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首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >Bone metastasis and poor performance status are prognostic factors for survival of carcinoma of unknown primary site in patients treated with systematic chemotherapy.
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Bone metastasis and poor performance status are prognostic factors for survival of carcinoma of unknown primary site in patients treated with systematic chemotherapy.

机译:骨转移和较差的表现状态是接受系统化学疗法治疗的患者的原发灶未知癌生存的预后因素。

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摘要

BACKGROUND: Cancer of unknown primary site (CUP) generally has a poor prognosis, and there is no established standard therapy. There have been no reports of a prognostic model for CUP patients treated with a single regimen of systemic chemotherapy. METHODS: Univariate and multivariate prognostic factor analysis for overall survival (OS) were conducted retrospectively in 58 consecutive CUP patients treated with carboplatin plus paclitaxel (Taxol) therapy as a first-line treatment. RESULTS: Univariate prognostic factor analysis revealed baseline performance status (PS) of two or more, low serum albumin level, pleural effusion, bone metastasis, and liver metastasis as adverse prognostic factors. Cox proportional hazards analysis showed that poor PS and bone metastasis had the most powerful adverse impact on survival. We developed a prognostic model using those two variables-a good-risk group (PS 0-1 without bone metastasis) and a poor-risk group (PS > or =2 or bone metastasis). The poor-risk group showed significantly poorer OS than the good-risk group (1 year OS 36.8% versus 67.1%, P = 0.0003). CONCLUSIONS: Poor PS and bone metastasis were identified as independent adverse prognostic factors in CUP. A simple prognostic model was developed and seems useful for decision making as to whether chemotherapy is indicated for CUP patients.
机译:背景:原发灶未知的癌症(CUP)通常预后较差,目前尚无标准治疗方法。没有关于使用单一系统化疗方案治疗的CUP患者的预后模型的报道。方法:回顾性分析58例连续接受卡铂加紫杉醇(Taxol)治疗作为一线治疗的CUP患者的总生存期(OS)的单因素和多因素预后因素分析。结果:单因素预后因素分析显示基线表现状态(PS)为两个或多个,血清白蛋白水平低,胸腔积液,骨转移和肝转移为不良预后因素。 Cox比例风险分析表明,不良的PS和骨转移对生存的影响最大。我们使用这两个变量开发了一种预后模型:高风险组(PS 0-1无骨转移)和低风险组(PS>或= 2或骨转移)。与高风险组相比,低风险组的OS明显较差(1年OS为36.8%对67.1%,P = 0.0003)。结论:不良的PS和骨转移被确定为CUP的独立不良预后因素。建立了一个简单的预后模型,该模型对于决定是否对CUP患者进行化学疗法的决策似乎很有用。

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