# Cytogenetic Response to Asciminib in Chronic Myeloid Leukemia With the e19a2 Micro BCR::ABL1 Transcript: A Case Report

**Authors:** Takuya Terakawa, Yasuhiro Shingai, Yoshiki Matsuoka, Yuka Amemiya, Wataru Nakahara, Yuma Tada, Sayako Yuda, Shigeo Fuji, Jun Ishikawa, Takafumi Yokota

PMC · DOI: 10.7759/cureus.83363 · Cureus · 2025-05-02

## TL;DR

A CML patient with a rare e19a2 BCR::ABL1 transcript achieved a complete cytogenetic response with asciminib after failing other treatments.

## Contribution

This case report demonstrates asciminib's effectiveness in treating CML with the rare e19a2 BCR::ABL1 transcript.

## Key findings

- A CML patient with the e19a2 transcript achieved complete cytogenetic response with asciminib.
- Asciminib may be an effective treatment option for CML patients with the e19a2 BCR::ABL1 transcript.
- This case expands the potential use of asciminib beyond the major BCR::ABL1 transcript subtype.

## Abstract

Chronic myeloid leukemia (CML) is classified into three subtypes based on the BCR breakpoint, the rarest of which is micro BCR::ABL1 (also known as e19a2 BCR::ABL1), which encodes a P230 fusion protein. CML patients with the e19a2 transcript are known to have a poor prognosis. Although second-generation tyrosine kinase inhibitors (TKIs) may be effective for this subtype, asciminib, a novel BCR::ABL1 inhibitor that specifically targets the ABL1 myristoyl pocket, has only been shown to be effective in patients with the major BCR::ABL1 transcript, with limited data on the micro BCR::ABL1 subtype. Here, we report a case of a CML patient with the e19a2 transcript who was intolerant to four TKIs but achieved complete cytogenetic response with asciminib. Our case suggests that asciminib, in addition to showing promising outcomes in CML patients with the major BCR::ABL1 transcript, is an effective treatment option for CML patients with the e19a2 micro BCR::ABL1 transcript.

## Linked entities

- **Genes:** BCR (BCR activator of RhoGEF and GTPase) [NCBI Gene 613], ABL1 (ABL proto-oncogene 1, non-receptor tyrosine kinase) [NCBI Gene 25]
- **Chemicals:** asciminib (PubChem CID 72165228)
- **Diseases:** chronic myeloid leukemia (MONDO:0011996), CML (MONDO:0011996)

## Full-text entities

- **Genes:** GOLGA4 (golgin A4) [NCBI Gene 2803] {aka CRPF46, GCP2, GOLG, MU-RMS-40.18, p230}, BCR (BCR activator of RhoGEF and GTPase) [NCBI Gene 613] {aka ALL, BCR1, CML, D22S11, D22S662, PHL}
- **Diseases:** CML (MESH:D015464)
- **Chemicals:** Asciminib (MESH:C000621806)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12127035/full.md

## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC12127035/full.md

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Source: https://tomesphere.com/paper/PMC12127035