Evidence map›Paper›PMID 35615931›Full record

Trial reportHaematologica2022

Kinetics of early and late molecular recurrences after first-line imatinib cessation in chronic myeloid leukemia: updated results from the STIM2 trial.

Stéphanie Dulucq, Franck E Nicolini, Delphine Rea, Pascale Cony-Makhoul, Aude Charbonnier, Martine Escoffre-Barbe, Valérie Coiteux, Pascal Lenain, Françoise Rigal-Huguet, Jixing Liu and 20 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Haematologica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
2.2field-weighted citation impact, top 11% 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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it, 14 citations in OpenAlex.

  1. [Guideline for the diagnosis and treatment of chronic myeloid leukemia in China (2025)].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2025
    Guideline
  2. Guideline
  3. Observational
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
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  10. 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

30 authors at 17 institutions in 1 country.

Stéphanie DulucqLaboratory of Hematology, University Hospital of Bordeaux, Hôpital Haut Lévêque, Pessac, France; Groupe Fi-LMC, Centre Léon Bérard, Lyon, France. stephanie.dulucq@chu-bordeaux.fr.
Franck E NicoliniGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; INSERM U1052, Centre de Recherche de Cancérologie de Lyon, Centre Léon Bérard, Lyon, France; Hematology department, Centre Léon Bérard, Lyon, France.
Delphine ReaGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Adult Hematology Department, Hôpital Saint Louis, Paris, France.
Pascale Cony-MakhoulGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department and Clinical Investigation Center, Centre Hospitalier Annecy-Genevois, Metz-Tessy, Pringy, France.
Aude CharbonnierGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, Institut Paoli-Calmettes, Marseilles, France.
Martine Escoffre-BarbeGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, CHU de Pontchaillou, Rennes, France.
Valérie CoiteuxGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, CHU Huriez, Lille, France.
Pascal LenainGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, Institut Henri Becquerel, Rouen, France.
Françoise Rigal-HuguetGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, Institut Universitaire du Cancer, CHU de Toulouse, France.
Jixing LiuGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology and Oncology department, Centre Hospitalier de Valence, Valence, France.
Agnès Guerci-BreslerGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, CHRU Brabois, Nancy, France.
Laurence LegrosGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, Hôpital Bicêtre, Le Kremlin-Bicêtre, France.
Jean-Christophe IanottoGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, Morvan Hospital, CHU, Brest, France.
Martine GardembasGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, CHU, Angers, France.
Pascal TurlureGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, CHU Dupuytren, Limoges, France.
Viviane DubruilleGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, Hôtel Dieu, Nantes, France.
Philippe RousselotGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, Centre Hospitalier de Versailles, Le Chesnay, France.
Juliana MartiniucGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, Centre Hospitalier de Saint Brieuc, France.
Henry JardelGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, Centre Hospitalier de Bretagne, Vannes, France.
Hyacinthe Johnson-AnsahGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Institute of Normandy, CHU de la Côte de Nacre, Caën, France.
Bertrand JolyGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, CH Sud francilien, Corbeil-Essonne, France.
Tawfiq HenniGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, CHR La Réunion, France.
Emilie CayssialsGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, CHU de Poitiers, Poitiers, France.
Patricia ZunicGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, Centre Hospitalier, Saint Pierre de La Réunion, France.
Marc G BergerGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology (Biology) department, CHU Estaing, Clermont-Ferrand, France.
Bruno VillemagneGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Internal medicine and onco-hematology department, La Roche sur Yon, France.
Fanny RobbesynLaboratory of Hematology, University Hospital of Bordeaux, Hôpital Haut Lévêque, Pessac, France.
Stephane MorissetINSERM U1052, Centre de Recherche de Cancérologie de Lyon, Centre Léon Bérard, Lyon, France.
François-Xavier MahonGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, Institut Bergonié, Bordeaux, France.
Gabriel EtienneGroupe Fi-LMC, Centre Léon Bérard, Lyon, France; Hematology department, Institut Bergonié, Bordeaux, France.
Centre Léon Bérard · FRHôpital Cardiologique du Haut-Lévêque · FRHôpital Léon Bérard · FRInstitut Bergonié · FRBicêtre Hospital · FRCentre de Recherche en Cancérologie de Lyon · FRCentre hospitalier Bretagne Atlantique · FRCentre Hospitalier de Valence · FRCentre Hospitalier Sud Francilien · FRCentre Hospitalier Universitaire d'Angers · FRCentre Hospitalier Universitaire de La Réunion · FRCentre Hospitalier Universitaire de Toulouse · FRHôpital Claude Huriez · FRHôpital Dupuytren · FRInserm · FRInstitut Pprime · FRLaboratoire National Henri Becquerel · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Discontinuation of tyrosine kinase inhibitors in chronic phase chronic myeloid leukemia is feasible in clinical practice based on recently published international recommendations. Nevertheless, factors predictive of molecular recurrence have not been fully elucidated and long-term follow-up of patients enrolled in clinical studies are required in order to update knowledge on discontinuation attempts particularly in terms of the safety and durability of treatment-free remission (TFR). In the current study, we updated results from the STIM2 study in the light of the consensual criterion of molecular recurrence reported in different international recommendations. Among the 199 patients included in the perprotocol study, 108 patients lost a major molecular response. With a median follow-up of 40.8 months (5.5-111 months), the probability of treatment-free remission was 43.4% [36.3-50.4] at 5 years, 40.9% [32.8-47.3] at 7 years and 34.5% [25.6- 43.3] at 9 years. Molecular recurrence occurred between 0 to 6 months, 6 to 24 months and after 24 months in 75 patients (69%), 15 patients (14%) and 18 patients (17%), respectively. Notably, the kinetics of molecular recurrence differed significantly between these three subgroups with a median time from loss of MR4 (BCR::ABL1 IS≤0.01%) to loss of major molecular response of 1, 7 and 22 months, respectively. Predictive factors of molecular recurrence differed according to the time of occurrence of the molecular recurrence. Durations of imatinib treatment and deep molecular response as well as BCR::ABL1/ABL1 levels at cessation of tyrosine kinase inhibitor treatment, as quantified by reverse transcriptase droplet digital polymerase chain reaction, are involved in molecular recurrence occurring up to 24 months but not beyond. (ClinicalTrial. gov Identifier NCT#0134373).

Indexed as

Leukemia, Myelogenous, Chronic, BCR-ABL PositiveLeukemia, Myeloid, Chronic-PhaseFusion Proteins, bcr-ablHumansImatinib MesylateProtein Kinase InhibitorsRemission InductionStromal Interaction Molecule 2Treatment OutcomeFusion Proteins, bcr-ablImatinib MesylateProtein Kinase InhibitorsSTIM2 protein, humanStromal Interaction Molecule 2

Identifiers

PMID35615931
PMCPMC9713567
OpenAlexW4281553687

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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.