin lymphoma.

Vincent Camus, Aspasia Stamatoullas, Sylvain Mareschal, Pierre-Julien Viailly, Nasrin Sarafan-Vasseur, Elodie Bohers, Sydney Dubois, Jean Michel Picquenot, Philippe Ruminy, Catherine Maingonnat and 10 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Haematologica, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07060001 (Evaluation of the Efficacy of Hypomethylating Agent Versus Standard Intensive Chemotherapy Induction Based on 5hmC - a Novel, Blood Epigenetic Marker for Assessing Measurable Residual Disease in Patients With Acute Myeloid Leukemia), which is not on this map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
10.6field-weighted citation impact, top 1% 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.

NCT07060001 phase2not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Evaluation of the Efficacy of Hypomethylating Agent Versus Standard Intensive Chemotherapy Induction Based on 5hmC - a Novel, Blood Epigenetic Marker for Assessing Measurable Residual Disease in Patients With Acute Myeloid Leukemia

TypeinterventionalSponsorThe Methodist Hospital Research InstituteRan2026 to 2029Enrolled112ConditionsAcute Myeloid Leukemia (AML), Acute Myeloid Leukaemia (AML)Arms5hmC Biomarker, Venetoclax, Decitabine 20 mg/m²/day for 5 days, Azacitidine (AZA), Cytarabine (Ara-C)
3 · Its place in the literature

Who cites it

69 citing papers in PubMed, 118 citations in OpenAlex.

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  5. Article
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  7. Detection ofInternational journal of molecular sciences · 2025
    Article
  8. Liquid Biopsy in B and T Cell Lymphomas: From Bench to Bedside.International journal of molecular sciences · 2025
    Review
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  12. Review
  13. Article
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  20. Nuclear transport proteins: structure, function, and disease relevance.Signal transduction and targeted therapy · 2023
    Review

9 more citing papers are in PubMed but not listed here.

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

20 authors at 3 institutions in 1 country.

Vincent CamusDepartment of Hematology, Centre Henri Becquerel, Rouen, France INSERM U918, Centre Henri Becquerel, University of Rouen, Rouen, France.
Aspasia StamatoullasDepartment of Hematology, Centre Henri Becquerel, Rouen, France INSERM U918, Centre Henri Becquerel, University of Rouen, Rouen, France.
Sylvain MareschalINSERM U918, Centre Henri Becquerel, University of Rouen, Rouen, France.
Pierre-Julien ViaillyINSERM U918, Centre Henri Becquerel, University of Rouen, Rouen, France.
Nasrin Sarafan-VasseurINSERM U1079, University of Rouen, Rouen, France.
Elodie BohersINSERM U918, Centre Henri Becquerel, University of Rouen, Rouen, France.
Sydney DuboisINSERM U918, Centre Henri Becquerel, University of Rouen, Rouen, France.
Jean Michel PicquenotINSERM U918, Centre Henri Becquerel, University of Rouen, Rouen, France Department of Pathology, Centre Henri Becquerel, Rouen, France.
Philippe RuminyINSERM U918, Centre Henri Becquerel, University of Rouen, Rouen, France.
Catherine MaingonnatINSERM U918, Centre Henri Becquerel, University of Rouen, Rouen, France.
Philippe BertrandINSERM U918, Centre Henri Becquerel, University of Rouen, Rouen, France.
Marie CornicDepartment of Pathology, Centre Henri Becquerel, Rouen, France.
Valérie Tallon-SimonClinical Research Unit, Centre Henri Becquerel, Rouen, France.
Stéphanie BeckerDepartment of Nuclear Medicine and Radiology, Centre Henri Becquerel and QuantIF (Litis EA4108 - FR CNRS 3638), Rouen, France.
Liana VeresezanDepartment of Pathology, Centre Henri Becquerel, Rouen, France.
Thierry FrebourgINSERM U1079, University of Rouen, Rouen, France.
Pierre VeraDepartment of Nuclear Medicine and Radiology, Centre Henri Becquerel and QuantIF (Litis EA4108 - FR CNRS 3638), Rouen, France.
Christian BastardINSERM U918, Centre Henri Becquerel, University of Rouen, Rouen, France Department of Genetic Oncology, Centre Henri Becquerel, Rouen, France.
Hervé TillyDepartment of Hematology, Centre Henri Becquerel, Rouen, France INSERM U918, Centre Henri Becquerel, University of Rouen, Rouen, France.
Fabrice JardinDepartment of Hematology, Centre Henri Becquerel, Rouen, France INSERM U918, Centre Henri Becquerel, University of Rouen, Rouen, France fabrice.jardin@chb.unicancer.fr.
Inserm · FRCentre Henri BecquerelCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Classical Hodgkin lymphoma is one of the most common lymphomas and shares clinical and genetic features with primary mediastinal B-cell lymphoma. In this retrospective study, we analyzed the recurrent hotspot mutation of the exportin 1 (XPO1, p.E571K) gene, previously identified in primary mediastinal B-cell lymphoma, in biopsies and plasma circulating cell-free DNA from patients with classical Hodgkin lymphoma using a highly sensitive digital PCR technique. A total of 94 patients were included in the present study. This widely expressed XPO1 E571K mutation is present in one quarter of classical Hodgkin lymphoma patients (24.2%). Mutated and wild-type classical Hodgkin lymphomas were similar regarding the main clinical features. Patients with a detectable XPO1 mutation at the end of treatment displayed a tendency toward shorter progression-free survival, as compared to patients with undetectable mutation in plasma cell-free DNA (2-year progression-free survival: 57.1%, 95% confidence interval: 30.1-100% versus 2-year progression-free survival: 90.5%, 95% confidence interval: 78.8-100%, respectively, P=0.0601). To conclude, the detection of the XPO1 E571K mutation in biopsy and plasma cell-free DNA by digital PCR may be used as a novel biomarker in classical Hodgkin lymphoma for both diagnosis and minimal residual disease, and pinpoints a crucial role of XPO1 in classical Hodgkin lymphoma pathogenesis. The detection of somatic mutation in the plasma cell-free DNA of patients represents a major technological advance in the context of liquid biopsies and noninvasive management of classical Hodgkin lymphoma.

Indexed as

MutationAdultAmino Acid SubstitutionBiomarkers, TumorCell Line, TumorCodonCombined Modality TherapyDNA, NeoplasmExportin 1 ProteinFemaleHigh-Throughput Nucleotide SequencingHodgkin DiseaseHumansKaryopherinsMaleMiddle AgedBiomarkers, TumorCodonDNA, NeoplasmExportin 1 ProteinKaryopherinsReceptors, Cytoplasmic and Nuclear

Identifiers

PMID27479820
PMCPMC5060026
OpenAlexW2429689347

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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.