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非小细胞肺癌患者 PET-CT 中原发灶 FDG 摄取与临床分期的关系:一项观察。

Relationship between primary lesion FDG uptake and clinical stage at PET-CT for non-small cell lung cancer patients: An observation.

机构信息

Department of Radiation Oncology, Shandong Cancer Hospital & Institute, Jiyan Road 440, Jinan 250117, Shandong Province, China.

出版信息

Lung Cancer. 2010 Jun;68(3):394-7. doi: 10.1016/j.lungcan.2009.07.009. Epub 2009 Aug 14.

DOI:10.1016/j.lungcan.2009.07.009
PMID:19683358
Abstract

The aim of the present study was to investigate the relationship between FDG uptake and clinical stage for non-small cell lung cancer. The patients who were histologically or cytologically proven to be adenocarcinoma (AC) or squamous cell carcinoma (SCC) lung cancer and conducted FDG PET/CT staging were retrospectively reviewed. The FDG uptake was quantified as the maximum standardized uptake value (SUVmax). And the T-N-M status was determined mainly by FDG PET-CT imaging according to the 1997 update of the international staging system for lung cancer. From December 2003 to November 2007, 266 cases (194 men and 72 women; age range 31-90 years, median 62 years) were analyzed, which included 161 AC and 105 SCC patients. The present study showed that both size (3.23+/-1.68cm vs 2.63+/-1.33cm, P=0.004) and SUVmax (9.82+/-5.08 vs 8.43+/-4.21, P=0.016) were significantly greater for SCC compared to AC. There was positive correlation between the SUVmax and size for both SCC and AC (r=0.651, 0.632, respectively; both P=0.000). Significant difference is found among different stages in SUVmax for AC (F=11.693, P=0.000) but not for SCC (F=1.514, P=0.216). After controlling the size factor, a significant correlation was found between tumor stage and FDG uptake value for AC (r=0.323, P=0.000), but not for SCC (r=0.113, P=0.252). In conclusion, this observation showed that tumor size and histologic subtype had influences upon FDG uptake in non-small cell lung cancer. It demonstrated significant correlation between clinical stage and SUVmax for AC, but not for SCC.

摘要

本研究旨在探讨非小细胞肺癌(NSCLC)的 FDG 摄取与临床分期之间的关系。回顾性分析了经组织学或细胞学证实为腺癌(AC)或鳞状细胞癌(SCC)肺癌并进行 FDG PET/CT 分期的患者。FDG 摄取量通过最大标准化摄取值(SUVmax)进行量化。T-N-M 分期主要根据 1997 年国际肺癌分期系统的更新,通过 FDG PET-CT 成像确定。2003 年 12 月至 2007 年 11 月,共分析了 266 例患者(194 例男性和 72 例女性;年龄 31-90 岁,中位数 62 岁),其中包括 161 例 AC 和 105 例 SCC 患者。本研究表明,SCC 的大小(3.23+/-1.68cm 比 2.63+/-1.33cm,P=0.004)和 SUVmax(9.82+/-5.08 比 8.43+/-4.21,P=0.016)均明显大于 AC。SCC 和 AC 的 SUVmax 与大小之间均存在正相关(r=0.651,0.632,均 P=0.000)。AC 的不同分期之间 SUVmax 存在显著差异(F=11.693,P=0.000),但 SCC 则没有(F=1.514,P=0.216)。在控制大小因素后,AC 的肿瘤分期与 FDG 摄取值之间存在显著相关性(r=0.323,P=0.000),但 SCC 则没有(r=0.113,P=0.252)。综上所述,该观察结果表明,肿瘤大小和组织学亚型对非小细胞肺癌的 FDG 摄取有影响。AC 的临床分期与 SUVmax 之间存在显著相关性,但 SCC 则没有。

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