首页> 外文期刊>Journal of Clinical Oncology >Clinical outcome of children with newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia treated between 1995 and 2005
【24h】

Clinical outcome of children with newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia treated between 1995 and 2005

机译:1995年至2005年治疗的新诊断为费城染色体阳性的急性淋巴细胞白血病儿童的临床结局

获取原文
获取原文并翻译 | 示例
           

摘要

Purpose: In a previous analysis of 326 children with Philadelphia chromosome (Ph) -positive acute lymphoblastic leukemia (ALL) treated between 1986 and 1996, hematopoietic stem-cell transplantation from HLA-matched related donors, but not from unrelated donors, offered a superior outcome than chemotherapy alone. To evaluate the impact of recent improvements in chemotherapy and transplantation, we performed a similar analysis on patients treated in the following decade. Patients and Methods: We analyzed 610 patients with Ph-positive ALL treated between 1995 and 2005 without tyrosine kinase inhibitor therapy. The median follow-up duration was 6.3 years. Results: Complete remission was achieved in 89% of patients. The 7-year event-free survival and overall survival rates were superior in the present cohort compared with the previous cohort (32.0% ± 2.0% v 25.0% ± 3.0, respectively, P = .007; and 44.9% ± 2.2% v 36.0% ± 3.0%, respectively, P = .017). Compared with chemotherapy alone, transplantation with matched related donors or unrelated donors in first remission (325 patients) showed an advantage with increasing follow-up, suggesting greater protection against late relapses (hazard ratio at 5 years, 0.37; P < .001). In the multivariate Cox regression analysis accounting for treatment (transplantation v no transplantation), age, leukocyte count, and early response had independent impact on treatment outcome. Conclusion: Clinical outcome of children and adolescents with Ph-positive ALL has improved with advances in transplantation and chemotherapy. Transplantations with matched related donors and unrelated donors were equivalent and offered better disease control compared with chemotherapy alone. Age, leukocyte count, and early treatment response were independent prognostic indicators. The results of this study will serve as a historical reference to evaluate the therapeutic impact of tyrosine kinase inhibitors on the outcome of Ph-positive ALL.
机译:目的:在先前对1986年至1996年间治疗的326例费城染色体(Ph)阳性急性淋巴细胞白血病(ALL)儿童的分析中,从HLA匹配的相关供体而非非相关供体的造血干细胞移植提供了更好的结果比单纯化疗要好。为了评估近期化疗和移植的改善所产生的影响,我们对接下来的十年中接受治疗的患者进行了类似的分析。患者和方法:我们分析了1995年至2005年之间未经酪氨酸激酶抑制剂治疗的610例Ph阳性ALL患者。中位随访时间为6。3年。结果:89%的患者完全缓解。与先前的队列相比,当前队列的7年无事件生存率和总体生存率更高(分别为32.0%±2.0%v 25.0%±3.0,P = .007;和44.9%±2.2%v 36.0分别为%±3.0%,P = .017)。与单纯化疗相比,首次缓解时(325例患者)采用相匹配的相关供体或不相关供体进行的移植在随访方面显示出优势,表明对晚期复发的防护更大(5年时的危险比,0.37; P <.001)。在多因素Cox回归分析中,考虑治疗(移植与不移植),年龄,白细胞计数和早期反应对治疗结局具有独立影响。结论:随着移植和化疗的进展,Ph阳性的儿童和青少年的临床结局得到改善。相匹配的相关供体和无关供体的移植是同等的,与单纯化疗相比,可以更好地控制疾病。年龄,白细胞计数和早期治疗反应是独立的预后指标。这项研究的结果将作为历史参考,以评估酪氨酸激酶抑制剂对Ph阳性ALL结果的治疗作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号