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Pollheimer, MJ; Kornprat, P; Lindtner, RA; Harbaum, L; Schlemmer, A; Rehak, P; Langner, C.
Tumor necrosis is a new promising prognostic factor in colorectal cancer.
Hum Pathol. 2010; 41(12):1749-1757
Doi: 10.1016/j.humpath.2010.04.018
Web of Science
PubMed
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- Führende Autor*innen der Med Uni Graz
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Langner Cord
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Pollheimer Marion
- Co-Autor*innen der Med Uni Graz
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Kornprat Peter
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Rehak Peter
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Schlemmer Andrea
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- Abstract:
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The prognostic significance of tumor necrosis in colorectal cancer is unclear. Our study aimed to analyze the prognostic value of tumor necrosis with respect to progression-free and cancer-specific survival and to relate findings to expression of proteins involved in the control of cancer cell death, such as p53 and bcl-2. A total of 381 colorectal cancer specimens were retrospectively reevaluated. The extent of tumor necrosis was semiquantitatively assessed and recorded as either absent, focal (≤10% of the tumor area), moderate (10%-30%), or extensive (≥30%). Expression of p53 and bcl-2 was assessed immunohistochemically and recorded as either positive (using a cutoff value of 10%) or negative. In addition, mismatch repair protein status was assessed by immunohistochemistry using antibodies directed against hMLH1, hMSH2, and hMSH6. Tumor necrosis was observed in 365 (96%) cases, with 180 (47%) tumors showing focal necrosis, 119 (31%) moderate necrosis, and 66 (17%) extensive necrosis, respectively. Extent of necrosis was significantly associated with high T classification (P < .001), high N classification (P = .005), high International Union Against Cancer stage (P < .001), poor tumor differentiation (P < .001), large tumor size (P < .001), and blood vessel invasion (P = .01). No association of tumor necrosis with expression of p53, bcl-2, and mismatch repair protein status was observed. Tumor necrosis proved to be an independent prognostic variable with respect to progression-free and cancer-specific survival. In conclusion, tumor necrosis showed significant impact on prognosis of colorectal cancer patients. Its presence is readily assessable in hematoxylin and eosin-stained sections and should therefore routinely be commented upon in the pathology report.
Copyright © 2010 Elsevier Inc. All rights reserved.
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Adenocarcinoma - metabolism Adenocarcinoma - mortality Adenocarcinoma - pathology
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Adult -
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Aged -
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Aged, 80 and over -
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Aged, 80 and over - epidemiology
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Biomarkers, Tumor - metabolism
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Colorectal Neoplasms - metabolism Colorectal Neoplasms - mortality Colorectal Neoplasms - pathology
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DNA-Binding Proteins - metabolism
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Disease Progression -
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Female -
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Humans -
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Immunohistochemistry -
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Male -
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Middle Aged -
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Necrosis -
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Prognosis -
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Proto-Oncogene Proteins c-bcl-2 - metabolism
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Survival Rate -
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Tissue Array Analysis -
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Tumor Suppressor Protein p53 - metabolism
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Colorectal cancer
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Tumor necrosis
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Immunohistochemistry
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Prognosis
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Survival