Evidence map›Paper›PMID 26626993›Full record

Trial reportBlood2016

Effect of lenalidomide treatment on clonal architecture of myelodysplastic syndromes without 5q deletion.

Virginie Chesnais, Aline Renneville, Andrea Toma, Jérôme Lambert, Marie Passet, Florent Dumont, Sylvie Chevret, Julie Lejeune, Anna Raimbault, Aspasia Stamatoullas and 10 more

Registry-linked trialAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Blood, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01718379 (A Phase II Study Evaluating the Efficacy/Safety of Lenalidomide With or Without Epoetin Beta in Transfusion-dependent ESA-resistant Patients With IPSS Low- and Intermediate-1 Risk Myelodysplastic Syndromes Without Chromosome 5 Abnormality.), which is not on this map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
–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.

NCT01718379 phase2completednot on this map

A Phase II Study Evaluating the Efficacy/Safety of Lenalidomide With or Without Epoetin Beta in Transfusion-dependent ESA-resistant Patients With IPSS Low- and Intermediate-1 Risk Myelodysplastic Syndromes Without Chromosome 5 Abnormality.

TypeinterventionalSponsorGroupe Francophone des MyelodysplasiesRan2010 to 2016Enrolled132ConditionsMyelodysplastic SyndromesArmsLenalidomide, Epoetin beta
3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. A variant erythroferrone disrupts iron homeostasis inScience translational medicine · 2019
    Trial
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  4. Review
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  15. Article
  16. Dynamics ofClinical epigenetics · 2018
    Article
  17. Article
  18. Splicing factor mutations in MDS RARS and MDS/MPN-RS-T.International journal of hematology · 2017
    Review
  19. Article
  20. Review
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.

Virginie ChesnaisAssistance Publique-Hôpitaux de Paris, Service d'Hématologie Biologique, Hôpitaux Universitaires Paris Centre, Paris, France; Institut Cochin, INSERM U1016, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 8104, Université Paris Descartes, Paris, France;
Aline RennevilleLaboratoire d'Hématologie, Centre Hospitalier Régional Universitaire de Lille, Lille, France;
Andrea TomaAssistance Publique-Hôpitaux de Paris, Service d'Hématologie Clinique, Hôpital Henri-Mondor, Créteil, France;
Jérôme LambertService de Biostatistique et d'Information Médicale, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris, Paris, France; Epidémiologie Clinique et Statistiques pour la Recherche en Santé, Unité Mixte de Recherche 1153, INSERM, Université Paris Diderot, Sorbonne Paris Cité, France;
Marie PassetAssistance Publique-Hôpitaux de Paris, Service d'Hématologie Biologique, Hôpitaux Universitaires Paris Centre, Paris, France;
Florent DumontInstitut Cochin, INSERM U1016, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 8104, Université Paris Descartes, Paris, France;
Sylvie ChevretService de Biostatistique et d'Information Médicale, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris, Paris, France; Epidémiologie Clinique et Statistiques pour la Recherche en Santé, Unité Mixte de Recherche 1153, INSERM, Université Paris Diderot, Sorbonne Paris Cité, France;
Julie LejeuneService de Biostatistique et d'Information Médicale, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris, Paris, France; Epidémiologie Clinique et Statistiques pour la Recherche en Santé, Unité Mixte de Recherche 1153, INSERM, Université Paris Diderot, Sorbonne Paris Cité, France;
Anna RaimbaultAssistance Publique-Hôpitaux de Paris, Service d'Hématologie Biologique, Hôpitaux Universitaires Paris Centre, Paris, France; Institut Cochin, INSERM U1016, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 8104, Université Paris Descartes, Paris, France;
Aspasia StamatoullasCentre de Lutte contre le Cancer Henri-Becquerel, Rouen, France;
Christian RoseService d'Hématologie, Hôpital Saint Vincent de Paul, Université Catholique de Lille, Lille, France;
Odile Beyne-RauzyService de Médecine Interne, Institut Universitaire du Cancer, Toulouse, France;
Jacques DelaunayService d'Hématologie, Centre Hospitalier Universitaire, Nantes, France;
Eric SolaryInstitut Gustave Roussy, INSERM 1009, Université Paris Sud, Villejuif, France; and.
Pierre FenauxAssistance Publique-Hôpitaux de Paris, Service d'Hématologie Senior, Hôpital Saint-Louis, Paris, France.
François DreyfusInstitut Cochin, INSERM U1016, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 8104, Université Paris Descartes, Paris, France;
Claude PreudhommeLaboratoire d'Hématologie, Centre Hospitalier Régional Universitaire de Lille, Lille, France;
Olivier KosmiderAssistance Publique-Hôpitaux de Paris, Service d'Hématologie Biologique, Hôpitaux Universitaires Paris Centre, Paris, France; Institut Cochin, INSERM U1016, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 8104, Université Paris Descartes, Paris, France;
Michaela FontenayAssistance Publique-Hôpitaux de Paris, Service d'Hématologie Biologique, Hôpitaux Universitaires Paris Centre, Paris, France; Institut Cochin, INSERM U1016, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 8104, Université Paris Descartes, Paris, France;
Groupe Francophone des Myélodysplasies

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-del(5q) transfusion-dependent low/intermediate-1 myelodysplastic syndrome (MDS) patients achieve an erythroid response with lenalidomide in 25% of cases. Addition of an erythropoiesis-stimulating agent could improve response rate. The impact of recurrent somatic mutations identified in the diseased clone in response to lenalidomide and the drug's effects on clonal evolution remain unknown. We investigated recurrent mutations by next-generation sequencing in 94 non-del(5q) MDS patients randomized in the GFM-Len-Epo-08 clinical trial to lenalidomide or lenalidomide plus epoetin β. Clonal evolution was analyzed after 4 cycles of treatment in 42 cases and reanalyzed at later time points in 18 cases. The fate of clonal architecture of single CD34(+)CD38(-) hematopoietic stem cells was also determined in 5 cases. Mutation frequency was >10%: SF3B1 (74.5%), TET2 (45.7%), DNMT3A (20.2%), and ASXL1 (19.1%). Analysis of variant allele frequencies indicated a decrease of major mutations in 15 of 20 responders compared with 10 of 22 nonresponders after 4 cycles. The decrease in the variant allele frequency of major mutations was more significant in responders than in nonresponders (P < .001). Genotyping of single CD34(+)CD38(-) cell-derived colonies showed that the decrease in the size of dominant subclones could be associated with the rise of founding clones or of hematopoietic stem cells devoid of recurrent mutations. These effects remained transient, and disease escape was associated with the re-emergence of the dominant subclones. In conclusion, we show that, although the drug initially modulates the distribution of subclones, loss of treatment efficacy coincides with the re-expansion of the dominant subclone. This trial was registered at www.clinicaltrials.gov as #NCT01718379.

Indexed as

AgedAnemia, MacrocyticAntineoplastic Combined Chemotherapy ProtocolsCell ProliferationChromosome DeletionChromosomes, Human, Pair 5Clonal EvolutionClone CellsDNA Mutational AnalysisErythropoietinFemaleHumansLenalidomideMaleMyelodysplastic SyndromesRecombinant Proteinsepoetin betaErythropoietinLenalidomideRecombinant ProteinsThalidomide

Identifiers

PMID26626993
PMCPMC4937206

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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.