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1.
Clin Positron Imaging ; 3(3): 85-90, 2000 May.
Artigo em Inglês | MEDLINE | ID: mdl-11008097

RESUMO

Purpose: Yttrium-86 has been proposed for use as a quantitative positron emission tomography imaging agent to determine the in vivo distribution of therapeutic pharmaceuticals labeled with yttrium-90, a pure beta minus emitter. This study identifies, and proposes a solution for, an artifact, which interferes with quantitation.Procedures: Yttrium-86 is a 14.7-hour halflife positron emitter (33% abundance) with multiple high energy gamma rays in cascade. Phantom measurements with a GE Advance PET scanner using standard attenuation and scatter corrections, demonstrated anomalous apparent activity in inactive higher density regions.Results: Apparent activity up to 30% of the surrounding true activity was observed in a bone equivalent material. Even higher activities were observed if the scatter correction was omitted. This phenomenon was determined to result from the effect of attenuation correction on true coincidences between one gamma ray and a second gamma ray or annihilation photon.Conclusion: A simple additional correction based on sinogram tail subtraction improves accuracy significantly.

2.
Clin Positron Imaging ; 3(3): 107-114, 2000 May.
Artigo em Inglês | MEDLINE | ID: mdl-11008100

RESUMO

Purpose: To assess the clinical accuracy of whole-body 2-[F-18]-fluoro-2-deoxy-D-glucose-positron emission tomography (FDG-PET) in the diagnosis of recurrent colorectal carcinoma in comparison to conventional computed tomography (CT).Materials and methods: Forty patients with suspected recurrent colorectal carcinoma based on either progressive serial carcinoemrbyonic antigen (CEA) serum elevation or positive/equivocal CT findings underwent whole-body FDG-PET. PET results were compared with those of CT and correlated to the final histopathological and clinical findings.Results: A final diagnosis was obtained at 93 sites in 35 patients by histology and in 5 patients by clinical follow up of at least 6 months. Of the 93 sites, 53 were determined to be malignant and 40 benign. FDG-PET evaluated on a 5-point scale (0-4) showed a positive and negative predictive value in the range of 96-98% and 83-93% respectively as the threshold for positivity was moved from 0 through 3. By comparison, CT, also evaluated on a 5-point scale showed a positive and negative predictive value in the range of 75-88% and 67-71% respectively. The area under the fitted receiver operating characteristic curve for PET: A(PET) = 0.96 +/- 0.02 was significantly greater (P < 0.001) than that observed for CT: A(CT) = 0.77 +/- 0.06. The distribution of maximum standardized uptake value (SUVmax) showed that all negative lesions have SUVmax below 5.0 whereas 75% of positive lesions were above 5.0 pointing to the fact that disease positivity is more likely in lesions with high SUV values.Conclusion: The results of this study confirm that whole-body FDG-PET is more accurate than conventional CT in the staging of patients with suspected recurrent colorectal carcinoma.

3.
Clin Positron Imaging ; 3(2): 57-65, 2000 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-10838401

RESUMO

Objective: In patients with advanced cancer, total tumor burden affects the likelihood of tumor response and has important implications for prognosis. The aim of this study was to select the optimum 2-[F-18]fluoro-2-deoxy-D-glucose-positron emission tomography (FDG PET) tumor uptake parameter to accurately measure tumor burden in advanced metastatic renal cell cancer, in comparison with volumes measured with computed tomography (CT), as a reference test.Materials and Methods: Six patients with metastatic renal cell carcinoma measurable on CT were studied. CT and FDG PET scans were carried out on all patients within 4 weeks prior to their entry into a phase I-II radioimmunotherapy trial. CT-based evaluation of disease extent (tumor volume) and 4 PET-based measurements (standardized uptake value[SUVmax], SUVav, volume, and total lesion glycolysis [TLG]) were performed independently by a radiologist (VN) and a nuclear medicine physician (TA). The degree of correlation between conventional (CT) extent of disease and parameters describing tumor concentration of FDG was then determined.Results: Fifty-seven CT-measurable metastatic lesions in lung, abdomen, and scalp were evaluated in 6 patients. There was a high correlation between CT and FDG PET volume estimates for lesions greater than 5 cm(3) in size. However, a PET-derived parameter that embodies both FDG uptake and lesion size, the TLG, correlated better with CT-derived tumor volume than did FDG PET volume alone.Conclusion: Using CT volume as a gold standard, the optimal PET-based estimate of total tumor burden in patients with metastatic renal cancer is the sum over all lesions of the total lesion glycolysis.

