Evidence map›Paper›PMID 32241844›Full record

ArticleHaematologica2021

Diagnosis and prognosis are supported by integrated assessment of next-generation sequencing in chronic myeloid malignancies. A real-life study.

Sophie Vantyghem, Pierre Peterlin, Sylvain Thépot, Audrey Ménard, Viviane Dubruille, Camille Debord, Thierry Guillaume, Alice Garnier, Amandine Le Bourgeois, Soraya Wuilleme and 27 more

Abstract readMulticenter Study
In one paragraph

Article in Haematologica, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Review
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  9. International journal of molecular sciences · 2020
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

37 authors.

Sophie VantyghemHematology Clinic, Nantes University Hospital, Nantes
Pierre PeterlinHematology Clinic, Nantes University Hospital, Nantes
Sylvain ThépotHematology Clinic, Angers University Hospital, Angers
Audrey MénardHematology Biology, Nantes University Hospital, Nantes
Viviane DubruilleHematology Clinic, Nantes University Hospital, Nantes
Camille DebordHematology Biology, Nantes University Hospital, Nantes
Thierry GuillaumeHematology Clinic, Nantes University Hospital, Nantes
Alice GarnierHematology Clinic, Nantes University Hospital, Nantes
Amandine Le BourgeoisHematology Clinic, Nantes University Hospital, Nantes
Soraya WuillemeHematology Biology, Nantes University Hospital, Nantes
Catherine GodonHematology Biology, Nantes University Hospital, Nantes
Olivier TheisenHematology Biology, Nantes University Hospital, Nantes
Marion EveillardCRCINA, INSERM, CNRS, Université de Nantes, Université d'Angers, Pays de la Loire
Jacques DelaunayLe Confluent, Nantes
Hervé MaisonneuveHematology Clinic, Vendée Hospital Center, La Roche sur Yon
Nadine MorineauLe Confluent, Nantes
Bruno VillemagneHematology Clinic, Vendée Hospital Center, La Roche sur Yon
Stéphane VigourouxHematology Clinic, Vendée Hospital Center, La Roche sur Yon
François SubigerBiology Laboratory, Vendée Hospital Center, La Roche sur Yon
Elsa LestangHematology Clinic, Saint Nazaire Hospital, Saint Nazaire
Marion LoiratHematology Clinic, Saint Nazaire Hospital, Saint Nazaire
Anne ParcelierHematology Clinic, Bretagne Atlantique Hospital, Vannes
Pascal GodmerHematology Clinic, Bretagne Atlantique Hospital, Vannes
Mélanie MercierHematology Clinic, Bretagne Atlantique Hospital, Vannes
Adrien TrebouetHematology Clinic, Bretagne Sud Hospital, Lorient
Damien Luque PazCRCINA, INSERM, CNRS, Université de Nantes, Université d'Angers, Pays de la Loire
Ronan Le CallochHematology Clinic, Quimper Hospital, Quimper
Lenaig Le ClechHematology Clinic, Quimper Hospital, Quimper
Céline BossardPathology Department, Nantes University Hospital, Nantes, France
Anne MoreauPathology Department, Nantes University Hospital, Nantes, France
Valérie UgoCRCINA, INSERM, CNRS, Université de Nantes, Université d'Angers, Pays de la Loire
Mathilde HunaultHematology Clinic, Angers University Hospital, Angers
Philippe MoreauHematology Clinic, Nantes University Hospital, Nantes
Steven Le GouillHematology Clinic, Nantes University Hospital, Nantes
Patrice ChevallierHematology Clinic, Nantes University Hospital, Nantes
Marie C BénéCRCINA, INSERM, CNRS, Université de Nantes, Université d'Angers, Pays de la Loire
Yannick Le BrisCRCINA, INSERM, CNRS, Université de Nantes, Université d'Angers, Pays de la Loire

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Next-generation sequencing (NGS) is used to investigate the presence of somatic mutations. The utility of incorporating routine sequencing to guide diagnosis and therapeutic decisions remains unclear. We report the findings of an observational, multicenter study that aimed to assess the impact of somatic mutation testing by NGS in a reallife setting of chronic myeloid malignancies. A total of 177 patients were enrolled, partitioned into two overlapping groups. In group A (n=94), the indication was to search for clonal hematopoiesis, in a context of suspected myelodysplastic syndrome or myeloproliferative neoplasia. In group B (n=95), the theranostic impact of somatic mutations was studied. A panel of 34 genes was used on DNA extracted from blood or bone marrow samples. Within group A, the detection of clonal hematopoiesis supported the diagnosis of chronic myeloid malignancies for 31 patients while the absence of clonal hematopoiesis ruled out the suspected diagnosis in 47 patients. Within group B, NGS identified prognostically relevant somatic mutations in 32 patients, which had a therapeutic impact in 18 cases. By determining the presence or absence of somatic mutations, the application of NGS in daily practice was found to be useful for an integrated final diagnosis in 83% of the patients. Moreover, the search for somatic mutations had a prognostic impact that led to treatment modification in 19% of the cases. This study outlines the fact that adequate implementation of new investigations may have a significant positive medico-economic impact by enabling appropriate management of patients.

Indexed as

Myelodysplastic SyndromesMyeloproliferative DisordersNeoplasmsHigh-Throughput Nucleotide SequencingHumansMutationPrognosis

Identifiers

PMID32241844
PMCPMC7927891

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.