Abstract
The phase 3 ENESTPath study investigated treatment-free remission (TFR) rates in patients with chronic Philadelphia chromosome-positive (Ph+) and/or BCR::ABL1+ chronic myeloid leukemia who had not achieved deep molecular response (DMR) after >2 years of imatinib treatment and were switched to nilotinib 300 mg twice daily (BID). After 24 months of treatment, patients with a stable DMR were randomized to either enter the TFR phase (Arm 1) or continue nilotinib consolidation for an additional 12 months and then enter the TFR phase if in stable DMR (Arm 2). The primary endpoint was the proportion of patients who remained in TFR (≥MR4.0 [BCR::ABL1IS ≤ 0.01%]) without molecular relapse at the end of 12 months. Of the 620 patients enrolled, 239 (38.5%) achieved stable MR4.0 and were randomized to Arm 1 (n = 120) or Arm 2 (n = 119). In the TFR phase, MR4.0 rates at 12 months (Arm 1: 31.9%, Arm 2: 37.5%; p = 0.383) and 24 months (Arm 1: 29.4%, Arm 2: 30.8%) revealed no differences in TFR success between 2 and 3 years of nilotinib. Irrespective of the consolidation duration, switching to nilotinib 300 mg BID provided the opportunity to achieve TFR if patients were unable to reach stable DMR with first-line imatinib.
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Novartis is committed to sharing with qualified external researchers access to patient-level data and supporting clinical documents from eligible studies. These requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided are anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations. The availability of this trial data is according to the criteria and process described on www.clinicalstudydatarequest.com.
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Acknowledgements
The authors thank the patients who participated in the ENESTPath clinical trial, investigators, and staff at each participating study site. The authors acknowledge the extraordinary contribution of Dr. Michele Baccarani, who sadly passed away in December 2021. The authors also thank Rajendra Sarkar and Mahmudul Khan for providing their intellectual review for this manuscript and Sanchika Agarwal and Khalid Rahman, employees of Novartis Healthcare Private Limited, Hyderabad, India, as well as Timothy Harries of Novartis Pharmaceuticals, London, UK, for medical writing assistance funded by Novartis Pharma AG, Basel, Switzerland, in accordance with the Good Publication Practice (GPP) 2022 guidelines (https://www.ismpp.org/gpp-2022).
Funding
Financial support for medical writing assistance was provided by Novartis Pharma AG. This study was funded by Novartis Pharma AG.
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DR contributed to data interpretation, drafting and approval of the final manuscript, and is accountable for all aspects of the work. SK contributed to data interpretation, drafting and approval of the final manuscript, and is accountable for all aspects of the work. PS contributed to data interpretation, drafting and approval of the final manuscript, and is accountable for all aspects of the work. JM contributed to data interpretation, drafting and approval of the final manuscript, and is accountable for all aspects of the work. AI contributed to data interpretation, drafting and approval of the final manuscript, and is accountable for all aspects of the work. AAK contributed to data interpretation, drafting and approval of the final manuscript, and is accountable for all aspects of the work. AK contributed to data interpretation, drafting and approval of the final manuscript, and is accountable for all aspects of the work. AC contributed to data interpretation, drafting and approval of the final manuscript, and is accountable for all aspects of the work. TM contributed to data interpretation, drafting and approval of the final manuscript, and is accountable for all aspects of the work. LS contributed to data interpretation, drafting and approval of the final manuscript, and is accountable for all aspects of the work. JS contributed to data interpretation, drafting and approval of the final manuscript, and is accountable for all aspects of the work. GS contributed to data interpretation, drafting and approval of the final manuscript, and is accountable for all aspects of the work. AH contributed to data interpretation, drafting and approval of the final manuscript, and is accountable for all aspects of the work. DN contributed to data interpretation, drafting and approval of the final manuscript, and is accountable for all aspects of the work. P Schuld contributed to data analysis, drafting and approval of the final manuscript, and is accountable for all aspects of the work. GR contributed to data interpretation, drafting and approval of the final manuscript, and is accountable for all aspects of the work.
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DR is on the advisory board for Novartis, Enliven, TERNS, and Ascentage Pharma and is a consultant for TERNS and Novartis. JM received research support from Novartis. AI received consulting fees from Janssen, Swixx, Takeda, Astrazeneca, Astellas, Eli Lilly, Roche; honoraria from Astrazeneca, Astellas, Eli Lilly, Roche, Sobi; travel/meeting support from AbbVie, Sobi; Is on data monitoring/ advisory board at Sobi, Bristol-Myers Squibb, Johnson & Johnson, Novartis, AbbVie, Astellas, Roche, Astrazeneca. AK declared Novartis honoraria membership on an entity’s board of directors or advisory committees, research funding, and speakers bureau. AC has served on advisory boards and has acted as a speaker for Bristol-Myers Squibb, Incyte, Novartis, and Pfizer. PS declared that he is an employee of Novartis. LS received consulting fees from Xspray Pharma Sweden. The remaining authors declare no competing financial interests.
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Rea, D., Kyrcz-Krzemien, S., Sportoletti, P. et al. Treatment-free remission after two nilotinib consolidation durations in chronic myeloid leukemia treated with imatinib: Phase 3 ENESTPath results. Leukemia 40, 553–561 (2026). https://doi.org/10.1038/s41375-025-02847-5
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DOI: https://doi.org/10.1038/s41375-025-02847-5


