两种不同的以顺铂为基础的化疗方案对晚期非小细胞肺癌的影响。

Changgeng yi xue za zhi Pub Date : 1999-06-01
C H Chen, C T Yang, W J Chang, C C Liaw, T C Tsao
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引用次数: 0

摘要

背景:在以往的研究中,许多不同的以顺铂为基础的方案被用于晚期非小细胞肺癌(NSCLC),但在台湾很少有这样的文献。在这项研究中,我们评估了5-氟尿嘧啶、亚叶酸钙、依托泊苷和顺铂(FLEP)以及顺铂、依托泊苷和顺丝裂霉素(PEM)两种不同方案治疗晚期NSCLC患者的疗效和毒性。方法:回顾性分析1995年2月至1998年4月间符合入选标准的44例非小细胞肺癌患者。所有患者均经组织学检查证实为晚期,即IIIB期或IV期。22例患者接受了FLEP治疗,22例患者接受了PEM治疗。结果:3例FLEP治疗和3例PEM治疗均有部分缓解。没有患者完全缓解。两组有效率分别为13.6%。FLEP治疗患者的中位生存期为160 +/- 30(中位+ SD)天,PEM治疗患者的中位生存期为263 +/- 104天。在所有患者中,与更长的生存期相关的因素包括反应(疾病稳定vs疾病进展p = 0.004,部分反应vs疾病进展p = 0.047)和化疗方案(PEM vs FLEP p = 0.008)。主要的临床毒性是骨髓抑制。结论:在我们的研究组中,对FLEP和PEM方案的反应较低,可能是由于我们的方案中顺铂和依托泊苷的剂量较低。对化疗和PEM治疗有反应的患者比接受FLEP治疗的患者的中位生存期更长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effects of two different cisplatin-based chemotherapy regimens on advanced non-small cell lung cancer.

Background: Many different cisplatin-based regimens have been used on advanced non-small cell lung cancer (NSCLC) in previous studies but there have been few such references in Taiwan. In this study, we evaluated the efficacy and toxicity of two different regimens including 5-Fluorouracil, Leucovorin, Etoposide and cisPlatin (FLEP) and cisPlatin, Etoposide and Mitomycin (PEM) in the treatment of patients with advanced NSCLC.

Methods: We retrospectively analyzed the records of 44 patients with NSCLC who met the selection criteria from February 1995 through April 1998. All of them were confirmed, using histologic tests, that they were in advanced stages, i.e. stage IIIB or IV. Twenty-two patients received FLEP and 22 patients received PEM.

Results: Three patients with FLEP therapy and 3 patients with PEM therapy had partial response. No patient had complete response. The response rate was 13.6% in both groups, respectively. The median survival was 160 +/- 30 (median + SD) days for patients with FLEP therapy and 263 +/- 104 days for patients with PEM therapy. The factors that were associated with longer survival in all patients included response (Stable Disease vs Disease Progression p = 0.004, Partial Response vs Disease Progression p = 0.047) and regimen of chemotherapy (PEM vs FLEP p = 0.008). The major clinically significant toxicity was myelosupression.

Conclusion: The responses to regimens, FLEP and PEM, were low in our study groups that might be due to the low dose of cisplatin and etoposide in our regimens. The patients with response to chemotherapy and PEM therapy had longer median survival than those who underwent FLEP therapy.

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