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重组人内皮抑素联合化疗治疗晚期NSCLC近期疗效观察[J]. 肿瘤防治研究, 2009, 36(10): 869-871. DOI: 10.3971/j.issn.1000-8578.2009.10.015
引用本文: 重组人内皮抑素联合化疗治疗晚期NSCLC近期疗效观察[J]. 肿瘤防治研究, 2009, 36(10): 869-871. DOI: 10.3971/j.issn.1000-8578.2009.10.015
Rh-endostatin in Combination with Chemotherapy in Patients with Advanced Non-small Cell Lung Cancer[J]. Cancer Research on Prevention and Treatment, 2009, 36(10): 869-871. DOI: 10.3971/j.issn.1000-8578.2009.10.015
Citation: Rh-endostatin in Combination with Chemotherapy in Patients with Advanced Non-small Cell Lung Cancer[J]. Cancer Research on Prevention and Treatment, 2009, 36(10): 869-871. DOI: 10.3971/j.issn.1000-8578.2009.10.015

重组人内皮抑素联合化疗治疗晚期NSCLC近期疗效观察

Rh-endostatin in Combination with Chemotherapy in Patients with Advanced Non-small Cell Lung Cancer

  • 摘要: 目的 观察抗肿瘤新药重组人血管内皮抑素注射液联合化疗治疗晚期NSCLC的有效性和安全性。 方法 经组织学或细胞学确诊的Ⅳ期NSCLC患者34例接受重组人血管内皮抑素加常规化疗药物联合治疗,重组人血管内皮抑素剂量为(8.3~10)mg/m2,总量15 mg,加入生理盐水500 ml中缓慢静脉滴注(3~4)小时,滴注过程中给予心电监护,第1~14天连续给药;同时联合给予NCCN指南推荐的化疗药物治疗,每3周重复。按照RECIST标准评价近期客观疗效,按照NCI CTC 3.0版的分级标准评价药物毒性。治疗1周期后评价毒性,2周期后评价疗效。 结果 所有34例患者均可评价疗效,其中PR9例,SD19例,PD6例,临床有效率为26.47%(9/34),临床受益率为82.35%(28/34),初治和复治患者的RR率为42.86%和15%(P<0.05),CBR率分别为92.86%和75%(P<0.05),未出现严重不良反应。 结论 重组人内皮抑素联合化疗治疗晚期NSCLC耐受性好,可以提高化疗的有效率,用于一线治疗时疗效提高更为显著。

     

    Abstract: Objective To evaluate the treatment efficacy and safety with the combination of rh-endostatin(YH-16) and chemotherapy in patients with advanced non-small cell lung cancer(NSCLC). Methods 34 patients with advanced non-small cell lung cancer confirmed by histopathology or cytopathology were administrated with YH-16 7.5mg/m2 (day 1~14) and routine chemotherapy every 3 weeks.The dosage of (8.3~10)mg/m2 (15mg/time) of rh-endostatin solved in 500ml normal saline was slowly intravenously dropped for 3~4 hours from 1 to 14 days, repeated after 7days. The overall response and toxicity were observed. Results Totally, 34 patients were entered and all of these patients were evaluated.Partial response was observed in 9 patients,stable disease was observed in 19 patients and progressive disease was observed in 6 patients. Overall response rate was 26.47%(9/34), Clinical benefit rate was 82.35%(28/34).For the untreated patients and the pretreated patients,the response rate was 42.86% and 15%(P<0.05), Clinical benefit rate was 92.86% and 75%(P<0.05), respectively.No serious adverse event was observed. Conclusion The rh-endostatin combined with chemotherapy tends to show a better treatment efficacy than chemotherapy alone and is well tolerated in patients with advanced non-small cell lung cancer patients,especially in the front line treatment.

     

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