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Laboratory and Animal Investigations |

Tumor Necrosis Correlates With Angiogenesis and Is a Predictor of Poor Prognosis in Malignant Mesothelioma*

John G. Edwards; Daniel E. B. Swinson; J. Louise Jones; Salli Muller; David A. Waller; Kenneth J. O’Byrne
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*From the Departments of Oncology (Drs. Edwards, Swinson, and O’Byrne) and Pathology (Dr. Jones), University of Leicester, Leicester; and Departments of Respiratory Medicine and Thoracic Surgery (Dr. Waller) and Pathology (Dr. Muller), University Hospitals Leicester NHS Trust, Leicester, UK.

Correspondence to: Kenneth J. O’Byrne, MD, Department of Oncology, Osborne Building, Leicester Royal Infirmary, Leicester, LE1 5WW, UK; e-mail: ken.obyrne@uhl-tr.nhs.uk



Chest. 2003;124(5):1916-1923. doi:10.1378/chest.124.5.1916
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Objectives: Malignant mesothelioma (MM) is a fatal tumor of increasing incidence related to asbestos exposure. Microscopic tumor necrosis (TN) is a poor prognostic factor in solid tumors, but it has not been characterized in MM. We wished to evaluate the incidence of TN in MM and its correlations with clinicopathologic factors, angiogenesis, and survival.

Methods: TN was graded in 171 routine formalin-fixed, paraffin-embedded hematoxylin-eosin–stained tumor sections by two independent observers. Angiogenesis was assessed by the microvessel count (MVC) of CD34 immunostained sections. TN was correlated with survival by Kaplan-Meier and log-rank analysis, and stepwise, multivariate Cox models were used to compare TN with angiogenesis and established prognostic factors and prognostic scoring systems.

Results: TN was identified in 39 cases (22.8%) and correlated with low hemoglobin (p = 0.01), thrombocytosis (p = 0.04), and high MVC (p = 0.02). TN was a poor prognostic factor in univariate analysis (p = 0.008). Patients with TN had a median survival of 5.3 months vs 8.3 months in negative cases. Independent indicators of poor prognosis in multivariate analysis were nonepithelioid cell type (p = 0.0001), performance status > 0 (p = 0.007), and increasing MVC (p = 0.004) but not TN. TN contributed independently to the European Organisation for Research and Treatment of Cancer (EORTC) [p = 0.03] and to the Cancer and Leukemia Group B (CALGB) [p = 0.03] prognostic groups in respective multivariate Cox analyses.

Conclusions: TN correlates with angiogenesis and is a poor prognostic factor in MM. TN contributes to the EORTC and CALGB prognostic scoring systems.

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