Frasci Giuseppe, Comella Pasquale, Thomas Renato, Di Bonito Maurizio, Lapenta Liliana, Capasso Immacolata, Botti Gerardo, Vallone Paolo, De Rosa Vincenzo, D'Aiuto Giuseppe, Comella Giuseppe
SICOG, c/o National Tumor Institute, Via M Semmola 80131 Naples, Italy.
Cancer Chemother Pharmacol. 2004 Jan;53(1):25-32. doi: 10.1007/s00280-003-0669-x. Epub 2003 Sep 26.
Docetaxel (DTX) has been shown to be a very active drug in both breast cancer (BC) and non-small-cell lung cancer (NSCLC). Irinotecan (CPT-11) is also active in NSCLC, and has shown promising antitumor activity in pretreated BC. PURPOSE. To define the MTDs of these two drugs given together every other week with the use of filgrastim support in pretreated BC and NSCLC patients.
Patients (aged 18-70 years, performance status < or =2) with advanced NSCLC or BC who had received at least one prior chemotherapy regimen were candidates for this phase I study. The starting DTX and CPT-11 doses were 60 mg/m(2) and 80 mg/m(2). Doses were alternately escalated at each step by 10 mg/m(2) for both drugs. Filgrastim 300 microg/day was given subcutaneously from days 4 through 7 of each cycle.
From April 2000, 41 patients were included in the trial (27 BC, 14 NSCLC). All BC patients had received epirubicin plus paclitaxel (with or without cisplatin) as first-line treatment. Of the 14 NSCLC patients, 12 had received cisplatin-based first-line therapy, and 8 patients had been pretreated with paclitaxel. The dose escalation proceeded through five dose levels up to DTX and CPT-11 doses of 80 mg/m(2) and 100 mg/m(2), respectively. Overall, ten patients showed dose-limiting toxicity during the first cycle, diarrhea in seven and neutropenia in the remaining three. Considering all 218 cycles delivered, grade 3 or 4 neutropenia occurred in 14 patients (34%), with only one episode of neutropenic fever, while severe diarrhea was observed in 9 patients (23%). A total of 21 objective responses were registered (four complete) for an overall response rate of 51% [95% CI 35-67]. A major response was seen in 16 of the 27 BC patients (59%) and in 5 of the 14 NSCLC patients (36%).
DTX and CPT-11 can be safely given together biweekly at adequate doses, with filgrastim support. In view of the promising activity data in both groups, phase II studies testing this combination in pretreated BC and NSCLC patients are ongoing.
多西他赛(DTX)已被证明在乳腺癌(BC)和非小细胞肺癌(NSCLC)中都是一种非常有效的药物。伊立替康(CPT - 11)在NSCLC中也有活性,并且在预处理的BC中已显示出有前景的抗肿瘤活性。目的:确定在预处理的BC和NSCLC患者中,使用非格司亭支持,每隔一周联合给予这两种药物的最大耐受剂量(MTD)。
年龄在18 - 70岁、体能状态≤2的晚期NSCLC或BC患者,若之前至少接受过一种化疗方案,则为本I期研究的候选对象。DTX和CPT - 11的起始剂量分别为60mg/m²和80mg/m²。两种药物在每一步均交替递增10mg/m²。在每个周期的第4天至第7天皮下给予非格司亭300μg/天。
从2000年4月起,41例患者纳入试验(27例BC,14例NSCLC)。所有BC患者均接受表柔比星加紫杉醇(有或无顺铂)作为一线治疗。14例NSCLC患者中,12例接受了以顺铂为基础的一线治疗,8例曾接受过紫杉醇预处理。剂量递增至五个剂量水平,直至DTX和CPT - 11剂量分别达到80mg/m²和100mg/m²。总体而言,10例患者在第一个周期出现剂量限制性毒性,7例为腹泻,其余3例为中性粒细胞减少。考虑所有218个给药周期,14例患者(34%)发生3级或4级中性粒细胞减少,仅1例中性粒细胞减少性发热,9例患者(23%)出现严重腹泻。共记录到21例客观缓解(4例完全缓解),总缓解率为51%[95%可信区间35 - 67]。27例BC患者中有16例(59%)出现主要缓解,14例NSCLC患者中有5例(36%)出现主要缓解。
在非格司亭支持下,DTX和CPT - 11可以安全地每两周联合给予适当剂量。鉴于两组均有有前景的活性数据,正在进行在预处理的BC和NSCLC患者中测试这种联合用药的II期研究。