4.
Clin Positron Imaging ; 3(4): 131-136, 2000 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-11150744

RESUMO

Purpose: PET can be useful in determining the progression of malignant disease over time as well as the response to therapy. To achieve this, the physician must be able to unambiguously identify and characterize individual tumors among several different scans.Methods: We have developed a coordinate system for identifying individual tumor sites on PET scans, selecting the carina on the transmission scan as a point of origin. Using this system, each tumor is given a set of spherical coordinates that identifies its position: a rho (rho, displacement from carina), a theta (θ, angle between the A-P axis and the tumor), and a phi (φ, angle between the polar axis and the tumor). We tested this method on a patient with metastatic thyroid cancer, who underwent 18FDG and 124I-Iodide PET scans in the same week. This sytem was also used on a patient with metastatic prostate cancer, who had two FDG scans done 7 weeks apart. The patient underwent chemotherapy treatment during this period, and the scans were performed to assess therapy response.Results: The patient with thyroid cancer had a total of 90 tumors, 82 of them identified in the 18FDG scan and 35 in the 124I-Iodide scan, with 27 tumors identified in both. For rho, θ, and φ among the 27 matching pairs of tumors, the mean differences were 6.80 +/- 5 mm, 6.22 +/- 4.54 degrees, and 5.51 +/- 5.81 degrees, respectively. The disparity in coordinate values between corresponding tumors can be explained by the distinctive uptake patterns of the radiopharmaceuticals. The patient with prostate cancer had 9 tumors identifiable in both the pre- and post-therapy scans. The mean differences for rho, θ, and φ among the 9 pairs of tumors were 1.93 +/- 1.65 mm, 6.67 +/- 5.53 degrees, and 2.04 +/- 2.02 degrees, respectively. After thorough analysis, we have determined that corresponding tumors with rho < 15 mm, θ and φ < 15 degrees difference usually indicate a match.Conclusion: This coordinate system facilitates the identification and characterization of individual tumors among multiple scans, thus aiding in both the assessment of diagnostic capabilities of different tracers, and the tracking of tumors following therapy.

5.
Clin Positron Imaging ; 3(4): 162, 2000 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-11150765

RESUMO

Purpose: PET can be useful in determining the progression of malignant disease over time as well as the response to therapy. To achieve this, the physician must be able to unambiguously identify and characterize individual tumors among several different scans.Methods: We have developed a spherical coordinate system for identifying individual tumor sites on PET scans, using the carina on the transmission scan as a point of origin. Using this system, each tumor is given a set of spherical coordinates that identifies its position: a rho (rho, displacement from carina), a theta (θ, angle between the A-P axis and the tumor), and a phi (φ, angle between the cranial-caudal axis and the tumor).Results: We tested this method on a patient with metastatic thyroid cancer, who underwent 18FDG and 124I-Iodide PET scans in the same week. The patient had a total of 90 tumors, 82 of them identified in the 18FDG scan and 35 in the 124I-Iodide scan, with 27 tumors identified in both. For rho, θ, and φ among the 27 matching pairs of tumors, the mean differences were 6.80 + 5 mm, 6.22 + 4.54 degrees, and 5.51 + 5.81 degrees, respectively. After thorough analysis, we have determined that corresponding tumors with rho < 15 mm, θ and φ < 15 degrees difference usually indicate a match. The disparity in coordinate values between corresponding tumors can be explained by the distinctive uptake patterns of the radiopharmaceuticals.Conclusion: Within a mean difference of 6.8 mm and 6 degrees, this spherical coordinate system facilitates the identification and characterization of individual tumors among multiple scans, thus aiding in both the assessment of diagnostic capabilities of different tracers, and the tracking of tumors following therapy.

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