Gervais R, Le Guen Y, Le Caer H, Paillotin D, Chouaid C
Centre Régional de Lutte Contre le Cancer François Baclesse, Caen, France.
Rev Mal Respir. 2007 May;24(5):653-8. doi: 10.1016/s0761-8425(07)91136-5.
There is no standard second-line treatment for small cell lung cancer (SCLC). The prognosis of these patients is poor and special attention should be paid to both quality of life and economic factors.
The aim of this phase II randomised trial (GFPC0501) is to compare, in patients with progressive SCLC after first-line platinum based chemotherapy, oral multi drug chemotherapy (CCNU, cyclophosphamide, etoposide) and classical intravenous chemotherapy with cyclophosphamide, doxorubicin and vincristine (CAV) in terms of tolerability, efficacy (response rate, median one year survival and overall survival), quality of life and consumption of health care resources. Based on a two-stage Bryant and Day approach, this study will require a total of 138 patients with an interim analysis of the first 38.
This trial will provide information on several aspects of second-line chemotherapy for patients with SCLC. Thirty six patients have been enrolled in 16 centres by December 2006 and the results of the interim analysis will be available in June 2007.
小细胞肺癌(SCLC)尚无标准的二线治疗方案。这些患者预后较差,应特别关注生活质量和经济因素。
这项II期随机试验(GFPC0501)的目的是,在一线铂类化疗后病情进展的SCLC患者中,比较口服多药化疗(洛莫司汀、环磷酰胺、依托泊苷)与经典的环磷酰胺、多柔比星和长春新碱静脉化疗(CAV)在耐受性、疗效(缓解率、一年中位生存期和总生存期)、生活质量及医疗资源消耗方面的差异。基于两阶段的布莱恩特和戴方法,本研究共需要138例患者,先对前38例进行中期分析。
本试验将提供有关SCLC患者二线化疗几个方面的信息。截至2006年12月,已有36例患者在16个中心入组,中期分析结果将于2007年6月公布。