Hematology/Oncology, Medical College of Wisconsin, Froedtert/MCW Cancer Center, 4th Floor, 9200 W. Wisconsin Ave., Milwaukee, WI, 53226, USA.
Curr Treat Options Oncol. 2018 Oct 25;19(12):65. doi: 10.1007/s11864-018-0586-1.
Soft tissue sarcoma (STS) is a heterogeneous disease, in terms of histologic subtype, body site of presentation, and behavior. Localized soft tissue sarcoma may be cured with complete tumor excision, but overall, outcomes are sub-optimal. Metastatic disease is associated with shortened survival. Systemic therapy has been studied for several decades as adjunctive therapy, but the use of adjuvant and neo-adjuvant chemotherapy remains controversial. The heterogeneity of patients included in clinical trials, and of sarcoma in general, has made it difficult to draw conclusions about which patients with localized STS should be treated with chemotherapy. Over time, published outcomes for STS of the extremities have improved, and one of the factors that contributes to this improvement may be selection of patients most likely to benefit from the prescribed treatment. Recent studies of neo-adjuvant and adjuvant chemotherapy have recruited patients with the highest recurrence risk-those with large, high-grade, deep tumors. It is reasonable, in practice, to apply similar criteria in deciding whether to recommend treatment. Looking ahead, it will be important to refine our ability to identify patients at highest risk of recurrence, and to develop tools to predict which patients and tumors will respond to chemotherapy.
软组织肉瘤(STS)是一种异质性疾病,在组织学亚型、病变部位和行为方面均具有异质性。局限性软组织肉瘤可以通过完全肿瘤切除治愈,但总体而言,预后并不理想。转移性疾病与生存期缩短相关。几十年来,人们一直在研究全身性治疗作为辅助治疗,但辅助和新辅助化疗的应用仍存在争议。临床试验中纳入的患者异质性,以及肉瘤的总体异质性,使得难以确定哪些局限性 STS 患者应接受化疗治疗。随着时间的推移,肢体 STS 的发表结果得到了改善,促成这一改善的因素之一可能是选择最有可能从规定治疗中获益的患者。最近关于新辅助和辅助化疗的研究招募了复发风险最高的患者——那些肿瘤较大、分级较高、较深的患者。在实践中,根据相似的标准来决定是否推荐治疗是合理的。展望未来,重要的是要提高我们识别复发风险最高的患者的能力,并开发预测哪些患者和肿瘤对化疗有反应的工具。