# Therapeutic positioning of asciminib in chronic myeloid leukemia patients previously treated with multiple tyrosine kinase inhibitors in Qatar

**Authors:** Rola Ghasoub, Anas Hamad, Susanna El Akiki, Shehab Fareed, Anil Ellahie, Omar Ismael, Mohamed A. Yassin

PMC · DOI: 10.1007/s12672-025-03759-7 · Discover Oncology · 2025-10-23

## TL;DR

This paper discusses the use of asciminib as a treatment for chronic myeloid leukemia in Qatar, considering its effectiveness, safety, and cost.

## Contribution

The paper evaluates asciminib's therapeutic positioning in CML patients in Qatar, emphasizing its cardiovascular safety and cost-effectiveness.

## Key findings

- Asciminib achieves higher major molecular response rates than bosutinib.
- Asciminib has a better cardiovascular safety profile than ponatinib.
- Cost-effectiveness analyses support asciminib adoption in Qatar.

## Abstract

Chronic phase-chronic myeloid leukemia (CP-CML) in Qatar presents unique epidemiological and clinical challenges compared with those in the Western population, including nearly half of the affected patients being under 40 years of age. Additionally, the high prevalence of cardiovascular comorbidities in this region significantly influences treatment decisions. This position statement presents an evaluation of the therapeutic role of asciminib in patients previously treated with two or more tyrosine kinase inhibitors and its relevance within Qatar’s healthcare system. Studies have demonstrated asciminib’s superior efficacy in achieving higher rates of major molecular response than bosutinib. Furthermore, compared with ponatinib, asciminib offers a favorable cardiovascular safety profile, making it a preferred option for patients at risk of cardiovascular complications. Cost-effectiveness analyses further support its adoption as a viable treatment alternative in Qatar. Given these considerations, asciminib emerges as a promising therapeutic option for patients with CP-CML requiring third-line treatment, striking a balance between efficacy, safety, and economic feasibility within the local healthcare framework.

The online version contains supplementary material available at 10.1007/s12672-025-03759-7.

## Linked entities

- **Chemicals:** asciminib (PubChem CID 72165228), bosutinib (PubChem CID 5328940), ponatinib (PubChem CID 24826799)
- **Diseases:** chronic myeloid leukemia (MONDO:0011996)

## Full-text entities

- **Diseases:** chronic myeloid leukemia (MESH:D015464)
- **Chemicals:** asciminib (MESH:C000621806)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12550086/full.md

## References

13 references — full list in the complete paper: https://tomesphere.com/paper/PMC12550086/full.md

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Source: https://tomesphere.com/paper/PMC12550086