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首页> 外文期刊>Journal of Clinical Oncology >Maintenance chemotherapy with daily oral etoposide following salvage therapy in patients with germ cell tumors.
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Maintenance chemotherapy with daily oral etoposide following salvage therapy in patients with germ cell tumors.

机译:生殖细胞肿瘤患者抢救治疗后,每天口服依托泊苷维持化疗。

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PURPOSE: To evaluate the role of maintenance daily oral etoposide (VP-16) chemotherapy for germ cell patients who had a response to salvage therapy. PATIENTS AND METHODS: Thirty-seven patients were entered onto this trial, and 34 were fully assessable. This was as heavily pretreated patient population, with a median of two prior salvage regimens. The salvage treatment that immediately preceded oral VP-16 consisted of autologous bone marrow transplantation in 14 patients (41%), surgery in 10 (29%), and standard-dose salvage chemotherapy in 10 (29%). Daily oral VP-16 was administered at a dose of 50 mg/m2 for 21 consecutive days every 4 weeks for three cycles. RESULTS: The major toxicity with daily oral VP-16 was leukopenia. Three patients had grade III and two grade IV leukopenia. Two of these patients had granulocytopenic fever. Other grade III toxicities included thrombocytopenia (n = 1) and mucositis (n = 2). Twenty-three patients started daily oral VP-16 while in complete remission (CR) following salvage therapy. Seventeen (74%) remain continuously disease-free, with a median follow-up time of 36 months (range, 26 to 49) from initiation of daily oral VP-16. Eleven patients started daily oral VP-16 while in partial remission (PR) following salvage therapy. Three of these 11 patients converted to CR, but all three subsequently relapsed. CONCLUSION: Maintenance oral VP-16 was well tolerated in this heavily treated patient population. Results in this poor-risk population were encouraging.
机译:目的:评估维持性口服依托泊苷(VP-16)化疗对于对挽救疗法有反应的生殖细胞患者的作用。患者与方法:37例患者参加了该试验,其中34例可完全评估。这是经过大量治疗的患者人群,中位值为两种先前的挽救方案。口服VP-16之前的抢救治疗包括14例患者(41%)的自体骨髓移植,10例(29%)的手术和10例(29%)的标准剂量抢救化疗。每4周连续21天以50 mg / m2的剂量每日口服VP-16,共三个周期。结果:每日口服VP-16的主要毒性反应是白细胞减少症。三名患者患有三级白细胞减少症,三名患者具有四级白细胞减少症。这些患者中有两名患有粒细胞减少症。其他III级毒性包括血小板减少症(n = 1)和粘膜炎(n = 2)。 23例患者在挽救治疗后完全缓解(CR)时开始每日口服VP-16。从每日口服VP-16开始,十七名(74%)持续无病,平均随访时间为36个月(范围26至49)。 11名患者在挽救治疗后部分缓解(PR)期间开始每日口服VP-16。这11例患者中有3例转化为CR,但随后全部3例复发。结论:在这个经过严格治疗的患者人群中,维持口服VP-16耐受性良好。这一低风险人群的研究结果令人鼓舞。

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