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不可切除或转移性软组织肉瘤的系统治疗:过去、现在和未来。

Systematic therapy for unresectable or metastatic soft-tissue sarcomas: past, present, and future.

机构信息

Melanoma/Sarcoma Research Program, Arizona Cancer Center, University of Arizona, Tucson, AZ, USA.

出版信息

Curr Oncol Rep. 2011 Aug;13(4):331-49. doi: 10.1007/s11912-011-0182-z.

Abstract

Unresectable or metastatic disease occurs in 40% to 60% of soft-tissue sarcoma (STS) patients and portends a poor prognosis. For decades, doxorubicin has formed the backbone of systemic treatment, with response rates of approximately 26%. Patients progressing following first-line therapy were left with few proven options. No other cytotoxic chemotherapy agent or combination has demonstrated superiority to doxorubicin. Advances in targeted therapy of STS have been hindered by STS heterogeneity and poorly understood disease biology. Despite challenges, progress has been made in specific STS subtypes. Here, we highlight the challenges, progress, and lessons learned from STS trials published in the last 20 to 25 years.

摘要

约 40% 至 60%的软组织肉瘤(STS)患者发生不可切除或转移性疾病,预后不良。几十年来,阿霉素一直是系统治疗的基础,其缓解率约为 26%。一线治疗后进展的患者几乎没有经过验证的选择。没有其他细胞毒性化疗药物或联合用药显示优于阿霉素。STS 靶向治疗的进展受到 STS 异质性和疾病生物学认识不足的阻碍。尽管存在挑战,但在特定的 STS 亚型中已经取得了进展。在这里,我们重点介绍过去 20 到 25 年发表的 STS 试验中遇到的挑战、取得的进展和吸取的经验教训。

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