Evidence map›Paper›PMID 41751307›Full record

ReviewBiomedicines2026

Evolving Therapeutic Algorithms in Chronic Myeloid Leukemia: Integrating Efficacy, Safety, and Survivorship.

Yan Leyfman, Ahmed Hashim Azeez, Taha Kassim Dohadwala, Soumiya Nadar, Riya Vaishnav, Sumaiya Khan, Vraj JigarKumar Rangrej, Viviana Cortiana, Chandler Park

Abstract readReview
In one paragraph

Review in Biomedicines, 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

9 authors.

Yan LeyfmanNewYork Presbyterian Hospital, Brooklyn, NY 11215, USA.ORCID 0000-0002-9331-1857
Ahmed Hashim AzeezDepartment of Medicine, Tbilisi State Medical University, Tbilisi 0186, Georgia.
Taha Kassim DohadwalaDepartment of Medicine, David Tvildiani Medical University, Tbilisi 0159, Georgia.ORCID 0009-0005-3456-3148
Soumiya NadarDepartment of Medicine, Tbilisi State Medical University, Tbilisi 0186, Georgia.ORCID 0009-0000-6044-8294
Riya VaishnavDepartment of Medicine, Medical College Baroda, Vadodara 390001, Gujrat, India.ORCID 0009-0008-9026-8831
Sumaiya KhanDepartment of Medicine, Yerevan State Medical University, Yerevan 0025, Armenia.
Vraj JigarKumar RangrejDepartment of Medicine, GMERS Medical College Gotri, Vadodara 390021, Gujrat, India.ORCID 0009-0002-3356-1114
Viviana CortianaDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, 40126 Bologna, Italy.
Chandler ParkNorton Cancer Institute, Louisville, KY 40202, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic myeloid leukemia (CML) has undergone a significant shift over the past two decades, transitioning from a fatal malignancy to a chronic, highly manageable disease with near-normal life expectancy for most patients. This transformation has been driven by the development of BCR-ABL1-targeted tyrosine kinase inhibitors (TKIs), which have enabled durable disease control and deep molecular responses (DMRs) in the majority of patients with chronic-phase CML. As long-term survival outcomes have plateaued across available agents, contemporary management has shifted beyond disease suppression toward optimizing long-term safety, quality of life, and the achievement of treatment-free remission (TFR). This review summarizes current evidence on molecular monitoring strategies, the comparative efficacy and toxicity profiles of first-, second-, and third-generation TKIs, and emerging advances in response assessment. Patient-centered TKI selection is discussed in the context of cardiovascular risk, comorbidities, treatment tolerability, and survivorship goals, reflecting the growing emphasis on individualized therapy in chronic-phase CML. Molecular monitoring strategies are examined in parallel, highlighting the clinical importance of early and sustained DMRs in guiding therapeutic decisions and TFR eligibility. Although RT-qPCR remains the standard for molecular monitoring, emerging high-sensitivity techniques such as digital droplet PCR and next-generation sequencing provide complementary value by improving the detection of low-level residual disease, refining risk stratification, and enabling earlier identification of resistance. Emerging therapeutic strategies and advances in response assessment further highlight ongoing efforts to enhance the depth and durability of remission while minimizing long-term toxicity. These developments support a more precise, individualized, and outcome-driven approach to modern CML management.

Indexed as

chronic myeloid leukemiadeep molecular responsemolecular monitoringtreatment-free remissiontyrosine kinase inhibitors

Identifiers

PMID41751307
PMCPMC12938702

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.