Eiermann W, Achterrath W, Lenaz L, Hepp H
Klinikum Grosshadern der Universität, München, Federal Republic of Germany.
Cancer Chemother Pharmacol. 1991;27(5):389-93. doi: 10.1007/BF00688863.
In a pilot study, 18 patients with advanced ovarian cancer were evaluated for tolerance and response to a combination treatment with a fixed dose of carboplatin (350 mg/m2 given i.v. on day 1) and escalated doses of etoposide (70-130 mg/m2 daily given i.v. on days 1-3) as first-line chemotherapy. The maximum tolerated dose of etoposide was 130 mg/m2 when given i.v. on days 1-3 in combination with 350 mg/m2 carboplatin given i.v. every 4 weeks. At these dose levels, bone marrow toxicity was manageable and did not appear to be cumulative. In all, 12 objective responses, including 9 complete responses (CRs) and 3 partial responses (PRs), were achieved in 18 patients; 6 of the 9 CRs were confirmed as pathological CRs by second-look surgery.
在一项初步研究中,对18例晚期卵巢癌患者进行了评估,以确定其对卡铂(第1天静脉注射350mg/m²)和递增剂量依托泊苷(第1 - 3天每天静脉注射70 - 130mg/m²)联合治疗作为一线化疗的耐受性和反应。当依托泊苷在第1 - 3天静脉注射并与每4周静脉注射350mg/m²卡铂联合使用时,其最大耐受剂量为130mg/m²。在这些剂量水平下,骨髓毒性可控且似乎无累积性。18例患者中共有12例出现客观反应,包括9例完全缓解(CR)和3例部分缓解(PR);9例CR中有6例经二次探查手术确认为病理CR。