[Progress in the treatment of soft tissue sarcoma in the 2023 annual meeting of the American Society of Clinical Oncology].

J L Zhao, W F Liu
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Abstract

Soft tissue sarcoma (STS) is a group of rare malignant tumors originating from mesenchymal tissue, with a high degree of malignancy and a wide range of pathological subtypes. The prognosis varies among different subtypes, and treatment increasingly relies on selecting appropriate treatment methods for different subtypes. Surgical treatment is still the main treatment method at present, and the development of immune and targeted therapy also brings new hope for the treatment of soft tissue sarcoma. Immune checkpoint inhibitors, oncolytic viruses and T cell therapy have shown well safety and efficacy in clinical trials. Targeted drugs such as trabectedin and lenvatinib have changed the treatment pattern of soft tissue sarcoma. Currently, chemotherapy based on doxorubicin and ifosfamide is still the first line treatment for patients with advanced soft tissue sarcoma who have distant metastasis. However, the adverse reactions of doxorubicin limit its application in elderly patients, and trofosfamide has shown good efficacy and safety as an alternative in clinical trials. The efficacy of postoperative radiotherapy has been confirmed, which can reduce the local recurrence rate after surgical resection of soft tissue sarcoma. In summary, multimodal comprehensive treatment has become the main strategy for the treatment of soft tissue sarcoma. The combination of different treatment methods can generate synergistic effects and help patients obtain more clinical benefits, such as the combination of doxorubicin and immune checkpoint inhibitors, and the combination of antiangiogenic drugs and chemotherapy drugs. At the 2023 annual meeting of the American Society of Clinical Oncology (ASCO), oncologists from all over the world reported many researches related to the treatment of soft tissue sarcoma. This article aims to review the new progress in the treatment of soft tissue sarcoma in the 2023 annual meeting of ASCO.

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[美国临床肿瘤学会 2023 年年会上的软组织肉瘤治疗进展]。
软组织肉瘤(STS)是一类罕见的恶性肿瘤,起源于间质组织,恶性程度高,病理亚型繁多。不同亚型的预后各不相同,治疗越来越依赖于针对不同亚型选择合适的治疗方法。目前,手术治疗仍是主要的治疗方法,而免疫疗法和靶向疗法的发展也为软组织肉瘤的治疗带来了新的希望。免疫检查点抑制剂、溶瘤病毒和T细胞疗法在临床试验中显示出良好的安全性和有效性。曲贝替丁(trabectedin)和来伐替尼(lenvatinib)等靶向药物改变了软组织肉瘤的治疗模式。目前,以多柔比星和伊佛酰胺为基础的化疗仍是有远处转移的晚期软组织肉瘤患者的一线治疗方案。然而,多柔比星的不良反应限制了其在老年患者中的应用,而特罗磷酰胺作为一种替代疗法,在临床试验中显示出良好的疗效和安全性。术后放疗的疗效已得到证实,可降低软组织肉瘤手术切除后的局部复发率。总之,多模式综合治疗已成为治疗软组织肉瘤的主要策略。不同治疗方法的联合应用可产生协同效应,帮助患者获得更多临床获益,如多柔比星与免疫检查点抑制剂的联合应用、抗血管生成药物与化疗药物的联合应用等。在2023年美国临床肿瘤学会(ASCO)年会上,来自世界各地的肿瘤学家报告了许多与软组织肉瘤治疗相关的研究。本文旨在回顾2023年ASCO年会上软组织肉瘤治疗的新进展。
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来源期刊
中华肿瘤杂志
中华肿瘤杂志 Medicine-Medicine (all)
CiteScore
1.40
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0.00%
发文量
10433
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