Evidence map›Paper›PMID 42577849›Full record

ReviewEJHaem2026

Meta-Analysis of Imatinib Resistance in Chronic Myeloid Leukemia due to BIM Gene Deletion and Single Nucleotide Polymorphisms Reveals Ethnic Variations in Prevalence.

Abhinav Bhattarai, Dimitri Kountouris, Sanjit Sah, Rachana Mehta, Ranjit Sah

Abstract readReview
In one paragraph

Review in EJHaem, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Abhinav BhattaraiIrell & Manella Graduate School of Biological Sciences Beckman Research Institute City of Hope Duarte California USA.ORCID https://orcid.org/0000-0002-2232-4124
Dimitri KountourisIrell & Manella Graduate School of Biological Sciences Beckman Research Institute City of Hope Duarte California USA.
Sanjit SahSR Sanjeevani Hospital Kalyanpur Nepal.
Rachana MehtaSR Sanjeevani Hospital Kalyanpur Nepal.
Ranjit SahBMC Health System Boston Massachusetts USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aim: Deletion and single nucleotide polymorphisms in the BIM gene have been proposed as a potential contributor of intrinsic resistance to imatinib in patients with chronic myeloid leukemia (CML). Individual studies, particularly in East Asian population, have reported higher frequency of these gene variants and have suggested higher resistance rates, however, results remain varied across other non-East Asian cohorts. We aimed to determine the pooled prevalence of BIM deletion and polymorphisms across East Asian and non-East Asian populations and to evaluate their pooled association with imatinib resistance in CML. Methods: A meta-analysis was performed using R Studio 2024.12.0. PubMed, Embase, and Scopus were searched through October 2025. Studies reporting BIM deletion or polymorphisms and imatinib treatment response outcomes in CML patients were included. Random-effects models were applied to estimate pooled prevalence and odds ratios (ORs) for resistance. Subgroup analyses were performed by ethnicity: East Asians versus non-East Asians to compare the differences in prevalence of gene variants. Results: Ten studies comprising 1,614 CML patients were included. The pooled prevalence of BIM deletion was significantly higher in East Asians (12%, 95% CI: 10%-15%) compared to non-East Asians (4%, 95% CI: 0%-11%, Conclusion: Although BIM deletion has a significantly higher prevalence in East Asian populations, pooled evidence does not support a statistically significant association with imatinib resistance. However, large, prospective, multi-ethnic studies incorporating standardized response criteria and integrated molecular profiling will be essential to clarify whether BIM genotyping holds additive value in the risk stratification for TKI resistance. Trial Registration: The authors have confirmed clinical trial registration is not applicable for this submission.

Indexed as

allo‐HSCTBIM gene deletionCMLimatinibTKI resistance

Identifiers

PMID42577849
PMCPMC13455542

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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.