Evidence map›Paper›PMID 37141403›Full record

Trial reportThe oncologist2023

The EMA Assessment of Asciminib for the Treatment of Adult Patients With Philadelphia Chromosome-Positive Chronic Myeloid Leukemia in Chronic Phase Who Were Previously Treated With at Least Two Tyrosine Kinase Inhibitors.

C Mircea S Tesileanu, Sotirios Michaleas, Rocio Gonzalo Ruiz, Segundo Mariz, Babs O Fabriek, Paula B van Hennik, Jutta Dedorath, Bruna Dekic, Christoph Unkrig, Andreas Brandt and 4 more

Open access · goldAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in The oncologist, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 38% of its field
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

14 authors at 3 institutions in 3 countries.

C Mircea S TesileanuOncology and Hematology Office, European Medicines Agency, Amsterdam, The Netherlands.ORCID 0000-0003-3541-9242
Sotirios MichaleasOncology and Hematology Office, European Medicines Agency, Amsterdam, The Netherlands.
Rocio Gonzalo RuizOncology and Hematology Office, European Medicines Agency, Amsterdam, The Netherlands.
Segundo MarizOrphan Medicines Office, European Medicines Agency, Amsterdam, The Netherlands.
Babs O FabriekMedicines Evaluation Board, Utrecht, The Netherlands.
Paula B van HennikMedicines Evaluation Board, Utrecht, The Netherlands.
Jutta DedorathFederal Institute for Drugs and Medical Devices, Bonn, Germany.
Bruna DekicFederal Institute for Drugs and Medical Devices, Bonn, Germany.
Christoph UnkrigFederal Institute for Drugs and Medical Devices, Bonn, Germany.
Andreas BrandtFederal Institute for Drugs and Medical Devices, Bonn, Germany.
Janet KoenigCommittee for Medicinal Products for Human Use (CHMP), European Medicines Agency, Amsterdam, The Netherlands.
Harald EnzmannCommittee for Medicinal Products for Human Use (CHMP), European Medicines Agency, Amsterdam, The Netherlands.
Julio DelgadoOncology and Hematology Office, European Medicines Agency, Amsterdam, The Netherlands.ORCID 0000-0002-5157-4376
Francesco PignattiOncology and Hematology Office, European Medicines Agency, Amsterdam, The Netherlands.
European Medicines Agency · NLFederal Institute for Drugs and Medical Devices · DEMedicines Evaluation Board · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Asciminib is an allosteric high-affinity tyrosine kinase inhibitor (TKI) of the BCR-ABL1 protein kinase. This kinase is translated from the Philadelphia chromosome in chronic myeloid leukemia (CML). Marketing authorization for asciminib was granted on August 25, 2022 by the European Commission. The approved indication was for patients with Philadelphia chromosome-positive CML in the chronic phase which have previously been treated with at least 2 TKIs. Clinical efficacy and safety of asciminib were evaluated in the open-label, randomized, phase III ASCEMBL study. The primary endpoint of this trial was major molecular response (MMR) rate at 24 weeks. A significant difference in MRR rate was shown between the asciminib treated population and the bosutinib control group (25.5% vs. 13.2%, respectively, P = .029). In the asciminib cohort, adverse reactions of at least grade 3 with an incidence ≥ 5% were thrombocytopenia, neutropenia, increased pancreatic enzymes, hypertension, and anemia. The aim of this article is to summarize the scientific review of the application which led to the positive opinion by the European Medicines Agency's Committee for Medicinal Products for Human Use.

Indexed as

Antineoplastic AgentsLeukemia, Myelogenous, Chronic, BCR-ABL PositiveAdultDrug Resistance, NeoplasmFusion Proteins, bcr-ablHumansNiacinamidePhiladelphia ChromosomeProtein Kinase InhibitorsPyrazolesTyrosine Kinase InhibitorsAntineoplastic AgentsasciminibFusion Proteins, bcr-ablNiacinamideProtein Kinase InhibitorsPyrazolesTyrosine Kinase InhibitorsasciminibBCR-ABL1chronic myeloid leukemiaEMAtyrosine kinase inhibitor

Identifiers

PMID37141403
PMCPMC10322123
OpenAlexW4368342832

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.