Chen Gigi, Huynh Minh, Fehrenbacher Lou, West Howard, Lara Primo N, Yavorkovsky Leonid L, Russin Michael, Goldstein Desiree, Gandara David, Lau Derick
University of California, Davis Cancer Center, Sacramento, CA 95817, USA.
J Clin Oncol. 2009 Mar 20;27(9):1401-4. doi: 10.1200/JCO.2008.20.2127. Epub 2009 Feb 9.
The regimens of weekly irinotecan with platinum have been used for treatment of metastatic small-cell lung cancer (SCLC). We conducted a multi-institution phase II trial to evaluate a novel 21-day schedule of irinotecan and carboplatin in patients with relapsed or extensive SCLC.
Eighty patients were enrolled with the following characteristics: 39 male patients, 41 female patients; median age, 65 years; and Zubrod performance status, 0 to 1 in 85% and 2 in 15% of patients. Dosing schemas were based on the maximum-tolerated dose derived in a previous phase I study. Chemotherapy-naive patients with extensive SCLC were treated with irinotecan 200 mg/m(2) and carboplatin area under the curve (AUC) of 5 (arm A). Patients, who had previously been treated with chemotherapy and had relapsed disease received irinotecan 150 mg/m(2) and carboplatin AUC of 5 (arm B). In each study arm, the treatment was given every 21 days for up to six cycles.
The most common grade 3 to 4 toxicities included neutropenia (54%), thrombocytopenia (22%), anemia (13%), diarrhea (22%), and nausea/emesis (11%) in both study arms. There were three treatment-related deaths owing to neutropenic sepsis. Among 72 assessable patients, response rates of 65% and 50% were observed, respectively, for arm A and arm B. The median survival for both study arms was identical at 10 months (95% CI, 6 to 14 months). A response rate of 65% was observed in the intracranial disease of 14 patients with known brain metastases.
This 21-day regimen of irinotecan and carboplatin seems promising for the treatment of relapsed SCLC.
每周使用伊立替康联合铂类的方案已用于治疗转移性小细胞肺癌(SCLC)。我们开展了一项多机构II期试验,以评估伊立替康和卡铂用于复发或广泛期SCLC患者的新型21天给药方案。
80例患者入组,其特征如下:男性39例,女性41例;中位年龄65岁;Zubrod体能状态,85%的患者为0至1级,15%的患者为2级。给药方案基于先前I期研究得出的最大耐受剂量。初治的广泛期SCLC患者接受伊立替康200mg/m²和卡铂曲线下面积(AUC)为5的治疗(A组)。先前接受过化疗且疾病复发的患者接受伊立替康150mg/m²和卡铂AUC为5的治疗(B组)。在每个研究组中,每21天给药一次,最多6个周期。
两个研究组中最常见的3至4级毒性包括中性粒细胞减少(54%)、血小板减少(22%)、贫血(13%)、腹泻(22%)和恶心/呕吐(11%)。有3例与治疗相关的死亡,原因是中性粒细胞减少性败血症。在72例可评估患者中,A组和B组的缓解率分别为65%和50%。两个研究组的中位生存期均为10个月(95%CI,6至14个月)。14例已知脑转移患者的颅内疾病缓解率为65%。
这种伊立替康和卡铂的21天给药方案似乎有望用于复发SCLC的治疗。