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Article type: Research Article
Authors: Wƚodarczyk, Marcin* | Kasprzyk, Jakub | Sobolewska-Wƚodarczyk, Aleksandra | Wƚodarczyk, Jakub | Tchórzewski, Marcin | Dziki, Adam | Dziki, Ƚukasz
Affiliations: Department of General and Colorectal Surgery, Medical University of Lodz, Lodz, Poland
Correspondence: [*] Corresponding author: Marcin Wƚodarczyk, Department of General and Colorectal Surgery, Medical University of Lodz, Haller Sq. 1, 90-647 Lodz, Poland. Tel./Fax: +48 42 639 30 49; E-mail:dr.mwlodarczyk@gmail.com
Abstract: BACKGROUND: Rectal cancer is a major cause of death and an early diagnosis is crucial in decreasing mortality. Previous studies found a relation between chronic inflammation and increased risk of rectal cancer. It was shown that mean platelet volume (MPV) level might be a marker of subclinical inflammatory process in gastrointestinal tract. OBJECTIVE: To determinate whether MPV could be a useful biomarker of tumor progression in the rectal cancer. METHODS: One hundred and three patients with rectal cancer who underwent surgical resection of tumor were enrolled in the study. The control group consisted of 98 healthy subjects. RESULTS: The association between MPV, tumor stage and clinical status were assessed. The analysis proved that pre-operative MPV level was significantly lower in rectal cancer vs. healthy individuals (10.65 ± 0.79 vs. 11.41 ± 0.76 fL; p < 0.001).Receiver-operating characteristic curve analysis suggested 11.3 as the cut-off value for MPV (sensitivity = 83%; specificity = 54%; AUC = 0.745). Surgical resection of tumor resulted in the increase of the MPV level with statistical significance (10.65 ± 0.79 fL vs. 11.21 ± 0.82 fL; p < 0.001). No relationship was found between the post-operative MPV level in cancer patients and control subjects. CONLUSION: MPV level may be potentially useful and easily available biomarker for monitoring subclinical inflammation related to rectal cancer and predicting tumor progression.
Keywords: Biomarker, mean platelet volume, rectal cancer, tumor progression, inflammation
DOI: 10.3233/CBM-160657
Journal: Cancer Biomarkers, vol. 17, no. 4, pp. 411-417, 2016
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