Alberts David S, Liu P Y, Wilczynski Sharon P, Clouser Mary C, Lopez Ana Maria, Michelin David P, Lanzotti Victor J, Markman Maurie
University of Arizona Cancer Center, Tucson, AZ 85724-5024, USA.
Gynecol Oncol. 2008 Jan;108(1):90-4. doi: 10.1016/j.ygyno.2007.08.075. Epub 2007 Oct 18.
Because debate continues over the role of combination, platinum-based chemotherapy for platinum-sensitive (PS), recurrent ovarian cancer (OC), we compared overall survival (OS), progression-free survival (PFS), confirmed complete response rate and time to treatment failure in this population.
Patients with recurrent stage III or IV OC, a progression-free and platinum-free interval of 6-24 months after first-line platinum-based chemotherapy and up to 12 courses of a non-platinum containing consolidation treatment were eligible. Patients were randomized to i.v. pegylated liposomal doxorubicin (PLD) (30 mg/m2) plus i.v. carboplatin (AUC=5 mg/mL min) once every 4 weeks (PLD arm) or i.v. carboplatin alone (AUC=5 mg/mL min) once every 4 weeks.
The PLD arm enrolled 31 patients and the carboplatin alone arm 30 for a total of 61 patients out of 900 planned. Response rates were 67% for the PLD arm and 32% for the carboplatin only arm (Fisher's exact p=0.02). The estimated median PFS was 12 and 8 months for PLD versus carboplatin alone. The estimated median OS on the PLD arm was 26 months and 18 months on the carboplatin only arm (p=0.02). Twenty-six percent of the patients on the PLD arm reported grade 4 toxicities, all hematological in nature.
This study was closed early because of slow patient accrual. The response rate, median PFS and OS results are intriguing. These data suggest that there may be an advantage to the PLD plus carboplatin combination treatment in patients with PS, recurrent OC. The regimen should be further tested.
由于对于铂类敏感的复发性卵巢癌采用铂类联合化疗的作用仍存在争议,我们比较了该人群的总生存期(OS)、无进展生存期(PFS)、确认的完全缓解率以及至治疗失败时间。
复发性III期或IV期卵巢癌患者,一线铂类化疗后无进展且铂类药物洗脱期为6 - 24个月,并且接受了最多12个疗程不含铂的巩固治疗,符合入组条件。患者被随机分为静脉注射聚乙二醇化脂质体阿霉素(PLD)(30mg/m²)加静脉注射卡铂(AUC = 5mg/mL·min),每4周一次(PLD组),或仅静脉注射卡铂(AUC = 5mg/mL·min),每4周一次。
PLD组入组31例患者,单纯卡铂组入组30例患者,共61例患者,原计划入组900例。PLD组的缓解率为67%,单纯卡铂组为32%(Fisher精确检验p = 0.02)。PLD组和单纯卡铂组的估计中位PFS分别为12个月和8个月。PLD组的估计中位OS为26个月,单纯卡铂组为18个月(p = 0.02)。PLD组26%的患者报告有4级毒性反应,均为血液学毒性。
由于患者入组缓慢,本研究提前结束。缓解率、中位PFS和OS结果令人感兴趣。这些数据表明,对于铂类敏感的复发性卵巢癌患者,PLD加卡铂联合治疗可能具有优势。该方案应进一步进行试验。