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Article type: Research Article
Authors: Yazici, Pinar* | Demir, Uygar | Bozkurt, Emre | Isil, Gurhan R. | Mihmanli, Mehmet
Affiliations: Department of General Surgery, Sisli Etfal Training and Research Hospital, Istanbul, Turkey
Correspondence: [*] Corresponding author: Pinar Yazici, Sisli Etfal Training and Research Hospital, Halaskargazi Cad. Etfal Sokak, 34371, Istanbul, Turkey. Tel.: +90 212 373 5000; Fax: +90 212 224 07 72; E-mail:drpinaryazici@gmail.com
Abstract: BACKGROUND: Although the red cell distribution width (RDW) has been reported as a reliable predictor of prognosis in several types of cancer, to our knowledge the prognostic value of RDW in gastric carcinoma has not been studied, so far. OBJECTIVE: We aimed to investigate the role of red cell distribution width (RDW) in predicting prognosis in gastric cancer patients. METHODS: All gastric cancer patients who underwent curative surgery (n= 172, 110M/62F) over a five-year study period were evaluated. Data on demographics, preoperative RDW levels, tumor characteristics (early stage: I and II, advanced stage: IIIA-B-C), disease-free (DFS) and overall survival (OS) were retrospectively reviewed. Patients were classified as high RDW group (RDW ≥ 16, n= 62) or low RDW group (RDW < 16, n= 110). RESULTS: Overall mortality and postoperative 60-day mortality in both groups were 55% and 14%, respectively. A borderline significant association between RDW (0.063) and mortality was noted. Preoperative RDW levels were significantly higher in patients with short-term mortality (17.9 ± 4.3 vs. 16 ± 3.2, p= 0.015). In high RDW group, the incidence of advanced gastric cancer was significantly higher (75 vs. 51%, p= 0.002), whereas DFS (0.035) and OS (p= 0.04) were lower. CONCLUSION: The frequency of advanced cancer was high in patients with high RDWvalues. High RDW values were strongly associated with short-term mortality although only a borderline relationship with overall survival was observed.
Keywords: Gastric cancer, red cell distribution width, staging, prognosis
DOI: 10.3233/CBM-160668
Journal: Cancer Biomarkers, vol. 18, no. 1, pp. 19-25, 2017
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