Avelumab和全脑放疗(WBRT)治疗实体肿瘤轻脑膜病(LMD)患者的IB期研究:结果和分子分析

IF 13.4 1区 医学 Q1 CLINICAL NEUROLOGY
Yolanda Piña, Vincent Law, Solmaz Sahebjam, Nam Tran, Navya Siddarajappa, Jiannong Li, Qianxing Mo, Manali S Phadke, John Arrington, Robert Macaulay, Sepideh Mokhtari, Brittany Evernden, Kamran A Ahmed, Inna Smalley, Michael Yu, Keiran S M Smalley, Peter A Forsyth
{"title":"Avelumab和全脑放疗(WBRT)治疗实体肿瘤轻脑膜病(LMD)患者的IB期研究:结果和分子分析","authors":"Yolanda Piña, Vincent Law, Solmaz Sahebjam, Nam Tran, Navya Siddarajappa, Jiannong Li, Qianxing Mo, Manali S Phadke, John Arrington, Robert Macaulay, Sepideh Mokhtari, Brittany Evernden, Kamran A Ahmed, Inna Smalley, Michael Yu, Keiran S M Smalley, Peter A Forsyth","doi":"10.1093/neuonc/noaf183","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Leptomeningeal disease (LMD) from solid tumors has a dismal prognosis, even following treatment with anti-PD-1 therapy. We performed a phase IB study evaluating the safety of Avelumab with whole brain radiotherapy (WBRT) in LMD (NCT03719768).</p><p><strong>Methods: </strong>Fifteen patients were enrolled with LMD from breast, lung, nasopharyngeal, ovary, and pancreatic tumors. Patients were treated with Avelumab with WBRT, with first infusion of Avelumab starting 14 days pre-WBRT and continuing during and post-WBRT for up to 5 cycles. Primary endpoints were safety and 3-month OS (OS3). Secondary endpoints included assessment of immune cells in the cerebrospinal fluid (CSF) using single cell RNA-sequencing (scRNA-Seq) pre- and post-last treatment of Avelumab.</p><p><strong>Results: </strong>DLTs occurred in 2 patients, i.e., adrenal insufficiency, hypothyroidism, and pneumonitis. Treatment-related toxicities happened in 5 patients with grade 1/2 and 5 patients with grade 3/4. Immune-related adverse events occurred in 5 patients with grade 1/2 and 3 patients with grade 3/4. The OS3 was 67% (10 of 15; 95% CI: 38 - 84%). Median-OS was 3.85 months (95%CI: 0.9-34.4 months) and median-PFS 3.85months (95%CI: 0.9-12.1 months). scRNA-Seq analysis of CSF pre- and post-last-treatment showed Avelumab+WBRT stimulated an adaptive immune response associated with decrease regulatory T cells (Tregs), among other changes in the expression of immune checkpoints on CD8+ T cells and macrophages.</p><p><strong>Conclusion: </strong>The combination of Avelumab and WBRT is safe and demonstrates activity in patients with LMD. The identification of high levels of Tregs and macrophages in the CSF of LMD patients offers future avenues for therapeutic development.</p>","PeriodicalId":19377,"journal":{"name":"Neuro-oncology","volume":" ","pages":""},"PeriodicalIF":13.4000,"publicationDate":"2025-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Phase IB Study of Avelumab and Whole Brain Radiotherapy (WBRT) in Patients with Leptomeningeal Disease (LMD) from Solid Tumors: Results and Molecular Analyses.\",\"authors\":\"Yolanda Piña, Vincent Law, Solmaz Sahebjam, Nam Tran, Navya Siddarajappa, Jiannong Li, Qianxing Mo, Manali S Phadke, John Arrington, Robert Macaulay, Sepideh Mokhtari, Brittany Evernden, Kamran A Ahmed, Inna Smalley, Michael Yu, Keiran S M Smalley, Peter A Forsyth\",\"doi\":\"10.1093/neuonc/noaf183\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Leptomeningeal disease (LMD) from solid tumors has a dismal prognosis, even following treatment with anti-PD-1 therapy. We performed a phase IB study evaluating the safety of Avelumab with whole brain radiotherapy (WBRT) in LMD (NCT03719768).</p><p><strong>Methods: </strong>Fifteen patients were enrolled with LMD from breast, lung, nasopharyngeal, ovary, and pancreatic tumors. Patients were treated with Avelumab with WBRT, with first infusion of Avelumab starting 14 days pre-WBRT and continuing during and post-WBRT for up to 5 cycles. Primary endpoints were safety and 3-month OS (OS3). Secondary endpoints included assessment of immune cells in the cerebrospinal fluid (CSF) using single cell RNA-sequencing (scRNA-Seq) pre- and post-last treatment of Avelumab.</p><p><strong>Results: </strong>DLTs occurred in 2 patients, i.e., adrenal insufficiency, hypothyroidism, and pneumonitis. Treatment-related toxicities happened in 5 patients with grade 1/2 and 5 patients with grade 3/4. Immune-related adverse events occurred in 5 patients with grade 1/2 and 3 patients with grade 3/4. The OS3 was 67% (10 of 15; 95% CI: 38 - 84%). Median-OS was 3.85 months (95%CI: 0.9-34.4 months) and median-PFS 3.85months (95%CI: 0.9-12.1 months). scRNA-Seq analysis of CSF pre- and post-last-treatment showed Avelumab+WBRT stimulated an adaptive immune response associated with decrease regulatory T cells (Tregs), among other changes in the expression of immune checkpoints on CD8+ T cells and macrophages.</p><p><strong>Conclusion: </strong>The combination of Avelumab and WBRT is safe and demonstrates activity in patients with LMD. The identification of high levels of Tregs and macrophages in the CSF of LMD patients offers future avenues for therapeutic development.</p>\",\"PeriodicalId\":19377,\"journal\":{\"name\":\"Neuro-oncology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":13.4000,\"publicationDate\":\"2025-08-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Neuro-oncology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1093/neuonc/noaf183\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuro-oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/neuonc/noaf183","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景:实体肿瘤引起的轻脑膜病(LMD)预后不佳,即使在接受抗pd -1治疗后也是如此。我们进行了一项IB期研究,评估Avelumab与LMD (NCT03719768)全脑放疗(WBRT)的安全性。方法:纳入15例来自乳腺、肺、鼻咽、卵巢和胰腺肿瘤的LMD患者。患者接受Avelumab与WBRT联合治疗,在WBRT前14天开始首次输注Avelumab,并在WBRT期间和之后持续最多5个周期。主要终点为安全性和3个月OS (OS3)。次要终点包括使用单细胞rna测序(scRNA-Seq)在Avelumab治疗前后评估脑脊液(CSF)中的免疫细胞。结果:2例患者发生dlt,分别为肾上腺功能不全、甲状腺功能减退和肺炎。治疗相关毒性发生在5例1/2级患者和5例3/4级患者。免疫相关不良事件发生在5例1/2级患者和3例3/4级患者中。OS3为67% (10 / 15;95% CI: 38 - 84%)。中位os为3.85个月(95%CI: 0.9-34.4个月),中位pfs为3.85个月(95%CI: 0.9-12.1个月)。脑脊液治疗前后的scRNA-Seq分析显示,Avelumab+WBRT刺激了适应性免疫反应,与调节性T细胞(Tregs)减少相关,以及CD8+ T细胞和巨噬细胞免疫检查点表达的其他变化。结论:Avelumab联合WBRT在LMD患者中是安全的,并且显示出活性。LMD患者脑脊液中高水平Tregs和巨噬细胞的鉴定为未来的治疗发展提供了途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phase IB Study of Avelumab and Whole Brain Radiotherapy (WBRT) in Patients with Leptomeningeal Disease (LMD) from Solid Tumors: Results and Molecular Analyses.

