4.3 Article

Comparison of Nuclear Grade, Necrosis, and Histologic Subtype Between Biopsy and Resection in Pleural Malignant Mesothelioma An International Multi-Institutional Analysis

Journal

AMERICAN JOURNAL OF CLINICAL PATHOLOGY
Volume 156, Issue 6, Pages 989-999

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/ajcp/aqab054

Keywords

Malignant mesothelioma; Histology; Nuclear grading

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This study compared histologic subtype, nuclear grade, and necrosis in paired biopsy and resection specimens of pleural MM, showing moderate agreement in these pathologic parameters. The findings may be useful for guiding postbiopsy management and patient triage in MM cases.
Objectives: Numerous studies on malignant mesothelioma (MM) highlight the prognostic importance of histologic subtype, nuclear grade, and necrosis. This study compares these parameters in paired biopsy and resection specimens of pleural MM. Methods: Histologic subtype, percentage of epithelioid morphology, nuclear grade, and the presence or absence of necrosis were compared in 429 paired biopsies and resection specimens of pleural MM from 19 institutions. Results: Histologic subtype was concordant in 81% of cases (kappa = 0.58). When compared with resection specimens, epithelioid morphology at biopsy had a positive predictive value (PPV) of 78.9% and a negative predictive value (NPV) of 93.5%; sarcomatoid morphology showed high PPV (92.9%) and NPV (99.3%), and biphasic morphology PPV was 89.7% and NPV was 79.7%. Agreement of the percentage of epithelioid morphology was fair (kappa = 0.27). Nuclear grade and necrosis were concordant in 75% (kappa = 0.59) and 81% (kappa = 0.53) of cases, respectively. Nuclear grade showed moderate (kappa = 0.53) and substantial (kappa = 0.67) agreement from patients with and without neoadjuvant therapy, respectively, and necrosis showed moderate (kappa = 0.47 and kappa = 0.60) agreement, respectively, in the same subsets of paired specimens. Conclusions: Paired biopsy-resection specimens from pleural MM show overall moderate agreement in pathologic parameters. These findings may help guide postbiopsy management and triage of patients with MM.

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