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1.
Nucl Med Commun ; 23(9): 857-64, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12195090

ABSTRACT

The presence of distant metastases is the main prognostic factor in patients with breast cancer and has a significant influence in the choice of therapy. Therefore, chest X-ray, bone scintigraphy and ultrasound of the abdomen are performed to detect distant metastases at diagnosis and follow-up. Fluorodeoxyglucose positron emission tomography (FDG PET) has been shown to provide sensitive detection of primary tumour and metastases for many tumour entities, but little information is available about the diagnostic value for breast cancer patients. This study retrospectively compared FDG PET for detection of metastatic disease with chest X-ray, bone scintigraphy and ultrasound of the abdomen, referred to as "conventional diagnostic procedures" (CDPs), in 50 breast cancer patients. Imaging procedures were analysed in a blinded fashion with the results classified as "no evidence of metastases", "equivocal" and "evidence of metastases". Clinical follow-up and the results of other imaging modalities including computed tomography and magnetic resonance imaging were used to determine if metastases were present. FDG PET identified metastatic disease with a sensitivity and specificity of 86% and 90% as compared to 36% and 95% for CDPs, respectively. Regarding "equivocal" and "evidence of metastases" as positive, the sensitivity of CDPs increased to 57% with a corresponding specificity of 81%, whereas sensitivity and specificity of FDG PET remained unchanged. Regarding different localities of metastases the sensitivity of FDG PET was superior in the detection of pulmonary metastases and especially of lymph node metastases of the mediastinum in comparison to chest X-ray, whereas the sensitivity of FDG PET in the detection of bone and liver metastases was of the same magnitude as compared with bone scintigraphy and ultrasound of the abdomen.


Subject(s)
Breast Neoplasms/diagnosis , Carcinoma, Ductal, Breast/diagnosis , Carcinoma, Ductal, Breast/secondary , Carcinoma, Lobular/diagnosis , Carcinoma, Lobular/secondary , Diagnostic Imaging/methods , Tomography, Emission-Computed , Adult , Aged , Aged, 80 and over , False Negative Reactions , False Positive Reactions , Female , Fluorodeoxyglucose F18 , Humans , Lymphatic Metastasis , Middle Aged , Radiopharmaceuticals , Retrospective Studies , Sensitivity and Specificity , Single-Blind Method
2.
Strahlenther Onkol ; 175 Suppl 4: 6-12, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10584133

ABSTRACT

BACKGROUND AND PURPOSE: Parenchymal impairment of salivary glands following high-dose radioiodine treatment is a well-known side effect in general caused by free radicals. Therefore, the radioprotective effect of the radical scavenger amifostine was evaluated prospectively in patients receiving high-dose radioiodine treatment. PATIENTS AND METHODS: Parenchymal function was assessed by quantitative salivary gland scintigraphy performed in 50 patients with differentiated thyroid cancer prior to and 3 months after high-dose radioiodine treatment with either 3 GBq 131I (n = 21) or 6 GBq 131I (n = 29) in a double-blinded, placebo-controlled study. Twenty-five patients treated with 500 mg/m2 amifostine intravenously prior to high-dose radioiodine treatment were compared to 25 control patients receiving physiological saline solution. Xerostomia was graded according to WHO-criteria. RESULTS: In 25 control patients high-dose radioiodine treatment significantly (p < 0.001) reduced parenchymal function of parotid and submandibular glands by 40.2 +/- 14.1% and 39.9 +/- 15.3%, respectively. Nine out of these 25 patients developed Grade I and 2 Grade II xerostomia. In contrast, in 25 amifostine-treated patients there was no significant (p = 0.691) decrease in parenchymal function following high-dose radioiodine treatment, and xerostomia did not occur in any of them. CONCLUSION: Parenchymal damage of salivary glands induced by high-dose radioiodine treatment can be significantly reduced by amifostine which may improve quality of life of patients with differentiated thyroid cancer.


Subject(s)
Adenocarcinoma, Follicular/radiotherapy , Amifostine/pharmacology , Carcinoma, Papillary/radiotherapy , Iodine Radioisotopes/therapeutic use , Radiation-Protective Agents/pharmacology , Salivary Glands/drug effects , Salivary Glands/radiation effects , Thyroid Neoplasms/radiotherapy , Adult , Aged , Aged, 80 and over , Double-Blind Method , Female , Humans , Iodine Radioisotopes/adverse effects , Male , Middle Aged , Parotid Gland/drug effects , Parotid Gland/radiation effects , Placebos , Prospective Studies , Radionuclide Imaging , Radiotherapy Dosage , Salivary Glands/diagnostic imaging , Submandibular Gland/drug effects , Submandibular Gland/radiation effects , Time Factors , Xerostomia/etiology , Xerostomia/prevention & control
3.
Rofo ; 171(1): 49-53, 1999 Jul.
Article in German | MEDLINE | ID: mdl-10464505

ABSTRACT

PURPOSE: Search for focus in patients with fever of unknown origin (FUO). MATERIAL AND METHODS: In four patients with the above mentioned problem, F-18-FDG-PET was performed, following the common imaging methods, which were without evidence for a focus. RESULTS: The origin of FUO was verified in all patients by PET: Tuberculosis, pneumocystis-carinii pneumonia, chronic inflammatory hematoma, aortitis. CONCLUSION: Successful implementation of F-18-FDG-PET as additional imaging method in patients with FUO seems reasonable. This has to be verified by further prospective studies.


