Rose P G, Blessing J A, Mayer A R, Homesley H D
Department of Obstetrics and Gynecology, University Hospitals of Cleveland, Case Western Reserve University, OH, USA.
J Clin Oncol. 1998 Feb;16(2):405-10. doi: 10.1200/JCO.1998.16.2.405.
A phase II trial was conducted to determine the activity of prolonged oral etoposide in platinum-resistant and platinum-sensitive ovarian carcinoma.
Platinum-resistant disease was defined as progression on platinum-based chemotherapy or recurrence within 6 months of completing therapy. The starting dose was 50 mg/m2/d (30 mg/m2/d for prior radiotherapy) for 21 days, every 28 days. A dose escalation to a maximum dose of 60 mg/m2/d was prescribed.
Of 99 patients entered, 97 were assessable for toxicity and 82 were assessable for response. Among 41 platinum-resistant patients a 26.8% response rate (7.3% complete response [CR] and 19.5% partial response [PR] rate) occurred. The median response duration was 4.3 months (range, 1.3 to 8.7), median progression-free interval (PFI) was 5.7 months (range, 0.8 to 30.8+), and median survival time was 10.8 months (range, 1.9 to 45.8). Twenty-five of 41 platinum-resistant patients had also previously received paclitaxel; of which eight (32%) responded. Among 41 platinum-sensitive patients, a 34.1% response rate (14.6% CR and 19.5% PR rate) occurred. The median response duration was 7.5 months (range, 1.9 to 15.2+), median PFI was 6.3+ months (range, 0.9 to 20.4), and median survival time was 16.5+ months (range, 0.9 to 34.8). Of 97 patients assessable for toxicity, grade 3 or 4 hematologic toxicity was common, with leukopenia occurring in 41.2% (grade 3, 29%; grade 4, 12%), neutropenia in 45.4% (grade 3, 20%; grade 4, 25%), thrombocytopenia in 9% (grade 3, 5%; grade 4, 4%), and anemia in 13.4%. Three treatment-related deaths occurred: two from neutropenic sepsis and one from thrombocytopenic bleeding after an overdose. One patient developed leukemia.
This regimen is active in platinum-resistant and platinum-sensitive ovarian carcinoma. Additionally, the regimen is active in paclitaxel-resistant ovarian carcinoma.
开展一项II期试验,以确定长期口服依托泊苷对铂耐药和铂敏感卵巢癌的活性。
铂耐药疾病定义为铂类化疗期间病情进展或完成治疗后6个月内复发。起始剂量为50mg/m²/天(既往接受过放疗者为30mg/m²/天),持续21天,每28天为一周期。规定剂量可逐步增至最大剂量60mg/m²/天。
入组的99例患者中,97例可评估毒性,82例可评估疗效。41例铂耐药患者的缓解率为26.8%(完全缓解[CR]率7.3%,部分缓解[PR]率19.5%)。中位缓解持续时间为4.3个月(范围1.3至8.7个月),中位无进展生存期(PFI)为5.7个月(范围0.8至30.8+个月),中位生存时间为10.8个月(范围1.9至45.8个月)。41例铂耐药患者中有25例此前也接受过紫杉醇治疗;其中8例(32%)有反应。41例铂敏感患者的缓解率为34.1%(CR率14.6%,PR率19.5%)。中位缓解持续时间为7.5个月(范围1.9至15.2+个月),中位PFI为6.3+个月(范围0.9至20.4个月),中位生存时间为16.5+个月(范围0.9至34.8个月)。在97例可评估毒性的患者中,3或4级血液学毒性很常见,白细胞减少发生率为41.2%(3级29%,4级12%),中性粒细胞减少发生率为45.4%(3级20%,4级25%),血小板减少发生率为9%(3级5%,4级4%),贫血发生率为13.4%。发生了3例与治疗相关的死亡:2例死于中性粒细胞减少性败血症,1例死于过量用药后的血小板减少性出血。1例患者发生白血病。
该方案对铂耐药和铂敏感卵巢癌均有活性。此外,该方案对紫杉醇耐药的卵巢癌也有活性。