Sohn Joo Hyuk, Choi Hye Jin, Chang Joon, Kim Se Kyu, Lee Chang Geal, Chung Kyung Young, Kim Dae Joon, Cho Byoung Chul, Shin Sang Joon, Moon Yong Wha, Kim Joo-Hang
Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea.
Lung Cancer. 2006 Dec;54(3):365-70. doi: 10.1016/j.lungcan.2006.08.014. Epub 2006 Sep 29.
Irinotecan plus cisplatin has been previously documented to be effective in the treatment of extensive-disease small cell lung cancer (ED-SCLC). This study was undertaken to investigate the efficacy and feasibility of combination chemotherapy of irinotecan and carboplatin in previously untreated ED-SCLC.
From December 2002 to October 2005, 39 patients with previously untreated ED-SCLC were enrolled. Patients were treated with irinotecan (50mg/m(2) IV on days 1, 8, and 15) and carboplatin (target AUC=5 IV on day 1) every 4 weeks for up to six cycles.
Thirty-four patients (87.2%) were male and the median age was 65 years. ECOG performance status was 0-1 in 20 (51.3%) patients and 2 in 19 (48.7%) patients. The median number of chemotherapy cycles was six (range: 1-6 cycles). Thirty-five patients were assessable for response evaluation. The overall response rate was 69.2% (1 CR, 26 PR) under the intent-to-treat analysis. After a median follow-up of 22.7 months, the median time to progression was 6.4 months (95% confidence interval [CI]: 5.7-7.1 months) and median overall survival was 11.0 months (95% CI: 9.9-12.0 months). The estimated 1-year survival rate was 42.5%. In terms of toxicities, Grade 3/4 neutropenia and thrombocytopenia occurred in eight (25.6%) and five (15.4%) patients, respectively. Grade 3/4 non-hematologic toxicities included diarrhea (10.3%), anorexia (7.7%), infection (10.3%), and neutropenic fever (12.8%). There was one treatment-related death due to superimposed infection on the broncho-pleural fistula.
The combination chemotherapy of irinotecan and carboplatin was effective and tolerable in previously untreated ED-SCLC patients.
先前已证明伊立替康联合顺铂对广泛期小细胞肺癌(ED-SCLC)治疗有效。本研究旨在探讨伊立替康与卡铂联合化疗用于既往未治疗的ED-SCLC的疗效和可行性。
2002年12月至2005年10月,纳入39例既往未治疗的ED-SCLC患者。患者接受伊立替康(第1、8和15天静脉注射50mg/m²)和卡铂(第1天静脉注射,目标AUC = 5)治疗,每4周进行1次,最多6个周期。
34例(87.2%)患者为男性,中位年龄65岁。20例(51.3%)患者的东部肿瘤协作组(ECOG)体能状态为0 - 1,19例(48.7%)患者为2。化疗周期的中位数为6个(范围:1 - 6个周期)。35例患者可进行疗效评估。在意向性分析下,总缓解率为69.2%(1例完全缓解,26例部分缓解)。中位随访22.7个月后,中位疾病进展时间为6.4个月(95%置信区间[CI]:5.7 - 7.1个月),中位总生存期为11.0个月(95% CI:9.9 - 12.0个月)。估计1年生存率为42.5%。在毒性方面,8例(25.6%)患者发生3/4级中性粒细胞减少,5例(15.4%)患者发生3/4级血小板减少。3/4级非血液学毒性包括腹泻(10.3%)、厌食(7.7%)、感染(10.3%)和中性粒细胞减少性发热(12.8%)。有1例与治疗相关的死亡,原因是支气管胸膜瘘并发感染。
伊立替康与卡铂联合化疗对既往未治疗的ED-SCLC患者有效且耐受性良好。