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Trial result
Chronic myeloid leukemia

Asciminib (STAMP inhibitor; ABL myristoyl-pocket) delivers rapid MR2/MR3 with low discontinuation in 1L US CML-CP RWE

Cancer type
Chronic Myelogenous Leukemia (CML)
Published in
DOUBLE ISSUE: New in Oncology - July 8, 2026

Asciminib (SCEMBLIX) is a first-in-class BCR::ABL1 “STAMP” inhibitor that binds the ABL myristoyl pocket (allosteric), here used as first-line therapy for newly diagnosed Ph+ CML-CP (no T315I) in a US retrospective physician-panel chart review (n=98; Jan–Oct 2024 starts; median follow-up 51.3 weeks). By 48 weeks, Kaplan–Meier cumulative molecular response rates were MR2 (BCR::ABL1≤1%) 91.0% (median 17.0 weeks), MMR/MR3 (≤0.1%) 70.4% (median 32.1 weeks), and MR4 (≤0.01%) 42.6% (median not reached), with 7.3% discontinuation and no discontinuations for AEs; cardiovascular AEs were uncommon (e.g., hypertension 4.1%, heart failure 3.1%, QTc prolongation 2.0%) and no progressions/deaths observed—numerically consistent with ASC4FIRST week-48 MMR 67.7% and discontinuation for AEs 4.5%, and higher than historical imatinib MMR at 12 months (40%).

Take home

If these real-world kinetics hold up with longer follow-up, asciminib’s ~70% MMR by ~1 year with very low AE-driven discontinuation could make “frontline STAMP” a pragmatic default for many US CML-CP patients—though this chart-review design (non-randomized, short follow-up) can easily underestimate rare vascular/metabolic toxicity and can’t yet speak to long-term durability, TFR eligibility, or OS.

Source: Read the original publication

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