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[采用LSH II方案治疗朗格汉斯细胞组织细胞增多症的结果]

[Treatment results of Langerhans cell histiocytosis with LSH II protocol].

作者信息

Mottl H, Ganevová M, Radvanská J, Chánová M, Smelhaus V, Kodet R, Mrhalová M, Tichý M

机构信息

Klinika dĕtské hematologie a onkologie 2. LF UK a FNM, Praha.

出版信息

Cas Lek Cesk. 2005;144(11):753-5.

Abstract

BACKGROUND

The aim of study was to evaluate outcome of international treatment protocol LCH II for children with Langerhans cell histiocytosis treated in FN Motol.

METHODS AND RESULTS

Between November 1995 and December 2003, 46 children were treated, sex ratio M:F 29:17 and median age at diagnosis 6 years 8 months. 28 children (60.9%) suffered from monosystem disease with majority of bone lesions (23 times) with skull predominance (16 times). Surgery was primary treatment modality for monosystem disease. Five children with recurrence were successfully treated by protocol LCH II - LR (3x) and LCH III - LR /G2/, respectively. Eighteen children (39.1%) suffered from multisystem disease. 6 out of 18 patients were treated according to low-risk protocol LCH II - LR and 12 children by high-risk scheme LCH II - HR at the non-randomized branch included etoposide. Recurrence was revealed in 11 patients and 10 of them reached 2nd or 3rd complete remission (CR) by 2 - chlorodeoxyadenosine (CDA) monotherapy, and 1 child reached 2nd CR by LCH II - HR scheme. Two children underwent irradiation after bone lesion excision as well as 1 child as supplemental treatment. Totally, 29 children (63.0%) achieved 1st CR, 14 (30.4%) 2nd CR, 2 (4.4%) 3rd CR, and 1 child died because of LCH progression. There were no severe side effects of chemotherapy. Follow-up median time was 5 years 8 months (range 9 months - 9 years 6 months).

CONCLUSIONS

LCH II protocol is safe and effective. Results revealed that treatment of patients with multisystem disease might demand some treatment modification.

摘要

背景

本研究旨在评估在FN莫托尔医院接受治疗的朗格汉斯细胞组织细胞增多症患儿采用国际治疗方案LCH II的治疗效果。

方法与结果

1995年11月至2003年12月期间,共治疗46例患儿,男女比例为29:17,诊断时的中位年龄为6岁8个月。28例患儿(60.9%)患有单系统疾病,多数为骨病变(23次),以颅骨病变为主(16次)。手术是单系统疾病的主要治疗方式。5例复发患儿分别通过LCH II - LR方案(3例)和LCH III - LR /G2/方案成功治疗。18例患儿(39.1%)患有多系统疾病。18例患者中有6例根据低风险方案LCH II - LR进行治疗,12例患儿通过包含依托泊苷的非随机分组高风险方案LCH II - HR进行治疗。11例患者出现复发,其中10例通过2 - 氯脱氧腺苷(CDA)单一疗法达到第二次或第三次完全缓解(CR),1例患儿通过LCH II - HR方案达到第二次CR。2例患儿在骨病变切除后接受了放疗,1例患儿接受放疗作为补充治疗。总体而言,29例患儿(63.0%)达到第一次CR,14例(30.4%)达到第二次CR,2例(4.4%)达到第三次CR,1例患儿因LCH病情进展死亡。化疗未出现严重副作用。中位随访时间为5年8个月(范围9个月 - 9年6个月)。

结论

LCH II方案安全有效。结果显示,多系统疾病患者的治疗可能需要进行一些治疗调整。

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