Evidence map›Paper›PMID 41496461›Full record

ArticleCancer reports (Hoboken, N.J.)2026

Predictors of Response to Imatinib Therapy and Long-Term Outcomes in Paediatric and Adolescent Patients With Chronic Myeloid Leukaemia.

Souvik Saha, Sanjeev Yadav, Manish Kumar Singh, Khaliqur Rahman, Dinesh Chandra, Ruchi Gupta, Rajesh Kashyap

Abstract read
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2026. 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. 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

7 authors.

Souvik SahaDepartment of Hematology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.ORCID 0000-0002-7971-9776
Sanjeev YadavDepartment of Hematology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
Manish Kumar SinghDepartment of Hematology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.ORCID 0000-0001-7558-2656
Khaliqur RahmanDepartment of Hematology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.ORCID 0000-0002-8285-2092
Dinesh ChandraDepartment of Hematology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
Ruchi GuptaDepartment of Hematology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
Rajesh KashyapDepartment of Hematology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.ORCID 0000-0002-6645-8052

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic myeloid leukaemia (CML) is an infrequent myeloproliferative neoplasm in the paediatric population as compared to adults. Despite vast progress in understanding the disease biology and therapy of CML-chronic phase (CML CP), the applicability of risk scoring systems in practice and prognostic factors in children remain grey areas. Hence, we tried to analyse disease characteristics, molecular response to frontline imatinib therapy and its clinical predictors along with long-term outcomes in our population. MATERIALS AND

methodsIn this study, we retrospectively analysed 104 paediatric patients aged ≤ 18 years, diagnosed with CML CP, treated at our centre between 2007 and 2024. Their baseline demographic profile, clinical characteristics, haematological parameters and molecular transcripts as diagnosed by RT-PCR were recorded. The follow-up response assessments, including haematological response, molecular response and long-term survival, were collected from medical records. Risk scores were computed and correlated with clinical outcomes.

resultsOur study included 104 paediatric patients presenting with CML CP. Splenomegaly was a universal feature with a median size of 10 cm below costal margin. The majority of patients belonged to the low-risk group according to Sokal, EUTOS and ELTS systems. Imatinib was initiated in all of them and was followed up for a median duration of 72 months. Overall, 95.2% patients achieved complete hematologic response (CHR) at 3 months. A total of 42.5% (43/101) patients achieved MMR at 12 months and 54.4% (55/101) patients achieved MMR at 18 months. Sokal scoring system and EMR at 3 months were significantly correlated with the achievement of MMR at 12 months. A total of 11 patients progressed to blast crisis and 10 patients expired in due course of the disease. The 2- and 10-year PFS was 96% and 82%, respectively. CHR at 3 months was significantly predictive of PFS. None of the scoring systems had predictive value for PFS.

conclusionThis is one of the largest reported data on Indian paediatric CML CP patients with long-term outcomes. The dynamics of adult CML, including risk scores, do not perfectly fit the scenario of paediatric patients. Hence, further studies and newer strategies are required for optimal management of paediatric CML patients.

Indexed as

Antineoplastic AgentsImatinib MesylateLeukemia, Myelogenous, Chronic, BCR-ABL PositiveProtein Kinase InhibitorsAdolescentChildChild, PreschoolFemaleFollow-Up StudiesHumansMalePrognosisRetrospective StudiesTreatment OutcomeAntineoplastic AgentsImatinib MesylateProtein Kinase Inhibitorschronic myeloid leukaemiaimatinibIndiapaediatric

Identifiers

PMID41496461
PMCPMC12775581

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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.