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免疫疗法治疗合并皮质类固醇暴露的黑色素瘤脑转移患者的疗效。

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

机构信息

Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

Department of Epidemiology & Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

出版信息

CNS Oncol. 2023 Mar 1;12(1):CNS93. doi: 10.2217/cns-2022-0014. Epub 2023 Feb 20.

Abstract

Immune checkpoint inhibitor (ICI) efficacy is undefined for melanoma brain metastases (MBM) with concurrent corticosteroid exposure. 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. 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. In the largest reported ICI+corticosteroid cohort, we identify size dependent MBM response.

摘要

免疫检查点抑制剂(ICI)在伴皮质类固醇暴露的黑色素瘤脑转移(MBM)中的疗效尚未确定。我们回顾性评估了在 ICI 治疗后 30 天内接受皮质类固醇(≥1.5mg 地塞米松等效物)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)。采用重复测量模型评估病灶大小反应相关性。共评估了 109 例 MBM。患者颅内反应率为 41%。中位 iPFS 为 2.3 个月,总生存期为 13.4 个月。较大的病灶更有可能进展,直径>2.05cm 的病灶最具进展预测性(OR:18.9;95%CI:2.6-139.5;p=0.004)。ICI 治疗前后皮质类固醇暴露对 iPFS 无影响。在报告的最大 ICI+皮质类固醇队列中,我们确定了与肿瘤大小相关的 MBM 反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc25/9996406/11330a5ec3ee/cns-12-93-g1.jpg

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