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儿童多系统朗格汉斯细胞组织细胞增生症:当前治疗与未来方向

Multisystem Langerhans cell histiocytosis in children: current treatment and future directions.

机构信息

Department of Outpatient Hematology/Oncology, St Anna Children's Hospital, Kinderspitalgasse 6, Vienna, Austria.

出版信息

Paediatr Drugs. 2011 Apr 1;13(2):75-86. doi: 10.2165/11538540-000000000-00000.

Abstract

Langerhans cell histiocytosis (LCH) is a rare (about 3-5 cases per million children aged 0-14 years), non-malignant disease characterized by proliferation and accumulation of clonal dendritic cells, extreme clinical heterogeneity, and an unpredictable course. Three large-scale, international, prospective therapeutic studies (LCH-I to III) for multisystem LCH (MS-LCH) have been conducted by the Histiocyte Society since 1991. The cumulative lessons from these studies are summarized in this review. Patients with MS-LCH represent a heterogeneous group with respect to disease severity and outcome, therefore treatment stratification and risk-tailored treatment are mandatory. The risk for mortality can be predicted based on involvement of 'risk organs' (e.g. hematopoietic system, liver, and/or spleen) at diagnosis and on response to initial therapy (assessed after 6-12 weeks of treatment). Thus, patients without involvement of risk organs (low-risk group) are not at risk for mortality but need systemic therapy in order to control the disease activity and avoid reactivations and permanent consequences. Patients with risk organ involvement (risk group) are at risk for mortality, and lack of therapy response defines a subgroup with a particularly dismal prognosis (high-risk group). Those patients in the risk group who respond to therapy and survive are at risk for reactivations and permanent consequences. The LCH-I study compared the efficacy of vinblastine and etoposide, and concluded that they are equivalent single-agent treatments for children with MS-LCH. However, the results of this trial were inferior with respect to response rate at week 6, disease reactivation rate, and sequelae, when compared with historical trials using more intensive regimens. The combination of prednisolone and vinblastine was established as a standard first-line treatment through the LCH-II and LCH-III studies. The regimen consists of one to two 6-week courses (continuous oral corticosteroids 40 mg/m2/day for 4 weeks, tapered over 2 weeks plus weekly vinblastine intravenous push) of initial therapy, followed by a continuation phase (three weekly pulses of oral prednisolone 40 mg/m2/day for 5 days plus a vinblastine injection). The addition of a third drug to the standard combination (etoposide in LCH-II and methotrexate in LCH-III) failed to significantly improve survival in the risk group. The remaining mortality in the risk group is about 20%, and up to 40% in the high-risk group. Concerning low-risk MS-LCH, comparison of results of the LCH-II study with historical data suggested that the remaining reactivation rate of about 50% (and possibly permanent consequences) could be reduced by prolongation of the total treatment duration. To study this hypothesis, in the low-risk group of the LCH-III study standard maintenance therapy was randomly given for a total treatment duration of 6 and 12 months. Unpublished preliminary data from this recently closed trial suggested that prolongation of the treatment duration may significantly improve reactivation-free survival. In summary, several studies have shown that systemic therapy is indicated for all patients with MS-LCH. A standard two-drug regimen consisting of an initial 'intensive' phase for 6-12 weeks, followed by a less intensive 'maintenance phase' for a total treatment duration of at least 12 months is recommended for patients treated outside of clinical trials. Non-responders, particularly those with progressive disease in risk organs, are eligible for experimental salvage approaches. Remaining questions will be addressed in the upcoming LCH-IV trial, which is in the process of intensive preparation.

摘要

朗格汉斯细胞组织细胞增生症(LCH)是一种罕见的疾病(每 100 万 0-14 岁儿童中约有 3-5 例),其特征是非恶性疾病,表现为克隆性树突细胞的增殖和积累,临床表现呈极端的异质性,且具有不可预测的病程。自 1991 年以来,组织细胞协会开展了三项针对多系统 LCH(MS-LCH)的大型、国际、前瞻性治疗研究(LCH-I 至 III)。这些研究的累积经验教训在本综述中进行了总结。患有 MS-LCH 的患者在疾病严重程度和预后方面表现出异质性,因此需要进行治疗分层和风险分层治疗。根据诊断时是否存在“风险器官”(如造血系统、肝脏和/或脾脏)以及对初始治疗的反应(在治疗 6-12 周后评估),可以预测死亡率的风险。因此,没有风险器官受累的患者(低危组)没有死亡风险,但需要全身治疗以控制疾病活动并避免复发和永久性后果。有风险器官受累的患者(高危组)有死亡风险,且缺乏治疗反应定义了一个预后特别差的亚组(高危组)。那些在高危组中对治疗有反应并存活的患者有复发和永久性后果的风险。LCH-I 研究比较了长春新碱和依托泊苷的疗效,得出它们是治疗 MS-LCH 儿童的等效单药治疗。然而,与使用更强化方案的历史试验相比,该试验在第 6 周的反应率、疾病复发率和后遗症方面的结果较差。通过 LCH-II 和 LCH-III 研究,泼尼松龙和长春新碱的联合被确立为标准一线治疗方案。该方案包括一至两个 6 周疗程(连续口服泼尼松龙 40mg/m2/天 4 周,2 周内逐渐减量,每周长春新碱静脉推注),随后是维持期(连续口服泼尼松龙 40mg/m2/天 5 天,每周 3 次,同时给予长春新碱注射)。在标准联合治疗中加入第三种药物(LCH-II 中的依托泊苷和 LCH-III 中的甲氨蝶呤)未能显著改善高危组的生存率。高危组的剩余死亡率约为 20%,高危组的死亡率高达 40%。对于低危 MS-LCH,LCH-II 研究的结果与历史数据的比较表明,延长总治疗时间可能会降低约 50%(可能会有永久性后果)的复发率。为了研究这一假设,在 LCH-III 研究的低危组中,随机给予标准维持治疗,总治疗时间为 6 个月或 12 个月。最近结束的这项试验的未公开初步数据表明,延长治疗时间可能会显著改善无复发生存。综上所述,多项研究表明,所有患有 MS-LCH 的患者均需要进行全身治疗。推荐在临床试验之外使用包含初始“强化”期 6-12 周和随后至少 12 个月的非强化“维持”期的标准两药方案治疗患者。非应答者,特别是风险器官有进展性疾病的患者,有资格接受实验性挽救治疗方法。即将进行的 LCH-IV 试验将解决其他问题,该试验正在进行紧张的准备。

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