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TKI 治疗持续时间对慢性髓性白血病无治疗缓解的重要性:D-FREE 研究结果。

Importance of TKI treatment duration in treatment-free remission of chronic myeloid leukemia: results of the D-FREE study.

机构信息

Department of Hematology, National Hospital Organization Mito Medical Center, 280 Sakuranosato, Ibarakimachi, Higashiibarakigun, Ibaraki, 311-3193, Japan.

Department of Hematology, Nippon Medical School, Tokyo, Japan.

出版信息

Int J Hematol. 2023 May;117(5):694-705. doi: 10.1007/s12185-023-03549-3. Epub 2023 Feb 4.

DOI:10.1007/s12185-023-03549-3
PMID:36739328
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10121524/
Abstract

Treatment-free remission (TFR) is a new goal for patients with chronic myeloid leukemia in chronic phase (CML-CP) with a sustained deep molecular response (DMR) to treatment with tyrosine kinase inhibitors (TKIs). However, optimal conditions for successful TFR in patients treated with second-generation (2G)-TKIs are not fully defined. In this D-FREE study, treatment discontinuation was attempted in newly diagnosed CML-CP patients treated with the 2G-TKI dasatinib who achieved BCR-ABL1 levels of ≤ 0.0032% (MR4.5) on the international scale (BCR-ABL1) and maintained these levels for exactly 1 year. Of the 173 patients who received dasatinib induction therapy for up to 2 years, 123 completed and 60 (48.8%) reached MR 4.5. Among the first 21 patients who maintained MR4.5 for 1 year and discontinued dasatinib, 17 experienced molecular relapse defined as loss of major molecular response (BCR-ABL1 > 0.1%) confirmed once, or loss of MR4 (BCR-ABL1 > 0.01%) confirmed on 2 consecutive assessments. The estimated molecular relapse-free survival rate was 16.7% at 12 months. This study was prematurely terminated according to the protocol's safety monitoring criteria. The conclusion was that sustained DMR for just 1 year is insufficient for TFR in CML-CP patients receiving dasatinib for less than a total of 3 years of treatment.

摘要

无治疗缓解(TFR)是慢性期慢性髓性白血病(CML-CP)患者的一个新目标,这些患者对酪氨酸激酶抑制剂(TKI)治疗有持续的深度分子反应(DMR)。然而,用第二代(2G)TKI 治疗的患者成功实现 TFR 的最佳条件尚未完全确定。在这项 D-FREE 研究中,尝试对接受 2G-TKI 达沙替尼治疗、达到国际标准(BCR-ABL1)BCR-ABL1 水平 ≤ 0.0032%(MR4.5)且持续 1 年的新诊断 CML-CP 患者停止治疗。在接受达沙替尼诱导治疗长达 2 年的 173 名患者中,123 名完成治疗,60 名(48.8%)达到 MR4.5。在最初的 21 名患者中,有 17 名患者在维持 MR4.5 1 年后停止使用达沙替尼,其中 17 名患者的分子复发定义为主要分子反应丧失(BCR-ABL1 > 0.1%),1 次确认或在连续 2 次评估中失去 MR4(BCR-ABL1 > 0.01%)。12 个月时的估计分子无复发存活率为 16.7%。根据方案的安全监测标准,该研究提前终止。结论是,在不到 3 年的总治疗时间内接受达沙替尼治疗的 CML-CP 患者,持续 DMR 仅 1 年不足以实现 TFR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e934/10121524/7255b9c8f2e9/12185_2023_3549_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e934/10121524/d0a837f678eb/12185_2023_3549_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e934/10121524/b11c2bea59fd/12185_2023_3549_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e934/10121524/95a38d5c9028/12185_2023_3549_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e934/10121524/7255b9c8f2e9/12185_2023_3549_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e934/10121524/d0a837f678eb/12185_2023_3549_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e934/10121524/b11c2bea59fd/12185_2023_3549_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e934/10121524/95a38d5c9028/12185_2023_3549_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e934/10121524/7255b9c8f2e9/12185_2023_3549_Fig4_HTML.jpg

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