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异基因造血干细胞移植是慢性髓性白血病晚期患者或酪氨酸激酶抑制剂治疗失败患者的一种有效挽救疗法。

Allogeneic Hematopoietic Stem Cell Transplantation Is an Effective Salvage Therapy for Patients with Chronic Myeloid Leukemia Presenting with Advanced Disease or Failing Treatment with Tyrosine Kinase Inhibitors.

作者信息

Nair Anish P, Barnett Michael J, Broady Raewyn C, Hogge Donna E, Song Kevin W, Toze Cynthia L, Nantel Stephen H, Power Maryse M, Sutherland Heather J, Nevill Thomas J, Abou Mourad Yasser, Narayanan Sujaatha, Gerrie Alina S, Forrest Donna L

机构信息

Leukemia/BMT Program of British Columbia, Division of Hematology, Vancouver General Hospital, British Columbia Cancer Agency, and University of British Columbia, Vancouver, British Columbia, Canada.

Leukemia/BMT Program of British Columbia, Division of Hematology, Vancouver General Hospital, British Columbia Cancer Agency, and University of British Columbia, Vancouver, British Columbia, Canada.

出版信息

Biol Blood Marrow Transplant. 2015 Aug;21(8):1437-44. doi: 10.1016/j.bbmt.2015.04.005. Epub 2015 Apr 10.

Abstract

Allogeneic hematopoietic stem cell transplantation (HSCT) remains the only known curative therapy for chronic myeloid leukemia (CML); however, it is rarely utilized given the excellent long-term results with tyrosine kinase inhibitor (TKI) treatment. The purpose of this study is to examine HSCT outcomes for patients with CML who failed TKI therapy or presented in advanced phase and to identify predictors of survival, relapse, and nonrelapse mortality (NRM). Fifty-one patients with CML underwent HSCT for advanced disease at diagnosis (n = 15), TKI resistance as defined by the European LeukemiaNet guidelines (n = 30), TKI intolerance (n = 2), or physician preference (n = 4). At a median follow-up of 71.9 months, the 8-year overall survival (OS), event-free survival (EFS), relapse, and NRM were 68%, 46%, 41%, and 23%, respectively. In univariate analysis, predictors of OS included first chronic phase (CP1) disease status at HSCT (P = .0005), European Society for Blood and Marrow Transplantation score 1 to 4 (P = .04), and complete molecular response (CMR) to HSCT (P < .0001). Donor (female) to patient (male) gender combination (P = .02) and CMR to HSCT (P < .0001) predicted lower relapse. In multivariate analysis, CMR to HSCT remained an independent predictor of OS (odds ratio [OR], 43), EFS (OR, 56) and relapse (OR, 29). This report indicates that the outlook is excellent for those patients who remain in CP1 at the time of HSCT and achieve a CMR after HSCT. However, only approximately 50% of those in advanced phase at HSCT are long-term survivors. This highlights the ongoing need to try to identify patients earlier, before disease progression, who are destined to fail this treatment to optimize transplantation outcomes.

摘要

异基因造血干细胞移植(HSCT)仍然是慢性髓性白血病(CML)唯一已知的治愈性疗法;然而,鉴于酪氨酸激酶抑制剂(TKI)治疗具有出色的长期疗效,HSCT很少被采用。本研究的目的是检查TKI治疗失败或处于晚期的CML患者接受HSCT的结果,并确定生存、复发和非复发死亡率(NRM)的预测因素。51例CML患者因诊断时疾病处于晚期(n = 15)、根据欧洲白血病网络指南定义的TKI耐药(n = 30)、TKI不耐受(n = 2)或医生偏好(n = 4)而接受HSCT。中位随访71.9个月时,8年总生存率(OS)、无事件生存率(EFS)、复发率和NRM分别为68%、46%、41%和23%。单因素分析中,OS的预测因素包括HSCT时处于首次慢性期(CP1)疾病状态(P = .0005)、欧洲血液和骨髓移植学会评分1至4(P = .04)以及HSCT后的完全分子反应(CMR)(P < .0001)。供体(女性)与患者(男性)的性别组合(P = .02)以及HSCT后的CMR(P < .0001)预测较低的复发率。多因素分析中,HSCT后的CMR仍然是OS(比值比[OR],43)、EFS(OR,56)和复发(OR, 29)的独立预测因素。本报告表明,对于那些在HSCT时仍处于CP1且HSCT后实现CMR的患者,前景良好。然而,HSCT时处于晚期的患者中只有约50%是长期幸存者。这凸显了持续需要在疾病进展之前更早地识别那些注定会治疗失败的患者,以优化移植结果。

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