首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >Primary metastatic Ewing's family tumors: Results of the Italian Sarcoma Group and Scandinavian Sarcoma Group ISG/SSG IV Study including myeloablative chemotherapy and total-lung irradiation
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Primary metastatic Ewing's family tumors: Results of the Italian Sarcoma Group and Scandinavian Sarcoma Group ISG/SSG IV Study including myeloablative chemotherapy and total-lung irradiation

机译:转移性尤文氏家族肿瘤:意大利肉瘤组和斯堪的纳维亚肉瘤组ISG / SSG IV研究的结果,包括清髓化学疗法和全肺照射

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Background: The Italian Sarcoma Group and the Scandinavian Sarcoma Group designed a joint study to improve the prognosis for patients with Ewing's family tumors and synchronous metastatic disease limited to the lungs, or the pleura, or a single bone. Patients and methods: The study was opened in 1999 and closed to the enrollment in 2008. The program consisted of intensive five-drug combination chemotherapy, surgery and/or radiotherapy as local treatment, and consolidation treatment with high-dose busulfan/melphalan plus autologous stem cell rescue and total-lung irradiation. Results: During the study period, 102 consecutive patients were enrolled. The median follow-up was 62 months (range 24-124). The 5-year event-free survival probability was 0.43 [standard deviation (SD) = 0.05] and the 5-year overall survival probability was 0.52 (SD = 0.052). Unfavorable prognostic factors emerging on multivariate analysis were a poor histological/radiological response at the site of the primary tumor [relative risk (RR) = 3.4], and incomplete radiological remission of lung metastases after primary chemotherapy (RR = 2.6). One toxic death and one secondary leukemia were recorded. Conclusions: This intensive approach is feasible and long-term survival is achievable in ~50% of patients. New treatment approaches are warranted for patients responding poorly to primary chemotherapy.
机译:背景:意大利肉瘤小组和斯堪的纳维亚肉瘤小组设计了一项联合研究,以改善患有尤因氏家族肿瘤和局限于肺,胸膜或单个骨骼的同时转移性疾病的患者的预后。患者和方法:该研究于1999年开始,于2008年停止招募。该计划包括密集的五药联合化疗,手术和/或放疗作为局部治疗,以及大剂量白消安/美法仑加自体加药的合并治疗干细胞抢救和全肺照射。结果:在研究期间,连续入选了102名患者。中位随访时间为62个月(范围24-124)。 5年无事件生存概率为0.43 [标准偏差(SD)= 0.05],而5年总生存概率为0.52(SD = 0.052)。在多因素分析中出现的不良预后因素是原发肿瘤部位的组织学/放射学反应较差[相对风险(RR)= 3.4],以及原发化疗后肺转移的放射学不完全缓解(RR = 2.6)。记录了1例中毒死亡和1例继发性白血病。结论:这种强化治疗方法是可行的,约50%的患者可实现长期生存。对于原发化疗反应较差的患者,应采取新的治疗方法。

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