软组织肉瘤少转移性疾病的治疗

Marcos R. Gonzalez
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摘要

少转移性软组织肉瘤是一种介于局部和播散性疾病之间的中间状态。联合手术、放疗和全身治疗可显著改善预后,5年总生存率高达50%。由于肺转移的高发病率,大多数手术证据都集中在肺转移切除术上。手术转移切除术的决定仍然取决于最佳的患者选择。术后足够的肺功能、无肺外转移、原发肿瘤的控制以及达到阴性切缘的可行性是患者手术成功的主要标准。足够的切缘、较长的无病间隔、单侧、数量有限(≤2)、异时性和小(< 2 cm)肺转移是提高生存率的一些因素。放射治疗,特别是SBRT,是一种有效的疾病控制治疗方法,其作为(新)辅助治疗已显示出良好的效果。然而,比较放疗与手术的研究缺失,放疗独立于手术的疗效尚不清楚。介入放射学技术,如经皮热消融(PTA)或动脉栓塞也被认为是不适合手术的候选人的潜在治疗选择。传统的全身治疗包括以蒽环类药物(阿霉素)为基础的方案,在某些情况下添加异环磷酰胺。最近在全身治疗方面的进展包括在(低)转移性STS中使用靶向治疗和免疫治疗。然而,除了某些组织学外,大多数STS亚型是耐药的,对全身治疗的反应很差。
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Management of oligometastatic disease in soft tissue sarcomas
Oligometastatic soft tissue sarcoma represents an intermediate state between localized and disseminated disease. Combination A combination of surgery, radiotherapy and systemic treatment significantly improves prognosis, with a 5-year overall survival as high as 50%. Due to the high prevalence of lung metastases, most of the surgical evidence is centered around lung metastasectomy. The decision to perform surgical metastasectomy remains dependent on optimal patient selection. Adequate post-surgical lung function, absence of extrapulmonary metastases, control of the primary tumor, and feasibility of achieving negative margins are major criteria for patients to undergo successful surgery. Adequate margins, longer disease-free interval, unilateral, limited number (≤ 2), metachronous and small (< 2 cm) pulmonary metastasis are some factors associated with improved survival. Radiotherapy, especially SBRT, is an effective treatment for disease control, and its use as (neo)-adjuvant therapy has shown promising results. However, studies comparing radiotherapy against surgery are missing and the efficacy of radiotherapy independent of surgery is not yet clear. Interventional radiology techniques such as percutaneous thermal ablation (PTA) or arterial embolization have also been described as potential treatment alternatives in candidates deemed not fit for surgery. Systemic treatment has traditionally consisted of an anthracycline (doxorubicin)-based regimen with the addition of ifosfamide in certain cases. Recent advances in systemic treatment include the use of targeted therapy and immunotherapy in (oligo)-metastatic STS. However, except for certain histologies, most STS subtypes are chemoresistant, and the response to systemic treatment is poor.
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3.20
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5.30%
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460
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