Evidence map›Paper›PMID 41126742›Full record

ArticleHaematologica2026

Children with chronic-phase chronic myeloid leukemia: characteristics and outcomes from the International Registry of Childhood CML.

Frédéric Millot, Joe De Keizer, Markus Metzler, Krzysztof Kalwak, Adalet Meral Günes, Barbara De Moerloose, Maaike Luesink, Antonio Molines Honrubia, Petr Sedlacek, Julia Yajima and 11 more

Registry-linked trialAbstract readMulticenter Study
In one paragraph

Article in Haematologica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01281735 (INTERNATIONAL STUDY of Chronic Myeloid Leukaemia), which is not on this 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.

NCT01281735 recruitingnot on this map

INTERNATIONAL STUDY of Chronic Myeloid Leukaemia (CML) Treatment and Outcomes in Children and Adolescents

TypeobservationalSponsorPoitiers University HospitalRan2011 to 2028Enrolled750ConditionsChronic Myeloid Leukemia
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. 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

21 authors.

Frédéric MillotInserm CIC 1402, University Hospital, Poitiers. f.millot@chu-poitiers.fr.
Joe De KeizerInserm CIC 1402, University Hospital, Poitiers.
Markus MetzlerPediatric Oncology and Hematology, Department of Pediatrics and Adolescent Medicine, University Hospital Erlangen.
Krzysztof KalwakDepartment of Pediatric Hematology Oncology and BMT, Wroclaw Medical University, Wroclaw.
Adalet Meral GünesPediatric Hematology and Oncology Hospital Gorukle, Nilufer/Bursa.
Barbara De MoerlooseDepartment of Pediatric Hematology-Oncology, Ghent University Hospital.
Maaike LuesinkDutch Childhood Oncology Group, Princess Maxima Center for Pediatric Oncology, Utrecht.
Antonio Molines HonrubiaCHU Insular Materno-infantil Las Palmas de Gran Canaria.
Petr SedlacekDepartment of Pediatric Hematology-Oncology, University Hospital Motol, Charles University, Prague.
Julia YajimaCentro Infantil Boldrini, Sao Paulo.
Mirella AmpatzidouDepartment of Pediatric Hematology Oncology, Aghia Sophia Children's Hospital, Athens.
Michael DworzakChildren's Cancer Research Institute and St. Anna Children's Hospital, Vienna.
Birgitte LausenDepartment of Pediatrics, Rigshospitalet, University Hospital, Copenhagen.
Marina BorisevichBelarusian Research Center for Pediatric Oncology, Hematology and Immunology, Minsk.
Chi Kong LiDepartment of Pediatrics, Prince of Wales Hospital, Hong Kong.
Alexandra KolenovaDepartment of Pediatric Oncology of University Children's Hospital, Bratislava, Slovakia.
Gordana JakovljevicDepartment of Pediatric Hematology Oncology, Children's Hospital, Zagreb, Croatia.
Roula FarahDepartment of Pediatrics, LAU Medical Center Rizk Hospital Beirut.
Lisa DurocherInserm CIC 1402, University Hospital, Poitiers.
André BaruchelDepartment of Pediatric Hematology, Robert Debre Hospital, Paris.
Meinolf SuttorpPediatric Hematology and Oncology, Medical Faculty, TU Dresden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Five hundred and thirty-five patients (median age 12.2 years; range, 8 months to 18 years; N=303 males, N=232 females) diagnosed with chronic myeloid leukemia (CML) in chronic phase were registered in the International Registry of Childhood CML (clinicaltrials gov. Identifier: NCT01281735). Clinical signs of leukostasis or bleeding were observed in 16.5% and 20% of the patients, respectively. The spleen was palpable in 76% of patients with a median of 9 cm (range, 1-32) below the costal margin. The median leukocyte count was 222x109/L (interquartile range, 95-353). First-line therapy consisted of imatinib in 482 children. Among them, 40% remained on imatinib with a median follow-up 3.8 years (95% confidence interval [CI]: 3.2- 4.3 years); 3.1% died and 3.9% progressed to advanced-phase disease. The overall survival rate at 36 months was 97.4% (95% CI: 95-99%). Progression-free survival rate at 3-years was 97.1% (95% CI: 94.9-99.2%), 91.7% (95% CI:84.5-98.3%) and 72.0% (95% CI: 59-87.9%) in the Eutos Long-Term Survival (ELTS) low-, intermediate-, and high-risk group, respectively (P log rank <0.001). Pediatric CML is characterized by bulky disease (large splenomegaly, high leukocyte counts) and the ELTS score can identify children with the poorest outcome.

Indexed as

Leukemia, Myeloid, Chronic-PhaseAdolescentChildChild, PreschoolFemaleFollow-Up StudiesHumansImatinib MesylateInfantMaleRegistriesSurvival RateTreatment OutcomeImatinib Mesylate

Identifiers

PMID41126742
PMCPMC13040177

What OpenQuestion holds

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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.