Combination of lymphocyte count and albumin concentration as a new prognostic biomarker for rectal cancer

Although numerous studies have highlighted the prognostic values of various inflammation-related markers, clinical significance remains to be elucidated. The prognostic values of inflammation-related biomarkers for rectal cancer were investigated in this study. A total of 448 patients with stage II/...

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Veröffentlicht in:Scientific reports 2021-03, Vol.11 (1), p.5027-10, Article 5027
Hauptverfasser: Yamamoto, Takehito, Kawada, Kenji, Hida, Koya, Matsusue, Ryo, Itatani, Yoshiro, Mizuno, Rei, Yamaguchi, Takashi, Ikai, Iwao, Sakai, Yoshiharu
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Sprache:eng
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Zusammenfassung:Although numerous studies have highlighted the prognostic values of various inflammation-related markers, clinical significance remains to be elucidated. The prognostic values of inflammation-related biomarkers for rectal cancer were investigated in this study. A total of 448 patients with stage II/III rectal cancer undergoing curative resection were enrolled from the discovery cohort (n = 240) and validation cohort (n = 208). We comprehensively compared the prognostic values of 11 inflammation-related markers-derived from neutrophil, lymphocyte, platelet, monocyte, albumin, and C-reactive protein for overall survival (OS) and recurrence-free survival (RFS). Among 11 inflammation-related markers, only “lymphocyte × albumin (LA)” was significantly associated with both OS and RFS in the discovery cohort ( P  = 0.007 and 0.015, respectively). Multivariate analysis indicated that low LA was significantly associated with poor OS (hazard ratio [HR] 2.19, 95% confidence interval [CI] 1.09–4.58, P  = 0.025), and poor RFS (HR 1.61, 95% CI 1.01–2.80, P  = 0.048). Furthermore, using the discovery cohort, we confirmed that low LA was significantly associated with poor OS (HR 2.89, 95% CI 1.42–6.00, P  = 0.002), and poor RFS (HR 1.79, 95% CI 1.04–2.95, P  = 0.034). LA can be a novel prognostic biomarker for stage II/III rectal cancer.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-021-84475-4