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吉西他滨联合卡铂用于晚期鼻咽癌二线治疗的临床观察[J]. 肿瘤防治研究, 2007, 34(12): 962-964. DOI: 10.3971/j.issn.1000-8578.1703
引用本文: 吉西他滨联合卡铂用于晚期鼻咽癌二线治疗的临床观察[J]. 肿瘤防治研究, 2007, 34(12): 962-964. DOI: 10.3971/j.issn.1000-8578.1703
Gemcitabine Plus Carboplatin as Second-line Chemotherapy in Patients with Advanced Nasopharyngeal Carcinoma[J]. Cancer Research on Prevention and Treatment, 2007, 34(12): 962-964. DOI: 10.3971/j.issn.1000-8578.1703
Citation: Gemcitabine Plus Carboplatin as Second-line Chemotherapy in Patients with Advanced Nasopharyngeal Carcinoma[J]. Cancer Research on Prevention and Treatment, 2007, 34(12): 962-964. DOI: 10.3971/j.issn.1000-8578.1703

吉西他滨联合卡铂用于晚期鼻咽癌二线治疗的临床观察

Gemcitabine Plus Carboplatin as Second-line Chemotherapy in Patients with Advanced Nasopharyngeal Carcinoma

  • 摘要: 目的 观察吉西他滨(泽菲国产吉西他滨)联合卡铂的联合方案治疗晚期复治鼻咽癌的近期疗效及毒性反应。方法 32例均为一线含顺铂方案化疗失败的晚期鼻咽癌病人。吉西他滨1000mg/m2,d1.8;卡铂400mg/m2,d1;21天为1周期。完成2周期后评价疗效及毒性。结果 32例中CR4例,占12.5%;PR16例,占50.0%;总缓解率(CR+PR)62.5%。SD8例(25%),PD4例(12.5%)。中位缓解时间4.5个月。骨髓抑制为主要毒性:Ⅲ/Ⅳ度白细胞下降为43.6%,4例合并感染发热;Ⅲ/Ⅳ度血小板下降为21.8%。胃肠道反应轻微。结论 吉西他滨与卡铂的联合方案对一线含顺铂方案化疗失败的晚期鼻咽癌有较高的缓解率,毒性反应轻,值得作为二线方案推广使用。

     

    Abstract: Objective  To evaluate the efficacy and toxicity of gemcitabine in combination with carboplatin as second-line treatment in the patients with advanced nasopharyngeal carcinoma (NPC) . Methods  Eligibale patients with advanced NPC failed to previous cisplatin-based chemotherapy were analysed retrospectively. These patients had a performance status of 0 to 2, and adequate liver or renal function, as well as measurabale disease. Chemotherapy was administered with gemcitabine, 1, 000mg/ m2, int ravenously infusion for 30 minutes in d1 and d8, followed by carboplatin, 400mg/ m2, int ravenously infusion for 2 hours in day 1 ;treatment was repeated every 21 days. Efficacy and toxicity would be evaluated after the completion of two cycles of chemoyherapy. Results  A total of 32 patients t reated in the period of January, 2004 to March, 2007 were involved in this study. Complete remission ( CR) was observed in 4 patients (12. 5 %), 16 patients (50. 0 %) achieved partial remission, giving a total response rate of 62. 5 %. 8 patients achieved a stable status, 4 patients suffered from progressive disease. Median time to progression ( TTP) was 4. 5 months. . Hematological toxicities were the predominant side effects with grade 3/ 4 leukopenia, thrombocytopenia were observed in 43. 6 %, 21. 8 %of patient s, respectively, 4 febrile neut ropenia occurred. Non-hematological toxicity was mild. Conclusion  The combination of gemcitabine and carboplatin showed a promising result s as second-line chemotherapy in patients with advanced NPC, which merits the further study in a prospective clinical trial.

     

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