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艾迪联合GP方案治疗晚期非小细胞肺癌的近期疗效与毒性观察 被引量:2

Aidi Plus Gemcitabine and Cisplatin for Patients with Advanced Non-Small Cell Lung Cancer
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摘要 目的观察艾迪注射液联合GP方案(泽菲,顺铂)治疗晚期非小细胞肺癌的近期疗效和毒副反应。方法39例经病理学或细胞学证实的晚期非小细胞肺癌患者分为对照组(GP方案)和观察组(艾迪联合GP方案)。对照组应用泽菲1000mg/m^2,静滴,d1,8;顺铂80mg/m^2,分割为第1~3天,静滴;观察组在此基础上加用艾迪注射液50mL静滴,d1-14;21d为1周期,完成2~4周期后进行疗效评价。结果对照组:PR46.1%(6/13),SD30.8%(4/13),PD23.1%(3/13),总有效率为46.1%;观察组:PR50.0%(13/26),SD42.3%(11/26),PD7.7%(2/26),总有效率为50.0%;近期疗效差异无统计学意义(P〉0.05)。临床受益反应:观察组治疗后KPS评分增加〉20分占76.9%,体重增加〉7%占57.6%,止痛药用量减少50%占42.3%,而对照组分别为38.4%、30.7%和38.4%,二者差异均有统计学意义(P〈0.05)。毒副反应主要为轻微的血液学毒性。结论艾迪注射液联合化疗具有改善生活质量和明显协同、增效、减毒作用,且毒副反应轻微,可以作为化疗的重要辅助用药。 Objective To observe the efficacy and adverse reactions of Aidi and GP( gemcitabine, cisplatin) for patients with advanced nonsmall cell lung cancer. Methods The patients for GP: gemcitabine 1 000 mg/m^2 , d1,8 plus cisplatin 80 mg/m^2 , division d〉3 ; Aidi and GP: add Aidi 50 mL/d, d1-14 ; interval between each cycle was 21 days and the clinical response and the toxicity were assessed after 2-4 cycles. Results GP: overall response rates ( CR + PR) were 46. 1% ; Aidi and GP: overall response rates ( CR + PR) we:re 50.0% ( P 〉 0.05); CBR:Aidi and GP: KPS〉20, 76.9% , weight augment〉7% , 57.6%, anodyne reduce 50. 0% : 42.3% and 3g. 4%, 30.7%, 38.4% for GP(P 〈 0. 05). The major adverse reaction was mild hematology toxicity. Conclusion Aidi plus gemcitabine and cisplatin is an effective and mild toxicity combined with chemotherapy for advanced non-small cell lung cancer.
出处 《肿瘤基础与临床》 2008年第4期305-307,共3页 journal of basic and clinical oncology
关键词 艾迪 化疗 晚期肺癌 泽菲 顺铂 Aidi chemotherapy advanced non-small cell lung cancer gemcitabine cisplatin
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