Thatcher Nicholas, Qian Wendi, Clark Peter I, Hopwood Penelope, Sambrook Robert J, Owens Robert, Stephens Richard J, Girling David J
Medical Research Council Clinical Trials Unit, London NW1 2DA, United Kingdom.
J Clin Oncol. 2005 Nov 20;23(33):8371-9. doi: 10.1200/JCO.2004.00.9969.
Ifosfamide, carboplatin, etoposide, and vincristine, alone and in combination, are highly active against small-cell lung cancer (SCLC). This trial was designed to investigate whether survival could be improved by a regimen of all four drugs (ICE-V) compared with standard chemotherapy in patients with SCLC and good performance status, and to assess the patients' quality of life (QL).
Patients were randomly assigned to receive six cycles of either ICE-V at 4-week intervals without dose reduction or standard chemotherapy administered according to local practice. The recommended standard control regimens were cyclophosphamide, doxorubicin, and etoposide; and cisplatin and etoposide.
A total of 402 patients were randomly assigned, and 350 (87%) patients have died. Overall survival was longer in the ICE-V group (hazard ratio, 0.74; 95% CI, 0.60 to 0.91; P = .0049), median survival was 15.6 months in the ICE-V group and 11.6 months in the control group, and 2-year survival rates were 20% and 11%, respectively. There was no evidence that the relative survival benefit for ICE-V was less in extensive-stage than in limited-stage patients. An increased rate of septicemia was reported in the ICE-V group (15% v 7% in the control group), but this did not result in an increase in reported treatment-related deaths (four patients [2%] in both groups). The findings on QL were broadly similar in both groups, with some benefit in favor of ICE-V.
Compared with standard chemotherapy, the ICE-V regimen improves overall survival without QL penalties, despite an increased but manageable level of toxicity.
异环磷酰胺、卡铂、依托泊苷和长春新碱,单独使用或联合使用时,对小细胞肺癌(SCLC)均具有高活性。本试验旨在研究与标准化疗相比,对于体能状态良好的SCLC患者,使用包含这四种药物的方案(ICE-V)是否能提高生存率,并评估患者的生活质量(QL)。
患者被随机分配接受以下两种治疗之一,即每4周进行1次共6个周期的ICE-V治疗且不进行剂量减少,或根据当地实际情况给予标准化疗。推荐的标准对照方案为环磷酰胺、多柔比星和依托泊苷;以及顺铂和依托泊苷。
共有402例患者被随机分配,其中350例(87%)患者死亡。ICE-V组的总生存期更长(风险比,0.74;95%置信区间,0.60至0.91;P = 0.0049),ICE-V组的中位生存期为15.6个月,对照组为11.6个月,2年生存率分别为20%和11%。没有证据表明ICE-V在广泛期患者中的相对生存获益低于局限期患者。ICE-V组报告的败血症发生率有所增加(15%,对照组为7%),但这并未导致报告的治疗相关死亡增加(两组均为4例患者[2%])。两组在QL方面的结果大致相似,ICE-V组有一些优势。
与标准化疗相比,ICE-V方案可提高总生存期且不影响生活质量,尽管毒性有所增加但仍可控制。