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Adjuvant chemotherapy in localized soft tissue sarcomas: still not proven.

机译:局部软组织肉瘤的辅助化疗:尚无证据。

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Soft tissue sarcoma is a rare and heterogeneous group of tumors in terms of histological subtypes, molecular alterations, clinical presentation, and prognosis. Yet, these tumors are most often treated similarly in the localized phase. The standard treatment of these patients requires multidisciplinary management, in particular, careful diagnostic procedures and surgery by an expert physician, preceded or followed by external radiotherapy. The utility of adjuvant chemotherapy has been explored in 14 trials comparing adjuvant chemotherapy with no treatment. Several trials reported a lower risk for local relapse and lower risk for metastatic relapse, but only a few small trials reported longer overall survival. A meta-analysis of all trials failed to demonstrate a significant difference in the relapse-free survival (RFS) or overall survival rates. Two additional trials, reported afterward, presented conflicting results, with a significant benefit in terms of the RFS rate for the trial of the Italian Sarcoma Group, but no difference in the RFS or overall survival rate in the most recent European Organization for Research and Treatment of Cancer trial. We conclude that adjuvant chemotherapy has not been proven to improve the outcome of an unselected population of patients. Several hypotheses are proposed to account for this observation.
机译:就组织学亚型,分子改变,临床表现和预后而言,软组织肉瘤是一种罕见的异质性肿瘤。然而,这些肿瘤最经常在局部阶段被相似地治疗。这些患者的标准治疗需要多学科的管理,尤其是在外部放疗之前或之后进行仔细的诊断程序和由专业医生进行的手术。辅助化疗的效用已在14项试验中进行了比较,比较了未经治疗的辅助化疗。几项试验报告了局部复发的风险较低,而转移性复发的风险较低,但只有少数小试验报告了更长的总生存期。所有试验的荟萃分析均未能证明无复发生存期(RFS)或总体生存率存在显着差异。后来报道的另外两项试验显示出矛盾的结果,就意大利肉瘤集团的试验而言,RFS率具有显着优势,但在最新的欧洲研究与治疗组织中,RFS或总体生存率没有差异癌症试验。我们得出的结论是,尚未证明辅助化疗可改善未经选择的患者人群的预后。提出了几种假设来解释这种观察。

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