Tumor Necrosis and >20 mitoses Per 50 High-Power Fields can Distinguish ‘Very High-Risk’ and ‘Highest-Risk’ within ‘High-Risk’ Gastric Gastrointestinal Stromal Tumor
Author(s) -
Jiabin Zheng,
Renjie Li,
Haibo Qiu,
Tao Chen,
Yongjian Zhou,
ChangMing Huang,
Guoxin Li,
Zhiwei Zhou,
Yong Li
Publication year - 2018
Publication title -
future oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.857
H-Index - 72
eISSN - 1744-8301
pISSN - 1479-6694
DOI - 10.2217/fon-2017-0509
Subject(s) - univariate , medicine , necrosis , stromal cell , univariate analysis , mitotic index , multivariate analysis , multivariate statistics , oncology , high power field , gastroenterology , pathology , mitosis , immunohistochemistry , biology , statistics , mathematics , microbiology and biotechnology
Aim: We aimed to investigate the optimal criteria for classifying higher risk forms of gastric gastrointestinal stromal tumor (gGIST). Materials & methods: A total of 246 high-risk gGIST patients were enrolled. Univariate and multivariate analyses were conducted to determine the association between clinicopathological features and overall survival. Appropriate cut-off values were calculated to identify those at higher risk of gGIST. Results: Multivariate and univariate analyses revealed that tumor necrosis and mitotic counts are independent risk factors for overall survival. The optimal cut-off value of mitotic counts was 20. Patients with both necrosis and >20 mitoses/50 high-power fields were worse than those with either one. Conclusion: Tumor necrosis and >20 mitoses/50 high-power fields are independent risk factors for high-risk gGIST. Patients with both risk factors indicate worse prognosis.
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