非小细胞肺癌的PET/CT表现和肿瘤/患者特征的预后价值

O. Demirhan, Z. Balta, G. A. Tosun, S. Erturan, K. Sonmezoglu
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引用次数: 0

摘要

背景/目的:尽管非小细胞肺癌(NSCLC)的预后因素众多,但仍需要更好的非侵入性标志物。FDG-PET是一种非侵入性诊断工具,在肺癌诊断中应用越来越广泛。本研究评估了PET/CT定义的SUV测量和其他患者/肿瘤特征在新诊断的IIIB和IV期非小细胞肺癌中的预后价值。方法:本回顾性研究纳入了2005年至2006年间收治的111例IIIB期和IV期NSCLC患者,这些患者的诊断通过活检和PET/CT分期得到证实。采用生存分析分析原发性病变的标准摄取值(SUV)和其他患者/肿瘤特征的预后价值。结果:发现SUV与生存无关。仅发现远处转移的存在、转移类型(骨、脑或对侧肺)和使用的放射治疗类型(治愈性或姑息性)与生存有关。表皮样癌的SUV值明显高于腺癌(分别为16.15±7.18和12.32±5.52,p = 0.021)。结论:我们的研究结果不支持不能手术的非小细胞肺癌原发病变的SUV对生存有预后价值。这种情况可能是由于纳入了已知生存率低、死亡率高的明显晚期NSCLC患者,以及样本量相对较小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic Values of PET/CT Findings and Tumor/Patient Characteristics with Non-Small Cell Lung Cancer
Background/Aim: Although numerous prognostic factors have been described for non-small cell lung cancer (NSCLC), there is still a requirement for better and non-invasive markers. FDG-PET is a non invasive diagnostic tool that is being used increasingly in the diagnosis of lung cancer. This study evaluates the prognostic values of PET/CT defined SUV measurements and other patient/tumor characteristics in newly diagnosed stage IIIB and IV NSCLC. Method: This retrospective study included 111 patients admitted between 2005 and 2006 with stage IIIB and IV NSCLC, whose diagnoses were verified with biopsy and staging performed with PET/CT. The prognostic values of standart uptake values (SUV) of the primary lesion on PET/CT, and other patient/tumor characteristics were analyzed using survival analysis. Results: SUV was found to be unrelated with survival. Only the presence of distant metastasis, type of metastasis (bone, brain, or the contralateral lung) and the type of radiotherapy used (curative or palliative) were found to be related to survival. SUV values in epidermoid carcinoma were found to be significantly higher compared to adenocarcinoma (16.15 ± 7.18 and 12.32 ± 5.52, respectively, p = 0.021). Conclusion: Our findings do not support that SUV of the primary lesion in inoperable NSCLC has a prognostic value with respect to survival. This condition may be explained by the inclusion of significantly advanced NSCLC patients who are known to have a low survival and a high mortality, and also the relatively small sampling size.
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