Zamagni C, Martoni A, Cacciari N, Gentile A, Pannuti F
Division of Medical Oncology, S. Orsola-Malpighi Hospital, Bologna, Italy.
Am J Clin Oncol. 1998 Oct;21(5):491-7. doi: 10.1097/00000421-199810000-00015.
The combination of paclitaxel 135 mg/m2 (24-hour infusion) and cisplatin 75 mg/m2 is now considered the standard treatment in first-line chemotherapy for stage III suboptimally debulked and stage IV ovarian cancer. Interest is focused on the possibility of evaluating the combination of paclitaxel with carboplatin, because it was found to be less nefrotoxic and less neurotoxic than cisplatin. This study seeks to determine the maximum tolerated dose and to assess the antitumor activity of the combination of a 3-hour paclitaxel infusion followed by carboplatin. Thirty-three chemotherapy-naive patients with stage III-IV epithelial ovarian cancer entered this open, nonrandomized dose-finding study. The first dose level investigated was paclitaxel 125 mg/m2 and carboplatin 250 mg/m2: the dose level progression was performed by alternatively increasing paclitaxel 25 mg/m2 and carboplatin 50 mg/m2. Cycles were repeated every 28 days. At least three patients were treated at each dose level. Overall, 233 and 224 cycles, respectively, are evaluable for nonhematologic and hematologic toxicity. Dose-limiting toxicities (febrile neutropenia and severe fatigue) were observed in two of six patients at level VIII (paclitaxel 225 mg/m2 and carboplatin 400 mg/m2) and therefore the previous dose-level (paclitaxel 200 mg/m2 and carboplatin 400 mg/m2) was considered as the maximum tolerated dose. Neutropenia (grade 3-4 in 63% of cycles), neurotoxicity (grade 2 in 37.5% and grade 3 in 9% of patients), arthromyalgias (grade 2 in 53% of patients and grade 3 in 3% of patients), and grade 3 alopecia were the most common toxicities observed. The incidence of thrombocytopenia was low (grade 3 in 4% of cycles) and no renal toxicity was observed. An objective remission was documented in 74% of 31 evaluated patients, including eight complete remissions (26%) confirmed by second-look surgery. The combination of paclitaxel 200 mg/m2 3-hour infusion followed by carboplatin 400 mg/m2 (30-minute infusion) is a safe and active regimen as first-line chemotherapy for advanced ovarian cancer.
紫杉醇135mg/m²(24小时输注)与顺铂75mg/m²联合应用,目前被认为是Ⅲ期减瘤不充分及Ⅳ期卵巢癌一线化疗的标准治疗方案。人们的兴趣集中在评估紫杉醇与卡铂联合应用的可能性,因为已发现其肾毒性和神经毒性比顺铂小。本研究旨在确定最大耐受剂量,并评估先输注3小时紫杉醇随后给予卡铂这一联合方案的抗肿瘤活性。33例初治的Ⅲ - Ⅳ期上皮性卵巢癌患者进入了这项开放的、非随机的剂量探索研究。研究的首个剂量水平为紫杉醇125mg/m²和卡铂250mg/m²:剂量水平递增方式为交替增加紫杉醇25mg/m²和卡铂50mg/m²。每28天重复一个周期。每个剂量水平至少治疗3例患者。总体而言,分别有233个和224个周期可用于评估非血液学毒性和血液学毒性。在Ⅷ级水平(紫杉醇225mg/m²和卡铂400mg/m²)的6例患者中有2例观察到剂量限制性毒性(发热性中性粒细胞减少和严重疲劳),因此将前一个剂量水平(紫杉醇200mg/m²和卡铂400mg/m²)视为最大耐受剂量。中性粒细胞减少(63%的周期为3 - 4级)、神经毒性(37.5%的患者为2级,9%的患者为3级)、关节痛(53%的患者为2级,3%的患者为3级)以及3级脱发是观察到的最常见毒性。血小板减少的发生率较低(4%的周期为3级),未观察到肾毒性。在31例评估患者中有74%记录到客观缓解,包括经二次探查手术确认的8例完全缓解(26%)。先输注3小时紫杉醇200mg/m²随后给予卡铂400mg/m²(30分钟输注)的联合方案作为晚期卵巢癌的一线化疗是一种安全且有效的方案。