卡铂和伊立替康联合化疗并给予粒细胞集落刺激因子(G-CSF)支持治疗老年小细胞肺癌患者。
A combination chemotherapy of carboplatin and irinotecan with granulocyte colony-stimulating factor (G-CSF) support in elderly patients with small cell lung cancer.
作者信息
Okamoto Hiroaki, Naoki Katsuhiko, Narita Yusuke, Hida Naoya, Kunikane Hiroshi, Watanabe Koshiro
机构信息
Department of Respiratory Medicine, Yokohama Municipal Citizen's Hospital, Yokohama, Kanagawa, Japan.
出版信息
Lung Cancer. 2006 Aug;53(2):197-203. doi: 10.1016/j.lungcan.2006.05.004. Epub 2006 Jun 15.
BACKGROUND
We have previously reported that carboplatin plus etoposide is an effective and relatively non-toxic regimen in elderly patients with small cell lung cancer (SCLC). Recently, the Japan Clinical Oncology Group reported that irinotecan plus cisplatin was more effective than etoposide plus cisplatin in the treatment of non-elderly patients with extensive disease (ED)-SCLC. Therefore, we conducted a prospective feasibility study designed specifically to evaluate the efficacy of carboplatin (day 1) and irinotecan (days 1, 8, 15) with granulocyte colony-stimulating factor (G-CSF) support in elderly SCLC patients.
METHODS
Three carboplatin AUC and irinotecan dose levels were used: 4 mg/ml x min and 50 mg/m2, respectively (level 1); 5 mg/ml x min and 50 mg/m2, respectively (level 2), and 5 mg/ml x min and 60 mg/m2, respectively (level 3). Although a phase I trial using this drug combination against non-SCLC performed at our institution found that the recommended dose was level 3, as the current trial included only elderly patients, the starting dose used was level 2. However, if a patient had history of prior chemotherapy, performance status (PS) of 2, or was aged 75 years or more, the dose administered was reduced by 1 level. If a patient had a PS of 0, the dose was increased by 1 level. Cycles were repeated every 4 weeks, and patients aged 70 years or more with a PS of 0-2 were eligible.
RESULTS
Eighteen patients were enrolled, of which nine were given the level 1 dose, seven the level 2 dose, and two the level 3 dose. The patient group had a median age of 75 years, 8 patients had limited disease (LD) versus 10 with ED, 9 had received previous treatment for SCLC versus 9 previously untreated, and 13 had a PS of 0-1 versus 5 with a PS of 2. Seventeen (94%) patients received two or more cycles of chemotherapy, and the median actual delivery of irinotecan was 84% of the projected dose. Grade 3/4 neutropenia, anemia, and diarrhea occurred in 50%, 33% and 6% of patients, respectively. Other toxicities were mild and no treatment-related deaths occurred. The response rate was 89%, with two complete responses and 14 partial responses. The median survival time was 13.3 months and the 1-year survival rate was 62%.
CONCLUSIONS
The combination of carboplatin and irinotecan with G-CSF support was an effective and non-toxic regimen in elderly SCLC patients and should be further evaluated in phase III trials.
背景
我们之前曾报道,卡铂联合依托泊苷对于老年小细胞肺癌(SCLC)患者是一种有效且相对无毒的治疗方案。最近,日本临床肿瘤学组报告称,在治疗广泛期疾病(ED)-SCLC的非老年患者中,伊立替康联合顺铂比依托泊苷联合顺铂更有效。因此,我们开展了一项前瞻性可行性研究,专门评估卡铂(第1天)和伊立替康(第1、8、15天)联合粒细胞集落刺激因子(G-CSF)支持治疗老年SCLC患者的疗效。
方法
使用了三种卡铂曲线下面积(AUC)和伊立替康剂量水平:分别为4mg/ml·min和50mg/m²(1级);分别为5mg/ml·min和50mg/m²(2级),以及分别为5mg/ml·min和60mg/m²(3级)。尽管我们机构针对非SCLC使用这种药物组合进行的I期试验发现推荐剂量为3级,但由于当前试验仅纳入老年患者,起始使用的剂量为2级。然而,如果患者有既往化疗史、体能状态(PS)为2,或年龄在75岁及以上,则给药剂量降低1级。如果患者PS为0,则剂量增加1级。每4周重复一个周期,年龄在70岁及以上且PS为0 - 2的患者符合条件。
结果
共纳入18例患者,其中9例给予1级剂量,7例给予2级剂量,2例给予3级剂量。患者组的中位年龄为75岁,8例为局限期疾病(LD),10例为广泛期疾病(ED),9例曾接受过SCLC治疗,9例未曾接受过治疗,13例PS为0 - 1,5例PS为2。17例(94%)患者接受了两个或更多周期的化疗,伊立替康的实际给药中位剂量为预计剂量的84%。3/4级中性粒细胞减少、贫血和腹泻分别发生在50%、33%和6%的患者中。其他毒性反应较轻,未发生与治疗相关的死亡。缓解率为89%,2例完全缓解,14例部分缓解。中位生存时间为13.3个月,1年生存率为62%。
结论
卡铂和伊立替康联合G-CSF支持治疗对于老年SCLC患者是一种有效且无毒的治疗方案,应在III期试验中进一步评估。