School of Health Professions, University of Alabama at Birmingham, Birmingham, AL, USA.
InformedDNA, Inc., St. Petersburg, FL, USA.
Clin Trials. 2024 Feb;21(1):67-72. doi: 10.1177/17407745231178839. Epub 2023 Jun 2.
BACKGROUND/AIMS: More than 99% of individuals with neurofibromatosis 1 develop cutaneous neurofibromas, benign nerve sheath tumors that manifest as nodules on the skin. These cutaneous neurofibromas emerge with age, appearing most commonly in adolescence. Nevertheless, few data have been published on how adolescents with neurofibromatosis 1 feel about cutaneous neurofibromas. The purpose of this study was to assess the perspectives of adolescents with neurofibromatosis 1 and their caregivers regarding cutaneous neurofibroma morbidity, treatment options, and acceptable risks-benefits of treatment.
An online survey was distributed through the world's largest NF registry. Eligibility criteria included self-reported neurofibromatosis 1 diagnosis, adolescent child ages 12-17 years, ≥1 cutaneous neurofibroma, and ability to read English. The survey was designed to collect details about the adolescent's cutaneous neurofibromas, views on morbidity related to cutaneous neurofibromas, social and emotional impact of cutaneous neurofibromas, communication regarding cutaneous neurofibromas, and views regarding current and potential future cutaneous neurofibroma treatment.
Survey respondents included 28 adolescents and 32 caregivers. Adolescents reported having several negative feelings about cutaneous neurofibromas, particularly feeling worried about the potential progression of their cutaneous neurofibromas (50%). Pruritus (34%), location (34%), appearance (31%), and number (31%) were the most bothersome cutaneous neurofibroma features. Topical medication (77%-96%), followed by oral medication (54%-93%), was the most preferred treatment modality. Adolescents and caregivers most often replied that cutaneous neurofibroma treatment should be initiated when cutaneous neurofibromas become bothersome. The majority of respondents were willing to treat cutaneous neurofibromas for at least 1 year (64%-75%). Adolescent and caregivers were least willing to risk pain (72%-78%) and nausea/vomiting (59%-81%) as a cutaneous neurofibroma treatment side effect.
These data indicate that adolescents with neurofibromatosis 1 are negatively impacted by their cutaneous neurofibromas, and that both adolescents and their caregivers would be willing to try longer-term experimental treatments.
背景/目的:超过 99%的神经纤维瘤病 1 型患者会出现皮肤神经纤维瘤,这是一种良性的神经鞘肿瘤,表现为皮肤上的结节。这些皮肤神经纤维瘤随年龄增长而出现,最常见于青春期。然而,关于神经纤维瘤病 1 型青少年对皮肤神经纤维瘤的看法,发表的数据很少。本研究的目的是评估神经纤维瘤病 1 型青少年及其照顾者对皮肤神经纤维瘤发病率、治疗选择以及治疗可接受风险-效益的看法。
通过世界上最大的 NF 登记处在线分发调查。入选标准包括自我报告的神经纤维瘤病 1 型诊断、年龄在 12-17 岁的青少年、至少有 1 个皮肤神经纤维瘤和能够阅读英语。该调查旨在收集有关青少年皮肤神经纤维瘤的详细信息,对皮肤神经纤维瘤发病率相关的看法、皮肤神经纤维瘤对社交和情绪的影响、有关皮肤神经纤维瘤的沟通,以及对当前和潜在未来皮肤神经纤维瘤治疗的看法。
调查对象包括 28 名青少年和 32 名照顾者。青少年报告对皮肤神经纤维瘤有多种负面感受,尤其是担心皮肤神经纤维瘤的潜在进展(50%)。瘙痒(34%)、位置(34%)、外观(31%)和数量(31%)是最令人困扰的皮肤神经纤维瘤特征。局部用药(77%-96%),其次是口服药物(54%-93%),是最受欢迎的治疗方式。青少年和照顾者最常回答说,当皮肤神经纤维瘤变得令人困扰时,应开始治疗。大多数受访者愿意至少治疗 1 年的皮肤神经纤维瘤(64%-75%)。青少年和照顾者最不愿意因治疗皮肤神经纤维瘤而面临疼痛(72%-78%)和恶心/呕吐(59%-81%)的风险。
这些数据表明,神经纤维瘤病 1 型青少年受到皮肤神经纤维瘤的负面影响,青少年及其照顾者都愿意尝试更长期的实验性治疗。