Clinical Efficacy of Gemcitabine plus S-1 on Refractory Nasopharyngeal Carcinoma Patients and Their Influence on Immune Function

Autor: CHEN Jinghua, TAN Wenyong, XU Ruilian, XIA Junxian, ZHU Meiqin
Jazyk: čínština
Rok vydání: 2018
Předmět:
Zdroj: Zhongliu Fangzhi Yanjiu, Vol 45, Iss 12, Pp 1014-1019 (2018)
Druh dokumentu: article
ISSN: 1000-8578
DOI: 10.3971/j.issn.1000-8578.2018.18.0443
Popis: Objective To investigate the efficacy of gemcitabine plus S-1 on refractory nasopharyngeal carcinoma patients, and to detect the changes of T lymphocyte subsets in the peripheral blood before and after chemotherapy. Methods Forty-two refractory nasopharyngeal carcinoma patients received gemcitabine (1.0 g/m2 on day 1 and day 8) plus oral S-1 chemotherapy (40mg/m2 twice daily, d1-14). Each cycle was repeated every 21 days, two cycles at least for each patient. The peripheral blood samples were collected before and after chemotherapy respectively, then T lymphocyte subsets were analyzed by flow cytometry. Survival analysis included univariate model and multivariate Cox regression model. Results Forty-two patients had completed chemotherapy and follow-up. There was one case of complete response, 21 cases of partial responses, 12 cases of stable disease, 8 cases of progressive disease, the overall response rate was 52.4%(22/42), and the disease control rate was 81.0%(34/42). Median time to progression was 6.8 months and median survival was 14.6 months. The common adverse effects were myelosuppression, gastrointestinal tract reaction, rash and fatigue; no death occurred in relation to the therapy. Compared with PD group, the percentages of CD3+, CD3+CD4+ and CD4+/CD8+ ratios were increased significantly in the response group after chemotherapy. Liver metastasis was an independent prognostic factor for overall survival. Conclusion Gemcitabine plus S-1 are an effective therapy with tolerable toxicity profile for refractory NPC patients. Liver metastasis is an independent prognostic factor for overall survival. Effective chemotherapy influences T lymphocyte subsets obviously.
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