TY - JOUR
T1 - Changes in glucose metabolism during and after radiotherapy in non-small cell lung cancer
AU - Giovacchini, Giampiero
AU - Picchio, Maria
AU - Schipani, Stefano
AU - Landoni, Claudio
AU - Gianolli, Luigi
AU - Bettinardi, Valentino
AU - Muzio, Nadia Di
AU - Gilardi, Maria Carla
AU - Faziot, Ferruccio
AU - Messa, Cristina
PY - 2009/3
Y1 - 2009/3
N2 - Aims and background. Evaluation of the metabolic response to radiotherapy in non- small cell lung cancer patients is commonly performed about three months after the end of radiotherapy. The aim of the present study was to assess with positron emission tomography/computed tomography (PET/CT) and [
18F]fluorodeoxyglucose changes in glucose metabolism during and after radiotherapy in non-small cell lung cancer patients. Methods and study design. In 6 patients, PET/CT scans with [
18F]luorodeoxyglucose were performed before (PET
0), during (PET
1 at a median of 14 days before the end of radiotherapy) and after the end of radiotherapy (PET
2 and PET
3, at a median of 28 and 93 days, respectively). The metabolic response was scored according to visual and semiquantitative criteria. Results. Standardize maximum uptake at PET
1 (7.9 ± 4.8), PET
2 (5.1 ± 4.1) and PET
3 (2.7 ± 3.1) were all significantly (P 0 (16.1 ± 10.1). Standardized maximum uptake at PET, was significantly higher than at both PET
2 and PET
3. There were no significant differences in SUV
miX between PET
2 and PET
3. PET
3 identified 4 complete and 2 partial metabolic responses, whereas PET
1 identified 6 partial metabolic responses. Radiotherapy-induced increased [
18Fl]luorodeoxyglucose uptake could be visually distinguished from tumor uptake based on PET/CT integration and was less frequent at PET
1 (n = 2) than at PET
3 (n 6). Conclusions. In non-small cell lung cancer, radiotherapy induces a progressive decrease in glucose metabolism that is greater 3 months after the end of treatment but can be detected during the treatment itself. Glucose avid, radiotherapy-induced inflammation is more evident after the end of radiotherapy than during radiotherapy and does not preclude the interpretation of 1'8Flfluorodeoxyglucose images, particularly when using PET/CT.
AB - Aims and background. Evaluation of the metabolic response to radiotherapy in non- small cell lung cancer patients is commonly performed about three months after the end of radiotherapy. The aim of the present study was to assess with positron emission tomography/computed tomography (PET/CT) and [
18F]fluorodeoxyglucose changes in glucose metabolism during and after radiotherapy in non-small cell lung cancer patients. Methods and study design. In 6 patients, PET/CT scans with [
18F]luorodeoxyglucose were performed before (PET
0), during (PET
1 at a median of 14 days before the end of radiotherapy) and after the end of radiotherapy (PET
2 and PET
3, at a median of 28 and 93 days, respectively). The metabolic response was scored according to visual and semiquantitative criteria. Results. Standardize maximum uptake at PET
1 (7.9 ± 4.8), PET
2 (5.1 ± 4.1) and PET
3 (2.7 ± 3.1) were all significantly (P 0 (16.1 ± 10.1). Standardized maximum uptake at PET, was significantly higher than at both PET
2 and PET
3. There were no significant differences in SUV
miX between PET
2 and PET
3. PET
3 identified 4 complete and 2 partial metabolic responses, whereas PET
1 identified 6 partial metabolic responses. Radiotherapy-induced increased [
18Fl]luorodeoxyglucose uptake could be visually distinguished from tumor uptake based on PET/CT integration and was less frequent at PET
1 (n = 2) than at PET
3 (n 6). Conclusions. In non-small cell lung cancer, radiotherapy induces a progressive decrease in glucose metabolism that is greater 3 months after the end of treatment but can be detected during the treatment itself. Glucose avid, radiotherapy-induced inflammation is more evident after the end of radiotherapy than during radiotherapy and does not preclude the interpretation of 1'8Flfluorodeoxyglucose images, particularly when using PET/CT.
KW - Lung cancer
KW - Positron- emission tomography
KW - Radiotherapy
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M3 - Article
C2 - 19579863
AN - SCOPUS:67649127036
SN - 0300-8916
VL - 95
SP - 177
EP - 184
JO - Tumori
JF - Tumori
IS - 2
ER -