Evidence map›Paper›PMID 42026180›Full record

Trial reportLeukemia2026

ASC4OPT: asciminib treatment optimization study in patients with chronic myeloid leukemia in chronic phase previously treated with two or more tyrosine kinase inhibitors.

Andreas Hochhaus, Philipp le Coutre, Dragana Milojkovic, Dennis Dong Hwan Kim, Soo Min Lim, Carolina Pavlovsky, Thanh Nguyen, Franck Emmanuel Nicolini, Beatriz Moiraghi, Sebastian Grosicki and 13 more

Registry-linked trialAbstract readClinical Trial, Phase IIIMulticenter Study
In one paragraph

Trial report in Leukemia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04948333 (A Phase 3b, Multi-center, Open-label, Treatment Optimization Study of Oral Asciminib in Patients With Chronic Myelogenous Leukemia in Chronic Phase), which is not on this 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.

NCT04948333 phase3completednot on this map

A Phase 3b, Multi-center, Open-label, Treatment Optimization Study of Oral Asciminib in Patients With Chronic Myelogenous Leukemia in Chronic Phase (CML-CP) Previously Treated With 2 or More Tyrosine Kinase Inhibitors

TypeinterventionalSponsorNovartis PharmaceuticalsRan2021 to 2026Enrolled199ConditionsChronic Myelogenous LeukemiaArmsABL001 40mg BID, ABL001 80mg QD, ABL001 200mg QD
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

23 authors.

Andreas HochhausKlinik für Innere Medizin II, Hematology/Oncology, Universitätsklinikum Jena and Comprehensive Cancer Center Central Germany, Campus Jena, Jena, Germany. andreas.hochhaus@med.uni-jena.de.ORCID http://orcid.org/0000-0003-0626-0834
Philipp le CoutreDepartment of Oncology and Hematology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Dragana MilojkovicCentre for Haematology, Department of Immunology and Inflammation, Imperial College London, and Department of Clinical Haematology, Imperial College Healthcare NHS Trust, London, UK.
Dennis Dong Hwan KimPrincess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, ON, Canada.ORCID http://orcid.org/0000-0003-2640-4911
Soo Min LimSultanah Aminah Hospital, Johor Bahru, Malaysia.
Carolina PavlovskyFUNDALEU, Buenos Aires, Argentina.
Thanh NguyenNational Institute of Hematology and Blood Transfusion, Hanoi, Vietnam.
Franck Emmanuel NicoliniDepartment of Hematology, Centre Léon Bérard, and INSERM U1052, CRCL, Lyon, France.
Beatriz MoiraghiHospital Jose Maria Ramos Mejia, Buenos Aires, Argentina.
Sebastian GrosickiDepartment of Hematology and Cancer Prevention, Faculty of Health Sciences in Bytom, Medical University of Silesia, Katowice, Poland.ORCID http://orcid.org/0000-0003-2644-1050
Chi Dung PhuBlood Transfusion Hematology Hospital, Ho Chi Minh City, Vietnam.
Gabriel EtienneHematology Department, Institut Bergonié, Bordeaux, France.
Fernando Marco de LucasServicio de Hematología, Hospital Universitario Basurto, Osakidetza, Bilbao, Spain.
Rosa Maria Ayala DiazHaematological Malignancies Clinical Research Unit, Hospital 12 de Octubre Universidad Complutense, CNIO, CIBERONC and Spanish National Cancer Research Center (CNIO), Madrid, Spain.
Massimo BrecciaHematology, Department of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.ORCID http://orcid.org/0000-0003-1163-6162
Charles ChuahSingapore General Hospital, Singhealth Duke-NUS Medical School, Singapore, Singapore.
Roberto Abi RachedNovartis Pharma AG, Basel, Switzerland.
Himanshu PokhriyalNovartis Healthcare Pvt. Ltd., Salarpuria-Sattva Knowledge City, Hyderabad, India.ORCID http://orcid.org/0000-0002-6947-1535
Aswin IcNovartis Healthcare Pvt. Ltd., Salarpuria-Sattva Knowledge City, Hyderabad, India.
Peter SchuldNovartis Pharma AG, Basel, Switzerland.
Virginia PilipovicNovartis Pharma AG, Basel, Switzerland.
Franz AlischNovartis Pharma AG, Basel, Switzerland.
Carla Maria BoquimpaniHEMORIO, State Institute of Hematology Arthur de Siqueira Cavalcanti, Rio de Janeiro, Brazil.

Funding

Novartis N/A
6 · The paper itself

Abstract

The ASC4OPT non-comparative phase 3b study (NCT04948333) evaluates asciminib once daily (QD) or twice daily (BID) in chronic myeloid leukemia in chronic phase (CML-CP) treated with ≥2 tyrosine kinase inhibitors (TKIs). This study enrolled 169 patients not in major molecular response (MMR), with unsatisfactory response (intolerant, warning or failure) as defined by European LeukemiaNet (ELN) 2020 criteria. Patients intolerant to their most recent TKI and in MMR at baseline (n = 30) were also enrolled. The primary endpoint was the MMR rate at Week 48 for patients not in MMR at baseline. Results showed an overall MMR rate of 39.4% at Week 48 (40 mg BID, 43.4%; 80 mg QD, 35.4%) and 43.6% at Week 96 (40 mg BID, 45.8%; 80 mg QD, 41.5%) in patients not in MMR at baseline. Among 40 patients who had their asciminib dose escalated to 200 mg QD, 17.5% were in MMR at Week 96. Most patients in MMR at baseline remained in MMR at 48 and 96 weeks (93.3% and 86.7%, respectively). Safety for both dosing regimens was consistent with that of previous studies. Findings support asciminib as a potential standard of care for patients with CML-CP who have not responded optimally to prior TKI therapy.

Indexed as

Antineoplastic AgentsLeukemia, Myelogenous, Chronic, BCR-ABL PositiveLeukemia, Myeloid, Chronic-PhaseProtein Kinase InhibitorsAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedNiacinamidePyrazolesYoung AdultAntineoplastic AgentsasciminibNiacinamideProtein Kinase InhibitorsPyrazoles

Identifiers

PMID42026180
PMCPMC13233290

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Registered trials

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 OpenQuestion graph.