Vasey P A, Gore M, Wilson R, Rustin G, Gabra H, Guastalla J-P, Lauraine E P, Paul J, Carty K, Kaye S
CR-UK Clinical Trials Unit, Beatson Oncology Centre, Western Infirmary, Dumbarton Road, Glasgow, Scotland G11 6NT, UK.
Br J Cancer. 2008 Jun 3;98(11):1774-80. doi: 10.1038/sj.bjc.6604371. Epub 2008 May 27.
The safety and maximum tolerated dose (MTD) of erlotinib with docetaxel/carboplatin were assessed in patients with ovarian cancer. Chemonaive patients received intravenous docetaxel (75 mg m(-2)) and carboplatin (area under the curve 5) on day 1 of a 3-week cycle, and oral erlotinib at 50 (cohort 1), 100 (cohort 2a) or 75 mg day(-1) (cohort 2b) for up to six cycles. Dose-limiting toxicities were determined in cycle 1. Forty-five patients (median age 59 years) received treatment. Dose-limiting toxicities occurred in 1/5/5 patients (cohorts 1/2a/2b). The MTD of erlotinib in this regimen was determined to be 75 mg day(-1) (cohort 2b; the erlotinib dose was escalated to 100 mg day(-1) in 11 out of 19 patients from cycle 2 onwards). Neutropaenia was the predominant grade 3/4 haematological toxicity (85/100/95% respectively). Common non-haematological toxicities were diarrhoea, fatigue, nausea and rash. There were five complete and seven partial responses in 23 evaluable patients (52% response rate). Docetaxel/carboplatin had no measurable effect on erlotinib pharmacokinetics. In subsequent single-agent maintenance, erlotinib was given at 100-150 mg day(-1), with manageable toxicity, until tumour progression. Further investigation of erlotinib in epithelial ovarian carcinoma may be warranted, particularly as maintenance therapy.
在卵巢癌患者中评估了厄洛替尼与多西他赛/卡铂联合使用的安全性及最大耐受剂量(MTD)。初治患者在每3周周期的第1天接受静脉注射多西他赛(75 mg m⁻²)和卡铂(曲线下面积为5),并口服厄洛替尼,剂量分别为50 mg(队列1)、100 mg(队列2a)或75 mg/天(队列2b),最多进行6个周期。在第1周期确定剂量限制性毒性。45例患者(中位年龄59岁)接受了治疗。剂量限制性毒性分别发生在1/5/5例患者中(队列1/2a/2b)。该方案中厄洛替尼的MTD确定为75 mg/天(队列2b;从第2周期起,19例患者中有11例将厄洛替尼剂量增至100 mg/天)。中性粒细胞减少是主要的3/4级血液学毒性(分别为85%/100%/95%)。常见的非血液学毒性为腹泻、乏力、恶心和皮疹。23例可评估患者中有5例完全缓解和7例部分缓解(缓解率52%)。多西他赛/卡铂对厄洛替尼的药代动力学无显著影响。在随后的单药维持治疗中,给予厄洛替尼100 - 150 mg/天,毒性可控,直至肿瘤进展。厄洛替尼在上皮性卵巢癌中的进一步研究可能是必要的,尤其是作为维持治疗。