# Asciminib in patients with newly diagnosed chronic myeloid leukemia: results from the Japanese subgroup of ASC4FIRST

**Authors:** Naoto Takahashi, Yoshikane Kikushige, Hirohisa Nakamae, Tatsunori Goto, Akihiro Tomita, Michiko Ichii, Satoshi Ito, Takanori Teshima, Keita Kirito, Takayuki Ikezoe, Kaoru Hatano, Hirokazu Tanaka, Nobuhiro Hiramoto, Ryohei Osako, Makoto Aoki, Kamel Malek, Yasunori Ueda

PMC · DOI: 10.1007/s12185-025-04014-z · International Journal of Hematology · 2025-05-26

## TL;DR

A study found that asciminib is more effective and safer than other treatments for newly diagnosed chronic myeloid leukemia in Japanese patients.

## Contribution

This paper presents the first results of asciminib's efficacy and safety in Japanese patients with newly diagnosed CML.

## Key findings

- Asciminib achieved higher major molecular response rates compared to IS-TKI in Japanese patients.
- More Japanese patients on asciminib achieved deeper molecular responses (MR4.0 and MR4.5) than those on IS-TKI.
- Asciminib had fewer severe adverse events and treatment discontinuations compared to imatinib and 2G TKI.

## Abstract

The phase III ASC4FIRST study (NCT04971226) demonstrated superior efficacy and favorable safety and tolerability for asciminib against investigator-selected tyrosine kinase inhibitors (IS-TKI) in newly diagnosed chronic myeloid leukemia (CML). Results of a subgroup analysis in Japanese patients are presented here.

Adult patients were randomized 1:1 to asciminib or IS-TKI following stratification by European Treatment and Outcome Study long-term survival risk score and prerandomization-selected TKI (imatinib and second-generation [2G] TKI strata). At week 48, major molecular response (MMR) rate in all patients and imatinib stratum (primary endpoints) were assessed along with MR4.0, MR4.5, and safety (cutoff: November 28, 2023).

In Japanese patients (asciminib, n = 21; IS-TKI, n = 17 [imatinib/2G TKI, n = 8/9]), the MMR rate was higher with asciminib (81.0%) than IS-TKI (47.1%), and versus imatinib (asciminib: 100%; imatinib: 25.0% [imatinib stratum]). More patients on asciminib than IS-TKI achieved MR4.0 (57.1% vs. 11.8%) and MR4.5 (28.6% vs. 5.9%). Fewer grade ≥ 3 adverse events (AEs; 42.9%, 50.0%, and 55.6%) and AEs leading to treatment discontinuation (0%, 37.5%, and 11.1%) occurred with asciminib than imatinib or 2G TKI.

Outcomes in Japanese patients were consistent with the ASC4FIRST overall population. Asciminib may be a therapy of choice for Japanese patients with CML.

The online version contains supplementary material available at 10.1007/s12185-025-04014-z.

## Linked entities

- **Chemicals:** asciminib (PubChem CID 72165228), imatinib (PubChem CID 5291)
- **Diseases:** chronic myeloid leukemia (MONDO:0011996), CML (MONDO:0011996)

## Full-text entities

- **Diseases:** CML (MESH:D015464)
- **Chemicals:** Asciminib (MESH:C000621806), imatinib (MESH:D000068877), IS (MESH:D007455)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12572060/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12572060/full.md

## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC12572060/full.md

---
Source: https://tomesphere.com/paper/PMC12572060