MATERIALS AND METHODS

Case selection

Sixty-four patients with mesothelioma, 117 patients with reactive mesothelial hyperplasia, and 20 patients with FP who were diagnosed at our pathology clinic between January 2009 and March 2017 were included in the study. Diagnosis of the MM cases was made according to presence of deep-tissue invasion composed of mesothelial cells using immunohistochemically applied calretinin, WT1, and D2.40 stains of biopsy tissue. The cell blocks obtained from cytological material taken during biopsy were evaluated for the presence of mesothelial cells. The cell blocks, which were also stained with the same immunohistochemical markers, were also analyzed for this study.

We examined slides, paraffin blocks, and report archives of all the study cases where available. Cell blocks of cytological material and biopsy tissue were evaluated for suitability for immunohistochemical examination. Both cell blocks and tissue blocks that had sufficient mesothelial cells (≥20 cells) were immunohistochemically stained with BAP1 antibodies. For cases that did not have cell blocks or that had insufficient mesothelial cells in cell blocks, only tissue blocks were stained. Two pathologists, blinded from the diagnosis, evaluated results on light microscopy.

Immunohistochemical procedure

For immunohistochemical examination, 4-μm-thick sections prepared from formalin-fixed and paraffin-embedded tissues were used. Tissue sections were taken into electrostatically charged slides (Isotherm) and dried at 70°C for at least 1 hour. The whole immunohistochemical staining process, including deparaffinization and antigen release, was performed on a fully automated immunohistochemistry staining device (Ventana BenchMark XT, Ventana Medical Systems, Tucson, AZ, USA). We used a ready-made kit that is biotin-free, based on an horseradish peroxidase (HRP) multimer, and contains hydrogen peroxide substrate and 3,3'-diaminobenzidine tetrahydrochloride (DAB) chromogen (Catalog number 760-500, ultraView Universal DAB Detection Kit, Ventana Medical Systems) for this process. BAP1 antibody (1:100, Thermo Fisher Scientific, Rockford, IL, USA) was administered. Contrast staining with hemotoxylin and bluing solution was performed with a staining device; the procedure was completed manually with dehydration, transparency with xylene, and closure of the sections with lamel.

Inflammatory and stromal cells in the cell block of cytologic materials and biopsy materials were used as a positive internal control for BAP1 antibody. Mesothelial cells were evaluated via nuclear staining with BAP1 antibodies. Detection of nuclear staining was interpreted as “BAP1 normal expression” (Fig. 1A–D) and lack of staining as “loss of BAP1 expression” (Fig. 2A–D). Cytoplasmic staining, observed in some cases, was evaluated as nonspecific, and we took into account only nuclear staining.

Statistical analyses

Statistical analyses were performed using SPSS ver. 16.0 software (SPSS Inc., Chicago, IL, USA). Variables were evaluated for normality both visually (histogram and probability graphs) and statistically (Kolmogorov-Smirnov/Shapiro-Wilk tests). Descriptive analyses were performed using mean and standard deviations for normally distributed variables. In cases where the data were not normally distributed, the Mann-Whitney U test was used to compare two groups and the Kruskal-Wallis test was used to compare more than two groups. The chi-square and Fisher exact tests were used to compare nominal variables, e.g., biopsy results. Patient age was recategorized into ordinal groups and trend analysis was performed with meaningful parameters. Also, we used the Kappa test to determine the consistency of biopsy results with each other. A p-value <.05 was considered statistically significant.

RESULTS

Of 64 MM cases, 40 (62.5%) were male and 24 (37.5%) were female. The median age at diagnosis was 61 (±12.26) years, and 56.3% of the patients were between 40–64 years old. While 57 of the 64 cases (89.1%) originated in the pleura, six (9.4%) were from the peritoneum and one (1.5%) from the pericardium. In histological subtypes, 54 cases (84.4%) were epithelioid type, five cases (5.2%) sarcomatoid type, and 5 cases (5.2%) biphasic type. Asbestos exposure was detected in 35.9% of our MM cases.

