首页> 外文期刊>Radiation oncology >Definitive radiotherapy and Single-Agent radiosensitizing Ifosfamide in Patients with localized, irresectable Soft Tissue Sarcoma: A retrospective analysis
【24h】

Definitive radiotherapy and Single-Agent radiosensitizing Ifosfamide in Patients with localized, irresectable Soft Tissue Sarcoma: A retrospective analysis

机译:局部,不可切除的软组织肉瘤患者的明确放疗和单药放射增敏异环磷酰胺回顾性分析

获取原文
           

摘要

Background and Purpose Standard therapy for soft-tissue sarcomas remains complete resection. For primary radiotherapy local control rates of 30-45% have been reported. We analyzed retrospectively 11 cases of radiochemotherapy with single-agent ifosfamide in patients with macroscopic soft-tissue sarcomas. Patients and Methods The patients were treated in irresectable high risk situations. Radiation therapy was performed with median 60 Gy. During the first and fifth week the concomitant chemotherapy with ifosfamide was added. Two patients received trimodal therapy with additional regional hyperthermia. Results The therapy was completed in 73% of the patients. Average local control time was 91 months, median disease-free-survival/overall-survival was 8/26 months. Five-year rates for local control/disease free survival/overall survival were 70%/34%/34%. The limited prognosis is mainly caused by systemic treatment failure. Conclusions The data strongly suggest a better outcome of radiochemotherapy with ifosfamide compared to radiotherapy alone and radiotherapy in combination with other radiosensitizers.
机译:背景与目的软组织肉瘤的标准疗法仍为完全切除术。对于原发性放疗,据报道局部控制率为30-45%。我们回顾性分析了11例单药异环磷酰胺放疗的宏观软组织肉瘤患者。患者和方法患者在不可切除的高危情况下接受治疗。放射治疗的中位数为60 Gy。在第一周和第五周,伴随有异环磷酰胺的化疗。两名患者接受了三联疗法并伴有局部局部热疗。结果73%的患者完成了治疗。平均局部控制时间为91个月,中位无病生存/总体生存为8/26个月。五年的局部控制/无病生存/总生存率为70%/ 34%/ 34%。预后有限主要是由于全身治疗失败。结论数据强烈提示异环磷酰胺放疗比单独放疗和放疗联合其他放射增敏剂有更好的疗效。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号