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首页> 外文期刊>Journal of Clinical Oncology >Intensive therapy with growth factor support for patients with Ewing tumor metastatic at diagnosis: Pediatric Oncology Group/Children's Cancer Group Phase II Study 9457--a report from the Children's Oncology Group.
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Intensive therapy with growth factor support for patients with Ewing tumor metastatic at diagnosis: Pediatric Oncology Group/Children's Cancer Group Phase II Study 9457--a report from the Children's Oncology Group.

机译:生长因子支持的强化疗法对确诊为尤文肿瘤转移的患者的诊断:小儿肿瘤学组/儿童癌症组II期研究9457 –儿童肿瘤学组的报告。

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PURPOSE: Prognosis is poor for Ewing sarcoma patients with metastasis at diagnosis. We intensified a five-drug therapy (ifosfamide, etoposide alternated with vincristine, doxorubicin, and cyclophosphamide) using filgrastim but not stem-cell support. We studied topotecan alone and combined with cyclophosphamide in therapeutic windows before the five-drug therapy. A randomly assigned proportion of patients received amifostine as a cytoprotective agent. PATIENTS AND METHODS: Eligible patients were < or 30 years old and had histologically proven Ewing sarcoma or primitive neuroectodermal tumor (PNET) and metastasis at diagnosis. Chemotherapeutic cycles began every 21 days, after recovery from toxicities. RESULTS: One hundred ten of the 117 patients enrolled were eligible. Thirty-six patients received initial topotecan. Three had partial responses (PRs), and 17 had progressive disease (PD). Thirty-seven patients were administered topotecan and cyclophosphamide; 21 of these patients achieved PR, and one patient had PD. In a randomly assigned group of 69 patients, amifostine did not provide myeloprotection, which was measured by absolute neutrophil count, platelet count, or cycle intervals. The best responses to the overall therapy included 45 complete responses, 41 PRs, stable disease in 14 patients, and PD in five patients. For all patients, the 2-year event-free survival (EFS) rate was 24% (+/- 4%), and the overall survival rate was 46% (+/- 5%). For the 39 patients with isolated pulmonary metastases, the 2-year EFS rate was 31% (+/- 7%) compared with 20% (+/- 5%) for patients with more widespread disease. CONCLUSION: Topotecan had limited activity in patients with Ewing sarcoma or PNET metastatic at diagnosis. The topotecan-cyclophosphamide combination was active. Amifostine was not myeloprotective. Overall results showed no improvement compared with previous studies.
机译:目的:尤文肉瘤转移时确诊的预后较差。我们使用非格司亭而不是干细胞支持加强了五种药物疗法(异环磷酰胺,依托泊苷与长春新碱,阿霉素和环磷酰胺交替使用)。在五种药物治疗之前,我们单独研究了拓扑替康并与环磷酰胺联合在治疗窗中使用。随机分配的一部分患者接受氨磷汀作为细胞保护剂。患者和方法:符合条件的患者<30岁或30岁,经组织学证实为尤因肉瘤或原始神经外胚层肿瘤(PNET),并在诊断时发生转移。从毒性中恢复后,化学疗法周期每21天开始。结果:117名患者中有110名符合条件。三十六名患者接受了初始拓扑替康。其中3人具有部分反应(PR),而17人患有进行性疾病(PD)。三十七例患者接受了拓扑替康和环磷酰胺治疗;这些患者中有21位实现了PR,一名患者患有PD。在一个随机分配的69例患者中,氨磷汀没有提供骨髓保护,这是通过绝对中性粒细胞计数,血小板计数或周期间隔来衡量的。总体治疗的最佳反应包括45例完全缓解,41例PR,14例患者疾病稳定,5例PD。对于所有患者,2年无事件生存率(EFS)为24%(+/- 4%),总生存率为46%(+/- 5%)。对于39例孤立肺转移患者,其2年EFS率为31%(+/- 7%),而疾病更广泛的患者为20%(+/- 5%)。结论:托泊替康在诊断为尤因肉瘤或PNET转移的患者中活性有限。拓扑替康-环磷酰胺组合具有活性。氨磷汀没有骨髓保护作用。总体结果显示与以前的研究相比没有改善。

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