Evidence map›Paper›PMID 40344674›Full record

ArticleHematological oncology2025

Real-World Efficacy Profile of Compassionate Use of Asciminib in an Italian, Multi-Resistant Chronic-Phase Chronic Myeloid Leukemia (CML-CP) Patient Population.

Massimo Breccia, Antonella Russo Rossi, Valentina Giai, Bruno Martino, Carmen Fava, Mario Annunziata, Elisabetta Abruzzese, Gianni Binotto, Claudia Baratè, Aurelio Pio Nardozza and 36 more

Abstract read
In one paragraph

Article in Hematological oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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.

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

7 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. 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

46 authors.

Massimo BrecciaDivision of Hematology, Department of Translational and Precision Medicine, Azienda Policlinico Umberto I, Sapienza University, Rome, Italy.ORCID https://orcid.org/0000-0003-1163-6162
Antonella Russo RossiHematology and Transplantation Unit, University of Bari, Bari, Italy.
Valentina GiaiDivision of Haematology, A.O.U. Città della Salute e della Scienza, Turin, Italy.
Bruno MartinoDivision of Hematology, Azienda Ospedaliera "Bianchi Melacrino Morelli", Reggio Calabria, Italy.
Carmen FavaDepartment of Clinical and Biological Sciences, University of Turin, Turin, Italy.
Mario AnnunziataHematology Unit, Cardarelli Hospital, Napoli, Italy.
Elisabetta AbruzzeseHematology Unit, S. Eugenio Hospital, ASL Roma2, Tor Vergata University, Rome, Italy.
Gianni BinottoDepartment of Medicine, Unit of Hematology and Clinical Immunology, University of Padova, Padova, Italy.
Claudia BaratèDepartment of Clinical and Experimental Medicine, UO Hematology, Azienda Ospedaliero Universitaria Pisana, University of Pisa, Pisa, Italy.
Aurelio Pio NardozzaMedical Department, Novartis, Novartis Farma SpA, Milan, Italy.
Alessandra MistoMedical Department, Novartis, Novartis Farma SpA, Milan, Italy.
Paola CocoMedical Department, Novartis, Novartis Farma SpA, Milan, Italy.
Valeria CalafioreU.O. Oncoematologia, A.O.R. Villa Sofia - Vincenzo Cervello, Palermo, Italy.
Maria Cristina CarraroUOC Hematology and Transfusion Medicine, Ospedale Luigi Sacco, Milan, Italy.
Federica CattinaOncology Unit, Hospital Crema, Crema, Italy.
Francesco CavazziniHematology Unit, University of Ferrara, Ferrara, Italy.
Maria Teresa CorsettiHematology Division, Azienda Ospedaliera Santi Antonio e Biagio e Cesare Arrigo, Alessandria, Italy.
Lara CrucittiUnità Operativa Ematologia, Azienda Sanitaria Provinciale Trapani, Presidio Ospedaliero Castelvetrano, Trapani, Italy.
Monica CrugnolaHematology Unit and BMT Center University Hospital of Parma, Parma, Italy.
Ambra Di VeroliHematology, Belcolle Hospital, Viterbo, Italy.
Paolo DitonnoHaematology Unit, National Cancer Center, IRCCS Istituto Tumori "Giovanni Paolo II", Bari, Italy.
Anna ErmacoraHaematology Unit, Azienda Ospedaliera S. Maria Angeli, Pordenone, Italy.
Felicetto FerraraUOC Ematologia, AORN "A. Cardarelli", Napoli, Italy.ORCID https://orcid.org/0000-0003-3721-5403
Angelo GenuaHematology Unit, Azienda Ospedaliera Santa Maria di Terni, Terni, Italy.
Antonella GozziniDepartment of Cellular Therapies and Transfusion Medicine, AOU Careggi, Florence, Italy.
Stefana ImperaDivision of Oncology and Hematology, ARNAS Garibaldi-Nesima, Catania, Italy.
Alessandra IurloHematology Division, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.ORCID https://orcid.org/0000-0002-4401-0812
Luciano LevatoDepartment Hematology-Oncology, Azienda Ospedaliera Universitaria "Renato Dulbecco", Catanzaro, Italy.
Luigia LucianoHematology Unit, Federico II University of Naples, Naples, Italy.ORCID https://orcid.org/0000-0003-2255-9190
Maria Cristina MiggianoHematology Department, San Bortolo Hospital, Vicenza, Italy.
Marco De GobbiDepartment of Clinical and Biological Sciences, Internal Medicine With Hematological Focus, AOU San Luigi, University of Turin, Turin, Italy.
Marco SantoroUO Hematology, University Hospital Paolo Giaccone, Palermo, Italy.ORCID https://orcid.org/0000-0003-4390-8388
Barbara ScappiniHematology Unit, Azienda Ospedaliero-Universitaria Careggi, Florence, Italy.
Anna Rita ScortechiniHematology Unit, Azienda Ospedaliero Universitaria Ospedali Riuniti Ancona, Ancona, Italy.
Andrea PatriarcaDepartment of Translational Medicine, Hematology Unit, University of Eastern Piedmont and AOU Maggiore della Carità, Novara, Italy.
Serena RosatiOspedale Nuovo Santo Stefano, Prato, Italy.
Sabina RussoDipartimento di Patologia Umana dell'Adulto e dell'Età Evolutiva, Division of Hematology, Policlinico G. Martino, University of Messina, Messina, Italy.
Rosaria SancettaHematology Unit, ULSS 3, Dell'Angelo Hospital, Venezia-Mestre, Italy.
Grazia SanpaoloDepartment of Hematology and Stem Cell Transplantation Unit, IRCCS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy.
Teresa Maria SanteramoHematology Unit, Dimiccoli Hospital, Barletta, Italy.
Silvia SibillaUO di Ematologia e trapianto, Azienda Ospedaliera Cardinale G. Panico, Tricase, Italy.
Federica SoràDipartimento di Scienze di laboratorio ed ematologiche, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.ORCID https://orcid.org/0000-0002-9607-5298
Paolo SportolettiCentro Ricerche Emato-Oncologiche, Institute of Hematology, Ospedale S. Maria della Misericordia, University of Perugia, Perugia, Italy.
Fabio StagnoHematology Unit, AOU Policlinico "G. Martino", University of Messina, Messina, Italy.
Elena TrabacchiHematology Unit and BMT Center, Ospedale G. Saliceto, Piacenza, Italy.
Fausto CastagnettiInstitute of Hematology "Seràgnoli" IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.

