The diagnostic role of BAP1 in serous effusions

Hum Pathol. 2018 Sep:79:122-126. doi: 10.1016/j.humpath.2018.05.012. Epub 2018 May 24.

Abstract

The aim of this study was to analyze the diagnostic role of BAP1 in effusion cytology. Effusions (n = 258), consisting of 53 malignant mesotheliomas and 205 other cancers, the majority carcinomas (62 breast, 60 ovarian, 31 lung, 51 carcinomas of other origin, 1 melanoma), were analyzed for BAP1 expression using immunohistochemistry. BAP1 was lost in 46 (87%) mesotheliomas compared with 4 (2%) of 205 other cancers (P < .001), resulting in sensitivity and specificity of 87% and 98%, respectively. There was no significant difference between peritoneal (n = 14) and pleural (n = 39) mesotheliomas. The 4 carcinomas with loss of BAP1 included 1 ovarian, 1 breast, 1 uterine cervical, and 1 gastric carcinoma. The present study supports the role of BAP1 as a highly sensitive and specific marker for malignant mesothelioma in serous effusions and argues for inclusion of this test in all specimens in which this diagnosis is considered.

Keywords: BAP1; Carcinoma; Diagnosis; Effusions; Immunohistochemistry; Malignant mesothelioma.

Publication types

  • Comparative Study
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Ascitic Fluid / enzymology*
  • Ascitic Fluid / pathology
  • Biomarkers, Tumor / analysis*
  • Carcinoma / enzymology*
  • Carcinoma / pathology
  • Diagnosis, Differential
  • Europe
  • Female
  • Humans
  • Immunohistochemistry
  • Lung Neoplasms / enzymology*
  • Lung Neoplasms / pathology
  • Male
  • Mesothelioma / enzymology*
  • Mesothelioma / pathology
  • Mesothelioma, Malignant
  • Middle Aged
  • Pleural Effusion, Malignant / enzymology*
  • Pleural Effusion, Malignant / pathology
  • Predictive Value of Tests
  • Reproducibility of Results
  • Tumor Suppressor Proteins / analysis*
  • Ubiquitin Thiolesterase / analysis*

Substances

  • BAP1 protein, human
  • Biomarkers, Tumor
  • Tumor Suppressor Proteins
  • Ubiquitin Thiolesterase