Evidence map›Paper›PMID 33988316›Full record

ArticleCancer medicine2021

Relevance of treatment-free remission recommendations in chronic phase chronic leukemia patients treated with frontline tyrosine kinase inhibitors.

Gabriel Etienne, Carole Faberes, Fréderic Bauduer, Didier Adiko, François Lifermann, Corinne Dagada, Caroline Lenoir, Anna Schmitt, Emilie Klein, Marie-Pierre Fort and 12 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Cancer medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. 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

22 authors at 8 institutions in 1 country.

Gabriel EtienneDépartement d'Hématologie, Institut Bergonié, Bordeaux, France.ORCID 0000-0001-7600-4954
Carole FaberesDépartement d'Hématologie, Institut Bergonié, Bordeaux, France.
Fréderic BauduerGroupe France Intergroupe des Leucémies Myéloïdes Chroniques, Hôpital Haut-Lévêque, Pessac, France.
Didier AdikoGroupe France Intergroupe des Leucémies Myéloïdes Chroniques, Hôpital Haut-Lévêque, Pessac, France.
François LifermannService de Médecine Interne, Centre Hospitalier de Dax-Côte d'Argent, Dax, France.
Corinne DagadaService d'Oncologie-Hématologie, Centre Hospitalier de Pau, Pau, France.
Caroline LenoirService d'Hémato-Oncologie Radiothérapie, Polyclinique Bordeaux Nord Aquitaine, Bordeaux, France.
Anna SchmittDépartement d'Hématologie, Institut Bergonié, Bordeaux, France.
Emilie KleinLaboratoire d'Hématologie, Hôpital Haut Lévêque Centre Hospitalier Universitaire de Bordeaux, Pessac, France.ORCID 0000-0002-4983-5581
Marie-Pierre FortDépartement d'Hématologie, Institut Bergonié, Bordeaux, France.
Fontanet BijouDépartement d'Hématologie, Institut Bergonié, Bordeaux, France.
Beatrice TurcqInstitut National de la Santé et de la Recherche Médicale, U1218 ACTION, Université de Bordeaux, Bordeaux, France.
Fanny RobbesynLaboratoire d'Hématologie, Hôpital Haut Lévêque Centre Hospitalier Universitaire de Bordeaux, Pessac, France.
Françoise DurrieuDépartement d'Hématologie, Institut Bergonié, Bordeaux, France.
Laura VersméeDépartement d'Hématologie, Institut Bergonié, Bordeaux, France.ORCID 0000-0002-5423-0552
Samia MadeneService de Médecine Interne et Hématologie, Centre Hospitalier Intercommunal Mont-de-Marsan - Pays des Sources, Mont de Marsan, France.
Marius MoldovanHôpital de jour Hématologie-Oncologie, Centre Hospitalier de Périgueux, Périgueux, France.
Sandrine KatsahianUnité de Recherche Clinique et Centre Investigation Clinique-Epidémiologie, Hôpitaux Universitaires Paris-Ouest Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, Paris, France.
Anais Charles-NelsonUnité de Recherche Clinique et Centre Investigation Clinique-Epidémiologie, Hôpitaux Universitaires Paris-Ouest Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, Paris, France.
Axelle LascauxService Des Maladies du Sang, Hôpital Haut Lévêque Centre Hospitalier Universitaire de Bordeaux, Pessac, France.
François-Xavier MahonDépartement d'Hématologie, Institut Bergonié, Bordeaux, France.
Stéphanie DulucqGroupe France Intergroupe des Leucémies Myéloïdes Chroniques, Hôpital Haut-Lévêque, Pessac, France.
Institut Bergonié · FRCentre Hospitalier Universitaire de Bordeaux · FRUniversité de Bordeaux · FRInserm · FRCentre Hospitalier de Dax –Côte d’Argent · FRCentre Hospitalier De Pau · FRCentre Hospitalier de Valence · FRPolyclinique Bordeaux Nord Aquitaine · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTyrosine kinase inhibitors (TKI) can be safely discontinued in chronic phase chronic myeloid leukemia (CP-CML) patients who had achieved a sustained deep molecular response. Based on the results of discontinuation trials, recommendations regarding patient selection for a treatment-free remission (TFR) attempt had been proposed. The aims of this study were to evaluate the rate of patients eligible for TKI discontinuation and molecular recurrence-free survival (MRFS) after stop according to recommendations.

methodsOver a 10-year period, newly diagnosed CP-CML patients and treated with first-line TKI in the nine French participating centers were included. Eligibility to treatment discontinuation and MRFS were analyzed and compared according to selection criteria defined by recommendations and first-line treatments.

resultsFrom January 2006 to December 2015, 398 patients were considered. Among them, 73% and 27% of patients received imatinib or either second or third generation tyrosine kinase inhibitors as frontline treatment, respectively. Considering the selection criteria defined by recommendations, up to 55% of the patients were selected as optimal candidates for treatment discontinuation. Overall 95/398 (24%) discontinued treatment. MRFS was 51.8% [95% CI 41.41-62.19] at 2 years and 43.8% [31.45-56.15] at 5 years. Patients receiving frontline second-generation TKI and fulfilling the eligibility criteria suggested by recommendations had the lowest probability of molecular relapse after TKI stop when compare to others.

conclusionOne third of CP-CML patients treated with TKI frontline fulfilled the selection criteria suggested by European LeukemiaNet TFR recommendations. Meeting selection criteria and second-generation TKI frontline were associated with the highest MRFS.

Indexed as

Patient SelectionWithholding TreatmentAdultAgedAged, 80 and overFemaleFranceFusion Proteins, bcr-ablGuidelines as TopicHumansImatinib MesylateLeukemia, Myeloid, Chronic-PhaseMaleMiddle AgedProgression-Free SurvivalProtein Kinase InhibitorsFusion Proteins, bcr-ablImatinib MesylateProtein Kinase Inhibitorsmolecular recurrence-free survivalrecommendationstyrosine kinase inhibitor discontinuation

Identifiers

PMID33988316
PMCPMC8178499
OpenAlexW3161596058

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.