Laval University Cancer Research Center, Hôtel-Dieu-de-Québec, Centre Hospitalier Universitaire (CHU) de Québec, 11 Côte du Palais, Québec, Québec G1R 2J6, Canada; Department of Pathology/Applied Molecular Oncology, Toronto General Hospital, University Health Network, 200 Elizabeth Street, Toronto, Ontario M5G 2C4, Canada.
Gynecol Oncol. 2013 Nov;131(2):357-61. doi: 10.1016/j.ygyno.2013.08.019. Epub 2013 Aug 27.
A two-stage, single-arm, phase II study was conducted to assess the effectiveness and safety of an epigallocatechin gallate (EGCG)-enriched tea drink, the double-brewed green tea (DBGT), as a maintenance treatment in women with advanced stage serous or endometrioid ovarian cancer (clinicaltrials.gov, NCT00721890).
Eligible women had FIGO stage III-IV serous or endometrioid ovarian cancer. They had to undergo complete response after debulking surgery followed by 6 to 8 cycles of platinum/taxane chemotherapy at the Centre Hospitalier Universitaire de Québec. They all had to drink the DBGT, 500 mL daily until recurrence or during a follow-up of 18 months. The primary endpoint was the absence of recurrence at 18 months. Statistical analyses were done according to the principle of intention to treat. Using a two-stage design, the first stage consisted of 16 enrolled patients. At the end of the follow-up, if 7 or fewer patients were free of recurrence, the trial stopped. Otherwise, accrual would continue to a total of 46 patients.
During the first stage of the study, only 5 of the 16 women remained free of recurrence 18 months after complete response. Accordingly, the clinical trial was terminated. Women's adherence to DBGT was high (median daily intake during intervention, 98.1%, interquartile range: 89.7-100%), but 6 women discontinued the intervention before the end of their follow-up. No severe toxicity was reported.
DBGT supplementation does not appear to be a promising maintenance intervention in women with advanced stage ovarian cancer after standard treatment.
一项两阶段、单臂、二期研究旨在评估表没食子儿茶素没食子酸酯(EGCG)富集茶饮料——双蒸绿茶(DBGT)作为晚期浆液性或子宫内膜样卵巢癌女性维持治疗的有效性和安全性(clinicaltrials.gov,NCT00721890)。
符合条件的女性患有国际妇产科联盟(FIGO)分期 III-IV 期浆液性或子宫内膜样卵巢癌。她们必须在接受减瘤手术后完全缓解,然后在魁北克大学中心医院接受 6 至 8 个周期的铂类/紫杉烷化疗。所有患者均需饮用 DBGT,每天 500 毫升,直至复发或随访 18 个月。主要终点是 18 个月时无复发。统计分析根据意向治疗原则进行。采用两阶段设计,第一阶段纳入 16 名患者。随访结束时,如果 7 名或更少的患者无复发,则试验停止。否则,将继续招募总计 46 名患者。
在研究的第一阶段,16 名女性中只有 5 名在完全缓解后 18 个月无复发。因此,临床试验终止。女性对 DBGT 的依从性很高(干预期间的中位每日摄入量为 98.1%,四分位距:89.7-100%),但有 6 名女性在随访结束前停止了干预。未报告严重毒性。
DBGT 补充似乎不是晚期卵巢癌女性在标准治疗后有前途的维持干预措施。