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Targeted therapy for soft tissue sarcomas in adolescents and young adults

机译:针对青少年和年轻人的软组织肉瘤的靶向治疗

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摘要

Soft tissue sarcomas (STSs) are a heterogeneous group of tumors originating from the mesenchyme. Even though they affect individuals in all age groups, the prevalence of subtypes of STSs changes significantly from childhood through adolescence into adulthood. The mainstay of therapy is surgery, with or without the addition of chemotherapy and/or radiation therapy. These treatment modalities are associated, in many cases, with significant morbidity and, given the heterogeneity of tumor histologies encompassed by the term “STS”, have not uniformly improved outcomes. Moreover, some subgroups of STSs appear to be more, and others less, responsive to conventional chemotherapy agents. Over the last two decades, our understanding of the biology of STSs is slowly increasing, allowing for the development of more targeted therapies. We review the new treatment modalities that have been tested on patients with STSs, with a special focus on adolescents and young adults, a group of patients that is often underrepresented in clinical trials and has not received the dedicated attention it deserves, given the significant differences in biology and treatment response in comparison to children and adults.
机译:软组织肉瘤(STS)是起源于间充质的异质性肿瘤。即使它们影响所有年龄段的个体,STS亚型的患病率也从儿童期到青春期到成年期都有显着变化。治疗的主要手段是手术,有或没有增加化学疗法和/或放射疗法。在许多情况下,这些治疗方式与明显的发病率相关,并且鉴于术语“ STS”所涵盖的肿瘤组织学的异质性,其治疗效果并未得到统一改善。此外,STS的某些亚组似乎对常规化疗药物的反应更多,而另一些则更少。在过去的二十年中,我们对STS生物学的了解正在逐步增加,从而可以开发出更具针对性的疗法。我们回顾了已针对STS患者测试的新治疗方式,特别关注青少年和年轻人,这是一组患者,在临床试验中通常代表性不足,并且由于明显的差异而没有得到应有的关注与儿童和成人相比在生物学和治疗反应方面的优势。

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