Effect of respiratory gating on quantifying PET images of lung cancer.

UNLABELLED We have developed a new technique to gate lung 18F-FDG PET images in synchronization with the respiratory motion to reduce smearing due to breathing and improve quantitation of 18F-FDG uptake in lung lesions. METHODS A camera-based respiratory gating system, the real-time position management (RPM), is used to monitor the respiratory cycle. The RPM provides a trigger to the PET scanner to initiate the gating cycle. Each respiratory cycle is divided into discrete bins triggered at a defined amplitude or phase within the patient's breathing motion, into which PET data are acquired. The acquired data within the time bins correspond to different lesion positions within the breathing cycle. The study includes 5 patients with lung cancer. RESULTS Measurements of the lesions' volumes in the gated mode showed a reduction of up to 34% compared with that of the nongated measurement. This reduction in the lesion volume has been accompanied by an increase in the intensity in the 18F-FDG signal per voxel. This finding has resulted in an improvement in measurement of the maximum standardized uptake value (SUV(max)), which increased in 1 patient by as much as 159%. The total lesion glycolysis, defined as the product of the SUV(max) and the lesion volume, was also measured in gated and nongated modes and showed a consistency between the 2 measurements. CONCLUSION We have shown that image smearing can be reduced by gating 18F-FDG PET images in synchronization with the respiratory motion. This technique allows a more accurate definition of the lesion volume and improves the quantitation specific activity of the tracer (in this case, 18F-FDG), which are distorted because of the breathing motion.

[1]  R L Wahl,et al.  Fluorodeoxyglucose uptake in human cancer cell lines is increased by hypoxia. , 1995, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[2]  T K Lewellen,et al.  Quantifying regional hypoxia in human tumors with positron emission tomography of [18F]fluoromisonidazole: a pretherapy study of 37 patients. , 1996, International journal of radiation oncology, biology, physics.

[3]  P. Vaupel,et al.  Hypoxia and Radiation Response in Human Tumors. , 1996, Seminars in radiation oncology.

[4]  S M Larson,et al.  Segmentation of lung lesion volume by adaptive positron emission tomography image thresholding , 1997, Cancer.

[5]  G. Hanks,et al.  Measuring hypoxia and predicting tumor radioresistance with nuclear medicine assays. , 1998, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

[6]  D Delbeke,et al.  Prospective investigation of positron emission tomography in lung nodules. , 1998, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[7]  John L. Humm,et al.  Tumor Treatment Response Based on Visual and Quantitative Changes in Global Tumor Glycolysis Using PET-FDG Imaging. The Visual Response Score and the Change in Total Lesion Glycolysis. , 1999, Clinical positron imaging : official journal of the Institute for Clinical P.E.T.

[8]  H. Mostafavi,et al.  Breathing-synchronized radiotherapy program at the University of California Davis Cancer Center. , 2000, Medical physics.

[9]  C C Ling,et al.  Towards multidimensional radiotherapy (MD-CRT): biological imaging and biological conformality. , 2000, International journal of radiation oncology, biology, physics.

[10]  E. Nitzsche,et al.  Increased metabolic activity in the thymus gland studied with 18F-FDG PET: age dependency and frequency after chemotherapy. , 2001, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[11]  C. Ling,et al.  Hypoxia-Induced increase in FDG uptake in MCF7 cells. , 2001, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[12]  G. Hobbs,et al.  Mediastinal lymph node sampling following positron emission tomography with fluorodeoxyglucose imaging in lung cancer staging. , 2001, Chest.

[13]  T. Buettner,et al.  Copper-64-diacetyl-bis(N4-methylthiosemicarbazone): An agent for radiotherapy. , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[14]  C. Ling,et al.  Effect of respiratory gating on reducing lung motion artifacts in PET imaging of lung cancer. , 2002, Medical physics.