Seventy-four of 117 RMH cases (63.2%) and 15 of 20 FP cases (75%) were male, with median ages of 45 (±19.36) years and 59.5 (±16.07) years, respectively. Of the 137 non-MM cases (117 RMH and 20 FP), 103 biopsy specimens (75.1%) were taken from the pleura, 31 (22.6%) from the peritoneum, and 3 (2.3%) from the pericardium.

According to biopsy status, the BAP1 expression loss rate (76.6%) in patients diagnosed with MM was significantly higher than among other benign diseases (0%; p<.001). When MM cases were evaluated by histological subtype, the BAP1 expression loss rate was 81.5% in epithelioid-type MM cases, whereas no BAP1 expression loss was observed among sarcomatoid-type MM cases. BAP1 expression loss was observed in all five biphasic cases, but all expression loss was found in the epithelioid components, and no loss was found in the sarcomatoid components (Table 1). For MM diagnosis, the sensitivity and specificity of BAP1 expression loss in tissue biopsies were 76.56% and 100%, respectively.

Only the epithelioid histological subtype of malignant mesothelioma cases had sufficient cell block material. According to cell block status, expression loss was observed in all malignant mesothelioma cases (n=11), while there was no expression loss in any of the benign processes (8 RMH and 1 FP cases). The sensitivity and specificity of the BAP1 test were both 100% for cell block (Table 2).

When the consistency between cell block and tissue biopsy results for BAP1 expression status was examined, a high consistency (ĸ=0.90) and significant correlation were obtained (p< .001). Accordingly, 10 of the 11 patients (90.9%) who were found to have BAP1 expression loss in cell block also showed expression loss in biopsy, while all nine patients (100%) who did not show expression loss in cell block also showed no loss in biopsy (Table 3).

MM cases were evaluated in terms of BAP1 expression loss according to age, gender, asbestos exposure, additional cancer, and localization, and no significant differences were found (all p> .05) (Table 4).

DISCUSSION

Due to high tumor aggressiveness, distinguishing MM cases from reactive processes and diagnosing accurately as early as possible is of great importance [4-6]. However, the only reliable criterion for histopathological diagnosis is detection of fatty tissue invasion [8]. Unfortunately, these criteria cannot be evaluated in cytological materials. For this reason, numerous studies have been conducted to find an immunohistochemical marker that might aid MM diagnosis or even offer a definitive diagnosis.

Various studies have demonstrated that immunohistochemical evidence of BAP1 expression loss in mesothelial cells may be a clue to malignancy. Cozzi et al. [18] reported that BAP1 expression loss in cell blocks obtained from effusions had a sensitivity of 76% for MM diagnosis, and that BAP1 expression loss in biopsy samples had 48.7% sensitivity. Meanwhile, Cigognetti et al. [19] and Walts et al. [20] estimated 100% specificity for BAP1 expression loss. In our study, we estimated 76% sensitivity and 100% specificity from biopsy tissue, but 100% sensitivity and specificity from cell blocks obtained from effusion.

Cozzi et al. [18], who investigated the role of BAP1 expression loss in effusion diagnosis for MM, found that BAP1 expression loss was 76.5% prevalent in mesothelioma cases, while it was 11.7% in mesothelial hyperplasia cases. In the same study, looking at biopsy diagnosis, BAP1 expression loss was 47.5% prevalent in patients diagnosed with mesothelioma, but no BAP1 expression loss was observed in any cases diagnosed with mesothelial hyperplasia. In our study, BAP1 expression loss was 76.6% prevalent in biopsy materials and 100% in cell blocks. Furthermore, no BAP1 expression loss was observed in either cell block or biopsy materials in our mesothelial hyperplasia cases.