Funding

Novartis Farma Italy CABL001AIT01M
6 · The paper itself

Abstract

Chronic myeloid leukemia (CML) patients who have experienced failure and/or intolerance to multiple lines of treatment have limited therapeutic possibilities. Asciminib is a first-in-class tyrosine kinase inhibitor (TKI) that inhibits the ABL Myristoyl Pocket (STAMP or Specifically Targeting the ABL Myristoyl Pocket) within the BCR::ABL1 oncoprotein. This retrospective Italian analysis reports the efficacy and safety outcomes of asciminib in treating 77 CML patients in chronic phase (CML-CP) within a compassionate use setting. Patients were heavily pretreated with a median of 3 TKIs (55.8% had prior ponatinib exposure). Overall, 57.1% and 42.9% patients switched to asciminib because of resistance and intolerance, respectively. Asciminib maintained or improved molecular responses (MRs) in most patients: as best response, 41 patients (53%) achieved a MR3 or better, with 25 patients (32.5%) reaching deep molecular response (DMR). Greater percentages of intolerant patients achieved MR compared with resistant patients, although the probability of reaching at least a MR3 was not significant between the two groups (p = 0.116). Patients with the T315I mutation responded to asciminib, while ponatinib pre-treated patients showed lower MR improvements compared to naïve patients and had a lower probability to reach a MR3 versus naïve patients (p = 0.0262). These results highlight asciminib remarkable tolerability and efficacy in real-world CML-CP patient population, including heavily pretreated patients, those intolerant and resistant to previous TKIs, and presenting several comorbidities. TRAIL REGISTRATION: The identification code for the MAP is CABL001AIT01M.

Indexed as

Drug Resistance, NeoplasmLeukemia, Myeloid, Chronic-PhaseProtein Kinase InhibitorsPyrazolesAdultAgedAged, 80 and overCompassionate Use TrialsFemaleFusion Proteins, bcr-ablHumansItalyLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMaleMiddle AgedNiacinamideasciminibFusion Proteins, bcr-ablNiacinamideProtein Kinase InhibitorsPyrazolesasciminibchronic myeloid leukemia in chronic phase (CML‐CP)major molecular response (MMR)real‐worldTKI resistance/intolerancetyrosine kinase inhibitor (TKI)

Identifiers

PMID40344674
PMCPMC12064212

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.