Treatment‐free remission after dasatinib in patients with chronic myeloid leukaemia in chronic phase with deep molecular response: Final 5‐year analysis of DASFREE

达沙替尼 中止 医学 内科学 不利影响 毒品假日 慢性粒细胞白血病 外科 胃肠病学 伊马替尼 免疫学 髓系白血病 人类免疫缺陷病毒(HIV)
作者
Neil P. Shah,Valentín García‐Gutiérrez,Antonio Jiménez‐Velasco,Sarah Marie Larson,Susanne Saußele,Delphine Réa,François‐Xavier Mahon,Moshe Yair Levy,María Teresa Gómez‐Casares,Michael J. Mauro,Oumar Sy,Patricia Martin‐Regueira,Jeffrey Howard Lipton
出处
期刊:British Journal of Haematology [Wiley]
卷期号:202 (5): 942-952 被引量:28
标识
DOI:10.1111/bjh.18883
摘要

Patients with chronic myeloid leukaemia in chronic phase (CML-CP) who have a sustained deep molecular response (DMR) are eligible to discontinue treatment and attempt treatment-free remission (TFR). In the DASFREE study (ClinicalTrials.gov; NCT01850004), the 2-year TFR rate after dasatinib discontinuation was 46%; here we present the 5-year update. Patients with a stable DMR after ≥2 years of dasatinib therapy discontinued treatment and were followed for 5 years. At a minimum follow-up of 60 months, in 84 patients discontinuing dasatinib, the 5-year TFR rate was 44% (n = 37). No relapses occurred after month 39 and all evaluable patients who relapsed and restarted dasatinib (n = 46) regained a major molecular response in a median of 1.9 months. The most common adverse event during the off-treatment period was arthralgia (18%, 15/84); a total of 15 withdrawal events were reported in nine patients (11%). At the 5-year final follow-up, almost half of the patients who discontinued dasatinib after a sustained DMR maintained TFR. All evaluable patients who experienced a relapse quickly regained a DMR after restarting dasatinib, demonstrating that dasatinib discontinuation is a viable and potentially long-term option in patients with CML-CP. The safety profile is consistent with the previous report.
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