首页> 外文期刊>Pediatric Hematology and Oncology >Treatment outcome of pediatric acute lymphoblastic leukemia in Yeungnam region: Multicenter retrospective study of Study Alliance of Yeungnam Pediatric Hematology-Oncology (SAYPH)
【24h】

Treatment outcome of pediatric acute lymphoblastic leukemia in Yeungnam region: Multicenter retrospective study of Study Alliance of Yeungnam Pediatric Hematology-Oncology (SAYPH)

机译:埃文南地区小儿急性淋巴细胞白血病治疗结果:叶文新儿科血液学 - 肿瘤学研究联盟的多中心回顾性研究(SAYPH)

获取原文
获取原文并翻译 | 示例
       

摘要

Objectives: We aimed to evaluate treatment outcomes of pediatric acute lymphoblastic leukemia (ALL) subgroups by risk-stratification, in the Yeungnam region of Korea. Methods: We reviewed the courses of 409 newly diagnosed ALL patients from January 2004 to December 2013 in the Yeungnam region. Results: All patients were classified into three risk groups: standard risk (SR, n=212), high risk (HR, n=153) and very high risk (VHR, n=44). The mean follow-up time was 73.6 +/- 39.4 months. The 7-year event-free survival (EFS) and overall survival (OS) rates were 78.7 +/- 2.1% and 86.8 +/- 1.8%, respectively. Significant 7-year EFS and OS rates for SR (84.0 +/- 2.7%, 93.7 +/- 1.8%), HR (76.5 +/- 3.5%, 82.1 +/- 3.3%), and VHR (60.6 +/- 7.5%, 69.9 +/- 7.5%) were observed (P0.001), respectively. Relapse occurred in 52 patients, and the cumulative 7-year incidence of relapse differed according to risk groups (SR vs. HR vs. VHR=12.6% vs. 14.0% vs. 29.6%, P=0.003).For the 46 relapsed patients who were treated, the 3-year EFS and OS were 42.3 +/- 8.3%and 46.4 +/- 8.4%. Among the 44 VHR patients, EFS was not significantly different between the chemotherapy-treated patients and those received hematopoietic stem cell transplantation (P=0.533). The 7-year EFS of the hyperleukocytosis subgroup (24 cases, 14 under 10 years of age)showed a tendency for better prognosis than that of the other VHR subgroups (P=0.178). Conclusion: Our results revealed improved outcomes in pediatric ALL patients with risk-stratified therapy. The hyperleukocytosis subgroup without any combined chromosomal abnormalities may respond favorably to chemotherapy alone after first complete remission.
机译:目的:我们旨在评估韩国埃文南地区风险分层小儿急性淋巴细胞白血病(全)亚组的治疗结果。方法:我们审查了从2004年1月至2013年12月在埃文南部地区新诊断的患者新诊断的课程。结果:所有患者均分为三个风险群:标准风险(SR,N = 212),风险高风险(HR,N = 153),风险很高(VHR,N = 44)。平均随访时间为73.6 +/- 39.4个月。 7年的无前活生存(EFS)和整体生存率(OS)率分别为78.7 +/- 2.1%和86.8 +/- 1.8%。 SR的重要7年EFS和OS率(84.0 +/- 2.7%,93.7 +/- 1.8%),人力资源(76.5 +/- 3.5%,82.1 +/- 3.3%)和VHR(60.6 +/-观察到7.5%,69.9 +/- 7.5%(P <0.001)。 52名患者发生复发,累计7年的复发发生率根据风险群体(SR与HR与vHR = 12.6%与14.0%与29.6%,P = 0.003)。对于46名复发患者谁被治疗,3年的EFS和OS为42.3 +/- 8.3%和46.4 +/- 8.4%。在44例VHR患者中,化疗治疗的患者和那些接受造血干细胞移植的EF没有显着差异(P = 0.533)。 7年的高织益菌病亚组(24例,10岁以下的24例)表现出比其他VHR亚组更好的预后(P = 0.178)的趋势。结论:我们的结果显示小儿患者的患者患有风险分层治疗的患者的改善。没有任何组合的染色体异常的高织血菌病亚组可能在首次完全缓解后单独对化疗有利的化疗。

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