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酪氨酸激酶抑制剂在临床试验之外成功停药——基于人群的瑞典慢性髓性白血病登记处的数据。

Successful tyrosine kinase inhibitor discontinuation outside clinical trials - data from the population-based Swedish chronic myeloid leukaemia registry.

机构信息

Department of Medical Science and Division of Hematology, University Hospital, Uppsala, Sweden.

Regional Cancer Centre, Uppsala-Örebro, Sweden.

出版信息

Br J Haematol. 2021 Jun;193(5):915-921. doi: 10.1111/bjh.17392. Epub 2021 Mar 30.

DOI:10.1111/bjh.17392
PMID:33782950
Abstract

Clinical trials show that tyrosine kinase inhibitor (TKI) treatment can be discontinued in selected patients with chronic myeloid leukaemia (CML). Although updated CML guidelines support such procedure in clinical routine, data on TKI stopping outside clinical trials are limited. In this retrospective study utilising the Swedish CML registry, we examined TKI discontinuation in a population-based setting. Out of 584 patients diagnosed with chronic-phase CML (CML-CP) in 2007-2012, 548 had evaluable information on TKI discontinuation. With a median follow-up of nine years from diagnosis, 128 (23%) discontinued TKI therapy (≥1 month) due to achieving a DMR (deep molecular response) and 107 (20%) due to other causes (adverse events, allogeneic stem cell transplant, pregnancy, etc). Among those stopping in DMR, 49% re-initiated TKI treatment (median time to restart 4·8 months). In all, 38 patients stopped TKI within a clinical study and 90 outside a study. After 24 months 41·1% of patients discontinuing outside a study had re-initiated TKI treatment. TKI treatment duration pre-stop was longer and proportion treated with second-generation TKI slightly higher outside studies, conceivably affecting the clinical outcome. In summary we show that TKI discontinuation in CML in clinical practice is common and feasible and may be just as successful as when performed within a clinical trial.

摘要

临床试验表明,酪氨酸激酶抑制剂(TKI)治疗可在选定的慢性髓性白血病(CML)患者中停药。尽管更新的 CML 指南支持在临床常规中进行这种操作,但临床试验之外关于 TKI 停药的数据有限。在这项利用瑞典 CML 登记处的回顾性研究中,我们在基于人群的环境中检查了 TKI 的停药情况。在 2007-2012 年诊断为慢性期 CML(CML-CP)的 584 名患者中,有 548 名患者具有可评估的 TKI 停药信息。从诊断到中位随访 9 年,由于达到 DMR(深度分子反应),128 名(23%)患者停止了 TKI 治疗(≥1 个月),107 名(20%)患者因其他原因(不良事件、异基因干细胞移植、怀孕等)停止了 TKI 治疗。在因 DMR 停药的患者中,49%重新开始 TKI 治疗(重新开始治疗的中位时间为 4.8 个月)。共有 38 名患者在临床试验中停止 TKI 治疗,90 名患者在临床试验之外停止 TKI 治疗。停药后 24 个月,41.1%在临床试验之外停药的患者重新开始 TKI 治疗。停药前 TKI 治疗时间较长,在临床试验之外接受第二代 TKI 治疗的比例略高,这可能影响临床结局。总之,我们表明,在临床实践中,CML 中的 TKI 停药是常见且可行的,并且可能与在临床试验中一样成功。

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