Downey Robert J, Akhurst Timothy, Gonen Mithat, Park Bernard, Rusch Valerie
Thoracic Surgery Service, Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
J Thorac Cardiovasc Surg. 2007 Jun;133(6):1419-27. doi: 10.1016/j.jtcvs.2007.01.041. Epub 2007 May 2.
Positron emission tomographic maximal standardized uptake value has been shown to predict survival after resection of non-small cell lung cancer. The relative prognostic benefit of maximal standardized uptake value with respect to other clinical/pathologic variables has not been defined.
We reviewed patients who had positron emission tomographic imaging and an R0 resection for non-small cell lung cancer between January 1, 2000, and December 31, 2004, without induction or adjuvant therapy. The associations between overall survival, histology, pathologic TNM stage, pathologic tumor diameter, and standardized uptake value were tested.
Four hundred eighty-seven patients met the study criteria. Median follow-up was 25.8 months. By using the median values for tumor size (2.5 cm) and standardized uptake value (5.3), standardized uptake value was an independent predictor of survival (P = .03), adjusting for tumor size (P = .02) and histology (P < .01). The optimal standardized uptake value for stratification was identified as 4.4, and this value was identified as an independent predictor of survival (P = .03) after adjusting for clinical TNM stage. Standardized uptake value was not an independent predictor of survival (P = .09), adjusting for pathologic TNM stage (stage IA vs IB vs stage II-IV, P < .01).
Standardized uptake value does not add to the prognostic significance of pathologic TNM stage. Standardized uptake value was an independent prognostic factor from clinical TNM stage.
正电子发射断层扫描最大标准化摄取值已被证明可预测非小细胞肺癌切除术后的生存率。最大标准化摄取值相对于其他临床/病理变量的相对预后益处尚未明确。
我们回顾了2000年1月1日至2004年12月31日期间接受正电子发射断层扫描成像且接受非小细胞肺癌R0切除、未接受诱导或辅助治疗的患者。测试了总生存期、组织学、病理TNM分期、病理肿瘤直径和标准化摄取值之间的关联。
487例患者符合研究标准。中位随访时间为25.8个月。以肿瘤大小(2.5 cm)和标准化摄取值(5.3)的中位数为标准,在对肿瘤大小(P = 0.02)和组织学(P < 0.01)进行校正后,标准化摄取值是生存的独立预测因素(P = 0.03)。分层的最佳标准化摄取值确定为4.4,在对临床TNM分期进行校正后,该值被确定为生存的独立预测因素(P = 0.03)。在对病理TNM分期(IA期与IB期与II-IV期,P < 0.01)进行校正后,标准化摄取值不是生存的独立预测因素(P = 0.09)。
标准化摄取值并未增加病理TNM分期的预后意义。标准化摄取值是独立于临床TNM分期的预后因素。