Background: Leptomeningeal disease (LMD) from solid tumors has a dismal prognosis, even following treatment with anti-PD-1 therapy. We performed a phase IB study evaluating the safety of Avelumab with whole brain radiotherapy (WBRT) in LMD (NCT03719768).

Methods: Fifteen patients were enrolled with LMD from breast, lung, nasopharyngeal, ovary, and pancreatic tumors. Patients were treated with Avelumab with WBRT, with first infusion of Avelumab starting 14 days pre-WBRT and continuing during and post-WBRT for up to 5 cycles. Primary endpoints were safety and 3-month OS (OS3). Secondary endpoints included assessment of immune cells in the cerebrospinal fluid (CSF) using single cell RNA-sequencing (scRNA-Seq) pre- and post-last treatment of Avelumab.

Results: DLTs occurred in 2 patients, i.e., adrenal insufficiency, hypothyroidism, and pneumonitis. Treatment-related toxicities happened in 5 patients with grade 1/2 and 5 patients with grade 3/4. Immune-related adverse events occurred in 5 patients with grade 1/2 and 3 patients with grade 3/4. The OS3 was 67% (10 of 15; 95% CI: 38 - 84%). Median-OS was 3.85 months (95%CI: 0.9-34.4 months) and median-PFS 3.85months (95%CI: 0.9-12.1 months). scRNA-Seq analysis of CSF pre- and post-last-treatment showed Avelumab+WBRT stimulated an adaptive immune response associated with decrease regulatory T cells (Tregs), among other changes in the expression of immune checkpoints on CD8+ T cells and macrophages.

Conclusion: The combination of Avelumab and WBRT is safe and demonstrates activity in patients with LMD. The identification of high levels of Tregs and macrophages in the CSF of LMD patients offers future avenues for therapeutic development.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Neuro-oncology
Neuro-oncology 医学-临床神经学
CiteScore
27.20
自引率
6.30%
发文量
1434
审稿时长
3-8 weeks
期刊介绍: Neuro-Oncology, the official journal of the Society for Neuro-Oncology, has been published monthly since January 2010. Affiliated with the Japan Society for Neuro-Oncology and the European Association of Neuro-Oncology, it is a global leader in the field. The journal is committed to swiftly disseminating high-quality information across all areas of neuro-oncology. It features peer-reviewed articles, reviews, symposia on various topics, abstracts from annual meetings, and updates from neuro-oncology societies worldwide.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信