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Analysis of clinical efficacy, safety and prognosis of docetaxel combined with nedaplatin in local advanced nasopharyngeal carcinoma |
LIU Tongxin SUN Quanquan CHEN Jing LI Bin QIN Weifeng WANG Fangzheng FU Zhenfu HU Fujun |
Department of Radiation Oncology, Zhejiang Cancer Hospital, Zhejiang Province, Hangzhou 310022, China |
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Abstract Objective To evaluate the efficacy and safety of Docetaxel combined with Nedaplatin (TP) and Fluorouracil combined with Cisplatin (PF) in the treatment of locally advanced nasopharyngeal carcinoma. Methods Retrospective analysis of 271 patients who received TP or PF induction chemotherapy in Zhejiang Cancer Hospital from January 2012 to May 2014, 8 cases were lost to follow-up, and 263 cases were finally included in the analysis, including 92 cases in PF group and 171 cases in TP group. Efficacy, safety and prognosis of the two groups were compared. Results The 5-year overall survival rate (OS), progression-free survival rate (PFS), local recurrence free survival rate (LRFS), and distant metastasis free survival rate (DMFS) were compared, the differences were not statisticdly significant between the two groups (all P > 0.05). Further multivariate analysis showed that N staging was an independent prognostic factor for 5-year OS, PFS and DMFS (P < 0.05). Adverse reaction analysis showed that grade 3-4 leukopenia, neutrophilia and thrombocytopenia were more likely to occur in the TP group, while grade 3-4 nausea and vomiting were more likely to occur in the PF group, with statistically significant differences (P < 0.05). There were no statistically significant differences in other adverse reactions between the two groups (P > 0.05). Conclusion The efficacy of TP and PF induction chemotherapy in the treatment of locally advanced nasopharyngeal carcinoma is similar, and the adverse reactions are tolerable, which can be used in the treatment of locally advanced nasopharyngeal carcinoma.
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