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NKG2A 表达对停药后慢性髓性白血病患者的预后作用

英文原题:The prognostic role of NKG2A expression for patients with chronic myeloid leukemia after treatment discontinuation.

查看英文原题

The prognostic role of NKG2A expression for patients with chronic myeloid leukemia after treatment discontinuation.

PubMed 2022/06/25(内容时间) Leuk Lymphoma Q3 · IF 2.1(JCR 2025)

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中文摘要

本研究旨在评估获得持续深度分子学应答(DMR)的慢性髓性白血病(CML)患者停用酪氨酸激酶抑制剂(TKI)的可行性,并探讨自然杀伤(NK)细胞对治疗停药后缓解(TFR)的预后作用。研究纳入60名停用TKI的CML患者,并调查其中27名患者停药后的免疫特征。在60名患者中,估算12个月TFR率为60.8%(95%置信区间49.5%–74.8%)。TKI治疗时间较长、达到主要分子学应答以及维持DMR时间较长的患者,TFR率显著较高。多变量分析显示,NKG2A+ NK细胞及NKG2A+CD56明亮型CD16− NK细胞比例较高,是TFR的独立预后因素。结果提示停用TKI具有可行性;NK细胞计数稳定且细胞毒性和杀伤能力增强的患者,更可能获得持续的无治疗生存。

展开英文摘要原文

This study aims to evaluate the possibility of tyrosine kinase inhibitors (TKIs) discontinuation in chronic myeloid leukemia (CML) patients who obtained sustained deep molecular response (DMR) and to explore the prognostic role of NK cells in treatment-free remission (TFR). Sixty CML patients who discontinued TKI treatment were enrolled, and we also investigated the immune profiles in 27 CML patients after TKI cessation. Of the 60 patients, the estimated TFR rate was 60. 8% [95% CI: 49. 5-74. 8%] at 12 months.

Patients who had longer TKI duration, major molecular response, and DMR maintenance time had a significantly higher TFR rate. And a higher percentage of NKG2A + NK cells and NKG2A + CD56 bright CD16 - NK cells were independent prognostic factors of TFR in multivariate analysis. These results indicate the practicality of the cessation of TKIs and patients with stable NK cell counts accompanied by higher cytotoxicity and increased killing capacity are more inclined to get sustained treatment-free survival.

论文信息

作者
Xu Z、Yin J、Sun Q、Hu J、Hong M、Qian S、Liu W
单位
Department of Hematology, The First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, Nanjing, China.China
文献类型
非美国政府资助研究
期刊
Leukemia & lymphoma2022 Nov
原文标识
PubMed 35758278 · DOI 10.1080/10428194.2022.2090549