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Ifosfamide/etoposide alternating with high-dose methotrexate: evaluation of a chemotherapy regimen for poor-risk osteosarcoma

机译:异环磷酰胺/依托泊苷与大剂量甲氨蝶呤交替使用:评估低危骨肉瘤化疗方案

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摘要

Fifteen patients with relapsed osteosarcoma were treated with an intensive combination chemotherapy schedule. Ifosfamide 2.5 g m−2 daily and etoposide 150 mg m−2 daily coincidentally for 3 days and high-dose methotrexate 8 g m−2 (with folinic acid rescue) on days 10–14 in a planned 21-day cycle. Feasibility, toxicity and response to this alternative combination for the treatment of relapsed osteosarcoma was assessed. There were 98 evaluable cycles for toxicity and tolerability. The majority of cycles were well tolerated. Haematological toxicity of grade 3/4 (common toxicity criteria) was seen in all courses. Renal tubular loss of electrolytes, particularly magnesium, occurred in 71% of cycles. Thirteen per cent of cycles were repeated within 21 days and 61% within 28 days. In the thirteen patients evaluable for response, a partial response rate of 31% was seen after two cycles. However, patients with stable disease continued on therapy, and an overall consequent response rate of 62% was observed. Four patients were alive with no evidence of disease at 8–74 months. Three are alive with disease (at 8–19 months). There were six deaths, all disease related. This regimen exhibits an encouraging response rate in a group of children with poor prognosis disease, with a tolerable toxicity profile. © 1999 Cancer Research Campaign
机译:15例骨肉瘤复发患者接受了强化联合化疗方案的治疗。异环磷酰胺2.5 gm −2 每天和依托泊苷150 mg m −2 每天同时发生3天,高剂量甲氨蝶呤8 gm −2 (与在计划的21天周期中的第10-14天进行亚叶酸营救。评估了该替代组合治疗复发性骨肉瘤的可行性,毒性和反应。有98个可评估的毒性和耐受性周期。大多数循环耐受性良好。在所有课程中均观察到3/4级的血液学毒性(一般毒性标准)。肾小管的电解质,尤其是镁的肾小管丢失发生在71%的循环中。在21天内重复进行了13%的周期,在28天内重复进行了61%。在可评估反应的13例患者中,两个周期后发现部分反应率为31%。但是,病情稳定的患者继续接受治疗,因此总体反应率为62%。 4例患者在8-74个月时还没有任何疾病的迹象。三个还活着(8-19个月)。有六人死亡,所有疾病均与之相关。该方案在一组预后不良的儿童中表现出令人鼓舞的反应率,并且具有可耐受的毒性。 ©1999癌症研究运动

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