首页> 美国卫生研究院文献>Annals of Oncology >A randomized phase III study comparing standard dose BEP with sequential high-dose cisplatin etoposide and ifosfamide (VIP) plus stem-cell support in males with poor-prognosis germ-cell cancer. An intergroup study of EORTC GTCSG and Grupo Germinal (EORTC 30974)
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A randomized phase III study comparing standard dose BEP with sequential high-dose cisplatin etoposide and ifosfamide (VIP) plus stem-cell support in males with poor-prognosis germ-cell cancer. An intergroup study of EORTC GTCSG and Grupo Germinal (EORTC 30974)

机译:一项III期随机研究比较了标准剂量BEP与顺序高剂量顺铂依托泊苷和异环磷酰胺(VIP)加上干细胞支持的男性预后差的生殖细胞癌。 EORTCGTCSG和Grupo Germinal的小组间研究(EORTC 30974)

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摘要

>Background: To compare the efficacy of one cycle of standard dose cisplatin, etoposide, and ifosfamide (VIP) plus three cycles of high-dose VIP followed by stem-cell infusion [high-dose chemotherapy (HD-CT arm)] to four cycles of standard cisplatin, etoposide, and bleomycin (BEP) in patients with poor-prognosis germ-cell cancer (GCC).>Patient and methods: Patients with poor-prognosis GCC were assigned to receive either BEP or VIP followed by HD-CT. To show a 15% improvement in a 1-year failure-free survival (FFS), the study aimed to recruit 222 patients but closed with 137, due to slow accrual.>Results: One hundred thirty-one patients were included in this analysis. The complete response rates in the HD-CT and in the BEP arm did not differ: (intention to treat) 44.6% versus 33.3% (P = 0.18). There was no difference in FFS between the two treatment arms (P = 0.057, 66 events). At 2 years, the FFS rate was 44.8% [95% confidence interval (CI) 32.5–56.4] and 58.2%, respectively (95% CI 48.0–71.9); but this 16.3% (standard deviation 7.5%) difference was not statistically significant (P = 0.060). Overall survival did not differ between the two groups (log-rank P > 0.1, 47 deaths).>Conclusion: This study could not demonstrate that high-dose chemotherapy given as part of first-line therapy improves outcome in patients with poor-prognosis GCC.
机译:>背景:比较一轮标准剂量的顺铂,依托泊苷和异环磷酰胺(VIP)加上三轮大剂量VIP进行干细胞输注[大剂量化疗(HD- CT臂]]对预后差的生殖细胞癌(GCC)患者的标准顺铂,依托泊苷和博来霉素(BEP)进行四个周期治疗。>患者和方法:被分配接收BEP或VIP,然后接收HD-CT。为了显示1年无失败生存率(FFS)改善15%,该研究旨在招募222名患者,但由于应计缓慢而关闭了137名患者。>结果:患者包括在此分析中。 HD-CT和BEP组的完全缓解率没有差异:(治疗意向)44.6%和33.3%(P = 0.18)。两个治疗组之间的FFS没有差异(P = 0.057,66个事件)。在2年时,FFS率分别为44.8%[95%置信区间(CI)32.5-56.4]和58.2%(95%CI 48.0-71.9);但是这一16.3%(标准偏差7.5%)的差异在统计上并不显着(P = 0.060)。两组的总生存期无差异(log-rank P> 0.1,死亡47人)。>结论:该研究不能证明作为一线治疗一部分的大剂量化疗可以改善预后预后不良的GCC患者。

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