第一次尝试伊马替尼失败后第二次尝试达沙替尼无治疗缓解的TKI停药试验的最终报告:达沙替尼(TRAD)研究实现无治疗缓解。

IF 5.1 2区 医学 Q1 HEMATOLOGY British Journal of Haematology Pub Date : 2023-09-11 DOI:10.1111/bjh.19058
Maria Agustina Perusini, Igor Novitzky-Basso, Eshetu G. Atenafu, Donna Forrest, Isabelle Bence-Bruckler, Lynn Savoie, Mary-Margaret Keating, Lambert Busque, Robert Delage, Anargyros Xenocostas, Elena Liew, Pierre Laneuville, Kristjan Paulson, Tracy Stockley, Jeffrey H. Lipton, Brian Leber, Dennis Dong Hwan Kim
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引用次数: 0

摘要

多项研究报道,停止酪氨酸激酶抑制剂(TKI)治疗的慢性髓性白血病(CML)患者的无治疗缓解(TFR)率为50%-60%。然而,其余一半的患者仍然需要重新开始TKI治疗以控制白血病。对于第一次TFR (TFR1)尝试失败的患者,是否应该改用TKI药物进行再治疗尚不清楚。我们的研究试图确定伊马替尼停药后TFR1失败后达沙替尼治疗是否可以提高TFR2的可能性。在59例因TFR1停用伊马替尼而失去分子反应的患者中,55例(93.2%)患者接受了达沙替尼治疗,其中49例(89.1%)患者恢复了MR4.5或更高的反应,中位时间为1.85个月,达到MR4.5。35例患者因TFR2尝试停用达沙替尼,其中26例(74.28%)患者失去了MMR, 6例(17.14%)患者失去了MR4。达沙替尼停药后TFR2的风险因素分析表明有三个重要因素:(1)TFR1尝试后BCR::ABL1转录物翻倍时间,(2)达沙替尼治疗后快速恢复分子反应,(3)TFR2尝试前无法检测到BCR::ABL1转录物。目前的研究表明,达沙替尼一般不会增加TFR2率,但一组选定的患者可以从这种方法中受益。
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Final report of TKI discontinuation trial with dasatinib for the second attempt of treatment-free remission after failing the first attempt with imatinib: Treatment-free Remission Accomplished by Dasatinib (TRAD) study

Multiple studies have reported a significant treatment-free remission (TFR) rate of 50%–60% in patients with chronic myeloid leukaemia (CML) who discontinue tyrosine kinase inhibitor (TKI) therapy. However, the remaining half of these patients still require re-initiation of TKI therapy for leukaemia control. It remains unclear if TKI drugs should be switched for re-therapy in patients who failed the first TFR (TFR1) attempt. Our study attempted to determine whether dasatinib therapy after TFR1 failure post-imatinib discontinuation could improve the likelihood of TFR2. Of 59 patients who lost molecular response after imatinib discontinuation for TFR1, 55 patients (93.2%) were treated with dasatinib, of whom 49 (89.1%) regained MR4.5 or deeper response, with a median time of 1.85 months to achieve MR4.5. Dasatinib was discontinued in 35 patients for TFR2 attempt, of whom 26 patients (74.28%) lost MMR and 6 (17.14%) MR4. Risk factor analysis for the TFR2 after dasatinib discontinuation suggested three significant factors: (1) doubling time of BCR::ABL1 transcript following TFR1 attempt, (2) rapid regaining of molecular response following dasatinib therapy and (3) undetectable BCR::ABL1 transcript prior to TFR2 attempt. The present study showed that dasatinib does not increase the TFR2 rate in general, but a selected group of patients could benefit from this approach.

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来源期刊
CiteScore
8.60
自引率
4.60%
发文量
565
审稿时长
1 months
期刊介绍: The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. The Journal also features annotations, reviews, short reports, images in haematology and Letters to the Editor.
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