Department of Pediatrics, Jichi Medical University School of Medicine, 3311-1 Yakushi-ji, Shimotsuke, Tochigi, Japan.
Int J Hematol. 2013 Jan;97(1):103-8. doi: 10.1007/s12185-012-1245-0. Epub 2012 Dec 16.
Little information is available regarding effective systemic therapies for adult Langerhans cell histiocytosis (LCH). The Japan LCH Study Group has formulated an ambulatory treatment regimen for adult patients with LCH. In total, 14 patients (median age 43 years, range 20-70 years) with multifocal LCH with biopsy-confirmed histology were enrolled. None had received cytoreductive agents for LCH previously. Four had single system (SS) and ten had multi system (MS) disease. All were treated with the Special C regimen, which consists of vinblastine/prednisolone and methotrexate with daily 6-mercaptopurine for 36 weeks. At the end of the therapeutic regimen, all SS patients achieved no active disease (NAD), and six of the ten MS patients showed a response (NAD in two, partial response in four). At the last follow-up (median 34 months), 11 patients were alive (NAD in eight and active disease in three). Of the three deceased, one died of hemorrhage during the Special C treatment, and two of infections during subsequent therapy. Although this study is limited by the small sample size, this ambulatory regimen shows signs of efficacy for adult LCH. This was particularly evident for patients with multifocal SS disease, but half of those with MS disease also benefited.
关于成人朗格汉斯细胞组织细胞增生症(LCH)的有效全身治疗方法,信息有限。日本 LCH 研究组已经为成人 LCH 患者制定了一个门诊治疗方案。共有 14 名(中位年龄 43 岁,范围 20-70 岁)经活检证实为多灶性 LCH 的患者入组。这些患者以前均未接受过 LCH 的细胞减灭剂治疗。其中 4 名患者有单一系统(SS)疾病,10 名患者有多系统(MS)疾病。所有患者均接受了特殊 C 方案治疗,该方案包括长春碱/泼尼松龙和甲氨蝶呤,同时每日给予 6-巯基嘌呤 36 周。在治疗方案结束时,所有 SS 患者均达到无活动疾病(NAD),10 名 MS 患者中有 6 名显示出应答(2 名 NAD,4 名部分应答)。在最后一次随访(中位时间 34 个月)时,11 名患者存活(8 名 NAD,3 名活动疾病)。在 3 名死亡患者中,1 名在特殊 C 治疗期间因出血死亡,2 名在随后的治疗期间因感染死亡。尽管这项研究受到样本量小的限制,但这种门诊治疗方案显示出对成人 LCH 的疗效迹象。这在多灶性 SS 疾病患者中尤为明显,但一半的 MS 疾病患者也从中受益。