首页> 外文期刊>Cancer Biology >Prognostic Impact of pathological subtypes in children with Classic Hodgkin Lymphoma: A comprehensive analysis
【24h】

Prognostic Impact of pathological subtypes in children with Classic Hodgkin Lymphoma: A comprehensive analysis

机译:病理亚型对经典霍奇金淋巴瘤患儿的预后影响:综合分析

获取原文
       

摘要

Introduction: Hodgkin lymphoma (HL) is a highly curable malignancy. Different pathological subtypes of classic Hodgkin lymphoma (CHL) are all treated with the same multimodality treatment, although they all do not have the same outcome. Our aim in this retrospective study was to highlight the presentation and prognosis of lymphocyte-depleted subtype and to compare it with the rest of subtypes in childhood CHL. Patients and methods : The data of 1197 children with biopsy-proven Hodgkin's lymphoma diagnosed from 2007 till 2017 at children cancer hospital Egypt were revised retrospectively. The outcome of different pathological subtypes are compared with other subtypes. Results: From a total of 1197 children with HL, ten patients (0.835%) were diagnosed as Lymphocyte Depleted Classic Hodgkin′s Lymphoma (LDCHL). All patients with LDCHL were diagnosed as high risk or advanced stages (3B, 4A, or 4B). Patients presented more often with advanced (high risk) disease as compared to other subtypes (100% versus 29.7%, respectively) and B symptoms (70% versus 32.3%, respectively). Risk factors as large mediastinal mass (50% versus 19%, respectively), high ESR (5 Out of 6 had elevated ESR), and involvement of more than three lymph nodes (80%). LDCHL cases showed an involvement of bone marrow in 22% of cases. The 5 years overall (OS) and Event-free survival (EFS) for LDCHL is the worst as compared to other pathologic subtypes CHL, 68.57% and 48% respectively. Conclusion : Children with LDCHL had a much aggressive presentation, responds inadequately to standard therapy, as well as having the worst outcome of all pathological subtypes CHL. Our results denote that children with LDCHL should receive more intensive chemotherapy.
机译:简介:霍奇金淋巴瘤(HL)是高度可治愈的恶性肿瘤。尽管经典霍奇金淋巴瘤(CHL)的不同病理亚型的预后不同,但均采用相同的多模态治疗。我们在这项回顾性研究中的目的是强调淋巴细胞贫乏亚型的表现和预后,并将其与儿童期CHL中的其余亚型进行比较。患者和方法:回顾性地修订了2007年至2017年在埃及儿童癌症医院诊断为经活检证实的霍奇金淋巴瘤的1197例儿童的数据。将不同病理亚型的结果与其他亚型进行比较。结果:在总共1197例HL儿童中,有10例(0.835%)被诊断为淋巴细胞减少的经典霍奇金淋巴瘤(LDCHL)。所有患有LDCHL的患者均被诊断为高危或晚期(3B,4A或4B)。与其他亚型(分别为100%对29.7%)和B症状(分别为70%对32.3%)相比,患者更常出现晚期(高风险)疾病。危险因素包括大纵隔肿块(分别为50%和19%),高ESR(6个中的5个ESR升高)以及涉及三个以上淋巴结(80%)。 LDCHL病例显示有22%的病例累及骨髓。与其他病理亚型CHL相比,LDCHL的5年总体(OS)和无事件生存(EFS)最差,分别为68.57%和48%。结论:LDCHL儿童表现出侵略性,对标准疗法的反应不佳,并且在所有病理亚型CHL中结果最差。我们的结果表明,患有LDCHL的儿童应接受更强化的化疗。

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