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化疗前氟代脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(FDG PET/CT)无法识别单个食管肿瘤内残留的代谢活性区域。

Pre-Chemoradiotherapy FDG PET/CT cannot Identify Residual Metabolically-Active Volumes within Individual Esophageal Tumors.

作者信息

Lu W, Tan S, Chen W, Kligerman S, Feigenberg S J, Zhang H, Suntharalingam M, Kang M, D'Souza W D

机构信息

Department of Radiation Oncology, University of Maryland School of Medicine, Baltimore, USA.

Department of Radiation Oncology, University of Maryland School of Medicine, Baltimore, USA ; Department of Control Science and Engineering, Huazhong University of Science and Technology, Wuhan, China.

出版信息

J Nucl Med Radiat Ther. 2015 May;6(3). doi: 10.4172/2155-9619.1000226. Epub 2015 Apr 29.

Abstract

OBJECTIVE

To study whether subvolumes with a high pre-chemoradiotherapy (CRT) FDG uptake could identify residual metabolically-active volumes (MAVs) post-CRT within individual esophageal tumors. Accurate identification will allow simultaneous integrated boost to these subvolumes at higher risk to improve clinical outcomes.

METHODS

Twenty patients with esophageal cancer were treated with CRT plus surgery and underwent FDG PET/CT scans before and after CRT. The two scans were rigidly registered. Seven MAVs pre-CRT and four MAVs post-CRT within a tumor were defined with various SUV thresholds. The similarity and proximity between the MAVs pre-CRT and post-CRT were quantified with three metrics: fraction of post-CRT MAV included in pre-CRT MAV, volume overlap and centroid distance.

RESULTS

Eight patients had no residual MAV. Six patients had local residual MAV (SUV ≥2.5 post-CRT) within or adjoining the original MAV (SUV ≥2.5 pre-CRT). On average, less than 65% of any post-CRT MAVs was included in any pre-CRT MAVs, with a low volume overlap <45%, and large centroid distance >8.6 mm. In general, subvolumes with higher FDG-uptake pre-CRT or post-CRT had lower volume overlap and larger centroid distance. Six patients had new distant MAVs that were determined to be inflammation from radiation therapy.

CONCLUSIONS

Pre-CRT PET/CT cannot reliably identify the residual MAVs within individual esophageal tumors. Simultaneous integrated boost to subvolumes with high FDG uptake pre-CRT may not be feasible.

摘要

目的

研究化疗放疗(CRT)前氟代脱氧葡萄糖(FDG)摄取量高的子体积是否能够识别个体食管肿瘤CRT后的残留代谢活性体积(MAV)。准确识别将有助于对这些高风险子体积同时进行同步整合加量放疗,以改善临床结局。

方法

20例食管癌患者接受CRT加手术治疗,并在CRT前后接受FDG PET/CT扫描。对两次扫描进行刚性配准。通过不同的标准化摄取值(SUV)阈值定义肿瘤内CRT前的7个MAV和CRT后的4个MAV。用三个指标量化CRT前和CRT后的MAV之间的相似性和接近程度:CRT后MAV包含在CRT前MAV中的比例、体积重叠和质心距离。

结果

8例患者无残留MAV。6例患者在原MAV(CRT前SUV≥2.5)内或相邻处有局部残留MAV(CRT后SUV≥2.5)。平均而言,任何CRT后MAV中包含在任何CRT前MAV中的比例不到65%,体积重叠率低<45%,质心距离大>8.6 mm。一般来说,CRT前或CRT后FDG摄取量较高的子体积体积重叠率较低,质心距离较大。6例患者有新的远处MAV,经判定为放射治疗引起的炎症。

结论

CRT前PET/CT不能可靠地识别个体食管肿瘤内的残留MAV。对CRT前FDG摄取量高的子体积同时进行同步整合加量放疗可能不可行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ba3/4652953/2a976ff8977c/nihms736371f1.jpg

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