Suppr超能文献

异基因造血细胞移植后复发的 CML 患者中供者淋巴细胞输注与酪氨酸激酶抑制剂的长期疗效比较。

A comparison of long-term outcomes of donor lymphocyte infusions and tyrosine kinase inhibitors in patients with relapsed CML after allogeneic hematopoietic cell transplantation.

机构信息

Allogeneic Blood and Marrow Transplantation Program, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.

Allogeneic Blood and Marrow Transplantation Program, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.

出版信息

Clin Lymphoma Myeloma Leuk. 2014 Feb;14(1):87-92. doi: 10.1016/j.clml.2013.09.010. Epub 2013 Oct 1.

Abstract

BACKGROUND

Donor lymphocyte infusion (DLI) and tyrosine kinase inhibitors (TKIs) are the 2 standard treatment options in chronic myeloid leukemia (CML) that relapses after hematopoietic cell transplantation (HCT), but reports comparing long-term outcomes of these modalities are rare.

PATIENTS AND METHODS

A total of 46 patients were treated with either DLI (n = 28) or TKIs (n = 18) during a first relapse of CML after HCT between 1993 and 2012. The stage of relapse was the chronic phase in 37 patients and the advanced phase in 9 patients. All patients had myeloablative conditioning without T-cell depletion during HCT. The median interval between HCT and treatment for relapse was 34 (range, 2-197) months.

RESULTS

At a median follow-up of 146 and 70 months, respectively, 32% of the DLI group and 33% of the TKI group had died. Six (21%) patients initially treated with DLI received TKIs during a second relapse. In multivariable analyses, DLI was associated with inferior overall survival (OS) (hazard ratio [HR], 37.4; 95% confidence interval [CI], 2.2-625.4; P = .01), shorter failure-free survival (FFS) (HR, 21.15; 95% CI, 1.8-251; P = .02), higher cumulative incidence of failure (CIF) (HR, 19.5; 95% CI, 1.6-236.5; P = .02), and increased incidence of treatment-induced graft vs. host disease (GVHD) (68% vs. 6%; P = .001).

CONCLUSION

TKIs appear better than DLI in chronic-phase relapses after myeloablative non-T-cell-depleted HCT. Outcomes were poor in advanced-phase relapses irrespective of treatment modality.

摘要

背景

供者淋巴细胞输注(DLI)和酪氨酸激酶抑制剂(TKIs)是异基因造血细胞移植(HCT)后慢性髓性白血病(CML)复发的 2 种标准治疗选择,但比较这两种方法的长期疗效的报道很少。

患者和方法

1993 年至 2012 年间,共有 46 例患者在 HCT 后 CML 首次复发时接受 DLI(n = 28)或 TKI(n = 18)治疗。复发时的疾病分期为慢性期 37 例,晚期 9 例。所有患者在 HCT 时均未接受 T 细胞清除的清髓性预处理。HCT 与复发治疗之间的中位时间间隔为 34(范围,2-197)个月。

结果

中位随访 146 和 70 个月后,DLI 组和 TKI 组分别有 32%和 33%的患者死亡。最初接受 DLI 治疗的 6 例(21%)患者在第二次复发时接受了 TKI 治疗。多变量分析显示,DLI 与总体生存(OS)不良相关(风险比[HR],37.4;95%置信区间[CI],2.2-625.4;P =.01),无失败生存(FFS)较短(HR,21.15;95% CI,1.8-251;P =.02),失败累积发生率(CIF)较高(HR,19.5;95% CI,1.6-236.5;P =.02),以及治疗相关移植物抗宿主病(GVHD)发生率增加(68% vs. 6%;P =.001)。

结论

在非 T 细胞清除的清髓性 HCT 后慢性期复发的患者中,TKI 似乎优于 DLI。无论治疗方式如何,晚期复发患者的结局均较差。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验