Abstract:Objective The study investigates the feasibility of Capthesin B as a marker for evaluating the therapeutic efficiency of nasopharyngeal carcinoma (NPC) patients through detecting the expression of Capthesin B in NPC tissues and serum. Methods The tumor and adjacent normal tissue samples from 50 NPC patients were obtained through biopsy. Immunohistochemistry (IHC) was used to detect the expression of Capthesin B in the tissues of these samples, which were collected in Changsha Jinyu Medical Laboratory Center from August 2019 to February 2020. Serum samples from 40 healthy subjects and from 106 patients with NPC before and after treatment were collected in Hunan Cancer Hospital from July 2019 to March 2020. Capthesin B in the serum was detected by ELISA, and the serum concentrations of Capthesin B among the three groups were compared and analyzed. Results IHC results showed that the positive rate of Capthesin B in NPC tissues was significantly higher than that in adjacent tissues (P<0.01). ELISA data showed that the serum level of Capthesin B in nasopharyngeal carcinoma patients 1.23 (0.64, 2.27) ng/mL was significantly higher than that in healthy subjects (0.98 ±0.49) ng/mL (P<0.01). The serum Capthesin B of NPC patients after treatment 0.69 (0.39, 1.42) ng/mL was significantly lower than that before treatment 1.23 (0.64, 2.27) ng/mL (P<0.001). The area under the ROC curve (AUC) was 0.670 (P<0.05), which suggested that Capthesin B may be used as a reference for predicting the therapeutic efficiency of NPC. The serum Capthesin B of TNM stage III、IV NPC patients (2.09 ±1.50) ng/mL was significantly higher than that of TNM stage I、II NPC patients 1.14 (0.60, 2.12) ng/mL, which indicated that Capthesin B was significantly correlated with TNM stage (P<0.05). Serum Capthesin B in the metastatic group (2.63 ±1.67) ng/mL was remarkably higher than that in the non-metastatic group 1.10 (0.59,2.14) ng/mL (P<0.01), which suggested that serum Capthesin B may be used as a biomarker for predicting NPC metastasis. Conclusion The level of Capthesin B expression in NPC tissues and in NPC serum were significantly increased, but decreased after treatment of NPC, which suggested that Capthesin B is closely related to NPC development. Capthesin B was positively correlated with lymph node metastasis and TNM stage, which suggested that Capthesin B could be used as a biomarker for evaluating NPC prognosis.