Giovacchini Giampiero, Picchio Maria, Schipani Stefano, Landoni Claudio, Gianolli Luigi, Bettinardi Valentino, Di Muzio Nadia, Gilardi Maria Carla, Fazio Ferruccio, Messa Cristina
University of Milano-Bicocca, Milan, Italy.
Tumori. 2009 Mar-Apr;95(2):177-84. doi: 10.1177/030089160909500208.
Evaluation of the metabolic response to radiotherapy in nonsmall 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.
In 6 patients, PET/CT scans with [18F]fluorodeoxyglucose were performed before (PET0), during (PET1; at a median of 14 days before the end of radiotherapy) and after the end of radiotherapy (PET2 and PET3, at a median of 28 and 93 days, respectively). The metabolic response was scored according to visual and semiquantitative criteria.
Standardize maximum uptake at PET1 (7.9 +/- 4.8), PET2 (5.1 +/- 4.1) and PET3 (2.7 +/- 3.1) were all significantly (P < 0.05; ANOVA repeated measures) lower than at PET0 (16.1 +/- 10.1). Standardized maximum uptake at PET1 was significantly higher than at both PET2 and PET3. There were no significant differences in SUV(max) between PET2 and PET3. PET3 identified 4 complete and 2 partial metabolic responses, whereas PET1 identified 6 partial metabolic responses. Radiotherapy-induced increased [l8F]fluorodeoxyglucose uptake could be visually distinguished from tumor uptake based on PET/CT integration and was less frequent at PET1 (n = 2) than at PET3 (n = 6).
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 [18F]fluorodeoxyglucose images, particularly when using PET/CT.
非小细胞肺癌患者放疗代谢反应的评估通常在放疗结束后约三个月进行。本研究的目的是通过正电子发射断层扫描/计算机断层扫描(PET/CT)及[18F]氟脱氧葡萄糖评估非小细胞肺癌患者放疗期间及放疗后葡萄糖代谢的变化。
对6例患者在放疗前(PET0)、放疗期间(PET1;放疗结束前中位14天)及放疗结束后(PET2和PET3,分别为中位28天和93天)进行[18F]氟脱氧葡萄糖PET/CT扫描。根据视觉和半定量标准对代谢反应进行评分。
PET1(7.9±4.8)、PET2(5.1±4.1)和PET3(2.7±3.1)的标准化最大摄取值均显著低于PET0(16.1±10.1)(P<0.05;重复测量方差分析)。PET1的标准化最大摄取值显著高于PET2和PET3。PET2和PET3之间的SUV(max)无显著差异。PET3识别出4例完全代谢反应和2例部分代谢反应,而PET1识别出6例部分代谢反应。基于PET/CT融合,放疗诱导的[18F]氟脱氧葡萄糖摄取增加在视觉上可与肿瘤摄取区分开来,且在PET1(n=2)时比PET3(n=6)时更少见。
在非小细胞肺癌中,放疗可导致葡萄糖代谢逐渐降低,治疗结束3个月后降低更明显,但在治疗期间即可检测到。放疗诱导的葡萄糖摄取性炎症在放疗结束后比放疗期间更明显,且不影响[18F]氟脱氧葡萄糖图像的解读,尤其是在使用PET/CT时。