免疫治疗并发皮质类固醇暴露的黑色素瘤脑转移患者的疗效。

Q1 Medicine
CNS Oncology Pub Date : 2023-03-01 DOI:10.2217/cns-2022-0014
Kathryn R Tringale, Anne S Reiner, Ryka R Sehgal, Katherine Panageas, Allison S Betof Warner, Michael A Postow, Nelson S Moss
{"title":"免疫治疗并发皮质类固醇暴露的黑色素瘤脑转移患者的疗效。","authors":"Kathryn R Tringale,&nbsp;Anne S Reiner,&nbsp;Ryka R Sehgal,&nbsp;Katherine Panageas,&nbsp;Allison S Betof Warner,&nbsp;Michael A Postow,&nbsp;Nelson S Moss","doi":"10.2217/cns-2022-0014","DOIUrl":null,"url":null,"abstract":"<p><p><b>Aim:</b> Immune checkpoint inhibitor (ICI) efficacy is undefined for melanoma brain metastases (MBM) with concurrent corticosteroid exposure. <b>Materials & methods:</b> We retrospectively evaluated patients with untreated MBM who received corticosteroids (≥1.5 mg dexamethasone equivalent) within 30 days of ICI. mRECIST criteria and Kaplan-Meier methods defined intracranial progression-free survival (iPFS). The lesion size-response association was evaluated with repeated measures modeling. <b>Results:</b> A total of 109 MBM were evaluated. The patient level intracranial response rate was 41%. Median iPFS was 2.3 months and overall survival was 13.4 months. Larger lesions were more likely to progress, with diameter >2.05 cm most predictive of progression (OR: 18.9; 95% CI: 2.6-139.5; p = 0.004). There was no difference in iPFS with steroid exposure pre- versus post-ICI initiation. <b>Conclusion:</b> In the largest reported ICI+corticosteroid cohort, we identify size dependent MBM response.</p>","PeriodicalId":10469,"journal":{"name":"CNS Oncology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/58/84/cns-12-93.PMC9996406.pdf","citationCount":"1","resultStr":"{\"title\":\"Efficacy of immunotherapy for melanoma brain metastases in patients with concurrent corticosteroid exposure.\",\"authors\":\"Kathryn R Tringale,&nbsp;Anne S Reiner,&nbsp;Ryka R Sehgal,&nbsp;Katherine Panageas,&nbsp;Allison S Betof Warner,&nbsp;Michael A Postow,&nbsp;Nelson S Moss\",\"doi\":\"10.2217/cns-2022-0014\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Aim:</b> Immune checkpoint inhibitor (ICI) efficacy is undefined for melanoma brain metastases (MBM) with concurrent corticosteroid exposure. <b>Materials & methods:</b> We retrospectively evaluated patients with untreated MBM who received corticosteroids (≥1.5 mg dexamethasone equivalent) within 30 days of ICI. mRECIST criteria and Kaplan-Meier methods defined intracranial progression-free survival (iPFS). The lesion size-response association was evaluated with repeated measures modeling. <b>Results:</b> A total of 109 MBM were evaluated. The patient level intracranial response rate was 41%. Median iPFS was 2.3 months and overall survival was 13.4 months. Larger lesions were more likely to progress, with diameter >2.05 cm most predictive of progression (OR: 18.9; 95% CI: 2.6-139.5; p = 0.004). There was no difference in iPFS with steroid exposure pre- versus post-ICI initiation. <b>Conclusion:</b> In the largest reported ICI+corticosteroid cohort, we identify size dependent MBM response.</p>\",\"PeriodicalId\":10469,\"journal\":{\"name\":\"CNS Oncology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/58/84/cns-12-93.PMC9996406.pdf\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"CNS Oncology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2217/cns-2022-0014\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"CNS Oncology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2217/cns-2022-0014","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 1

摘要

目的:免疫检查点抑制剂(ICI)对并发皮质类固醇暴露的黑色素瘤脑转移(MBM)的疗效尚不明确。材料与方法:我们回顾性评估了在ICI治疗30天内接受皮质类固醇(≥1.5 mg地塞米松当量)治疗的未经治疗的MBM患者。mRECIST标准和Kaplan-Meier方法定义了颅内无进展生存期(iPFS)。用重复测量模型评估病变大小与反应的关联。结果:共评估109个MBM。患者水平颅内反应率为41%。中位iPFS为2.3个月,总生存期为13.4个月。较大的病变更容易进展,直径>2.05 cm最能预测进展(OR: 18.9;95% ci: 2.6-139.5;p = 0.004)。类固醇暴露在ici开始前和开始后的iPFS没有差异。结论:在最大的ICI+皮质类固醇队列中,我们确定了大小依赖的MBM反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Efficacy of immunotherapy for melanoma brain metastases in patients with concurrent corticosteroid exposure.

Efficacy of immunotherapy for melanoma brain metastases in patients with concurrent corticosteroid exposure.

Efficacy of immunotherapy for melanoma brain metastases in patients with concurrent corticosteroid exposure.

Efficacy of immunotherapy for melanoma brain metastases in patients with concurrent corticosteroid exposure.

Aim: Immune checkpoint inhibitor (ICI) efficacy is undefined for melanoma brain metastases (MBM) with concurrent corticosteroid exposure. Materials & methods: We retrospectively evaluated patients with untreated MBM who received corticosteroids (≥1.5 mg dexamethasone equivalent) within 30 days of ICI. mRECIST criteria and Kaplan-Meier methods defined intracranial progression-free survival (iPFS). The lesion size-response association was evaluated with repeated measures modeling. Results: A total of 109 MBM were evaluated. The patient level intracranial response rate was 41%. Median iPFS was 2.3 months and overall survival was 13.4 months. Larger lesions were more likely to progress, with diameter >2.05 cm most predictive of progression (OR: 18.9; 95% CI: 2.6-139.5; p = 0.004). There was no difference in iPFS with steroid exposure pre- versus post-ICI initiation. Conclusion: In the largest reported ICI+corticosteroid cohort, we identify size dependent MBM response.

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
CNS Oncology
CNS Oncology Medicine-Neurology (clinical)
CiteScore
3.80
自引率
0.00%
发文量
12
审稿时长
13 weeks
×
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:481959085
Book学术官方微信