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培美曲塞作为一线疗法用于中国晚期非鳞状非小细胞肺癌患者。

Pemetrexed as the first-line therapy for Chinese patients with advanced non-squamous non-small-cell lung cancer.

机构信息

Department of Medical Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, PR China.

出版信息

Biomed Pharmacother. 2013 Oct;67(8):763-9. doi: 10.1016/j.biopha.2013.04.013. Epub 2013 May 15.

Abstract

Non-small cell lung cancer (NSCLC) represents the most common cause of cancer mortality worldwide and counts for the greatest number of deaths from lung cancer in both men and women over age 60. Pemetrexed is a multi-targeted anti-metabolite and has shown comparable activity for Caucasian patients with advanced NSCLC. In this single-center retrospective study, we analyzed the outcome in 75 Chinese non-squamous NSCLC patients treated with pemetrexed as first-line therapy and assessed its efficacy and tolerability. The overall response rate was 9.3% (7/75) with 7 partial response s and no complete response. There were 44 (58.7%) stable diseases and 24 progressive diseases (32.0%). The median progression-free survival (PFS) was 6.79 months (95% CI 5.69-7.90 months), and the median overall survival (OS) was 11.67 months (95% CI 9.98-13.36 months). Good performance status and negative smoke history predicted better PFS and OS. Most side effects were generally mild and well tolerated. Taken together, pemetrexed was safe and effective in Chinese patients with non-squamous NSCLC. Pemetrexed alone or in combination with other efficacious drugs may serve as first-line therapy for this disease.

摘要

非小细胞肺癌(NSCLC)是全球癌症死亡的最常见原因,也是 60 岁以上男性和女性肺癌死亡人数最多的原因。培美曲塞是一种多靶点抗代谢药物,在晚期非鳞状 NSCLC 白种人群中显示出相当的活性。在这项单中心回顾性研究中,我们分析了 75 例接受培美曲塞作为一线治疗的中国非鳞状 NSCLC 患者的结果,并评估了其疗效和耐受性。总体缓解率为 9.3%(7/75),其中 7 例部分缓解,无完全缓解。有 44 例(58.7%)疾病稳定,24 例疾病进展(32.0%)。无进展生存期(PFS)的中位数为 6.79 个月(95%CI 5.69-7.90 个月),总生存期(OS)的中位数为 11.67 个月(95%CI 9.98-13.36 个月)。良好的体能状态和阴性吸烟史预测 PFS 和 OS 更好。大多数不良反应通常为轻度且可耐受。总之,培美曲塞在中国非鳞状 NSCLC 患者中安全有效。培美曲塞单独或与其他有效药物联合可能作为该疾病的一线治疗。

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