Department of Neurology, Research Institute and Hospital of National Cancer Center, Goyang, Korea.
Department of Laboratory Medicine, Research Institute and Hospital of National Cancer Center, Goyang, Korea.
Cancer Biomark. 2020;28(1):81-89. doi: 10.3233/CBM-190187.
To investigate the feasibility of cerebrospinal fluid (CSF) CYFRA 21-1 levels as a therapeutic monitoring biomarker in leptomeningeal carcinomatosis (LMC) patients undergoing ventriculo-lumbar perfusion (VLP) chemotherapy.
The levels of CYFRA 21-1 in 42 CSF samples from 15 LMC patients were analyzed using an electrochemiluminescence immunoassay. Samples were collected at individual time points during VLP chemotherapy. Therapeutic outcomes were measured as improvements in the Karnofsky Performance Status (KPS) score and decreasing intracranial pressure (ICP) as the main endpoint of VLP chemotherapy. Changes in CSF CYFRA 21-1 levels, protein levels, and cytology results were also investigated. We subsequently evaluated whether these changes were correlated with KPS score and ICP.
The CSF CYFRA 21-1 levels at individual time points were associated with KPS score and ICP. The KPS scores (p= 0.007) and ICP (p= 0.018) of patients with high CSF CYFRA 21-1 levels were significantly different from those of patients with low CSF CYFRA 21-1 levels. By contrast, CSF protein levels and cytological responses were not significantly associated with KPS scores and ICP.
CSF CYFRA 21-1 may have utility as a therapeutic monitoring biomarker to design personalized therapeutic strategies in LMC patients undergoing VLP chemotherapy.
为了研究脑脊液(CSF)CYFRA 21-1 水平作为脑室-腰椎灌注(VLP)化疗的脑膜转移瘤(LMC)患者治疗监测生物标志物的可行性。
采用电化学发光免疫分析法检测 15 例 LMC 患者 42 例 CSF 样本中的 CYFRA 21-1 水平。在 VLP 化疗期间的各个时间点采集样本。以 VLP 化疗的主要终点——卡氏行为状态(KPS)评分的提高和颅内压(ICP)的降低来衡量治疗效果。还研究了 CSF CYFRA 21-1 水平、蛋白水平和细胞学结果的变化。随后,我们评估了这些变化是否与 KPS 评分和 ICP 相关。
各时间点的 CSF CYFRA 21-1 水平与 KPS 评分和 ICP 相关。高 CSF CYFRA 21-1 水平患者的 KPS 评分(p=0.007)和 ICP(p=0.018)明显低于低 CSF CYFRA 21-1 水平患者。相比之下,CSF 蛋白水平和细胞学反应与 KPS 评分和 ICP 无显著相关性。
CSF CYFRA 21-1 可能可作为治疗监测生物标志物,用于设计接受 VLP 化疗的 LMC 患者的个性化治疗策略。