Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.
Hematopoietic Stem Cell Transplantation Department, Morozov Children Hospital, Moscow, Russia.
Blood Adv. 2023 Sep 26;7(18):5246-5257. doi: 10.1182/bloodadvances.2022009067.
Langerhans cell histiocytosis (LCH) is a disorder with a variety of clinical signs. The most severe forms affect risk organs (RO). The established role of the BRAF V600E mutation in LCH led to a targeted approach. However, targeted therapy cannot cure the disease, and cessation leads to quick relapses. Here, we combined cytosine-arabinoside (Ara-C) and 2'-chlorodeoxyadenosine (2-CdA) with targeted therapy to achieve stable remission. Nineteen children were enrolled in the study: 13 were RO-positive (RO+) and 6 RO-negative (RO-). Five patients received the therapy upfront, whereas the other 14 received it as a second or third line. The protocol starts with 28 days of vemurafenib (20 mg/kg), which is followed by 3 courses of Ara-C and 2-CdA (100 mg/m2 every 12 h, 6 mg/m2 per day, days 1-5) with concomitant vemurafenib therapy. After that, vemurafenib therapy was stopped, and 3 courses of mono 2-CdA followed. All patients rapidly responded to vemurafenib: the median disease activity score decreased from 13 to 2 points in the RO+ group and from 4.5 to 0 points in the RO- group on day 28. All patients except 1 received complete protocol treatment, and 15 of them did not have disease progression. The 2-year reactivation/progression-free survival (RFS) for RO+ was 76.9% with a median follow-up of 21 months and 83.3% with a median follow-up of 29 months for RO-. Overall survival is 100%. Importantly, 1 patient experienced secondary myelodysplastic syndrome after 14 months from vemurafenib cessation. Our study demonstrates that combined vemurafenib plus 2-CdA and Ara-C is effective in a cohort of children with LCH, and the toxicity is manageable. This trial is registered at www.clinicaltrials.gov as NCT03585686.
朗格汉斯细胞组织细胞增生症(LCH)是一种具有多种临床体征的疾病。最严重的形式会影响风险器官(RO)。BRAF V600E 突变在 LCH 中的既定作用导致了靶向治疗。然而,靶向治疗不能治愈这种疾病,停止治疗会导致快速复发。在这里,我们将阿糖胞苷(Ara-C)和 2'-氯脱氧腺苷(2-CdA)与靶向治疗相结合,以实现稳定的缓解。19 名儿童入组本研究:13 名 RO 阳性(RO+),6 名 RO 阴性(RO-)。5 名患者接受了初始治疗,而其余 14 名患者则接受了二线或三线治疗。该方案首先使用 28 天的维莫非尼(20mg/kg),随后使用 3 个疗程的 Ara-C 和 2-CdA(100mg/m2,每 12 小时一次,每天 6mg/m2,第 1-5 天),同时进行维莫非尼治疗。之后,停止维莫非尼治疗,然后进行 3 个疗程的单 2-CdA 治疗。所有患者对维莫非尼迅速反应:RO+组的疾病活动评分中位数从 28 天的 13 分降至 2 分,RO-组从 4.5 分降至 0 分。除 1 名患者外,所有患者均接受了完整的方案治疗,其中 15 名患者未出现疾病进展。RO+的 2 年复发/无进展生存率(RFS)为 76.9%,中位随访时间为 21 个月,RO-为 83.3%,中位随访时间为 29 个月。总体生存率为 100%。重要的是,1 名患者在停止维莫非尼治疗 14 个月后出现继发性骨髓增生异常综合征。我们的研究表明,在一组患有 LCH 的儿童中,联合维莫非尼加 2-CdA 和 Ara-C 是有效的,且毒性可管理。该试验在 www.clinicaltrials.gov 上注册为 NCT03585686。