PURPOSE: Cancer cells reportedly produce C-reactive protein (CRP) locally within tumors. The aim of this study was to determine whether tumoral CRP is associated with clinical outcome and recurrence in thoracic esophageal squamous cell cancer. METHODS: The subjects included 73 Japanese patients with thoracic esophageal squamous cell cancer (pathological Stage IIA-IV) that had not been treated preoperatively with either chemotherapy or radiotherapy. Tumoral CRP expression in resected specimens of tumor tissue was assessed by immunohistochemistry. The survival rate following surgery, the rates and patterns of recurrence, and the serum CRP levels before treatment and at recurrence were analyzed in patients with and without tumoral CRP expression. RESULTS: Fifty-nine percent of the study participants (43/73) were positive for tumoral CRP expression, and the remaining 41% (30/73) were negative. No significant difference in clinicopathological factors was observed between the tumoral CRP-positive and CRP-negative groups; however, patients expressing tumoral CRP showed significantly poorer survival and recurrence rates. A multivariate analysis showed that tumoral CRP expression was an independent factor contributing to the likelihood of a poor outcome. CONCLUSION: Tumoral CRP is associated with a poor outcome in thoracic esophageal squamous cell cancer. Tumoral CRP could therefore be an important target for the treatment of this disease.
PURPOSE: Cancer cells reportedly produce C-reactive protein (CRP) locally within tumors. The aim of this study was to determine whether tumoralCRP is associated with clinical outcome and recurrence in thoracic esophageal squamous cell cancer. METHODS: The subjects included 73 Japanese patients with thoracic esophageal squamous cell cancer (pathological Stage IIA-IV) that had not been treated preoperatively with either chemotherapy or radiotherapy. TumoralCRP expression in resected specimens of tumor tissue was assessed by immunohistochemistry. The survival rate following surgery, the rates and patterns of recurrence, and the serum CRP levels before treatment and at recurrence were analyzed in patients with and without tumoralCRP expression. RESULTS: Fifty-nine percent of the study participants (43/73) were positive for tumoralCRP expression, and the remaining 41% (30/73) were negative. No significant difference in clinicopathological factors was observed between the tumoralCRP-positive and CRP-negative groups; however, patients expressing tumoralCRP showed significantly poorer survival and recurrence rates. A multivariate analysis showed that tumoralCRP expression was an independent factor contributing to the likelihood of a poor outcome. CONCLUSION:TumoralCRP is associated with a poor outcome in thoracic esophageal squamous cell cancer. TumoralCRP could therefore be an important target for the treatment of this disease.
Authors: Sandra Steffens; Andreas Al Ghazal; Julie Steinestel; Rieke Lehmann; Gerd Wegener; Thomas J Schnoeller; Marcus V Cronauer; Florian Jentzmik; Mark Schrader; Markus A Kuczyk; Andres J Schrader Journal: BMC Cancer Date: 2013-05-03 Impact factor: 4.430
Authors: Andreas Al Ghazal; Sandra Steffens; Julie Steinestel; Rieke Lehmann; Thomas J Schnoeller; Anna Schulte-Hostede; Gerd Wegener; Florian Jentzmik; Mark Schrader; Markus A Kuczyk; Andres J Schrader Journal: BMC Urol Date: 2013-10-22 Impact factor: 2.264