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Adjuvant treatment of high-risk adult soft tissue sarcomas: a survey by the Italian Sarcoma Group.

机译:成人高危软组织肉瘤的辅助治疗:意大利肉瘤组织的一项调查。

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AIMS AND BACKGROUND: After the first adjuvant study on adult soft tissue sarcomas was concluded, the participating institutions continued to select and treat patients according to that protocol. The aim of this study was to test the protocol reproducibility when applied as a standard practice. METHODS: A call for retrospective data was launched in June 1999 (self-referral of consecutive unregistered patients); thereafter, a prospective follow-up was performed. The treatment regimen consisted of epirubicin (60 mg/m2 days 1 and 2), ifosfamide (3 g/m2/die for 3 days) and equimolar doses of 6-mercapto-ethansulfonate (MESNA), with 300 microg G-CSF administered subcutaneously from day +8 until recovery, every 3 weeks for a total of 5 cycles. RESULTS: From November 1996 to June 1999, 55 high-risk, adult patients were treated. The average median dose intensity was 89% of the planned program. Grade 3-4 toxicities were leukopenia (49%), thrombocytopenia (14%), transfusion requiring anemia in 7 patients (16%), and alopecia in all patients (100%). After a median follow-up of 70 months, 23 patients (41.8%) relapsed and 19 died. Median disease-free, local disease-free and overall survival rates have not yet been reached. The disease-free survival rates at 2 and 4 years were 73% and 57%, respectively; the corresponding overall survival rates were 91% and 70%, respectively. CONCLUSIONS: The feasibility and reproducibility of the original protocol were confirmed, since disease-specific overall survival and disease-free survival rates at the same period of observation and with the same prolonged follow-up did not differ.
机译:目的和背景:在完成对成人软组织肉瘤的第一项辅助研究后,参与机构继续根据该方案选择和治疗患者。这项研究的目的是测试作为标准做法使用时的协议可重复性。方法:1999年6月开始要求回顾性数据(连续转诊未登记患者的自我转诊);此后,进行了前瞻性随访。治疗方案包括表柔比星(60 mg / m2第1天和第2天),异环磷酰胺(3 g / m2 /死亡,共3天)和等摩尔剂量的6-巯基-乙磺酸盐(MESNA),皮下注射300微克G-CSF从第8天起直到恢复,每3周进行一次,共5个周期。结果:从1996年11月至1999年6月,共治疗了55名高危成人患者。平均中位剂量强度为计划程序的89%。 3-4级毒性反应是白细胞减少症(49%),血小板减少症(14%),需要贫血的输血7例(16%)和所有患者的脱发(100%)。中位随访70个月后,有23例患者(41.8%)复发,其中19例死亡。尚未达到中位无病,局部无病和总生存率。 2年和4年无病生存率分别为73%和57%。相应的总生存率分别为91%和70%。结论:证实了原始方案的可行性和可重复性,因为在相同的观察时间和相同的长期随访中,疾病特异性总体生存率和无疾病生存率没​​有差异。

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