[18F] fluorodeoxyglucose uptake by positron emission tomography predicts outcome of non-small-cell lung cancer

被引:243
作者
Sasaki, R
Komaki, R
Macapinlac, H
Erasmus, J
Allen, P
Forster, K
Putnam, JB
Herbst, RS
Moran, CA
Podoloff, DA
Roth, JA
Cox, JD
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Radiat Oncol, Unit 97, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Nucl Med, Houston, TX USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Thorac & Cardiovasc Surg, Houston, TX USA
[4] Univ Texas, MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Houston, TX USA
[5] Univ Texas, MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
[6] Kobe Univ, Grad Sch Med, Div Radiol, Kobe, Hyogo, Japan
关键词
D O I
10.1200/JCO.2005.06.129
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To determine whether the standardized uptake value (SUV) of [F-18]fluorodeoxyglucose uptake by positron emission tomography could be a prognostic factor for non-small-cell lung cancer (NSCLC). Patients and Methods One hundred sixty-two patients with stage I to IIIb NSCLC were analyzed. Overall survival (OS), disease-free survival (DFS), distant metastasis-free survival (DMFS), and local-regional control (LRC) were calculated by the Kaplan-Meier method and evaluated with the log-rank test. The prognostic significance was assessed by univariate and multivariate analyses. Results There were 93 patients treated with surgery and 69 patients treated with radiotherapy, A cutoff of 5 for the SLIV for the primary tumor showed the best discriminative value. The SUV for the primary tumor was a significant predictor of OS (P = .02) in both groups. Low SUVs (less than or equal to 5.0) showed significantly better DFS rates than those with high SUVs (> 5.0; surgery group, P = .02; radiotherapy group, P = .0005). Low SUVs (:! 5.0) indicated a significantly better DFS than those with high SUVs (>5.0; stage I or II, P = .02; stage IIIa or IIIb, P = .004). However, using the same cutoff point of 5, the SUV for regional lymph nodes was not a significant indicator for DFS (P = .19), LRC (P = .97), or DMFS (P = .17). The multivariate analysis showed that the SUV for the primary tumor was a significant prognostic factor for OS (P = .03) and DFS (P = .001). Conclusion The SUV of the primary tumor was the strongest prognostic factor among the patients treated by curative surgery or radiotherapy. (C) 2005 by American Society of Clinical Oncology.
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页码:1136 / 1143
页数:8
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