• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[儿童恶性淋巴瘤确诊病例中特定临床及实验室特征的治疗结果与预后意义]

[Treatment results and prognostic significance of selected clinical and laboratory features in children diagnosed with malignant lymphoma].

作者信息

Kamieńska E

机构信息

I Kliniki Chorób Dzieci Katedry Chorób Dzieci Pomorskiej Akademii Medycznej w Szczecinie.

出版信息

Ann Acad Med Stetin. 1996;42:105-22.

PMID:9199116
Abstract

The clinical picture and results of treating malignant lymphoma in children, diagnosed and treated at the Pediatric Institute of Pomeranian Medical Academy in Szczecin during the period between May 1979 and February 1992, were analyzed. The studied group consisted of 33 children (23 boys, 10 girls) aged between 41-169 months (median 112 months, mean 110 months) having Hodgkin's lymphoma (HL), and 35 children (26 boys, 9 girls), aged between 35-171 months (median 101 months, mean 104 months), with non-Hodgkin's lymphoma (NHL). Till 1987 the children with HL were treated according to MOPP program, and since 1988 with MVPP/B-DOPA. Two children were treated according to COMP and ABVD programs. The NHL children were treated till 1985 with LSA2L2 or COAMP, and from 1986 with BFM-NHL 86 with the modification of methotrexate doses. The duration of observation involving HL cases ranged from 2 to 156 months (median 76, mean 78 months), that covering NHL cases from 3 to 153 months (median 28 months, mean 44 months). It was proved that the results of HL treatment in the Pediatric Institute of Pomeranian Medical Academy in Szczecin were comparable with the results of other centers. The probability of event free survival (EFS) for the whole group was 0.818, for children treated by MOPP program was 0.888, for children with MVPP/B-DOPA was 0.900. Unfortunately, the results of NHL treatment in our center in Szczecin are worse than those of other hematologic-oncologic institutions. The EFS was 0.550. The reason why our results were poor in treating NHL in our center was: delay in beginning the remission-inducing treatment because of diagnostic difficulties (especially in smaller hospitals): prolongation of the first remission-inducing therapy over 14 days, mainly due to generalized infection, generalized diathesis haemorrhagica with bleeding from the alimentary tract, and finally the need of modifying the treatment program BFM 86 concerning primarily the lowering of methotrexate doses from 5 g/m2 to 0.5 g/m2. That was necessary in view of our inability of monitoring the level of methotrexate in blood. All of those findings suggest the necessity of: 1) earlier proper diagnosis; the physicians taking care of children should be aware of high incidence of such neoplasms in children, especially with atypical clinical presentation; 2) full realization of the therapeutic program (particularly remission-inducing one). A general real improvement of the treatment conditions in hospitals is indispensable. The actual work has proved that in HL the detrimental prognostic factors included; the age above 10 years and histological type of nodular sclerosis. Children older than 10 years had lower EFS (1.0 vs 0.65; p < 0.05). EFS in histological type of nodular sclerosis was also lower namely (0.925 vs 0.600; p < 0.05). In the NHL group the bad prognostic factors were the age over 10 years and proliferation of T-cells. Patients older than 10 years displayed statistically lower EFS (0.709 vs 0.288; p < 0.05). The children with T-NHL had also lower EFS (0.621 vs 0.187; p < 0.05). It is necessary that the prognosis in these children should be substantially improved by elaborating treatment programme being adjusted to cope with the risk factors.

摘要

对1979年5月至1992年2月期间在什切青的波美拉尼亚医科大学儿科研究所诊断和治疗的儿童恶性淋巴瘤的临床表现及治疗结果进行了分析。研究组包括33名年龄在41 - 169个月(中位数112个月,平均110个月)的儿童(23名男孩,10名女孩)患有霍奇金淋巴瘤(HL),以及35名年龄在35 - 171个月(中位数101个月,平均104个月)的儿童(26名男孩,9名女孩)患有非霍奇金淋巴瘤(NHL)。直到1987年,HL患儿按照MOPP方案进行治疗,自1988年起采用MVPP/B - DOPA方案。两名患儿按照COMP和ABVD方案进行治疗。NHL患儿在1985年之前采用LSA2L2或COAMP方案治疗,从1986年起采用BFM - NHL 86方案并调整了甲氨蝶呤剂量。HL病例的观察期为2至156个月(中位数76个月,平均78个月),NHL病例的观察期为3至153个月(中位数28个月,平均44个月)。事实证明,什切青的波美拉尼亚医科大学儿科研究所HL的治疗结果与其他中心的结果相当。整个组无事件生存(EFS)的概率为0.818,采用MOPP方案治疗的儿童为0.888,采用MVPP/B - DOPA方案治疗的儿童为0.900。不幸的是,我们什切青中心NHL的治疗结果比其他血液肿瘤机构的结果更差。EFS为0.550。我们中心治疗NHL结果不佳的原因是:由于诊断困难(尤其是在较小的医院)导致诱导缓解治疗开始延迟;首次诱导缓解治疗延长超过14天,主要是由于全身感染、全身出血素质伴消化道出血,最后需要修改BFM 86治疗方案,主要是将甲氨蝶呤剂量从5 g/m²降至0.5 g/m²。鉴于我们无法监测血液中甲氨蝶呤的水平,这是必要的。所有这些发现表明有必要:1)更早地进行正确诊断;照顾儿童的医生应意识到此类肿瘤在儿童中的高发病率,尤其是具有非典型临床表现的情况;2)充分实施治疗方案(尤其是诱导缓解方案)。医院治疗条件的全面切实改善是必不可少的。实际工作证明,在HL中不利的预后因素包括;10岁以上的年龄和结节硬化的组织学类型。10岁以上的儿童EFS较低(1.0对0.65;p < 0.05)。结节硬化组织学类型的EFS也较低,即(0.925对0.600;p < 0.05)。在NHL组中,不良预后因素是10岁以上的年龄和T细胞增殖。10岁以上的患者EFS在统计学上较低(0.709对0.288;p < 0.0

相似文献

1
[Treatment results and prognostic significance of selected clinical and laboratory features in children diagnosed with malignant lymphoma].[儿童恶性淋巴瘤确诊病例中特定临床及实验室特征的治疗结果与预后意义]
Ann Acad Med Stetin. 1996;42:105-22.
2
[Treatment of aggressive non-Hodgkin's lymphoma with the ProMACE- CytaBOM protocol].采用ProMACE-CytaBOM方案治疗侵袭性非霍奇金淋巴瘤
Srp Arh Celok Lek. 1998 Sep-Oct;126(9-10):345-8.
3
Perspectives of the management of childhood lymphoma: experience at Tygerberg Hospital, Western Cape, South Africa.儿童淋巴瘤的管理视角:南非西开普省泰格伯格医院的经验
Transfus Apher Sci. 2005 Feb;32(1):27-31. doi: 10.1016/j.transci.2004.10.003. Epub 2005 Jan 22.
4
[Influence of age on treatment results in children and adolescents with Hodgkin's disease].[年龄对儿童及青少年霍奇金淋巴瘤治疗结果的影响]
Przegl Lek. 2004;61 Suppl 2:40-4.
5
[Over 30-year experience of Polish Pediatric Leukemia/Lymphoma Study Group for treatment of Hodgkin's disease in children and adolescents: improvement curability and decrease of serious complications].[波兰儿童白血病/淋巴瘤研究组治疗儿童和青少年霍奇金病的30多年经验:提高治愈率并减少严重并发症]
Przegl Lek. 2004;61 Suppl 2:33-9.
6
Survival improvement of young patients, aged 16-23, with Hodgkin lymphoma (HL) during the last three decades.过去三十年中16至23岁霍奇金淋巴瘤(HL)年轻患者的生存改善情况。
Anticancer Res. 2007 Mar-Apr;27(2):1191-7.
7
Treatment of pediatric Hodgkin's disease with chemotherapy alone or combined modality therapy.单纯化疗或综合治疗小儿霍奇金病
Radiat Oncol Investig. 1999;7(6):365-73. doi: 10.1002/(SICI)1520-6823(1999)7:6<365::AID-ROI7>3.0.CO;2-W.
8
[Feasibility study of application of international prognostic score on prediction of prognosis for advanced Hodgkin's lymphoma].国际预后评分在晚期霍奇金淋巴瘤预后预测中的应用可行性研究
Ai Zheng. 2006 Aug;25(8):1013-8.
9
Comparison between hybrid MOPPABV and ABVD chemotherapy protocols for Hodgkin's lymphoma in public hospitals of the largest South American city: a retrospective 14-year study.南美最大城市公立医院中霍奇金淋巴瘤的混合MOPPABV与ABVD化疗方案比较:一项为期14年的回顾性研究
Ann Hematol. 2009 Jul;88(7):633-7. doi: 10.1007/s00277-008-0635-0. Epub 2008 Nov 8.
10
Treatment outcome and prognostic factors for relapse after high-dose chemotherapy and peripheral blood stem cell rescue for patients with poor risk high grade non-Hodgkin's lymphoma.高危高级别非霍奇金淋巴瘤患者大剂量化疗及外周血干细胞救援后的治疗结果及复发的预后因素
Bone Marrow Transplant. 1999 Aug;24(3):271-7. doi: 10.1038/sj.bmt.1701894.