Treatment-free remission after discontinuation of imatinib, dasatinib, and nilotinib in patients with chronic myeloid leukemia.

IF 2.3 Q2 HEMATOLOGY Blood Research Pub Date : 2023-04-30 DOI:10.5045/br.2023.2023035
Jae Joon Han
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引用次数: 1

Abstract

Patients with chronic myeloid leukemia (CML) in the chronic phase receiving tyrosine kinase inhibitor (TKI) therapy are expected to have long-term survival outcomes comparable to those of the general population. Many clinical trials have confirmed that some patients sustain molecular responses without continuing TKI therapy. Treatment-free remission (TFR) is a new goal in treating chronic CML. The safety and outcome of TFR were studied in clinical trials after discontinuing imatinib or the second-generation TKIs dasatinib or nilotinib. TFR was safe in approximately 50% of patients who achieved a deep molecular response to TKI therapy. Patients who relapsed after discontinuing TKI responded immediately to the reintroduction of TKI. The mechanism by which TFR increases the success rate still needs to be understood. The hypothesis that the modulation of immune function and targeting of leukemic stem cells could improve the TFR is under investigation. Despite the remaining questions, the TFR has become a routine consideration for clinicians in the practice of molecular remission in patients with CML.

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慢性髓性白血病患者停用伊马替尼、达沙替尼和尼洛替尼后的无治疗缓解。
接受酪氨酸激酶抑制剂(TKI)治疗的慢性髓性白血病(CML)慢性期患者的长期生存结果有望与普通人群相当。许多临床试验证实,一些患者在不继续TKI治疗的情况下仍能维持分子反应。无治疗缓解(TFR)是慢性CML治疗的新目标。在临床试验中研究了停用伊马替尼或第二代TKIs(达沙替尼或尼洛替尼)后TFR的安全性和结局。TFR在约50%对TKI治疗有深度分子反应的患者中是安全的。停用TKI后复发的患者对重新引入TKI立即有反应。TFR增加成功率的机制仍需了解。调节免疫功能和靶向白血病干细胞可以改善TFR的假说正在研究中。尽管仍存在问题,但TFR已成为临床医生在CML患者分子缓解实践中的常规考虑因素。
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来源期刊
Blood Research
Blood Research HEMATOLOGY-
CiteScore
3.70
自引率
0.00%
发文量
64
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