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Treatment free remission (TFR) after second-generation tyrosine kinase inhibitors (2G-TKIs) treatment in chronic myeloid leukemia (CML): from feasibility to safety.
Laganà, Alessandro; Scalzulli, Emilia; Bisegna, Maria Laura; Carmosino, Ida; Ielo, Claudia; Costa, Alessandro; Torrieri, Lorenzo; Totaro, Matteo; Martelli, Maurizio; Breccia, Massimo.
Affiliation
  • Laganà A; Hematology, Department of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.
  • Scalzulli E; Hematology, Department of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.
  • Bisegna ML; Hematology, Department of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.
  • Carmosino I; Hematology, Department of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.
  • Ielo C; Hematology, Department of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.
  • Costa A; Hematology Unit, Department of Medical Sciences and Public Health, Businco Hospital, University of Cagliari, Cagliari, Italy.
  • Torrieri L; Hematology, Department of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.
  • Totaro M; Hematology, Department of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.
  • Martelli M; Hematology, Department of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.
  • Breccia M; Hematology, Department of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.
Expert Opin Drug Saf ; 23(8): 969-979, 2024 Aug.
Article in En | MEDLINE | ID: mdl-38873693
ABSTRACT

INTRODUCTION:

Chronic myeloid leukemia (CML) prevalence is currently increasing due to the great efficacy of tyrosine kinase inhibitor (TKI) therapy. Discontinuation of treatment in the long-term, owing to avoid off-target side effects or treatment-free remission (TFR), has become an additional treatment goal in CML patients who achieved a deep molecular response (DMR). Second-generation TKIs (2 G-TKIs) have a significantly higher rate of DMR than imatinib. Hence, especially in young patients with a strategy of TFR, 2 G-TKIs are becoming the most frequently used TKIs and may increase TFR attempts in the future. AREAS COVERED In this review, the main findings extrapolated from clinical trials and real-life evidence regarding 2 G-TKIs discontinuation were discussed, through broad research on Medline, Embase, and archives from EHA and ASH congresses. EXPERT OPINION Overall, TFR rate after 2 G-TKIs is ranging from 40% to 60% for selected patients with sustained DMR and it can be considered a safe procedure, that have become, nowadays, a daily practice. However, many crucial aspects regarding treatment choices, timings, as well as predictive factors, patient communication, and optimal strategies need to be better clarified to improve successful TFR rate.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Remission Induction / Leukemia, Myelogenous, Chronic, BCR-ABL Positive / Protein Kinase Inhibitors / Antineoplastic Agents Limits: Humans Language: En Journal: Expert Opin Drug Saf Journal subject: FARMACOLOGIA / TERAPIA POR MEDICAMENTOS Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Remission Induction / Leukemia, Myelogenous, Chronic, BCR-ABL Positive / Protein Kinase Inhibitors / Antineoplastic Agents Limits: Humans Language: En Journal: Expert Opin Drug Saf Journal subject: FARMACOLOGIA / TERAPIA POR MEDICAMENTOS Year: 2024 Document type: Article Affiliation country: Country of publication: