• 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

多系统朗格汉斯细胞组织细胞增多症初始治疗的反应:一项重要的预后指标。

Response to initial treatment of multisystem Langerhans cell histiocytosis: an important prognostic indicator.

作者信息

Minkov Milen, Grois Nicole, Heitger Andreas, Pötschger Ulrike, Westermeier T, Gadner Helmut

机构信息

St. Anna Children's Hospital, Kinderspitalgasse 9, A-1090 Vienna, Austria.

出版信息

Med Pediatr Oncol. 2002 Dec;39(6):581-5. doi: 10.1002/mpo.10166.

DOI:10.1002/mpo.10166
PMID:12376981
Abstract

BACKGROUND

Reliable prediction of prognosis allowing risk-adapted therapy remains a major issue in the management of multisystem Langerhans cell histiocytosis (LCH). In a recent publication of the International LCH Study Group, response to initial therapy appears to be a reliable outcome predictor. The aim of this study is to test this observation in a cohort of patients treated with more intensive initial therapy. Furthermore, we compare the predictive value of response to initial therapy to some other well-established stratification systems.

PROCEDURE

Response to initial combination chemotherapy (prednisolone, vinblastine, and etoposide) at 6 weeks and its prognostic value was evaluated retrospectively in 63 patients with multisystem LCH from the DAL-HX 83 and 90 Studies, and correlated to some established scoring systems from the literature.

RESULTS

After 6 weeks of therapy, 50/63 (79%) patients qualified as responders, 4/63 (7%) patients showed intermediate response, and 9/63 (14%) patients did not respond. Probability of survival at 5 years was 0.94 +/- 0.03 for responders, 0.75 +/- 0.22 for patients with intermediate response, and only 0.11 +/- 0.10 for non-responders.

CONCLUSIONS

Response to initial therapy appears to be a reliable prognostic predictor. Compared to the published international LCH-I Study, our results suggest that more intensive initial treatment allows a better discrimination between responders and non-responders. This allows to identify a subgroup of patients with extremely poor prognosis (mortality rate 90%) relatively early in the disease course.

摘要

背景

对于多系统朗格汉斯细胞组织细胞增多症(LCH)的治疗而言,能够进行风险适应性治疗的可靠预后预测仍是一个主要问题。在国际LCH研究小组最近发表的一篇文章中,初始治疗的反应似乎是一个可靠的预后预测指标。本研究的目的是在一组接受更强化初始治疗的患者队列中验证这一观察结果。此外,我们将初始治疗反应的预测价值与其他一些成熟的分层系统进行比较。

程序

回顾性评估了来自DAL-HX 83和90研究的63例多系统LCH患者对初始联合化疗(泼尼松龙、长春碱和依托泊苷)6周时的反应及其预后价值,并与文献中一些既定的评分系统进行关联。

结果

治疗6周后,50/63(79%)例患者为反应者,4/63(7%)例患者表现为中度反应,9/63(14%)例患者无反应。反应者5年生存率为0.94±0.03,中度反应患者为0.75±0.22,无反应者仅为0.11±0.10。

结论

初始治疗反应似乎是一个可靠的预后预测指标。与已发表的国际LCH-I研究相比,我们的结果表明,更强化的初始治疗能够更好地区分反应者和无反应者。这使得能够在疾病进程相对早期识别出预后极差(死亡率90%)的患者亚组。

相似文献

1
Response to initial treatment of multisystem Langerhans cell histiocytosis: an important prognostic indicator.多系统朗格汉斯细胞组织细胞增多症初始治疗的反应:一项重要的预后指标。
Med Pediatr Oncol. 2002 Dec;39(6):581-5. doi: 10.1002/mpo.10166.
2
Treatment of multisystem Langerhans cell histiocytosis. Results of the DAL-HX 83 and DAL-HX 90 studies. DAL-HX Study Group.多系统朗格汉斯细胞组织细胞增多症的治疗。DAL-HX 83和DAL-HX 90研究结果。DAL-HX研究组。
Klin Padiatr. 2000 Jul-Aug;212(4):139-44. doi: 10.1055/s-2000-9667.
3
A randomized trial of treatment for multisystem Langerhans' cell histiocytosis.多系统朗格汉斯细胞组织细胞增多症治疗的随机试验。
J Pediatr. 2001 May;138(5):728-34. doi: 10.1067/mpd.2001.111331.
4
2'-Chlorodeoxyadenosine (2-CdA) as salvage therapy for Langerhans cell histiocytosis (LCH). results of the LCH-S-98 protocol of the Histiocyte Society.2'-氯脱氧腺苷(2-CdA)作为朗格汉斯细胞组织细胞增多症(LCH)的挽救治疗。组织细胞协会LCH-S-98方案的结果。
Pediatr Blood Cancer. 2009 Dec 15;53(7):1271-6. doi: 10.1002/pbc.22229.
5
Improved outcome in the treatment of pediatric multifocal Langerhans cell histiocytosis: Results from the Japan Langerhans Cell Histiocytosis Study Group-96 protocol study.儿童多灶性朗格汉斯细胞组织细胞增多症治疗效果的改善:日本朗格汉斯细胞组织细胞增多症研究组-96方案研究结果。
Cancer. 2006 Aug 1;107(3):613-9. doi: 10.1002/cncr.21985.
6
Langerhans cell histiocytosis: retrospective evaluation of 123 patients at a single institution.朗格汉斯细胞组织细胞增多症:单机构123例患者的回顾性评估
Pediatr Hematol Oncol. 1999 Sep-Oct;16(5):377-85. doi: 10.1080/088800199276921.
7
Pulmonary Langerhans cell histiocytosis: a variable disease in childhood.肺朗格汉斯细胞组织细胞增多症:一种儿童期的可变疾病。
Pediatr Blood Cancer. 2006 Dec;47(7):889-93. doi: 10.1002/pbc.20676.
8
Langerhans cell histiocytosis in neonates.新生儿朗格汉斯细胞组织细胞增多症
Pediatr Blood Cancer. 2005 Nov;45(6):802-7. doi: 10.1002/pbc.20362.
9
Nationwide survey of single-system single site Langerhans cell histiocytosis in Japan.日本全国性单系统单部位朗格汉斯细胞组织细胞增多症调查。
Pediatr Blood Cancer. 2010 Jan;54(1):98-102. doi: 10.1002/pbc.22224.
10
Predictors of outcome in children with Langerhans cell histiocytosis.朗格汉斯细胞组织细胞增多症患儿预后的预测因素
Pediatr Blood Cancer. 2005 Jul;45(1):37-42. doi: 10.1002/pbc.20364.

引用本文的文献

1
Advances in allogeneic hematopoietic stem cell transplantation for Langerhans cell histiocytosis in children.儿童朗格汉斯细胞组织细胞增多症异基因造血干细胞移植的进展
Front Immunol. 2025 Jan 28;16:1345855. doi: 10.3389/fimmu.2025.1345855. eCollection 2025.
2
High risk Langerhans cell histiocytosis in children: the role of salvage in improving the outcome. A single center experience.儿童高危朗格汉斯细胞组织细胞增生症:挽救治疗改善预后的作用。单中心经验。
Orphanet J Rare Dis. 2024 Jun 24;19(1):242. doi: 10.1186/s13023-024-03232-8.
3
Treatment of children with refractory/relapse high risk langerhans cell histiocytosis with the combination of cytarabine, vindesine and prednisone.
用阿糖胞苷、长春新碱和泼尼松联合治疗难治性/复发性高危朗格汉斯细胞组织细胞增生症患儿。
BMC Pediatr. 2024 Jan 3;24(1):1. doi: 10.1186/s12887-023-04465-5.
4
Cladribine and cytarabine in children refractory high risk multisystem Langerhans cell histiocytosis.克拉屈滨与阿糖胞苷治疗儿童难治性高危多系统朗格汉斯细胞组织细胞增多症
Heliyon. 2023 Aug 21;9(9):e19277. doi: 10.1016/j.heliyon.2023.e19277. eCollection 2023 Sep.
5
Langerhans Cell Histiocytosis with Good Response to Low-Dose Imatinib: Case Report and Literature Review.对低剂量伊马替尼反应良好的朗格汉斯细胞组织细胞增多症:病例报告及文献综述
Case Rep Oncol. 2023 Jul 12;16(1):511-518. doi: 10.1159/000531230. eCollection 2023 Jan-Dec.
6
Clinical and prognostic features of Langerhans cell histiocytosis in adults.成人朗格汉斯细胞组织细胞增生症的临床和预后特征。
Cancer Sci. 2023 Sep;114(9):3687-3697. doi: 10.1111/cas.15879. Epub 2023 Jun 26.
7
Experiences of a Single Center in One Hundred Ninety-Four Adult Patients With Langerhans Cell Histiocytosis.单中心194例成人朗格汉斯细胞组织细胞增多症患者的经验
J Hematol. 2022 Aug;11(4):131-141. doi: 10.14740/jh1020. Epub 2022 Aug 30.
8
Multisystem Langerhans Cell Histiocytosis in Younger Infants First Presenting in Skin: A Case Series.首发于皮肤的小婴儿多系统朗格汉斯细胞组织细胞增多症:病例系列
J Pers Med. 2022 Jun 22;12(7):1024. doi: 10.3390/jpm12071024.
9
Vemurafenib for Refractory Multisystem Langerhans Cell Histiocytosis in Children: An International Observational Study.维莫非尼治疗儿童难治性多系统朗格汉斯细胞组织细胞增生症:一项国际观察性研究。
J Clin Oncol. 2019 Nov 1;37(31):2857-2865. doi: 10.1200/JCO.19.00456. Epub 2019 Sep 12.
10
Enlargement of Langerhans cell histiocytosis of the hypothalamus with progression into the basal ganglia and white matter.下丘脑朗格汉斯细胞组织细胞增多症扩大并进展至基底神经节和白质。
Surg Neurol Int. 2018 Oct 3;9:197. doi: 10.4103/sni.sni_229_18. eCollection 2018.