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用克拉屈滨治疗朗格汉斯细胞组织细胞增多症,10名成年患者中有9名实现了长期完全缓解。

[Treatment of Langerhans cells histiocytosis by cladribin reached long-term complete remission in 9 out of 10 adult patients].

作者信息

Adam Z, Szturz P, Duraš J, Pour L, Krejčí M, Rehák Z, Koukalová R, Navrátil M, Hájek R, Král Z, Mayer J

机构信息

Interni hematoonkologicka klinika LF MU a FN Brno, Brno.

出版信息

Klin Onkol. 2012;25(4):255-61.

Abstract

BACKGROUND

The effectiveness of cladribine depends on the ratio of activating (deoxycytidine kinase) and inactivating (5-nucleotidase) enzymes. Not only is this ratio high in resting lymphocytes but also in Langerhans cells as well in some other histiocytic cells. Therefore, cladribine shows high effectiveness in patients with Langerhans cell histiocytosis (LCH). In 2003, the first report on excellent results with cladribine in first line treatment of patients with multisystem or multifocal LCH was published. That is why we use cladribine for adult patients with relapsing form of LCH and also for first line treatment of multifocal and multisystem LCH at our department.

PATIENTS AND METHODS

Since 2001, we have treated altogether 10 adults (9 male and 1 female) with cladribine. The median age at diagnosis was 31.5 years (range: 5-45). The multiorgan form of the disease was present in 8 patients, and 2 patients had the multifocal skeletal form with aggressive disease course. Cladribine at a dose of 5 mg/m2 SC per day was given as a 5-day course at 28-day intervals. In cases of insufficient effectiveness, in two patients after the 3rd cycle with cladribine monotherapy, we proceeded to combination therapy with cladribine of 5 mg/m2 per day, cyclophosphamide 150 mg/m2 per day and dexamethasone 20 mg per day, all on days 1-5. We planned 6 cycles at the most.

RESULTS

The median of cladribine cycles was 5 (range: 4-6). Altogether, 10 patients finished therapy; out of them 9 are in complete remission with the follow-up median of 26 months (range: 16-94). Treatment failure was noted only in 1 patient - in 60 days after therapy cessation the disease progressed and required further treatment (CHOEP, high-dose BEAM chemotherapy with autologous transplantation followed by Revlimid treatment and allogeneic transplantation). Treatment response - disappearance of infiltrate in the pituitary infundibulum - was observed in 2 patients with LCH affecting the pituitary infundibulum.

CONCLUSION

Cladribine is a suitable medication for multiorgan and multifocal forms of LCH. In our group of ten evaluated patients, cladribine therapy resulted in 90% of long-term complete remissions. Three patients had CNS involvement and in all three patients, treatment responses have been achieved.

摘要

背景

克拉屈滨的疗效取决于激活酶(脱氧胞苷激酶)和失活酶(5-核苷酸酶)的比例。不仅静止淋巴细胞中的这一比例较高,朗格汉斯细胞以及其他一些组织细胞中的比例也较高。因此,克拉屈滨在朗格汉斯细胞组织细胞增多症(LCH)患者中显示出高效性。2003年,发表了首篇关于克拉屈滨一线治疗多系统或多灶性LCH患者取得优异疗效的报告。这就是我们在科室将克拉屈滨用于复发型LCH成年患者以及多灶性和多系统LCH一线治疗的原因。

患者与方法

自2001年以来,我们共使用克拉屈滨治疗了10名成年患者(9名男性和1名女性)。诊断时的中位年龄为31.5岁(范围:5 - 45岁)。8名患者患有多器官型疾病,2名患者患有伴有侵袭性病程的多灶性骨骼型疾病。克拉屈滨以每天5 mg/m²皮下注射的剂量给药,为期5天,每间隔28天进行一个疗程。在疗效不佳的情况下,2名患者在接受克拉屈滨单药治疗的第3个周期后,我们采用了联合治疗,即每天5 mg/m²的克拉屈滨、每天150 mg/m²的环磷酰胺和每天20 mg的地塞米松,均在第1 - 5天使用。我们最多计划进行6个周期的治疗。

结果

克拉屈滨治疗周期的中位数为5(范围:4 - 6)。共有10名患者完成治疗;其中9名患者完全缓解,随访的中位时间为26个月(范围:16 - 94个月)。仅1名患者出现治疗失败——在治疗停止60天后疾病进展,需要进一步治疗(CHOEP、高剂量BEAM化疗联合自体移植,随后进行来那度胺治疗和异基因移植)。在2名累及垂体漏斗部的LCH患者中观察到治疗反应——垂体漏斗部浸润消失。

结论

克拉屈滨是治疗多器官型和多灶性LCH的合适药物。在我们评估的10名患者组中,克拉屈滨治疗导致90%的患者长期完全缓解。3名患者有中枢神经系统受累,所有3名患者均取得了治疗反应。

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