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识别神经纤维瘤病的挑战:一项改良 Delphi 程序。

Identifying challenges in neurofibromatosis: a modified Delphi procedure.

机构信息

Department of General Paediatrics, Sophia's Children's Hospital, Rotterdam, The Netherlands.

ENCORE, Erasmus MC, Rotterdam, The Netherlands.

出版信息

Eur J Hum Genet. 2021 Nov;29(11):1625-1633. doi: 10.1038/s41431-021-00892-z. Epub 2021 Apr 26.

Abstract

Neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2) and schwannomatosis (SWN) are rare conditions with pronounced variability of clinical expression. We aimed to reach consensus on the most important manifestations meriting the development of drug trials. The five-staged modified Delphi procedure consisted of two questionnaires and a consensus meeting for 40 NF experts, a survey for 63 patient representatives, and a final workshop. In the questionnaires, manifestations were scored on multiple items on a 4-point Likert scale. The highest average scores for NF experts deciding the 'need for new treatment' were for malignant peripheral nerve sheath tumour (MPNST) (4,0) and high grade glioma (HGG) (3,9) for NF1; meningioma (3,9) for NF2 and pain (3,9) for SWN. The patient representatives assigned high scores to all manifestations, with plexiform neurofibroma being highest in NF1 (4,0), vestibular schwannoma in NF2 (4,0), and pain in SWN (3,9). Twelve experts participated in the consensus meeting and prioritised manifestations. MPNST was ranked the highest for NF1, followed by benign peripheral nerve sheath tumours. Tumour manifestations received highest ranking in NF2, and pain was the most prominent problem for SWN. Patient representative ratings for NF1 were similar to the experts' opinions, except that they ranked HGG as the most important manifestation. For NF2 and SWN, the patient representatives agreed with the experts. We conclude that NF experts and patient representatives consent to prioritise development of drug trials for MPNST, benign peripheral nerve sheath tumours, cutaneous manifestations and HGG for NF1; tumours for NF2; and pain for SWN.

摘要

神经纤维瘤病 1 型(NF1)、神经纤维瘤病 2 型(NF2)和许旺细胞瘤病(SWN)是罕见疾病,临床表现明显多变。我们旨在就最值得开展药物试验的重要表现达成共识。五阶段改良 Delphi 程序包括两轮问卷和 40 名 NF 专家的共识会议、63 名患者代表的调查以及最终的研讨会。在问卷中,表现通过 4 分制的李克特量表进行多项评分。决定“需要新治疗”的 NF 专家的平均得分最高的是恶性外周神经鞘瘤(MPNST)(4.0)和高级别神经胶质瘤(HGG)(3.9),用于 NF1;脑膜瘤(3.9)用于 NF2 和疼痛(3.9)用于 SWN。患者代表对所有表现均给予高分,其中丛状神经纤维瘤在 NF1 中得分最高(4.0),前庭神经鞘瘤在 NF2 中得分最高(4.0),疼痛在 SWN 中得分最高(3.9)。12 名专家参加了共识会议,并对表现进行了优先排序。MPNST 在 NF1 中排名最高,其次是良性外周神经鞘肿瘤。肿瘤表现在 NF2 中排名最高,疼痛是 SWN 最突出的问题。NF1 患者代表的评分与专家意见相似,只是他们将 HGG 列为最重要的表现。对于 NF2 和 SWN,患者代表与专家意见一致。我们得出结论,NF 专家和患者代表同意优先为 NF1 中的 MPNST、良性外周神经鞘肿瘤、皮肤表现和 HGG、NF2 中的肿瘤以及 SWN 中的疼痛开发药物试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0dfd/8560751/734ef59b1e30/41431_2021_892_Fig1_HTML.jpg

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引用本文的文献

本文引用的文献

1
Clinicopathologic study of glioblastoma in children with neurofibromatosis type 1.
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