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
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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。

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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.

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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
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