Evidence map›Paper›PMID 41254114›Full record

Trial reportLeukemia2026

Nilotinib versus imatinib with early switch from imatinib to nilotinib to obtain treatment-free remission in newly diagnosed chronic myeloid leukemia patients: the analysis of the first co-primary endpoint.

Fausto Castagnetti, Massimo Breccia, Elisabetta Abruzzese, Renato Bassan, Gianni Binotto, Massimiliano Bonifacio, Giovanni Caocci, Isabella Capodanno, Francesco Cavazzini, Giuseppe Cimino and 20 more

Abstract readRandomized Controlled TrialComparative StudyMulticenter 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. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

30 authors.

Fausto Castagnetti *Department of Medical and Surgical Sciences, Institute of Hematology "Seràgnoli", IRCCS Azienda Ospedaliero-Universitaria di Bologna, University of Bologna, Bologna, Italy.ORCID http://orcid.org/0000-0002-0602-2628
Massimo Breccia *Department of Translational and Precision Medicine, Hematology Sapienza University, Rome, Italy.ORCID http://orcid.org/0000-0003-1163-6162
Elisabetta AbruzzeseHematology, S. Eugenio Hospital, Tor Vergata University, Rome, Italy.ORCID http://orcid.org/0000-0001-5228-6491
Renato BassanDivision of Hematology, Ospedale dell'Angelo, Mestre-Venice, Italy.ORCID http://orcid.org/0000-0001-8214-2894
Gianni BinottoDepartment of Medicine, Hematology Unit, University of Padova, Padova, Italy.
Massimiliano BonifacioDepartment of Engineering for Innovation Medicine, Section of Innovation BIomedicine, Hematology Area - University of Verona, Verona, Italy.ORCID http://orcid.org/0000-0003-0716-1686
Giovanni CaocciDepartment of Medical Sciences and Public Health, Businco Hospital, University of Cagliari, Cagliari, Italy.ORCID http://orcid.org/0000-0002-6585-5187
Isabella CapodannoSOC Ematologia Azienda USL-IRCSS di Reggio Emilia, Reggio Emilia, Italy.
Francesco CavazziniDivision of Hematology, University of Ferrara, Ferrara, Italy.
Giuseppe CiminoDepartment of Translation and Precision Medicine, University "La Sapienza", Rome, Italy.
Paola FaziGIMEMA Foundation, Data Center and Health Outcomes Research Unit, Rome, Italy.
Antonella GozziniHematology Unit, AOU Careggi, University of Florence, Florence, Italy.
Alessandra IurloHematology Division, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.ORCID http://orcid.org/0000-0002-4401-0812
Jeroen J W M JanssenDepartment of Hematology, Radboud University Medical Center, Nijmegen, The Netherlands.
Monia LunghiDivision of Hematology, Department of Translational Medicine, AOU Maggiore della Carità, Università del Piemonte Orientale, Novara, Italy.
Roberto MarascaHematology Unit, Department of Medical and Surgical Sciences, Azienda Ospedaliera Universitaria di Modena, University of Modena and Reggio Emilia, Modena, Italy.ORCID http://orcid.org/0000-0002-6431-6878
Bruno MartinoHematology Unit, Grande Ospedale Metropolitano "Bianchi-Melacrino-Morelli", Reggio Calabria, Italy.
Monica MessinaGIMEMA Foundation, Data Center and Health Outcomes Research Unit, Rome, Italy.
Francesco MurianoDepartment of Clinical Medicine and Surgery, Hematology Section, University of Naples "Federico II", Naples, Italy.ORCID http://orcid.org/0009-0001-4737-4451
Francesca PaoloniGIMEMA Data Center, Rome, Italy.
Alfonso PiciocchiGIMEMA Foundation, Data Center and Health Outcomes Research Unit, Rome, Italy.
Gianantonio RostiMedical Oncology Unit, IRST/IRCCS "Dino Amadori", Meldola, Italy.
Antonella Russo RossiHematology and Stem Cell Transplantation Unit, AOU Consorziale Policlinico, Bari, Italy.
Giuseppe SaglioDepartment of Clinical and Biological Sciences, University of Turin, Turin, Italy.ORCID http://orcid.org/0000-0002-1046-3514
Simona SicaHaematology Unit, Department of Radiological and Hematological Sciences, Università Cattolica del Sacro Cuore, Rome, Italy.ORCID http://orcid.org/0000-0003-2426-3465
Simona SoveriniDepartment of Medical and Surgical Sciences, Institute of Hematology "Seràgnoli", University of Bologna, Bologna, Italy.
Agostino TafuriDepartment of Clinical and Molecular Medicine and Hematology, Sant'Andrea - University Hospital - Sapienza, University of Rome, Rome, Italy.
Daniele VallisaCivic Hospital of Piacenza, Piacenza, Italy.
Peter E WesterweelDepartment of Internal Medicine, Albert Schweitzer Hospital, Dordrecht, The Netherlands.ORCID http://orcid.org/0000-0002-0746-7039
Fabrizio PaneDepartment of Oncology and Hematology, University Federico II of Naples, Naples, Italy. fabpane@unina.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Treatment-free remission is one of the most important goals of CML treatment but so far, the best treatment to reach this aim is still undefined, even though it is widely accepted that a sustained DMR is the prerequisite to discontinue TKI. Here we report on the depth of the molecular response, the first co-primary end point of the SUSTRENIM study, in a cohort of newly diagnosed CP-CML patients randomized 1:1 to be treated with nilotinib or with imatinib followed by switching to nilotinib in absence of optimal response. Of the 448 enrolled patients, 228 and 220 were randomized to the nilotinib (NIL) and imatinib (IM) arms, respectively, and followed for a median of 45.9 months. Eighty-two (37.2%) of the 220 patients on the IMarm did not fulfill the ELN criteria for optimal response of treatment and switched to nilotinib therapy. At the 24 months of follow-up, 107 of the 448 patients reached an MR4.5 response with a significantly higher frequency within the patients on the nilotinib arm (65 vs 42; p = 0.02). The analysis of the first primary endpoint indicates that, despite the early switch in the IM-randomized patients, NIL therapy is more effective to induce DMR.

Indexed as

Antineoplastic AgentsLeukemia, Myelogenous, Chronic, BCR-ABL PositivePiperazinesPyrimidinesAdolescentAdultAgedBenzamidesFemaleFollow-Up StudiesHumansImatinib MesylateMaleMiddle AgedProtein Kinase InhibitorsRemission InductionAntineoplastic AgentsBenzamidesImatinib MesylatenilotinibPiperazinesProtein Kinase InhibitorsPyrimidines

Identifiers

PMID41254114
PMCPMC12789014

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.