Department of Obstetrics and Gynecology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Department of Obstetrics and Gynecology, Keimyung University School of Medicine, Daegu, Korea.
Cancer Res Treat. 2018 Jan;50(1):195-203. doi: 10.4143/crt.2016.376. Epub 2017 Mar 21.
Genexol-PM is a biodegradable cremophor EL-free polymeric micelle formulation of paclitaxel. Here,we compared efficacy and safety of Genexol-PM plus carboplatin versus Genexol plus carboplatin for ovarian cancer treatment.
In this multicenter, randomized, phase II study, patients with International Federation of Gynecology and Obstetrics IC-IV epithelial ovarian cancer were randomly assigned (1:1) to receive Genexol-PM 260 mg/m or Genexol 175 mg/m with 5 area under the curve carboplatin every 3weeks (6 cycles). The primary endpointwas the carbohydrate antigen 125 and Response Evaluation Criteria In Solid Tumor composite overall response rate (ORR).
Of 131 enrolled patients, 98 were included in intention-to-treat analysis. Mean dosages were 260.00±0.00 mg/m Genexol-PM or 174.24±3.81 mg/m Genexol. Median followup was 18.0 months (range, 6.1 to 33.8 months). ORR was 88.0% (95% confidence interval [CI], 80.4 to 95.6) with Genexol-PM, and 77.1% (95% CI, 67.1 to 87.1) with Genexol (noninferiority threshold, 16.3%). Median time to progression was 14.8 months (95% CI, 11.3 to 20.2) with Genexol-PM and 15.4 months (95% CI, 13.2 to 29.6) with Genexol (p=0.550). Overall, six patients died. Neutropenia was the most common toxicity (incidences of 86.0% vs. 77.1%, p=0.120). Peripheral neuropathy incidences were 84.0% versus 64.6% (p= 0.148). Peripheral neuropathy of ≥ grade 3 occurred in one patient receiving Genexol. All toxicities were manageable.
Genexol-PM plus carboplatin as first-line treatment in patients with epithelial ovarian cancer demonstrated non-inferior efficacy and well-tolerated toxicities compared with the standard paclitaxel regimen. Further studies are warranted to optimize the dose and schedule, and to investigate long-term outcomes.
Genexol-PM 是一种紫杉醇的可生物降解的聚氧乙烯蓖麻油-free 聚合物胶束制剂。在这里,我们比较了 Genexol-PM 联合卡铂与 Genexol 联合卡铂治疗卵巢癌的疗效和安全性。
在这项多中心、随机、二期研究中,国际妇产科联合会(FIGO)IC-IV 上皮性卵巢癌患者被随机(1:1)分配接受 Genexol-PM 260mg/m 或 Genexol 175mg/m 联合每 3 周 5 个曲线下面积卡铂(6 个周期)。主要终点是碳水化合物抗原 125 和实体瘤反应评估标准的综合总缓解率(ORR)。
在 131 名入组患者中,98 名患者被纳入意向治疗分析。Genexol-PM 的平均剂量为 260.00±0.00mg/m,Genexol 的平均剂量为 174.24±3.81mg/m。中位随访时间为 18.0 个月(范围,6.1 至 33.8 个月)。Genexol-PM 的 ORR 为 88.0%(95%可信区间[CI],80.4 至 95.6),Genexol 为 77.1%(95% CI,67.1 至 87.1)(非劣效性阈值为 16.3%)。Genexol-PM 的中位无进展生存期为 14.8 个月(95% CI,11.3 至 20.2),Genexol 为 15.4 个月(95% CI,13.2 至 29.6)(p=0.550)。总的来说,有 6 名患者死亡。中性粒细胞减少是最常见的毒性(发生率分别为 86.0%和 77.1%,p=0.120)。周围神经病变的发生率分别为 84.0%和 64.6%(p=0.148)。一名接受 Genexol 治疗的患者出现 3 级以上的周围神经病变。所有毒性均可控制。
Genexol-PM 联合卡铂作为上皮性卵巢癌患者的一线治疗方案,与标准紫杉醇方案相比,疗效不劣且毒性可耐受。需要进一步的研究来优化剂量和方案,并研究长期结果。