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