Hermes Andreas, Bergman Bengt, Bremnes Roy, Ek Lars, Fluge Sverre, Sederholm Christer, Sundstrøm Stein, Thaning Lars, Vilsvik Jan, Aasebø Ulf, Sörenson Sverre
Department of Pulmonary Oncology, Grosshansdorf Hospital, Wöhrendamm 80, 22927 Grosshansdorf, Germany.
J Clin Oncol. 2008 Sep 10;26(26):4261-7. doi: 10.1200/JCO.2007.15.7545.
A Japanese randomized trial showed superior survival for patients with extensive-disease (ED) small-cell lung cancer (SCLC) receiving irinotecan plus cisplatin compared with etoposide plus cisplatin. The present trial evaluated the efficacy of irinotecan plus carboplatin (IC) compared with oral etoposide plus carboplatin (EC).
Patients with ED SCLC were randomly assigned to receive either IC, which consisted of carboplatin (area under the curve = 4; Chatelut formula) and irinotecan (175 mg/m2) intravenously both on day 1, or EC, which consisted of carboplatin as in IC and etoposide (120 mg/m(2)/d) orally on days 1 through 5. Courses were repeated every 3 weeks with four cycles planned. Doses were reduced by one third in patients with a WHO performance status (PS) of 3 to 4 and/or age older than 70 years. Primary end point was overall survival (OS). Secondary end points were quality of life (QOL) and complete response (CR) rate.
Of 220 randomly assigned patients, 209 were eligible for analysis (IC, n = 105; EC, n = 104). Thirty-five percent were older than 70 years, and 47% had a PS of 2 to 4. The groups were well balanced with respect to prognostic factors. OS was inferior in the EC group (hazard ratio = 1.41; 95% CI, 1.06 to 1.87; P = .02). Median survival time was 8.5 months for IC compared with 7.1 months for EC. One-year survival rate was 34% for IC and 24% for EC. CR was seen in 18 IC patients compared with seven EC patients (P = .02). There were no statistically significant differences in hematologic grade 3 or 4 toxicity. Grade 3 or 4 diarrhea was more common in the IC group. QOL differences were small, with a trend toward prolonged palliation with the IC regimen.
IC prolongs survival in ED SCLC with slightly better scores for QOL.
一项日本的随机试验表明,广泛期(ED)小细胞肺癌(SCLC)患者接受伊立替康联合顺铂治疗的生存期优于依托泊苷联合顺铂治疗。本试验评估了伊立替康联合卡铂(IC)与口服依托泊苷联合卡铂(EC)的疗效。
ED SCLC患者被随机分配接受IC方案,即第1天静脉注射卡铂(曲线下面积=4;Chatelut公式)和伊立替康(175mg/m²),或EC方案,即第1至5天口服卡铂(同IC方案)和依托泊苷(120mg/m²/d)。每3周重复一个疗程,计划进行4个周期。世界卫生组织体能状态(PS)为3至4分和/或年龄大于70岁的患者剂量减少三分之一。主要终点是总生存期(OS)。次要终点是生活质量(QOL)和完全缓解(CR)率。
220例随机分配的患者中,209例符合分析条件(IC组,n = 105;EC组,n = 104)。35%的患者年龄大于70岁,47%的患者PS评分为2至4分。两组在预后因素方面平衡良好。EC组的OS较差(风险比=1.41;95%CI,1.06至1.87;P = 0.02)。IC组的中位生存时间为8.5个月,而EC组为7.1个月。IC组的1年生存率为34%,EC组为24%。IC组有18例患者达到CR,而EC组有7例(P = 0.02)。血液学3级或4级毒性无统计学显著差异。3级或4级腹泻在IC组更常见。QOL差异较小,IC方案有延长缓解期的趋势。
IC可延长ED SCLC患者的生存期,且QOL评分略高。