紫杉醇-卡铂与贝伐单抗紫杉醇-卡铂治疗非小细胞肺癌

Waleed Hammam, Y. Saleh
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引用次数: 0

摘要

背景:肺癌被认为是癌症相关死亡的主要原因,约85%的肺癌患者为非小细胞肺癌(NSCLC),血管内皮生长因子(VEGF)在恶性肿瘤血管生成的调控中起主要作用。目的:本研究的目的是比较2013年3月至2016年2月期间在沙特-德国医院诊断为非鳞状非小细胞肺癌的患者单独化疗与联合抗vegf(贝伐单抗)化疗的反应率、无进展生存期和总生存期。患者和方法:本研究于2013年3月至2016年2月在沙特德国医院进行,我们进行了一项随机研究,其中40例复发或晚期非小细胞肺癌(IIIB或IV期)患者接受紫杉醇和卡铂(紫杉醇-卡铂组)(20例)紫杉醇和卡铂加贝伐单抗(紫杉醇-卡铂-贝伐单抗组)(20例)。结果:紫杉醇-卡铂-贝伐单抗组的中位总生存期为15.5个月,而紫杉醇-卡铂-贝伐单抗组为10.5个月(P=0.002),紫杉醇-卡铂-贝伐单抗组的中位无进展生存期也显著提高(8.4个月,紫杉醇-卡铂组为5.9个月),疾病进展的风险比为0.67 (95% CI, 0.57至0.77;P<0.001),贝伐单抗加入紫杉醇和卡铂提高了反应率,因为紫杉醇-卡铂组(25%)有反应,而紫杉醇-卡铂-贝伐单抗组(65%)有反应(P<0.001),并且紫杉醇-卡铂-贝伐单抗组的高血压、出血、血小板减少症、中性粒细胞减少症、发热性中性粒细胞减少症、蛋白尿的发生率显著高于紫杉醇-卡铂组。(P < 0.05)。结论:贝伐单抗联合化疗对非鳞状NSCLC患者在缓解率、无进展生存期和总生存期方面有显著的增加价值,但副作用明显。
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Paclitaxel-Carboplatin versus Bevacizumab Paclitaxel-Carboplatin for Treatment of Non-Small-Cell Lung Cancer
Background: Lung cancer is considered as the leading cause attributed to cancer related deaths and approximately 85% of lung cancer patients have non-small-cell lung cancer (NSCLC) and Vascular endothelial growth factor (VEGF) is used to play the major role in regulation of angiogenesis in malignancies. Aim: The aim of this study was to compare chemotherapy alone in comparison with addition of anti -vegf (bevacizumab) to chemotherapy and assessment of response rate , progression free survival, overall survival in patients diagnosed with nonsquamous non small cell lung cancer in Saudi German hospitals in the period between March 2013 and February 2016. Patients and methods: This study was held between March 2013 and February 2016 in Saudi German hospitals when we performed a randomized study in which 40 patients with recurrent or advanced nonsmall-cell lung cancer (stage IIIB or IV) received paclitaxel and carboplatin (paclitaxel-carboplatin arm) (20 patients) paclitaxel and carboplatin in addition to bevacizumab (paclitaxel-carboplatin-bevacizumab arm) (20 patients). Results: The median overall survival was 15.5 months in the paclitaxel-carboplatin-bevacizumab arm as compared with 10.5 months in the paclitaxelcarboplatin arm ( P=0.002) and the median progression-free survival was also significantly improved in the paclitaxel-carboplatin-bevacizumab arm reaching (8.4 months versus 5.9 in the paclitaxel-carboplatin arm) for a hazard ratio for disease progression of 0.67 (95% CI, 0.57 to 0.77; P<0.001) and the addition of bevacizumab to paclitaxel and carboplatin improved the response rate as (25 %) in the paclitaxel-carboplatin arm had a response versus (65%) in the paclitaxel-carboplatin-bevacizumab arm (P<0.001) and the rates of hypertension, bleeding, thrombocytopenia, neutropenia, febrile neutropenia, proteinuria were significantly higher in the paclitaxel-carboplatin-bevacizumab arm than in the paclitaxel-carboplatin arm. (P<0.05). Conclusion: The addition of bevacizumab to the chemotherapy added a significant value to the patients with non squamous NSCLC in terms of response rate, progression free survival and overall survival however with significant side effects.
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