University Hospital Southampton NHS Foundation Trust, Southampton General Hospital, Southampton, United Kingdom.
University Hospital Southampton NHS Foundation Trust, Southampton General Hospital, Southampton, United Kingdom.
Clin Genitourin Cancer. 2018 Dec;16(6):458-465.e2. doi: 10.1016/j.clgc.2018.07.006. Epub 2018 Jul 17.
Metastatic germ cell tumors remain potentially curable when treated with salvage chemotherapy at first relapse. In the present phase I/II study, we sought to improve on the response rate and duration of the TIP (paclitaxel, ifosfamide, cisplatin) regimen by adding gemcitabine (Gem-TIP).
Twenty patients were recruited after failure of first-line cisplatin-containing chemotherapy. The primary objectives were to determine the maximum tolerated dose of gemcitabine when combined with TIP and to establish the dose intensity of the TIP drugs in this combination. The secondary objectives were the response rates, failure-free survival, and overall survival.
The maximum tolerated dose of gemcitabine was 1200 mg/m. The mean relative dose intensity was 95% (95% confidence interval [CI], 90.2%-99.2%) for gemcitabine, 96% (95% CI, 92.9%-98.7%) for paclitaxel, 92% (95% CI, 84.5%-98.8%) for ifosfamide, and 94% (95% CI, 89.3%-99.0%) for cisplatin. The overall complete response rate was 50%; another 30% of the patients achieved a partial response. The 1-year failure-free survival and overall survival rates were 68% (95% CI, 43%-84%) and 89.5% (95% CI, 64%-97%), respectively.
Gemcitabine can be added to TIP chemotherapy at the full dose, with manageable toxicity and no detrimental effect on the dose intensity of the TIP drugs. The response rate and duration were improved compared with those reported from the Medical Research Council TIP trial; further evaluation is warranted.
转移性生殖细胞肿瘤在首次复发时接受挽救性化疗仍有治愈可能。在本 I/II 期研究中,我们试图通过添加吉西他滨(Gem-TIP)来提高 TIP(紫杉醇、异环磷酰胺、顺铂)方案的反应率和持续时间。
在一线含顺铂化疗失败后,招募了 20 名患者。主要目的是确定与 TIP 联合使用时吉西他滨的最大耐受剂量,并确定该联合用药中 TIP 药物的剂量强度。次要目标是反应率、无失败生存期和总生存期。
吉西他滨的最大耐受剂量为 1200mg/m。吉西他滨的平均相对剂量强度为 95%(95%置信区间[CI],90.2%-99.2%),紫杉醇为 96%(95% CI,92.9%-98.7%),异环磷酰胺为 92%(95% CI,84.5%-98.8%),顺铂为 94%(95% CI,89.3%-99.0%)。总完全缓解率为 50%;另外 30%的患者获得部分缓解。1 年无失败生存率和总生存率分别为 68%(95% CI,43%-84%)和 89.5%(95% CI,64%-97%)。
吉西他滨可在全剂量下添加到 TIP 化疗中,毒性可管理,且对 TIP 药物的剂量强度无不良影响。与医学研究委员会 TIP 试验报告的结果相比,反应率和持续时间有所提高;需要进一步评估。