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大剂量美法仑、依托泊苷、全身照射及自体干细胞重建作为高危尤因肉瘤的巩固治疗并不能改善预后。

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.

作者信息

Meyers P A, Krailo M D, Ladanyi M, Chan K W, Sailer S L, Dickman P S, Baker D L, Davis J H, Gerbing R B, Grovas A, Herzog C E, Lindsley K L, Liu-Mares W, Nachman J B, Sieger L, Wadman J, Gorlick R G

机构信息

Memorial Sloan-Kettering Cancer Center, New York, NY, USA.

出版信息

J Clin Oncol. 2001 Jun 1;19(11):2812-20. doi: 10.1200/JCO.2001.19.11.2812.

Abstract

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.

摘要

目的

确定采用大剂量美法仑、依托泊苷及全身照射(TBI)联合自体干细胞支持的巩固治疗是否能改善新诊断的转移性尤因肉瘤(ES)患者的预后。

患者与方法

32例新诊断为骨和/或骨髓转移的ES合格患者纳入本研究。治疗最初包括五个周期的诱导化疗(环磷酰胺、多柔比星和长春新碱与异环磷酰胺和依托泊苷交替使用)及局部控制。化疗第二周期后进行外周血干细胞采集,若骨髓持续受累则延迟采集。若患者对初始治疗反应良好,则继续接受美法仑、依托泊苷、TBI及干细胞支持的巩固治疗。

结果

32例合格患者中,23例进行了大剂量治疗巩固。未进行巩固治疗的9例患者中,4例继发于疾病进展,2例继发于毒性反应。3例患者在治疗的大剂量阶段死于毒性反应。接受大剂量巩固治疗的大多数患者出现复发并死于疾病进展。所有合格患者的2年无事件生存率(EFS)为20%。接受巩固治疗的23例患者亚组在干细胞重建后的2年EFS为24%。采用分子技术分析外周血干细胞采集的微小残留病,在所有有可用数据的3例患者中,至少部分样本存在肿瘤细胞污染。

结论

对于该组新诊断的转移性ES患者,采用大剂量美法仑、依托泊苷、TBI及自体干细胞支持的巩固治疗未能提高EFS概率。

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