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本文引用的文献

1
Classification of accelerated phase chronic myeloid leukemia in the era of the BCR::ABL1 tyrosine kinase inhibitors: A work in progress.BCR::ABL1酪氨酸激酶抑制剂时代慢性髓性白血病加速期的分类:一项正在进行的工作。
Am J Hematol. 2023 Sep;98(9):1350-1353. doi: 10.1002/ajh.27007. Epub 2023 Jun 26.
2
Chronic Myeloid Leukemia, from Pathophysiology to Treatment-Free Remission: A Narrative Literature Review.慢性髓性白血病:从病理生理学到无治疗缓解——一篇叙述性文献综述
J Blood Med. 2023 Apr 6;14:261-277. doi: 10.2147/JBM.S382090. eCollection 2023.
3
Treatment-free remission after discontinuation of imatinib, dasatinib, and nilotinib in patients with chronic myeloid leukemia.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
Blood Res. 2023 Apr 30;58(S1):S58-S65. doi: 10.5045/br.2023.2023035. Epub 2023 Apr 7.
4
Outcomes after allogeneic hematopoietic cell transplant in patients diagnosed with blast phase of myeloproliferative neoplasms: A retrospective study from the Chronic Malignancies Working Party of the European Society for Blood and Marrow Transplantation.异基因造血细胞移植治疗骨髓增生性肿瘤急变期患者的结局:欧洲血液和骨髓移植学会慢性恶性肿瘤工作组的一项回顾性研究。
Am J Hematol. 2023 Apr;98(4):628-638. doi: 10.1002/ajh.26833. Epub 2023 Jan 13.
5
Transplantation in CML in the TKI era: who, when, and how?TKI 时代的 CML 移植:谁、何时以及如何?
Hematology Am Soc Hematol Educ Program. 2022 Dec 9;2022(1):114-122. doi: 10.1182/hematology.2022000329.
6
Treatment of blast phase chronic myeloid leukaemia: A rare and challenging entity.急变期慢性髓性白血病的治疗:一种罕见且极具挑战性的疾病。
Br J Haematol. 2022 Dec;199(5):665-678. doi: 10.1111/bjh.18370. Epub 2022 Jul 22.
7
The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/Dendritic Neoplasms.世界卫生组织血液淋巴肿瘤分类第五版:髓系和组织细胞/树突状肿瘤。
Leukemia. 2022 Jul;36(7):1703-1719. doi: 10.1038/s41375-022-01613-1. Epub 2022 Jun 22.
8
Potential to Improve Therapy of Chronic Myeloid Leukemia (CML), Especially for Patients with Older Age: Incidence, Mortality, and Survival Rates of Patients with CML in Switzerland from 1995 to 2017.改善慢性髓性白血病(CML)治疗的潜力,尤其是对老年患者:1995年至2017年瑞士CML患者的发病率、死亡率和生存率
Cancers (Basel). 2021 Dec 14;13(24):6269. doi: 10.3390/cancers13246269.
9
Understanding the hematopoietic microenvironment in chronic myeloid leukemia: A concise review.理解慢性髓性白血病的造血微环境:简明综述。
Curr Res Transl Med. 2021 Jul;69(3):103295. doi: 10.1016/j.retram.2021.103295. Epub 2021 May 4.
10
Efficacy of Allogeneic Hematopoietic Cell Transplantation in Patients With Chronic Phase CML Resistant or Intolerant to Tyrosine Kinase Inhibitors.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期慢性粒细胞白血病患者的疗效
Hematol Oncol Stem Cell Ther. 2022 Mar 1;15(1):36-43. doi: 10.1016/j.hemonc.2021.02.003.

造血干细胞移植在慢性髓性白血病治疗中的当代作用:在所有情况下都相同吗?

The Contemporary Role of Hematopoietic Stem Cell Transplantation in the Management of Chronic Myeloid Leukemia: Is It the Same in All Settings?

作者信息

Elmakaty Ibrahim, Saglio Giuseppe, Al-Khabori Murtadha, Elsayed Abdelrahman, Elsayed Basant, Elmarasi Mohamed, Elsabagh Ahmed Adel, Alshurafa Awni, Ali Elrazi, Yassin Mohamed

机构信息

College of Medicine, QU Health, Qatar University, Doha P.O. Box 2713, Qatar.

Department of Clinical and Biological Sciences, University of Turin, 10124 Turin, Italy.

出版信息

Cancers (Basel). 2024 Feb 12;16(4):754. doi: 10.3390/cancers16040754.

DOI:10.3390/cancers16040754
PMID:38398145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10886670/
Abstract

Hematopoietic stem cell transplantation (HSCT) for chronic myeloid leukemia (CML) patients has transitioned from the standard of care to a treatment option limited to those with unsatisfactory tyrosine kinase inhibitor (TKI) responses and advanced disease stages. In recent years, the threshold for undergoing HSCT has increased. Most CML patients now have life expectancies comparable to the general population, and therefore, the goal of therapy is shifting toward achieving treatment-free remission (TFR). While TKI discontinuation trials in CML show potential for achieving TFR, relapse risk is high, affirming allogeneic HSCT as the sole curative treatment. HSCT should be incorporated into treatment algorithms from the time of diagnosis and, in some patients, evaluated as soon as possible. In this review, we will look at some of the recent advances in HSCT, as well as its indication in the era of aiming for TFR in the presence of TKIs in CML.

摘要

慢性粒细胞白血病(CML)患者的造血干细胞移植(HSCT)已从标准治疗转变为仅限于酪氨酸激酶抑制剂(TKI)反应不佳和疾病晚期患者的治疗选择。近年来,接受HSCT的门槛有所提高。现在大多数CML患者的预期寿命与普通人群相当,因此,治疗目标正转向实现无治疗缓解(TFR)。虽然CML的TKI停药试验显示出实现TFR的潜力,但复发风险很高,这肯定了异基因HSCT是唯一的治愈性治疗方法。HSCT应从诊断时起纳入治疗方案,对于一些患者,应尽快进行评估。在本综述中,我们将探讨HSCT的一些最新进展,以及在CML存在TKI的情况下,其在旨在实现TFR时代的适应症。