医学
细胞学
脑脊液
采样(信号处理)
癌症
病理
脑膜癌病
内科学
计算机视觉
计算机科学
滤波器(信号处理)
作者
Michael Glantz,Bernard F. Cole,Lisa Glantz,Janet Cobb,P. Mills,Andrew Lekos,Beverly C. Walters,Lawrence D. Recht
出处
期刊:Cancer
[Wiley]
日期:1998-02-15
卷期号:82 (4): 733-739
被引量:401
标识
DOI:10.1002/(sici)1097-0142(19980215)82:4<733::aid-cncr17>3.0.co;2-z
摘要
Detection of malignant cells on cytologic examination of the cerebrospinal fluid (CSF) is the diagnostic gold standard for leptomeningeal carcinomatosis. The absence of cells is a primary endpoint for most therapeutic trials. Unfortunately, false-negative results are common. Practical strategies are necessary to remedy this problem.Four physician-dependent variables (CSF sample volume, site of CSF sampling, processing time, and frequency of CSF sampling) were identified, and their contributions to the false-negative rate of CSF cytology were evaluated prospectively in 39 patients with leptomeningeal carcinomatosis. Retrospective data were analyzed to estimate the importance of these variables in daily practice.False-negative CSF cytology results correlated with small CSF volume (P < 0.001), delayed processing (P < 0.001), not obtaining CSF from a site of symptomatic or radiographically demonstrated disease (P = 0.02), and sampling fewer than two times (P < 0.001). In 1 year, 97% of CSF specimens at the study institution were of inadequate volume; >25% were processed too slowly.False-negative CSF cytology results are common, but can be minimized by: 1) withdrawing at least 10.5 mL of CSF for cytologic analysis; 2) processing the CSF specimen immediately; 3) obtaining CSF from a site of known leptomeningeal disease; and 4) repeating this procedure once if the initial cytology is negative.
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