Evidence map›Paper›PMID 28860339›Full record

ArticleHaematologica2017

Treatment outcome in a population-based, 'real-world' cohort of patients with chronic myeloid leukemia.

Inge G P Geelen, Noortje Thielen, Jeroen J W M Janssen, Mels Hoogendoorn, Tanja J A Roosma, Sten P Willemsen, Otto Visser, Jan J Cornelissen, Peter E Westerweel

Abstract read
In one paragraph

Article in Haematologica, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing 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.

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

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

  1. Patient-reported toxicity symptoms during tyrosine kinase inhibitor treatment in chronic myeloid leukemia: a systematic review and meta-analysis.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2025
    Pooled it
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  11. Evaluation of real-world versus clinical trial outcomes of tyrosine kinase inhibitor therapy for chronic myeloid leukemia.Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners · 2024
    Review
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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

9 authors.

Inge G P GeelenDepartment of Hematology, Albert Schweitzer Hospital, Dordrecht, the Netherlands.
Noortje ThielenDepartment of Hematology, VU University Medical Center, Amsterdam, the Netherlands.
Jeroen J W M JanssenDepartment of Hematology, VU University Medical Center, Amsterdam, the Netherlands.
Mels HoogendoornDepartment of Hematology, Medical Center Leeuwarden, the Netherlands.
Tanja J A RoosmaDepartment of Hematology, VU University Medical Center, Amsterdam, the Netherlands.
Sten P WillemsenDepartment of Biostatistics, Albert Schweitzer Hospital, Dordrecht, the Netherlands.
Otto VisserNetherlands Comprehensive Cancer Organisation (IKNL), Utrecht, the Netherlands.
Jan J CornelissenDepartment of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Peter E WesterweelDepartment of Hematology, Albert Schweitzer Hospital, Dordrecht, the Netherlands p.e.westerweel@asz.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evaluations of the 'real-world' efficacy and safety of tyrosine kinase inhibitors in patients with chronic myeloid leukemia are scarce. A nationwide, population-based, chronic myeloid leukemia registry was analyzed to evaluate (deep) response rates to first and subsequent treatment lines and eligibility for a treatment cessation attempt in adults diagnosed between January 2008 and April 2013 in the Netherlands. The registry covered 457 patients; 434 in chronic phase (95%) and 15 (3%) in advanced disease phase. Seventy-five percent of the patients in chronic phase were treated with imatinib and 25% with a second-generation tyrosine kinase inhibitor. At 3 years 44% of patients had discontinued their first-line treatment, mainly due to intolerance (21%) or treatment failure (19%). At 18 months 73% of patients had achieved a complete cytogenetic response and 63% a major molecular response. Deep molecular responses (MR

Indexed as

AdultAgedAntineoplastic Combined Chemotherapy ProtocolsCohort StudiesComorbidityDisease ProgressionDrug SubstitutionFemaleHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMaleMiddle AgedMolecular Targeted TherapyMortalityNetherlandsProtein Kinase InhibitorsProtein Kinase Inhibitors

Identifiers

PMID28860339
PMCPMC5664388

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.