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维莫非尼联合克拉屈滨和阿糖胞苷治疗儿科 BRAF V600E 阳性朗格汉斯细胞组织细胞增生症可获得持久缓解。

Vemurafenib combined with cladribine and cytarabine results in durable remission of pediatric BRAF V600E-positive LCH.

机构信息

Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.

Hematopoietic Stem Cell Transplantation Department, Morozov Children Hospital, Moscow, Russia.

出版信息

Blood Adv. 2023 Sep 26;7(18):5246-5257. doi: 10.1182/bloodadvances.2022009067.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40c0/10500470/68d8d64c87f1/BLOODA_ADV-2022-009067-ga1.jpg

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