Evidence map›Paper›PMID 39568222›Full record

ArticleAmerican journal of hematology2025

Treatment-Free Remissions in Children With Chronic Myeloid Leukemia (CML): A Prospective Study From the Tata Memorial Hospital (TMH) Pediatric CML (pCML) Cohort.

Nirmalya Roy Moulik, Swaminathan Keerthivasagam, Gaurav Chatterjee, Jayesh Agiwale, Pallavi Rane, Chetan Dhamne, Akanksha Chichra, Shyam Srinivasan, Purvi Mohanty, Hemani Jain and 7 more

Abstract read
In one paragraph

Article in American journal of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Targeted therapies in pediatric oncology: A start.Molecular therapy. Oncology · 2026
    Review
  2. Article
  3. Review
  4. Article
  5. [How I treat pediatric chronic myeloid leukemia].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2025
    Review
  6. 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

17 authors.

Nirmalya Roy MoulikTata Memorial Hospital, Pediatric Oncology, Mumbai, India.ORCID 0000-0001-5650-3115
Swaminathan KeerthivasagamTata Memorial Hospital, Pediatric Oncology, Mumbai, India.ORCID 0000-0003-2834-3868
Gaurav ChatterjeeHomi Bhabha National Institute, Mumbai, India.ORCID 0000-0002-6505-7898
Jayesh AgiwaleTata Memorial Hospital, Pediatric Oncology, Mumbai, India.
Pallavi RaneHomi Bhabha National Institute, Mumbai, India.
Chetan DhamneTata Memorial Hospital, Pediatric Oncology, Mumbai, India.
Akanksha ChichraTata Memorial Hospital, Pediatric Oncology, Mumbai, India.
Shyam SrinivasanTata Memorial Hospital, Pediatric Oncology, Mumbai, India.ORCID 0000-0003-2587-9181
Purvi MohantyHomi Bhabha National Institute, Mumbai, India.
Hemani JainHomi Bhabha National Institute, Mumbai, India.
Dhanlaxmi ShettyHomi Bhabha National Institute, Mumbai, India.
Sweta RajpalHomi Bhabha National Institute, Mumbai, India.
Prashant TembhareHomi Bhabha National Institute, Mumbai, India.ORCID 0000-0002-9030-0415
Nikhil PatkarHomi Bhabha National Institute, Mumbai, India.ORCID 0000-0001-9234-2857
Gaurav NarulaTata Memorial Hospital, Pediatric Oncology, Mumbai, India.
Papagudi G SubramanianHomi Bhabha National Institute, Mumbai, India.
Shripad BanavaliTata Memorial Hospital, Pediatric Oncology, Mumbai, India.

Funding

The Sohn Conference FoundationThe Sohn Conference Foundation. INR 1 672 000 (Equivalent to 20 400 USD)
6 · The paper itself

Abstract

Pediatric chronic myeloid leukemia (pCML) is a rare childhood malignancy, representing 2%-3% of all childhood leukemia. Tyrosine kinase inhibitors (TKIs) have greatly improved survival but pose challenges due to their long-term effects on growth and bone health in children. We prospectively studied treatment-free remission (TFR) in 45 children with pCML in chronic phase on imatinib. Eligibility criteria were as per current NCCN guidelines, with a less stringent qPCR monitoring scheduled every 3 months. TFR was successful in 71.1% (32 out of 45) of patients after a median follow-up of 25 (range: 6-42) months. The TFR rates at 12 and 24 months were 70% and 66%, respectively. Children under 5 years had a TFR rate of 88.9%, compared to 61.8% in those over 5 years (p = 0.18). Eleven of the 13 patients who lost MMR did so within 6 months of discontinuation. The cumulative incidence of loss in MMR at 6, 12, and 24 months was 26.4%, 27%, and 33%, respectively. Ten out of 13 (76.9%) patients with discontinuation failure (DF) regained MMR within 3 (2-20) months of restarting imatinib. A significant correlation was found between higher T-regulatory cell levels at baseline and DF (p = 0.005). More than half patients showed improved bone mineral density after 2 years of TFR. Our findings suggest that high TFR rates can be attained in pCML, with added benefits for bone health. Less frequent molecular monitoring was not associated with adverse outcomes and there seems to be a role of the immune system in sustaining TFR. The study is registered in the Clinical Trials Registry-India (CTRI/2020/11/029199).

Indexed as

Imatinib MesylateLeukemia, Myelogenous, Chronic, BCR-ABL PositiveRemission InductionAdolescentAntineoplastic AgentsChildChild, PreschoolFemaleFollow-Up StudiesHumansInfantMaleProspective StudiesProtein Kinase InhibitorsAntineoplastic AgentsImatinib MesylateProtein Kinase Inhibitorsimatinib discontinuationpediatric CMLTFR in pediatric CMLTKI discontinuation

Identifiers

PMID39568222
PMCPMC11705202

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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.