首页> 外文期刊>Journal of Clinical Oncology >High-dose melphalan, etoposide, total-body irradiation, and autologous stem-cell reconstitution as consolidation therapy for high-risk Ewing's sarcoma does not improve prognosis.
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High-dose melphalan, etoposide, total-body irradiation, and autologous stem-cell reconstitution as consolidation therapy for high-risk Ewing's sarcoma does not improve prognosis.

机译:大剂量美法仑,依托泊苷,全身照射和自体干细胞重建作为高危尤因肉瘤的巩固疗法不能改善预后。

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PURPOSE: To determine whether consolidation therapy with high-dose melphalan, etoposide, and total-body irradiation (TBI) with autologous stem-cell support would improve the prognosis for patients with newly diagnosed metastatic Ewing's sarcoma (ES). PATIENTS AND METHODS: Thirty-two eligible patients with newly diagnosed ES metastatic to bone and/or bone marrow were enrolled onto this study. Treatment was initially comprised of five cycles of induction chemotherapy (cyclophosphamide, doxorubicin, and vincristine alternating with ifosfamide and etoposide) and local control. Peripheral-blood stem-cell collection was performed after the second cycle of chemotherapy, with delay if the bone marrow was persistently involved. If patients had a good response to initial therapy, they proceeded to consolidation therapy with melphalan, etoposide, TBI, and stem-cell support. RESULTS: Of the 32 eligible patients, 23 proceeded to high-dose therapy consolidation. Of the nine patients who did not proceed to consolidation, four were secondary to progressive disease and two were secondary to toxicity. Three patients died from toxicity during the high-dose phase of the therapy. The majority of the patients who underwent high-dose consolidation therapy experienced relapse and died with progressive disease. Two-year event-free survival (EFS) for all eligible patients is 20%. The 2-year post-stem-cell reconstitution EFS for the subset of 23 patients who received consolidation therapy is 24%. Analysis of peripheral-blood stem-cell collections by molecular techniques for minimal residual disease showed contamination of at least some samples by tumor cells in all three patients with available data. CONCLUSION: Consolidation with high-dose melphalan, etoposide, TBI, and autologous stem-cell support failed to improve the probability of EFS in this cohort of patients with newly diagnosed metastatic ES.
机译:目的:确定采用大剂量美法仑,依托泊苷和全身放射(TBI)结合自体干细胞支持的巩固治疗是否可以改善新诊断为转移性尤因肉瘤(ES)的患者的预后。患者与方法:32例符合条件的患者被新诊断为ES转移至骨骼和/或骨髓。治疗最初包括五个周期的诱导化疗(环磷酰胺,阿霉素和长春新碱与异环磷酰胺和依托泊苷交替使用)和局部对照。在化疗的第二个周期后进行外周血干细胞收集,如果持续牵涉骨髓,则会延迟收集。如果患者对初始治疗有良好的反应,则可以进行美法仑,依托泊苷,TBI和干细胞支持的巩固治疗。结果:在32例合格患者中,有23例进行了大剂量巩固治疗。在没有进行巩固的9例患者中,有4例继发于进行性疾病,2例继发于毒性。在高剂量治疗期间,三名患者死于毒性。接受高剂量巩固治疗的大多数患者出现复发并死于进行性疾病。所有合格患者的两年无事件生存期(EFS)为20%。 23例接受巩固治疗的患者亚组中,干细胞重建后2年的EFS为24%。通过分子技术对外周血干细胞集合进行分析以最大程度地减少残留疾病,显示在所有三名患者中,至少有一些样品被肿瘤细胞污染,并具有可用数据。结论:大剂量美法仑,依托泊苷,TBI和自体干细胞支持的合并未能提高该组新诊断为转移性ES的患者发生EFS的可能性。

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