The use of CDKN2A deletion as a diagnostic marker for malignant mesothelioma in body cavity effusions Journal Article


Authors: Illei, P. B.; Ladanyi, M.; Rusch, V. W.; Zakowski, M. F.
Article Title: The use of CDKN2A deletion as a diagnostic marker for malignant mesothelioma in body cavity effusions
Abstract: BACKGROUND. The distinction between benign reactive mesothelial cells and malignant mesothelial cells in serous effusions is difficult and has an unusually high false negative rate. Unfortunately, there are no generally accepted markers to distinguish between benign reactive and malignant mesothelial cells. Homozygous deletion of CDKN2A is frequent in mesothelioma (present in > 70% of tumors). Therefore, detection of CDKN2A deletion by fluorescence in situ hybridization (FISH) was evaluated as an ancillary test in the cytologic diagnosis of malignant mesothelioma. METHODS. Dual-color FISH for CDKN2A and chromosome 9 centromere was performed on cytolyt-fixed Thinprep slides from 6 cytologically suspicious and 7 cytologically positive effusions (all with histologically confirmed mesothelioma) and in 19 cytologically benign effusions (14 pleural effusions, 3 pericardial effusions, and 2 abdominal fluid specimens). Specimens containing ≥ 15 nuclei that lacked signals for CDKN2A but showed at least 1 signal for chromosome 9 centromere were considered positive. In samples with negative cytology, the nuclei of at least 100 mesothelial cells were evaluated; whereas, in specimens with positive or suspicious cytology, counting nuclei was done only if < 15% of nuclei showed homozygous loss of CDKN2A. RESULTS. Homozygous deletion was detected in mesothelial cells in six of seven specimens with positive cytology and in six of six specimens with suspicious cytology. Cytologically, there were numerous tumor cells in a single positive specimen without homozygous deletion. All 19 cytologically negative specimens were negative for CDKN2A deletion. CONCLUSIONS. The detection of homozygous CDKN2A deletion by FISH would have been helpful in confirming a diagnosis of mesothelioma over reactive mesothelial cells in 12 of 13 samples with positive or suspicious cytology. Further studies on larger series of patients with suspicious cytology are needed to evaluate the validity and efficiency of this approach for improving the diagnostic accuracy of effusion cytology. © 2003 American Cancer Society.
Keywords: adult; clinical article; aged; aged, 80 and over; middle aged; human cell; gene deletion; clinical trial; diagnostic accuracy; sensitivity and specificity; gene; in situ hybridization, fluorescence; tumor marker; homozygosity; fluorescence in situ hybridization; cancer cytodiagnosis; malignant mesothelioma; mesothelioma; pleura effusion; pericardial effusion; cytopathology; ascitic fluid; genetic markers; cdkn2a; centromere; cytodiagnosis; chromosome 9; sensitivity; genes, p16; pleural effusion; cdkn2a gene; fluorescent in situ hybridization; humans; human; male; female; priority journal; article; effusions; reactive mesothelium; peritoneum exudate
Journal Title: Cancer Cytopathology
Volume: 99
Issue: 1
ISSN: 1934-662X
Publisher: John Wiley & Sons  
Date Published: 2003-02-25
Start Page: 51
End Page: 56
Language: English
DOI: 10.1002/cncr.10923
PUBMED: 12589646
PROVIDER: scopus
DOI/URL:
Notes: Export Date: 12 September 2014 -- Source: Scopus
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors
  1. Valerie W Rusch
    864 Rusch
  2. Peter Illei
    26 Illei
  3. Marc Ladanyi
    1326 Ladanyi
  4. Maureen F Zakowski
    289 Zakowski