There are some differences between MM subtypes in terms of nuclear BAP1 expression loss. Wu et al. [21] grouped 38 pleural MM cases as 29 biphasic and nine epithelioid types and then compared their BAP1 expression loss status and subtypes. In this study, we observed BAP1 expression loss in five of eight epithelioid-type MM cases (62.5%), while also observing loss in both sarcomatoid and epithelioid components in five of 13 biphasic-type MM cases (38.5%). Shinozaki-Ushiku et al. [17] studied 32 MM cases and found BAP1 expression loss in 53% (17/32), among which 14 were epithelioid and 3 were biphasic. Furthermore, two biphasic-type cases showed expression loss in both epithelioid and sarcomatoid components, while only 1 showed BAP1 expression persistence in the sarcomatoid component. In our study, BAP1 expression loss was observed in 81.5% of 54 epithelioid-type MM cases, whereas it was observed in all five biphasic-type MM cases (100%), all of which were detected in the epithelioid component. Moreover, no loss of BAP1 expression was observed in any of our five sarcomatoid-type MM cases.

Massive and recurrent effusions occur in the early stages of MM. Therefore, initial diagnosis is mostly based on cytological samples, especially in the epithelioid type [22]. However, in some cases, effusion material alone is not sufficient to diagnose MM. In such cases, diagnosis requires biopsy tissue from the patients. Although the diagnostic power of biopsies have been demonstrated by numerous studies, less invasive methods are preferred by both patients and surgeons.

Pulford et al. [14] included both cytological and biopsy materials of 83 MM cases and 18 cases with malignant pleural effusion due to metastatic adenocarcinoma. In addition to the diagnostic value and prognostic significance of BAP1 expression loss, they also measured the agreement of cytological and biopsy materials with the Kappa test. Pulford et al. [14] reported that BAP1 expression loss was observed in 59% of MM cases and the Kappa value was 0.85. Similarly, we applied BAP1 antibodies to the biopsies of cases with cytological samples and we calculated agreement with the Kappa test. Accordingly, the agreement between cytological and histological specimens for BAP1 expression loss was excellent (ĸ=0.90), and the correlation was significant (p<.001).

Environmental exposure to asbestos, especially for regions with abundant white soil, like some provinces of Turkey, is of great importance in MM development. Onder et al. [23] evaluated 88 MM cases from central Ankara, which is the nearest city to Cappadocia; they reported that 95% of the cases had been exposed to asbestos and no significant relationship was found between asbestos exposure and BAP1 expression loss. In our study, only 35.9% of MM cases were exposed to asbestos. We attribute this difference to the fact that the city where we work is far from Cappadocia, and we could not find as significant a relationship as Onder et al. [23] did.

There were some limitations to our work. Primarily, because of the retrospective nature of our study, it was not possible to obtain all of the cytological specimens from the biopsy materials analyzed by immunohistochemistry for BAP1 expression.

In conclusion, BAP1 expression loss was found in all the cytological materials of the cases whose diagnoses were confirmed by tissue biopsy, and the results were replicated for each case when BAP1 antibodies were applied to biopsy materials. This suggests that BAP1 expression loss is a robust criterion in achieving MM diagnosis from cytological materials. Effusion in the serosal cavity is a common early finding for MM. Furthermore, because cytologic examination is less invasive and easy to perform, it is likely to be the preferred diagnostic method, especially given the results reported here. In patients with only serous effusion and no radiological suspicion of MM but who show evidence of BAP1 expression loss by immunohistochemical analysis of cell blocks, we suggest that invasive MM may develop in the near future and, thus, these patients need strict clinical follow-up.

Fig. 1.

BRCA1-associated protein 1 (BAP1) immunohistochemistry results in reactive mesothelial hyperplasia. Biopsy material with hematoxylin and eosin staining (A) and BAP1 immunohistochemistry (B) with strong nuclear staining. Cell block material with BAP1 immunohistochemistry staining. (C) Note the strong nuclear and weak nonspecific cytoplasmic staining. (D) An example of a fibrinous pleuritis case with BAP1 staining.

Fig. 2.

BRCA1-associated protein 1 (BAP1) immunohistochemistry results in malignant mesothelioma. Biopsy material with hematoxylin and eosin staining (A) and loss of BAP1 expression (B) with inflammatory cells as a positive internal control in epithelioid mesothelioma. Cell block material with BAP1 staining (C). BAP1 normal expression in sarcomatoid mesothelioma (D).

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Figure & Data

References

Citations

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