BRAF and MEK inhibitor targeted therapy in papillary craniopharyngiomas: a cohort study.

IF 5.3 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM European Journal of Endocrinology Pub Date : 2024-08-05 DOI:10.1093/ejendo/lvae091
Dario De Alcubierre, Grigorios Gkasdaris, Margaux Mordrel, Anthony Joncour, Claire Briet, Fabien Almairac, Julien Boetto, Celine Mouly, Delphine Larrieu-Ciron, Alexandre Vasiljevic, Chiara Villa, Camille Sergeant, François Ducray, Loic Feuvret, Philippe Chanson, Bertrand Baussart, Gerald Raverot, Emmanuel Jouanneau
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Abstract

Objective: Targeted therapy (TT) with BRAF/MEK inhibitors has emerged as a potential treatment in papillary craniopharyngiomas (PCPs). However, standardized data on large cohorts are lacking. Our study aimed to assess real-life efficacy and safety of BRAF/MEK inhibition in patients with PCPs.

Design: Retrospective French multicenter study involving BRAF V600E-mutated PCP patients, treated with BRAF/MEK inhibitor combination dabrafenib and trametinib, from April 2019 to July 2023.

Methods: Objective response and clinical and safety outcomes were assessed after 3 months and at the last available follow-up during TT.

Results: Sixteen patients (8 females, mean age 50.5 ± 15.75 years), receiving either neoadjuvant therapy (NEO) for non-resectable tumors (n = 6), post-surgical adjuvant therapy (ADJ; n = 8), or palliative therapy (PAL) following failure of multimodal treatment (n = 2), were included.At the last follow-up (mean 7.6 ± 5.3 months), 12 patients showed subtotal response, 3 exhibited partial response, and 1 maintained stable disease. Mean volume reduction was 88.9 ± 4.4%, 73.3 ± 23.4%, and 91.8 ± 4.3% in the NEO, ADJ, and PAL groups, respectively.Targeted therapy resolved headaches in 5/5 patients and visual impairment in 6/9; 2/3 patients had improved neurological symptoms, 1/4 presented weight loss, and 2/14 recovered endocrine function.Targeted therapy was well-tolerated in 62.5% of cases; adverse events led to treatment discontinuation in 5 patients and definitive discontinuation in 3 cases.

Conclusions: In this study, 94% of patients showed partial response or better to TT. Adverse events were acceptable. Further research is needed to establish standardized protocols; however, these results advocate for a NEO approach in invasive PCPs.

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乳头状颅咽管瘤的 BRAF 和 MEK 抑制剂靶向治疗:一项队列研究。
目的:BRAF/MEK抑制剂靶向治疗(TT)已成为乳头状颅咽管瘤(PCP)的一种潜在治疗方法。然而,目前还缺乏大样本的标准化数据。我们的研究旨在评估BRAF/MEK抑制剂在乳头状颅咽管瘤患者中的实际疗效和安全性:回顾性法国多中心研究,涉及 BRAF V600E 突变的 PCP 患者,在 2019 年 4 月至 2023 年 7 月期间接受 BRAF/MEK 抑制剂联合达拉非尼和曲美替尼治疗:结果:16名患者(8名女性)接受了BRAF/MEK抑制剂联合达拉菲尼和曲美替尼的治疗:16名患者(8名女性,平均年龄(50.5±15.75)岁)接受了不可切除肿瘤的新辅助治疗(NEO)(n = 6)、手术后辅助治疗(ADJ;n = 8)或多模式治疗失败后的姑息治疗(PAL)(n = 2)。在最后一次随访(平均7.6±5.3个月)中,12名患者表现出次完全反应,3名患者表现出部分反应,1名患者病情保持稳定。NEO组、ADJ组和PAL组的平均体积缩小率分别为(88.9±4.4)%、(73.3±23.4)%和(91.8±4.3)%.靶向治疗解决了5/5例患者的头痛问题和6/9例患者的视力障碍问题;2/3例患者的神经症状得到改善,1/4例患者体重减轻,2/14例患者的内分泌功能得到恢复.62.5%的病例对靶向治疗耐受良好;不良反应导致5例患者停止治疗,3例患者最终停止治疗.结论:该研究发现,94%的患者对靶向治疗耐受良好:结论:在这项研究中,94%的患者对TT有部分或更好的反应。结论:在这项研究中,94% 的患者对 TT 有部分或更好的反应,不良反应是可以接受的。还需要进一步研究,以制定标准化方案;不过,这些结果主张在侵袭性五氯苯甲醚中采用 NEO 方法。
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来源期刊
European Journal of Endocrinology
European Journal of Endocrinology 医学-内分泌学与代谢
CiteScore
9.80
自引率
3.40%
发文量
354
审稿时长
1 months
期刊介绍: European Journal of Endocrinology is the official journal of the European Society of Endocrinology. Its predecessor journal is Acta Endocrinologica. The journal publishes high-quality original clinical and translational research papers and reviews in paediatric and adult endocrinology, as well as clinical practice guidelines, position statements and debates. Case reports will only be considered if they represent exceptional insights or advances in clinical endocrinology. Topics covered include, but are not limited to, Adrenal and Steroid, Bone and Mineral Metabolism, Hormones and Cancer, Pituitary and Hypothalamus, Thyroid and Reproduction. In the field of Diabetes, Obesity and Metabolism we welcome manuscripts addressing endocrine mechanisms of disease and its complications, management of obesity/diabetes in the context of other endocrine conditions, or aspects of complex disease management. Reports may encompass natural history studies, mechanistic studies, or clinical trials. Equal consideration is given to all manuscripts in English from any country.
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