尼莫司汀治疗转移性软组织肉瘤的II期研究

D.J.Th. Wagener , R. Somers , A. Santoro , J. Verweij , P.J. Woll , G. Blackledge , H.J. Schütte , M.A. Lentz , M. van Glabbeke , European Organization for Research and Treatment of Cancer Soft Tissue and Bone Sarcoma Group
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引用次数: 4

摘要

EORTC软组织和骨肉瘤组在33例符合条件的转移性软组织肉瘤患者中进行了一项II期试验,每6周使用尼莫司汀100mg /m2。在31例可评估的患者中,有3例(10%)部分缓解持续4.5、6和7.5个月,5例病情稳定。进展性疾病12例,早期进展性疾病11例。毒性主要表现为白细胞减少、血小板减少和恶心呕吐。结论:尼莫司汀在软组织肉瘤中仅具有微弱活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phase II study of nimustine in metastatic soft tissue sarcoma

The EORTC Soft Tissue and Bone Sarcoma Group has conducted a phase II trial in 33 eligible patients with metastatic soft tissue sarcoma with nimustine 100 mg/m2 every 6 weeks. In 31 evaluable patients there were 3 (10%) partial responses lasting 4.5,6 and 7.5 months, and 5 cases of stable disease. 12 patients had progressive disease and 11 patients early progressive disease. Toxicity consisted mainly of leukopenia and thrombocytopenia and nausea and vomiting. It is concluded that nimustine has only minor activity in soft tissue sarcoma.

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