Chemotherapy response evaluation with 18F-FDG PET in patients with non-small cell lung cancer

被引:103
作者
de Geus-Oei, Lioe-Fee [1 ]
van der Heijden, Henricus F. M. [2 ]
Visser, Eric P. [1 ]
Hermsen, Rick [1 ]
van Hoorn, Bas A. [1 ]
Timmer-Bonte, Johanna N. H. [2 ,3 ]
Willemsen, Antoon T. [4 ]
Pruim, Jan [4 ]
Corstens, Frans H. M. [1 ]
Krabbe, Paul F. M. [5 ]
Oyen, Wim J. G. [1 ]
机构
[1] Radboud Univ Nijmegen, Nijmegen Med Ctr, Dept Nucl Med, NL-6500 HB Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Nijmegen Med Ctr, Dept Pulm Dis, NL-6500 HB Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Nijmegen Med Ctr, Dept Med Oncol, NL-6500 HB Nijmegen, Netherlands
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Nucl Med & Mol Imaging, Groningen, Netherlands
[5] Radboud Univ Nijmegen, Nijmegen Med Ctr, Dept Med Technol Assessment, NL-6500 HB Nijmegen, Netherlands
关键词
chemotherapy response monitoring; F-18-FDG PET; non-small cell lung cancer; standardized uptake value; Patlak analysis;
D O I
10.2967/jnumed.107.043414
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
The aim of this prospective study was to evaluate the value of F-18-FDG PET for the assessment of chemotherapy response in patients with non-small cell lung cancer. Furthermore, part of the objective of this study was to compare 2 methods to quantify changes in glucose metabolism. Methods: In 51 patients, dynamic F-18-FDG PET was performed before and at 5-8 wk into treatment. Simplified methods to measure glucose metabolism (standardized uptake value [SUV]) and quantitative measures (metabolic rate of glucose [MRGlu]), derived from Patlak analysis, were evaluated. The overall survival and progression-free survival with respect to MRGlu and SUV were calculated using Kaplan-Meier estimates. Fractional changes in tumor glucose use were stratified by the median value and also the predefined EORTC (European Organization for Research and Treatment of Cancer) metabolic response criteria, and criteria applying cutoff levels similar to those of RECIST (Response Evaluation Criteria in Solid Tumors) were evaluated. Results: When stratifying at the median value of Delta MRGlu and Delta SUV, the difference in overall survival (P=0.017 for Delta MRGlu, P = 0.018 for Delta SUV) and progression-free survival (P = 0.002 for Delta MRGlu, P = 0.0009 for Delta SUV) was highly significant. When applying the predefined criteria for metabolic response, the cutoff levels as also used for size measurement (RECIST) showed significant differences for Delta SUV between response categories in progression-free survival (P = 0.0003) as well as overall survival (P = 0.027). Conclusion: The degree of chemotherapy-induced changes in tumor glucose metabolism as determined by 18F-FDG PET is highly predictive for patient outcome, stratifying patients into groups with widely differing overall survival and progression-free survival probabilities. The use of 18F-FDG PET for therapy monitoring seems clinically feasible, because simplified methods to measure tumor glucose use (SUV) are sufficiently reliable and can replace more complex, quantitative measures (MRGlu) in this patient population.
引用
收藏
页码:1592 / 1598
页数:7
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