Mahajan Amit, Goldberg Sarah L, Weiss Sarah A, Tran Thuy, Singh Kanwar, Joshi Kavita, Aboian Mariam S, Kluger Harriet M, Chiang Veronica L
Department of Radiology and Biomedical Imaging, Yale University School of Medicine, Neuroradiology Section, CB 30, 333, Cedar St, New Haven, CT, 06510, USA.
Department of Medicine (Medical Oncology), Yale University School of Medicine, New Haven, CT, USA.
J Neurooncol. 2024 Sep;169(3):555-561. doi: 10.1007/s11060-024-04754-8. Epub 2024 Jul 4.
Central nervous system (CNS) metastases from lung cancers and melanoma, significantly contribute to morbidity and mortality. Despite advances in local therapies, there is a need for effective systemic treatments. Pembrolizumab, a PD-1 inhibitor, has shown promise for some patients with untreated brain metastases from melanoma and non-small cell lung cancer (NSCLC). This study aims to analyze the response of brain metastasis to pembrolizumab and associate characteristics like size and location with treatment outcome.
This retrospective study used imaging data from a phase II trial of pembrolizumab in melanoma or NSCLC patients with untreated brain metastases. MRI evaluations were conducted at 2 month intervals, with each brain metastasis treated as a distinct tumor for response assessment, based on modified RECIST criteria (maximum 5 lesions, 5 mm target lesions).
Of 130 individual target metastases (> 5 mm), in 65 patients with NSCLC (90 metastases) and Melanoma (40 metastases), 32 (24.6%) demonstrated complete resolution, 24 (18.5%) had partial resolution, 32 (24.6%) were SD and 42 (32.3%) demonstrated PD. Those smaller than 10 mm were more likely to show complete resolution (p = 0.0218), while those ≥ 10 mm were more likely to have PR. There was no significant association between size, number or location (supratentorial vs. infratentorial) and lesion progression. The median time to metastatic lesion progression in the brain was 5.7-7 weeks.
Pembrolizumab is effective in brain metastases from NSCLC and melanoma, showing response (CR + PR) in 43% and progression (PD) in 32% of metastases. With the median time to CNS progression of 5.7-7 weeks, careful radiographic monitoring is essential to guide timely local treatment decisions.
肺癌和黑色素瘤的中枢神经系统(CNS)转移显著增加了发病率和死亡率。尽管局部治疗取得了进展,但仍需要有效的全身治疗。帕博利珠单抗是一种PD-1抑制剂,已显示出对一些未经治疗的黑色素瘤和非小细胞肺癌(NSCLC)脑转移患者有疗效。本研究旨在分析脑转移对帕博利珠单抗的反应,并将大小和位置等特征与治疗结果相关联。
这项回顾性研究使用了帕博利珠单抗治疗未经治疗的黑色素瘤或NSCLC脑转移患者的II期试验的影像数据。每2个月进行一次MRI评估,根据改良的RECIST标准(最多5个病灶,5毫米的靶病灶),将每个脑转移灶视为一个独立的肿瘤进行反应评估。
在130个单独≥5毫米的靶转移灶中,65例NSCLC患者(90个转移灶)和黑色素瘤患者(40个转移灶)中,32个(24.6%)完全消退,24个(18.5%)部分消退,32个(24.6%)病情稳定,42个(32.3%)病情进展。小于10毫米的转移灶更有可能完全消退(p = 0.0218),而≥10毫米的转移灶更有可能部分缓解。大小、数量或位置(幕上与幕下)与病灶进展之间无显著关联。脑转移灶进展的中位时间为5.7 - 7周。
帕博利珠单抗对NSCLC和黑色素瘤的脑转移有效,43%的转移灶有反应(完全缓解+部分缓解),32%的转移灶病情进展。由于中枢神经系统进展的中位时间为5.7 - 7周,仔细的影像学监测对于指导及时的局部治疗决策至关重要。