Triana Paloma, Miguel Miriam, Díaz Mercedes, Cabrera Marta, López Gutiérrez Juan Carlos
Department of Pediatric Surgery, La Paz Children's Hospital, Madrid, Spain.
Department of Pediatric Plastic Surgery, La Paz Children's Hospital, Madrid, Spain.
Lymphat Res Biol. 2019 Oct;17(5):504-511. doi: 10.1089/lrb.2018.0068. Epub 2019 Apr 13.
Mechanistic target of rapamycin (mTOR) inhibitors are being used off-label showing promising results in patients with vascular anomalies. Children with lymphatic malformations (LMs) involving the airway benefit from sirolimus therapy soon after birth, reducing the need of tracheostomy. Available information about efficacy and side effects in neonates remains poor. We present seven newborns with severe head and neck LM showing response to sirolimus with no significant toxicity. We performed a retrospective review of neonates with head and neck LM who received sirolimus between January 2014 and May 2018 with upper airway involvement needing ventilatory support. We analyzed type of LM, involved anatomical area, symptoms and response to sirolimus, including dosage, blood levels, response, side effects, and complications. Seven neonates received primary treatment with sirolimus in the context of cervical LM. Sirolimus was started at the recommended dose of 0.8 mg/m/12 h and adjusted to maintain blood levels between 4 and 12 ng/mL. Median follow-up was 32 months (4-43) with a median treatment duration of 12 months (3-43). One patient had complete resolution of the malformation, one had complete resolution of symptoms, and five had partial resolution of the malformation with significant improvement in their respiratory conditions. Two patients required additional subtotal surgical resection and one tracheostomy. Four patients remain under treatment. Toxicity was not observed. Sirolimus is a safe drug in neonates and can be considered the first therapeutical option in newborns at high risk of respiratory failure before sclerosis or surgery. Close follow-up is mandatory to identify side effects at long-term use.
雷帕霉素的机制性靶点(mTOR)抑制剂正在被用于非标签用途,在血管异常患者中显示出有前景的结果。患有累及气道的淋巴管畸形(LM)的儿童在出生后不久即从西罗莫司治疗中获益,减少了气管造口术的需求。关于新生儿疗效和副作用的现有信息仍然匮乏。我们报告了7例患有严重头颈部LM的新生儿,他们对西罗莫司有反应且无明显毒性。我们对2014年1月至2018年5月期间接受西罗莫司治疗且上气道受累需要通气支持的头颈部LM新生儿进行了回顾性研究。我们分析了LM的类型、受累解剖区域、症状以及对西罗莫司的反应,包括剂量、血药浓度、反应、副作用和并发症。7例新生儿在颈部LM的情况下接受了西罗莫司的初始治疗。西罗莫司起始剂量为推荐的0.8mg/m²/12小时,并进行调整以维持血药浓度在4至12ng/mL之间。中位随访时间为32个月(4 - 43个月),中位治疗持续时间为12个月(3 - 43个月)。1例患者畸形完全消退,1例症状完全消退,5例畸形部分消退且呼吸状况显著改善。2例患者需要额外进行次全手术切除,1例需要气管造口术。4例患者仍在接受治疗。未观察到毒性反应。西罗莫司在新生儿中是一种安全的药物,在硬化或手术前有呼吸衰竭高风险的新生儿中可被视为首选治疗方案。必须进行密切随访以识别长期使用时的副作用。