Khosravi Adnan, Salimi Babak, Esfahani-Monfared Zahra, Seifi Sharareh, Mirtavoos-Mahyari Hanifeh
Tobacco Prevention and Control Research Center, National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran. Email:
Asian Pac J Cancer Prev. 2018 Oct 26;19(10):2973-2978. doi: 10.22034/APJCP.2018.19.10.2973.
Background: This study performed to assess the efficacy and safety of Formeta (generic form of Pemetrexed) plus Carboplatin as first-line chemotherapy in advanced stage, non- squamous, non small cell lung cancer ( NSCLC) in Iran. Methods: This was a post marketing single-arm phase IV efficacy study of Formeta (manufactured by Oncomed.,Czech Republic ) and Carboplatin in chemo-naive advanced non-squamous NSCLC Iranian patients. Patients received up to six cycles of Formeta (500 mg/m2) combined with Carboplatin (area under the curve: AUC 5) every 3 weeks. The primary endpoint was the progression free survival (PFS) and secondary endpoints were safety and overall survival (OS). Results: Fifty-two patients were enrolled between June 2014 to January 2016, and 44 patients were evaluable for both safety and efficacy. Partial and complete responses were achieved in 19 (36.5 %) and 2 (3.8%) patients, respectively as well as stable disease in 8 patients (15.3 %). Median of PFS and OS were 7.9 ± 1.1 months and 12.43±0.6 months, respectively. Anemia was the most prevalent adverse events of this regimen. Grades 3 or 4 of adverse events were not observed in any patients. Non-hematologic and other grades of hematologic toxicities were generally mild, and there were no treatment-related deaths. Conclusion: The combination of Formeta and Carboplatin was effective in advanced non-squamous NSCLC and can be a suitable candidate as first-line treatment in these patient’s population.
本研究旨在评估培美曲塞(Pemetrexed的通用形式)联合卡铂作为伊朗晚期非鳞状非小细胞肺癌(NSCLC)一线化疗的疗效和安全性。方法:这是一项关于培美曲塞(由捷克Oncomed公司生产)和卡铂在未经化疗的晚期非鳞状NSCLC伊朗患者中的上市后单臂IV期疗效研究。患者每3周接受最多6个周期的培美曲塞(500mg/m²)联合卡铂(曲线下面积:AUC 5)治疗。主要终点是无进展生存期(PFS),次要终点是安全性和总生存期(OS)。结果:2014年6月至2016年1月共纳入52例患者,44例患者可进行安全性和疗效评估。分别有19例(36.5%)和2例(3.8%)患者达到部分缓解和完全缓解,8例患者(15.3%)病情稳定。PFS和OS的中位数分别为7.9±1.1个月和12.43±0.6个月。贫血是该治疗方案最常见的不良事件。未观察到任何患者出现3级或4级不良事件。非血液学和其他级别的血液学毒性一般较轻,且无治疗相关死亡。结论:培美曲塞和卡铂联合方案对晚期非鳞状NSCLC有效,可作为这些患者群体一线治疗的合适选择。