Department of Internal Medicine, Kangnam Sacred-Heart Hospital, Hallym University Medical Center, Hallym University College of Medicine, 948-1, Daerim-1-dong, Yeongdeungpo-gu, Seoul 150-950, Republic of Korea.
Cancer Chemother Pharmacol. 2013 Jun;71(6):1591-7. doi: 10.1007/s00280-013-2159-0. Epub 2013 Apr 9.
Platinum-based doublet chemotherapy has a major role in the treatment of patients with advanced non-small cell lung cancer (NSCLC). The weekly fractionated administration of cisplatin for patients with NSCLC has been shown to be active. Irinotecan and carboplatin are effective against NSCLC and demonstrated synergism with non-cross-resistance in preclinical studies. We conducted a phase II study of weekly combination of carboplatin and irinotecan as first-line chemotherapy for patients with advanced NSCLC.
From March 2009 to November 2011, 24 patients who were diagnosed with inoperable or metastatic NSCLC were enrolled. Treatment consisted of carboplatin at an AUC 2.5 mg/mL/min over 30-min intravenous infusion and irinotecan 65 mg/m(2) over 90-min intravenous infusion on day 1 and day 8, respectively. The treatment was repeated every 3 weeks.
One patient (4.2 %) achieved complete response, and seven (29.2 %) showed partial response. Overall response rate was 33.3 %, with median response duration of 4.55 months. Nine patients had stable disease, and disease control rate was 70.8 %. With median follow-up of 12.8 months, median progression-free survival was 4.5 months (95 % CI 1.8-7.2), and median overall survival was 15.5 months (95 % CI 6.9-24.1). Major toxicity was myelosuppression. Grade 3-4 neutropenia and thrombocytopenia occurred in 50 and 20.8 % of patients, respectively. Two patients experienced febrile neutropenia. Non-hematologic toxicities were generally mild. One patient suffered grade 4 diarrhea, and one treatment-related death due to pneumonia was occurred.
The weekly combination of carboplatin and irinotecan showed favorable activity and manageable toxicity profiles in chemo-naïve patients with advanced NSCLC. Our results suggest that this regimen can be a reasonable chemotherapeutic option for patients with advanced NSCLC.
铂类双联化疗在治疗晚期非小细胞肺癌(NSCLC)患者中具有重要作用。每周给予 NSCLC 患者顺铂分割剂量给药已显示出活性。伊立替康和卡铂对 NSCLC 有效,并在临床前研究中表现出协同作用,无交叉耐药性。我们进行了一项 II 期研究,评估每周联合卡铂和伊立替康作为晚期 NSCLC 患者的一线化疗。
从 2009 年 3 月至 2011 年 11 月,共纳入 24 例诊断为不可切除或转移性 NSCLC 的患者。治疗方案为卡铂 AUC 2.5 mg/mL/min,静脉输注 30 分钟,伊立替康 65 mg/m2,静脉输注 90 分钟,分别于第 1 天和第 8 天给药。每 3 周重复治疗。
1 例患者(4.2%)达到完全缓解,7 例(29.2%)显示部分缓解。总缓解率为 33.3%,中位缓解持续时间为 4.55 个月。9 例患者疾病稳定,疾病控制率为 70.8%。中位随访 12.8 个月时,中位无进展生存期为 4.5 个月(95%CI 1.8-7.2),中位总生存期为 15.5 个月(95%CI 6.9-24.1)。主要毒性为骨髓抑制。3-4 级中性粒细胞减少和血小板减少分别发生在 50%和 20.8%的患者中。2 例患者发生发热性中性粒细胞减少。非血液学毒性通常较轻。1 例患者发生 4 级腹泻,1 例治疗相关肺炎死亡。
卡铂联合伊立替康每周方案在未经化疗的晚期 NSCLC 患者中显示出良好的活性和可管理的毒性特征。我们的结果表明,该方案可作为晚期 NSCLC 患者的合理化疗选择。