异基因造血细胞移植治疗对酪氨酸激酶抑制剂耐药或不耐受的慢性粒细胞白血病的疗效。

Q1 Medicine
Farah Yassine, Tea Reljic, Muhamad Alhaj Moustafa, Madiha Iqbal, Hemant S Murthy, Ambuj Kumar, Mohamed A Kharfan-Dabaja
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引用次数: 2

摘要

大约15-20%的慢性髓性白血病(CML)患者因耐药或不耐受而未能接受酪氨酸激酶抑制剂(TKI)治疗。在tki之前的时代,前线同种异体造血细胞移植(allo- HCT)代表了慢性慢性粒细胞白血病(CP-CML)患者的标准方法,这些患者被认为适合耐受该手术,并且有一个人类白细胞抗原兼容的供体。目前,CP-CML患者只有在一次以上TKI失败和/或对药物不耐受的情况下才有资格接受allo-HCT治疗。我们对现有文献进行了系统回顾/荟萃分析,以评估allo-HCT治疗CP-CML患者疗效的证据。从符合条件的研究中提取与获益(总生存期[OS]、无进展生存期、无病生存期[DFS]、完全缓解期[CR]和分子反应期[MR])和危害(非复发死亡率[NRM]、复发、急性和慢性移植物抗宿主病)相关的数据,并按年龄分为成人组和儿科组。对于成人全hct受体,总OS、DFS、CR和MR分别为84%[95%置信区间(CI) 59-99%]、66% (95% CI 59-73%)、56% (95% CI 30-80%)和88% (95% CI 62-98%)。合并NRM和复发率分别为20% (95% CI 15-26%)和19% (95% CI 10-28%)。对于儿科组,一项研究报告的总生存率为91% (95% CI 72-99%)。我们的研究结果表明,allo-HCT是tki耐药或tki不耐受的CP-CML的有效治疗方法。移植后的策略仍然需要进一步降低复发的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of Allogeneic Hematopoietic Cell Transplantation in Patients With Chronic Phase CML Resistant or Intolerant to Tyrosine Kinase Inhibitors.

Approximately 15-20% of chronic myeloid leukemia (CML) patients fail tyrosine kinase inhibitor (TKI) therapy secondary to resistance or intolerance. In the pre-TKI era, front-line allogeneic hematopoietic cell transplantation (allo- HCT) represented the standard approach for patients with chronic phase-CML (CP-CML) who were deemed fit to tolerate the procedure and had a human leukocyte antigen compatible donor available. Currently, CP-CML patients are eligible for allo-HCT only if they fail more than one TKI and/or are intolerant to the drug. We performed a systematic review/meta-analysis of the available literature to assess the evidence regarding allo-HCT efficacy in CP-CML patients. Data from eligible studies were extracted in relation to benefits (overall survival [OS], progression-free survival, disease-free survival [DFS], complete remission [CR], and molecular response [MR]) and harms (nonrelapse mortality [NRM], relapse, and acute and chronic graft-versus-host disease), and stratified by age into adult and pediatric groups. For adult allo-HCT recipients, the pooled OS, DFS, CR and, MR were 84% [95% confidence interval (CI) 59-99%], 66% (95% CI 59-73%), 56% (95% CI 30-80%), and 88% (95% CI 62-98%), respectively. Pooled NRM and relapse were 20% (95% CI 15-26%) and 19% (95% CI 10-28%), respectively. For the pediatric group, the OS rate was reported in one study and was 91% (95% CI 72-99%). Our results suggest that allo-HCT is an effective treatment for TKI-resistant or TKI-intolerant CP-CML. Post-transplant strategies are still needed to further mitigate the risk of relapse.

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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
0
审稿时长
27 weeks
期刊介绍: Hematology Oncology and Stem Cell Therapy is an international, peer-reviewed, open access journal that provides a vehicle for publications of high-quality clinical as well as basic science research reports in hematology and oncology. The contents of the journal also emphasize the growing importance of hematopoietic stem cell therapy for treatment of various benign and malignant hematologic disorders and certain solid tumors.The journal prioritizes publication of original research articles but also would give consideration for brief reports, review articles, special communications, and unique case reports. It also offers a special section for clinically relevant images that provide an important educational value.
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