Irinotecan and Cisplatin Combination Chemotherapy Plus Concurrent Thoracic Irradiation for Patients with Limited Disease Small Cell Lung Cancer

Junshik Hong, Y. Park, S. Lee, K. Lee, S. Park, Jinny Park, S. Sym, E. Cho, D. Shin, J. H. Lee
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引用次数: 3

Abstract

Purpose: To evaluate the antitumor activity and safety of irinotecan plus cisplatin combination chemotherapy with concurrent thoracic radiotherapy (TRT) in patients with limited disease (LD) small cell lung cancer (SCLC). Materials and Methods: Patients with pathologically-confirmed LD SCLC with the following inclusion criteria were retrospectively analyzed: age ≥18 years; measurable lesion; Eastern Cooperative Oncology Group Performance Status 0 ∼2; chemotherapy naive; and adequate bone marrow and organ function. Patients received an intravenous (IV) infusion of irinotecan (35 mg/m 2 on days 1, 8, and 15) and cisplatin (60 mg/m 2 on day 1), which was repeated every 4 weeks for up to 6 cycles. Concurrent TRT was administered with the beginning of chemotherapy. Irinotecan was increased to 60 mg/m2 after completion of TRT. Patients with a complete response (CR) subsequently received prophylactic cranial irradiation. Results: Nineteen patients were analyzed. There were 8 patients (42.1%) with CR, 9 patients (47.4%) with partial response, and 1 patient each (5.3%) with stable disease and progressive disease (PD). The overall response rate was 89.5%. The median progression-free survival was 7.6 months (95% confidence interval [CI], 1.3 ∼14.0 months) and the median overall survival was 12.4 months (95% CI, 0.5∼24.2 months). The 2-year survival rate of the CR patients was 75.0%. No grade 4 hematologic toxicity was reported. Frequently reported toxicities were nausea (10 patients), radiation-induced pneumonitis (10 patients), and neutropenia (6 patients). Radiation-related severe toxicities were frequently reported. Three patients had treatment-related deaths. Conclusion: This study supports the activity and tolerability of irinotecan plus cisplatin with concurrent TRT in patients with LD SCLC. (J Lung Cancer 2011;10(1):49 �� 55)
伊立替康与顺铂联合化疗加同期胸部放疗治疗局限性小细胞肺癌
目的:评价伊立替康+顺铂联合化疗并发胸部放疗(TRT)对局限性疾病(LD)小细胞肺癌(SCLC)患者的抗肿瘤活性和安全性。材料和方法:回顾性分析病理证实的LD SCLC患者,符合以下入选标准:年龄≥18岁;可测量的损伤;东部肿瘤合作组绩效状况0 ~ 2;化疗天真;以及充足的骨髓和器官功能。患者接受静脉(IV)输注伊立替康(35mg / m2,第1、8和15天)和顺铂(60mg / m2,第1天),每4周重复一次,最多6个周期。化疗开始时同时给予TRT。完成TRT后伊立替康增加至60 mg/m2。完全缓解(CR)的患者随后接受预防性颅脑照射。结果:对19例患者进行分析。CR 8例(42.1%),部分缓解9例(47.4%),病情稳定和进展性疾病(PD)各1例(5.3%)。总有效率为89.5%。中位无进展生存期为7.6个月(95%可信区间[CI], 1.3 ~ 14.0个月),中位总生存期为12.4个月(95% CI, 0.5 ~ 24.2个月)。CR患者2年生存率为75.0%。无4级血液学毒性报告。常见的毒性反应是恶心(10例)、放射性肺炎(10例)和中性粒细胞减少(6例)。经常报告与辐射有关的严重毒性。3名患者因治疗而死亡。结论:本研究支持伊立替康联合顺铂并发TRT治疗LD SCLC患者的活性和耐受性。[J] .肺癌杂志;2011;10(1):49 - 55。
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