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Necrosis on FDG PET/CT correlates with prognosis and mortality in sarcomas.

机译:FDG PET / CT坏死与肉瘤的预后和死亡率相关。

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The purpose of this study was to determine if there is an association between necrosis as identified on staging (18)F-FDG PET/CT and overall survival (OS) and progression-free survival (PFS) in patients with sarcoma.Sixty-six patients with newly diagnosed limb and girdle sarcoma underwent PET/CT at our institution between June 2004 and July 2009 for sarcoma staging before treatment with curative intent. The tumor maximum standardized up-take values (SUVmax), the presence of necrosis, and the volume of necrosis were measured for each primary tumor and correlated with follow-up data. PFS and OS were analyzed using the Kaplan-Meier method. Proportional hazards models were used to estimate hazard ratios.Median patient age was 49 years, and 51.6% of the patients were men. Sarcomas were categorized as soft tissue (69.2%), bone (23.5%), or other (7.3%). Mean follow-up time was 33.3 months. During the follow-up interval, 53% of patients experienced disease progression, and 40.9% died. There was a statistically significant relationship between the presence of necrosis and OS (by log-rank test, p = 0.001), as well as PFS (by log-rank test, p = 0.0001). Twenty-four-month OS was 96%, 65%, and 38% in patients with tumors with absence necrosis, those with presence of necrosis, and with necrosis volume greater than 50%, respectively. Forty-eight-month OS was 81% in patients with absence of necrosis and 41% in patients with presence of necrosis. Twelve-month PFS was 96%, 60%, and 42% in patients with tumors with absence of necrosis, those with presence of necrosis, and those with necrosis volume greater than 50%, respectively. Twenty-four-month PFS was 83%, 38%, and 22%, respectively, in these groups.The presence of necrosis and the volume of necrosis, as identified on the staging FDG PET/CT and after adjusting for SUVmax, are strong independent adverse prognostic factors for disease recurrence and death in patients with limb and girdle sarcomas.
机译:这项研究的目的是确定在分期(18)F-FDG PET / CT上发现的坏死与肉瘤患者的总生存期(OS)和无进展生存期(PFS)之间是否存在关联。 2004年6月至2009年7月间,新诊断为肢体和腰带肉瘤的患者在我院接受PET / CT肉瘤分期,然后进行根治性治疗。测量每个原发肿瘤的肿瘤最大标准化摄取值(SUVmax),坏死的存在和坏死的体积,并与随访数据相关。使用Kaplan-Meier方法分析了PFS和OS。使用比例危害模型估算危害比,患者中位年龄为49岁,其中51.6%为男性。肉瘤分为软组织(69.2%),骨(23.5%)或其他(7.3%)。平均随访时间为33.3个月。在随访期间,53%的患者经历了疾病进展,40.9%的患者死亡。坏死的存在与OS(按对数检验,p = 0.001)以及PFS(按对数检验,p = 0.0001)之间存在统计学上的显着关系。没有坏死的肿瘤,有坏死的肿瘤和坏死体积大于50%的患者的24个月OS分别为96%,65%和38%。没有坏死的患者的48个月OS为81%,有坏死的患者为41%。没有坏死的肿瘤,有坏死的肿瘤和坏死体积大于50%的患者的十二个月PFS分别为96%,60%和42%。这些组的24个月PFS分别为83%,38%和22%。在分期FDG PET / CT上和调整SUVmax后确定的坏死的存在和坏死的体积很强肢体和腰带肉瘤患者疾病复发和死亡的独立不良预后因素。

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