首页> 美国卫生研究院文献>British Journal of Cancer >A phase II trial of TIP (paclitaxel ifosfamide and cisplatin) given as second-line (post-BEP) salvage chemotherapy for patients with metastatic germ cell cancer: a medical research council trial
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A phase II trial of TIP (paclitaxel ifosfamide and cisplatin) given as second-line (post-BEP) salvage chemotherapy for patients with metastatic germ cell cancer: a medical research council trial

机译:TIP(紫杉醇异环磷酰胺和顺铂)II期试验作为转移性生殖细胞癌患者的二线(BEP后)挽救性化疗:一项医学研究委员会试验

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摘要

This phase II trial describes the use of TIP chemotherapy (paclitaxel, ifosfamide and cisplatin) as salvage for patients with metastatic germ cell cancer (GCC) who have failed initial BEP (bleomycin, etoposide and cisplatin) chemotherapy. Patients with first relapse following BEP for metastatic GCC, confirmed by biopsy or sequentially rising markers, received four courses of TIP (paclitaxel 175 mg m−2 day 1, followed on days 1–5 by ifosfamide 1 g m−2 intravenously (i.v.) and cisplatin 20 mg2 i.v.) at 3-weekly intervals. The primary outcome measure was response to TIP. In all, 51 patients were registered, of whom 43 were eligible for response assessment. Eight achieved complete remission (CR) and 18 a partial remission with negative markers (PR−ve); favourable response rate (FRR=CR+PR−ve) 60%, 95% CI (44–75%); survival at 1 year was 70% (56–84%) and failure-free survival 36% (22–50%). In the group of 26 patients meeting the ‘good-risk' criteria described by the Memorial Hospital, the FRR was 73% (52–88%) compared with 41% (18–67%) for the 17 ‘poor-risk' patients. These results are inferior to those previously reported for TIP in a single-centre study when it was given more intensively, at higher dose and with growth factor support. Nonetheless, TIP as described here can cure a substantial proportion of patients.
机译:这项II期临床试验描述了TIP化疗(紫杉醇,异环磷酰胺和顺铂)用于治疗初始BEP化疗(博来霉素,依托泊苷和顺铂)失败的转移性生殖细胞癌(GCC)患者。 BEP后因转移性GCC首次复发的患者,经活检或依次上升的标志物证实,接受了四个疗程的TIP治疗(紫杉醇175 mg m -2 第1天,然后在1-5天服用异环磷酰胺1 g静脉(m)静脉注射m −2 (iv),每3周间隔注射顺铂20 mg 2 iv)。主要结局指标是对TIP的反应。总共登记了51名患者,其中43名有资格进行反应评估。 8例达到完全缓解(CR),18例达到部分缓解,并带有阴性标记(PR -ve );良好的响应率(FRR = CR + PR -ve )60%,95%CI(44–75%); 1年生存率为70%(56–84%),无故障生存率为36%(22–50%)。在满足纪念医院描述的“高风险”标准的26位患者中,FRR为73%(52–88%),而17位“低风险”患者为41%(18-67%) 。这些结果不如以前在单中心研究中报告的那些结果,后者是在更密集,更高剂量和生长因子支持下给予的。但是,如本文所述,TIP可以治愈大部分患者。

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