Evidence map›Paper›PMID 40778574›Full record

Trial reportHematological oncology2025

Treatment-Free Remission in Chronic Phase Chronic Myeloid Leukemia After Nilotinib De-Escalation: 96-Week Update of the DANTE Study.

Alessandra Iurlo, Massimo Breccia, Fabio Stagno, Elisabetta Abruzzese, Fabrizio Pane, Immacolata Attolico, Paolo Sportoletti, Marco Cerrano, Sara Galimberti, Barbara Scappini and 9 more

Abstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Hematological oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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

19 authors.

Alessandra IurloHematology Division, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.ORCID https://orcid.org/0000-0002-4401-0812
Massimo BrecciaHematology, Department of Translational and Precision Medicine, Policlinico Umberto I, Sapienza University, Rome, Italy.ORCID https://orcid.org/0000-0003-1163-6162
Fabio StagnoHematology Unit, AOU Policlinico "G. Martino", University of Messina, Messina, Italy.ORCID https://orcid.org/0000-0002-7947-158X
Elisabetta AbruzzeseHematology, S. Eugenio Hospital, Tor Vergata University, ASL Roma 2, Rome, Italy.ORCID https://orcid.org/0000-0001-5228-6491
Fabrizio PaneDepartment of Clinical Medicine and Surgery, Federico II University of Naples, Naples, Italy.ORCID https://orcid.org/0000-0003-2563-4125
Immacolata AttolicoDepartment of Emergency and Organ Transplantation (D.E.T.O.), University of Bari, Hematology Section, Bari, Italy.ORCID https://orcid.org/0000-0002-3527-3151
Paolo SportolettiCentro di Ricerca Emato-Oncologica (CREO), University of Perugia, Perugia, Italy.ORCID https://orcid.org/0000-0002-5630-9862
Marco CerranoHematology Unit, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza, Turin, Italy.ORCID https://orcid.org/0000-0003-1666-3100
Sara GalimbertiDepartment of Clinical and Experimental Medicine, Hematology Section, University of Pisa, Pisa, Italy.ORCID https://orcid.org/0000-0001-7899-5966
Barbara ScappiniHematology, AOU Careggi, University of Florence, Florence, Italy.ORCID https://orcid.org/0000-0002-4162-0009
Maurizio MiglinoHematology Clinic, IRCCS San Martino Hospital, Genoa, Italy.ORCID https://orcid.org/0009-0006-6577-2388
Sergio SiragusaPro.Mi.Se Department, University of Palermo, Palermo, Italy.ORCID https://orcid.org/0000-0002-1641-6508
Isabella CapodannoHematology Department, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, Reggio Emilia, Italy.ORCID https://orcid.org/0009-0009-7853-3310
Diletta ValsecchiNovartis Farma SpA, Milan, Italy.
Aurelio Pio NardozzaNovartis Farma SpA, Milan, Italy.ORCID https://orcid.org/0009-0004-2282-1990
Alessandra MistoNovartis Farma SpA, Milan, Italy.
Paola CocoNovartis Farma SpA, Milan, Italy.
Giuseppe SaglioDepartment of Clinical and Biological Sciences, University of Turin, Turin, Italy.ORCID https://orcid.org/0000-0002-1046-3514
Gianantonio RostiIRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.ORCID https://orcid.org/0000-0002-0310-4206

Funding

Novartis
6 · The paper itself

Abstract

Treatment-free remission (TFR) in chronic myeloid leukemia (CML) can be considered for patients in sustained deep molecular response (DMR) who can discontinue tyrosine kinase inhibitors (TKIs) while maintaining responses. Studies suggest that TKI de-escalation before TFR is feasible. This phase II study evaluated nilotinib de-escalation outcomes in adults with CML in chronic phase (CP) treated with first-line nilotinib for ≥ 3 years and in sustained DMR for ≥ 1 year. The study had four phases: screening, de-escalation (week 0-48), TFR (week 48-144) and follow-up. During de-escalation, patients received nilotinib 300 mg once daily, and those with sustained DMR entered TFR and discontinued nilotinib. Patients with major molecular response (MMR) but without sustained DMR continued nilotinib. At the data cut-off, 107 patients entered, and 98 (91.6%) completed de-escalation. TFR was entered by 90 patients (84.1%) with sustained DMR. At 96 weeks, 71/107 patients (66.4%) were in full TFR; 64/90 patients (71.1%) who entered TFR remained in ≥ MMR, and the median time-to-loss of MMR was not reached. During TFR, adverse events occurred in 64 patients (71.1%), including one serious event (pneumonia). Our data suggest that the de-escalation of nilotinib before a TFR attempt in CML-CP patients with sustained DMR can be a successful dose optimization strategy.

Indexed as

Leukemia, Myeloid, Chronic-PhaseProtein Kinase InhibitorsPyrimidinesAdultAgedAged, 80 and overFemaleFollow-Up StudiesHumansMaleMiddle AgedRemission InductionYoung AdultnilotinibProtein Kinase InhibitorsPyrimidineschronic myeloid leukemianilotinibsustained deep molecular responsetreatment‐free remission

Identifiers

PMID40778574
PMCPMC12333328

What OpenQuestion holds

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Registered trials

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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.