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[慢性髓性白血病中国患者在现实世界中停用酪氨酸激酶抑制剂的观察性研究]

[Observational study of chronic myeloid leukemia Chinese patients who discontinued tyrosine kinase inhibitors in the real-world].

作者信息

Zhao H F, Yang Y F, Liu B C, Li W M, Xu N, Liu X L, Jiang Q, Dang H B, Liang L X, Zhang Yanli, Song Y P

机构信息

Department of Hematology, Henan Cancer Hospital, the Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou 450008, China.

Department of Hematology, Institute of Hematology, West China Hospital, Sichuan University, Chengdu 610041, China.

出版信息

Zhonghua Xue Ye Xue Za Zhi. 2022 Aug 14;43(8):636-643. doi: 10.3760/cma.j.issn.0253-2727.2022.08.004.

DOI:10.3760/cma.j.issn.0253-2727.2022.08.004
PMID:36709147
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9593009/
Abstract

This study aimed to observe whether the treatment-free remission (TFR) of second-generation tyrosine kinase inhibitors (TKI) in chronic myeloid leukemia (CML) is better than imatinib (IM) . The clinical data of 274 CML patients who discontinued treatment and with complete clinical data were retrospectively studied from June 2013 to March 2021. Using both univariate and multivariate Cox proportional hazards regression models, risk factors influencing TFR outcomes after drug withdrawal in CML patients were assessed. A total of 274 patients were enrolled, 140 patients were women (51.1%) , with a median age of 48 (9-84) years at the time of TKI discontinuation. Prior to TKI discontinuation, 172 (62.8%) patients were treated with IM, and 102 (37.2%) had received second-generation TKI treatment, including 73 patients who had shifted from IM to a second-generation TKI and 29 patients who used second-generation TKI as the first-line treatment. The rationale for converting to a second-generation TKI are as follows: 37 patients aimed deep molecular response (DMR) to achieve TFR, seven patients changed due to IM intolerance, and 29 patients changed because of failure to achieve the optimal treatment response. The use of the last type of TKI included 96 patients (94.1%) with nilotinib, three patients (2.9%) with dasatinib, and two patients (2%) with flumatinib, including one patient who changed to IM due to second-generation TKI intolerance. No statistical differences were found in the median age at diagnosis and TKI discontinuation, sex, Sokal score, IFN treatment before TKI, median time of TKI treatment to achieve DMR, and the reasons for TKI discontinuation between the second TKI and IM (>0.05) .The median cumulative treatment time of TKI (71.5 months 88 months, <0.001) , the last TKI median treatment time (60 months 88 months, <0.001) , and the median duration of DMR (58 months 66 months, =0.002) were significantly shorter in the second-generation TKI compared with IM. In the median follow-up of 22 (6-118) months after TKI discontinuation, 88 patients (32.1%) had lost their MMR at a median of 6 (1-91) months; of the 53 patients (60.2%) who lost MMR within 6 months, the overall TFR rate was 67.9%, and the cumulative TFR rates at 12 and 24 months were 70.5% and 67.5%, respectively. Withdrawal syndrome occurred in 26 patients (9.5%) . For patients who restarted TKI treatment, 72 patients (83.7%) achieved DMR again at a median treatment of 4 (1 to 18) months. The univariate analysis showed that the TFR rate of patients treated with second-generation TKI was significantly higher than those who were treated with IM (77.5% 62.2%, =0.041) . A further subgroup analysis found that the TFR rate of the second-generation TKI patients was significantly higher than those treated with IM (80.8% 62.2%, =0.026) . No significant difference was found in the second-generation TKI used as the first line treatment compared with those who were treated with IM (69.0% 62.2%, =0.599) . The multivariate analysis results showed that second-generation TKI treatment was an independent prognostic factor affecting TFR in patients who discontinued TKI (=1.827, 95% 1.015-3.288, =0.044) . In the clinical setting, more CML patients rapidly achieved TFR using second-generation TKI than IM treatment.

摘要

本研究旨在观察慢性髓性白血病(CML)患者中第二代酪氨酸激酶抑制剂(TKI)的无治疗缓解(TFR)是否优于伊马替尼(IM)。回顾性研究了2013年6月至2021年3月期间274例停止治疗且临床资料完整的CML患者的临床数据。使用单变量和多变量Cox比例风险回归模型,评估影响CML患者停药后TFR结果的危险因素。共纳入274例患者,140例为女性(51.1%),TKI停药时的中位年龄为48岁(9 - 84岁)。在TKI停药前,172例(62.8%)患者接受IM治疗,102例(37.2%)接受第二代TKI治疗,其中73例从IM转换为第二代TKI,29例将第二代TKI作为一线治疗。转换为第二代TKI的理由如下:37例旨在获得深度分子反应(DMR)以实现TFR,7例因IM不耐受而更换,29例因未达到最佳治疗反应而更换。最后一种TKI的使用情况包括96例(94.1%)使用尼罗替尼,3例(2.9%)使用达沙替尼,2例(2%)使用氟马替尼,其中1例因第二代TKI不耐受而转换为IM。第二代TKI组和IM组在诊断时和TKI停药时的中位年龄、性别、Sokal评分、TKI治疗前的IFN治疗、达到DMR的TKI治疗中位时间以及TKI停药原因方面均无统计学差异(>0.05)。与IM相比,第二代TKI的TKI中位累积治疗时间(71.5个月对88个月,<0.001)、最后一种TKI的中位治疗时间(60个月对88个月,<0.001)以及DMR的中位持续时间(58个月对66个月,=0.002)均显著缩短。在TKI停药后的中位随访22个月(6 - 118个月)中,88例患者(32.1%)在中位6个月(1 - 91个月)时失去了主要分子反应(MMR);在6个月内失去MMR的53例患者(60.2%)中,总体TFR率为67.9%,12个月和24个月时的累积TFR率分别为70.5%和67.5%。26例患者(9.5%)出现停药综合征。对于重新开始TKI治疗的患者,72例(83.7%)在中位治疗4个月(1至18个月)时再次达到DMR。单变量分析显示,接受第二代TKI治疗的患者的TFR率显著高于接受IM治疗的患者(77.5%对62.2%,=0.041)。进一步的亚组分析发现,第二代TKI患者的TFR率显著高于接受IM治疗的患者(80.8%对62.2%,=0.026)。与接受IM治疗的患者相比,将第二代TKI作为一线治疗的患者之间无显著差异(69.0%对62.2%,=0.599)。多变量分析结果显示,第二代TKI治疗是影响停用TKI患者TFR的独立预后因素(=1.827,95% 1.015 - 3.288,=0.044)。在临床实践中,与IM治疗相比,更多的CML患者使用第二代TKI能快速实现TFR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d436/9593009/0bcd1567f030/cjh-43-08-636-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d436/9593009/d663de5b5375/cjh-43-08-636-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d436/9593009/0bcd1567f030/cjh-43-08-636-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d436/9593009/d663de5b5375/cjh-43-08-636-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d436/9593009/0bcd1567f030/cjh-43-08-636-g002.jpg

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