Evidence map›Paper›PMID 37877113›Full record

ArticleTurkish journal of haematology : official journal of Turkish Society of Haematology2023

Long-term Results of Imatinib Discontinuation in Patients with Chronic-phase Chronic Myeloid Leukemia: A National Multicenter Prospective Study

Emine Merve Savaş, Seda Yılmaz, Ayşe Asena Başer Dikyar, Zübeyde Nur Özkurt, Ramazan Öcal, Ferda Can, Sezgin Pepeler, Lale Aydın Kaynar, Sanem Gökçen, Abdulkerim Yıldız and 4 more

Abstract readMulticenter Study
In one paragraph

Article in Turkish journal of haematology : official journal of Turkish Society of Haematology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. CLINICAL VALIDATION OF ANKRD36 MUTATIONS AS A NOVEL BIOMARKER FOR MONITORING EARLY PROGRESSION AND TIMELY CLINICAL INTERVENTIONS IN BLAST CRISIS CML.Journal of population therapeutics and clinical pharmacology = Journal de la therapeutique des populations et de la pharmacologie clinique · 2022
    Article
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

14 authors.

Emine Merve SavaşGazi University Faculty of Medicine, Department of Hematology, Ankara, TürkiyeORCID 0000-0001-8295-9431
Seda YılmazKonya City Hospital, Department of Hematology, Konya, TürkiyeORCID 0000-0002-7222-499X
Ayşe Asena Başer DikyarAnkara Etlik City Hospital, Clinic of Hematology, Ankara, TürkiyeORCID 0000-0002-9108-876X
Zübeyde Nur ÖzkurtGazi University Faculty of Medicine, Department of Hematology, Ankara, TürkiyeORCID 0000-0001-9834-6058
Ramazan ÖcalLiv Hospital, Clinic of Hematology, Ankara, TürkiyeORCID 0000-0002-9172-9854
Ferda CanAnkara Bilkent City Hospital, Clinic of Hematology, Ankara, TürkiyeORCID 0000-0002-9899-1441
Sezgin PepelerAnkara Bilkent City Hospital, Clinic of Hematology, Ankara, TürkiyeORCID 0000-0002-2762-8573
Lale Aydın KaynarAnkara Etlik City Hospital, Clinic of Hematology, Ankara, TürkiyeORCID 0000-0003-1539-077X
Sanem GökçenGazi University Faculty of Medicine, Department of Hematology, Ankara, TürkiyeORCID 0000-0003-3436-5086
Abdulkerim YıldızUniversity of Health Sciences Türkiye, Hitit University Çorum Erol Olçok Training and Research Hospital, Clinic of Hematology, Çorum, TürkiyeORCID 0000-0002-9596-4042
Murat AlbayrakUniversity of Health Sciences Türkiye, Dışkapı Yıldırım Beyazıt Training and Research Hospital, Clinic of Hematology, Ankara, TürkiyeORCID 0000-0003-4025-741X
Sema KarakuşBaşkent University Faculty of Medicine, Department of Hematology, Ankara, TürkiyeORCID 0000-0001-7615-4581
Özcan ÇeneliNecmettin Erbakan University Faculty of Medicine, Department of Hematology, Konya, TürkiyeORCID 0000-0003-2541-1335
Münci YağcıGazi University Faculty of Medicine, Department of Hematology, Ankara, TürkiyeORCID 0000-0002-0458-2920

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: The discovery of imatinib was a milestone for chronic myeloid leukemia (CML). As the life expectancy of CML patients has approached that of the general population, research has shifted towards improving quality of life and economic considerations. After 2010, it was shown that some patients could maintain molecular response even after discontinuing imatinib. This national multicenter prospective cohort study aimed to observe the long-term consequences of discontinuing imatinib therapy in adult chronic-phase CML patients. Materials and Methods: We enrolled 41 CML patients from 4 different centers in this non-randomized single-arm trial. Molecular responses of all patients were re-evaluated using real-time polymerase chain reaction at a single center. The median follow-up time after imatinib discontinuation was 48 months (minimum-maximum: 6-81 months). Results: The rate of molecular relapse-free survival at 48 months was 33.2% (confidence interval: 48.2-18.2). Twenty-seven of 41 patients lost their major molecular response, treatment was started again, and deep molecular response was re-achieved with imatinib in all cases. There was no significant relationship between molecular relapse and clinical factors such as duration of treatment or molecular response status. Discontinuing imatinib resulted in savings of approximately 4,392,000 Turkish lira or 245,150 US dollars. Conclusion: Tyrosine kinase inhibitor discontinuation with close molecular monitoring is a safe option and provides important national economic benefits for chronic phase CML patients. This approach should be considered for all eligible patients. This is the first tyrosine kinase inhibitor discontinuation study from Türkiye.

Indexed as

Imatinib MesylateLeukemia, Myelogenous, Chronic, BCR-ABL PositiveLeukemia, Myeloid, Chronic-PhaseAdultAntineoplastic AgentsHumansProspective StudiesProtein Kinase InhibitorsQuality of LifeRecurrenceTreatment OutcomeAntineoplastic AgentsImatinib MesylateProtein Kinase InhibitorsChronic myeloid leukemiaMolecular relapse-free survivalTreatment-free survivalTyrosine kinase inhibitor

Identifiers

PMID37877113
PMCPMC10701319

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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.