徐杰, 齐大亮, 李绪斌, 王瑞霞. 重组人血管内皮抑制素联合化疗治疗非小细胞肺癌恶性胸腔积液的疗效观察[J]. 中国肿瘤临床, 2014, 41(24): 1573-1576. DOI: 10.3969/j.issn.1000-8179.20141512
引用本文: 徐杰, 齐大亮, 李绪斌, 王瑞霞. 重组人血管内皮抑制素联合化疗治疗非小细胞肺癌恶性胸腔积液的疗效观察[J]. 中国肿瘤临床, 2014, 41(24): 1573-1576. DOI: 10.3969/j.issn.1000-8179.20141512
XU Jie, QI Daliang, LI Xubin, WANG Ruixia. Efficacy of recombinant human endostatin (Endostar) combined with chemotherapy for malignant pleural effusion in non-small cell lung cancer patients[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2014, 41(24): 1573-1576. DOI: 10.3969/j.issn.1000-8179.20141512
Citation: XU Jie, QI Daliang, LI Xubin, WANG Ruixia. Efficacy of recombinant human endostatin (Endostar) combined with chemotherapy for malignant pleural effusion in non-small cell lung cancer patients[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2014, 41(24): 1573-1576. DOI: 10.3969/j.issn.1000-8179.20141512

重组人血管内皮抑制素联合化疗治疗非小细胞肺癌恶性胸腔积液的疗效观察

Efficacy of recombinant human endostatin (Endostar) combined with chemotherapy for malignant pleural effusion in non-small cell lung cancer patients

  • 摘要:
      目的  观察重组人血管内皮抑制素(恩度)联合化疗治疗非小细胞肺癌恶性胸腔积液的短期疗效及安全性。
      方法  70例恶性胸腔积液患者经皮穿刺置管彻底引流胸腔积液,随机分成两组,治疗组35例,重组人血管内皮抑制素60 mg联合奈达铂60 mg胸腔内注入;对照组35例为单纯奈达铂60 mg胸腔内注入。将重组人血管内皮抑制素及奈达铂经胸腔置管于胸腔内注射,每周1次,连用2周。1个月复查,比较两组的总有效率及不良反应发生率。
      结果  治疗组总有效率为74.28%,高于对照组的48.57%(P < 0.05)。两组均有恶心、呕吐、外周白细胞减少等不良反应,但差异均无统计学意义(P > 0.05)。
      结论  胸腔内灌注奈达铂联合重组人血管内皮抑制素疗效优于单纯奈达铂,且不增加治疗的不良反应,重组人血管内皮抑制素联合化疗治疗恶性胸腔积液是一种安全有效的治疗方法。

     

    Abstract:
      Objective  To study the efficacy and safety of the intrapleural injection of nedaplatin combined with recombinant hu-man endostatin (Endostar) in the treatment of malignant pleural effusion in non-small cell lung cancer (NSCLC) patients.
      Methods  Seventy patients diagnosed with NSCLC with malignant pleural effusion were treated by intrapleural injection. The subjects were divid-ed into two groups, as follows: 35 cases were injected with nedaplatin and Endostar (the treatment group) and 35 cases were injected with nedaplatin only (the control group). One month after the treatment, the clinical efficacy and toxicity were evaluated. The clinical ef-ficacy, quality of life, and toxic reaction were compared between the two groups.
      Results  The short-term clinical efficacy rate of the treatment group was 74.28%, whereas that of the control group was 48.57%, and the difference between the two groups was significant (P < 0.05). Adverse effects such as nausea vomiting and leukopenia, occurred in both groups, but no significant differences were found between the two groups (P > 0.05).
      Conclusion  The efficacy of the intrapleural injection of recombinant human endostatin combined with nedaplatin is superior to that of cisplatin alone in the treatment of malignant pleural effusion, without increasing chemotherapeutic toxicity.

     

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