Subject(s)
Fever of Unknown Origin/diagnostic imaging , Fluorodeoxyglucose F18 , Radiopharmaceuticals , Tomography, Emission-Computed/methods , Adolescent , Adult , Diagnosis, Differential , Female , Fever of Unknown Origin/etiology , Humans , Male , Middle Aged , Tomography, Emission-Computed/instrumentation , Whole-Body Counting/instrumentation , Whole-Body Counting/methods
4.
J Nucl Med Technol ; 27(1): 20-6, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10322570

ABSTRACT

OBJECTIVE: Uptake of 99mTc-pertechnetate in salivary glands reflects intact salivary gland parenchyma. However, no standardized protocol for an accurate quantification of parenchymal function has been established so far. METHODS: In this paper we report on a validated acquisition protocol supplying a normal database for standardized quantitative salivary gland scintigraphy. RESULTS: The major advantage of salivary gland scintigraphy, as compared to other imaging modalities, is that both parenchymal function and excretion fraction of all four major salivary glands (i.e., parotid and submandibular glands) can be simultaneously quantified with a single intravenous injection. CONCLUSION: Quantitative salivary gland scintigraphy is demonstrated to be a suitable imaging modality for research applications in evaluating the effects of radioprotective drugs on salivary glands. Salivary gland scintigraphy is easy to perform, reproducible and well-tolerated by the patient.


Subject(s)
Salivary Gland Diseases/diagnostic imaging , Salivary Glands/diagnostic imaging , Adolescent , Adult , Aged , Aged, 80 and over , Animals , Databases, Factual , Female , Humans , Male , Middle Aged , Rabbits , Radiation Injuries , Radionuclide Imaging/methods , Radiopharmaceuticals , Salivary Gland Calculi/diagnostic imaging , Sjogren's Syndrome/diagnostic imaging , Sodium Pertechnetate Tc 99m , Tomography, Emission-Computed, Single-Photon , Xerostomia/diagnostic imaging
5.
Nuklearmedizin ; 38(2): 56-60, 1999.
Article in German | MEDLINE | ID: mdl-10100232

ABSTRACT

AIM: Lesion detection and localization of 2-[18F]fluoro-2-deoxy-D-glucose (F-18-FDG) Onco-PET-Investigations are usually performed on-line at the computer display. The aim of the present study was to evaluate the clinical efficacy of a standardized film documentation as an alternative approach. METHODS: 100 Onco-PET-investigations without attenuation correction were analyzed with regard to number and localization of lesions suspicious of malignancy. A standardized documentation on film was developed including 1. transversal slices of the brain, 2. coronal slices and maximum-intensity-projections (MIPs) of the head/neck region and 3. of the trunk and 4. MIPs of the legs. These transparencies were analyzed at the light box. An additional analysis on the computer display was performed slice by slice in coronal, transversal and sagittal directions for the whole body. RESULTS: A total of 315 lesions were detected in 100 patients. In 96/100 patients the two modalities agreed both in number and localization of tumor-suspicious lesions. 7 lesions in the legs of 3 patients didn't show when interpreting the films (MIPs only). In 2/100 patients additional analysis on the computer display caused a change in the localization of 9/315 lesions. 8 of these were located in the legs. When adding coronal slices for the documentation of the lower extremities all the lesions were shown. Moreover, all lesions were localized correctly except one clinically non-relevant change of localization out of a total of 322 lesions. CONCLUSION: The newly developed standardized documentation supports the concept of film reading and reporting of onco-PET investigations, restricting an additional on-line analysis to rare cases only. Furthermore, the intention of the "Arbeitsgemeinschaft Standardisierung" (work group standardisation) are met, i.e. to ease analysis of follow-up studies acquired at different places.


Subject(s)
Fluorodeoxyglucose F18 , Image Processing, Computer-Assisted/methods , Neoplasms/diagnostic imaging , Radiopharmaceuticals , Tomography, Emission-Computed , Documentation/methods , Female , Humans , Lymphoma/diagnostic imaging , Online Systems
6.
Strahlenther Onkol ; 175(2): 57-61, 1999 Feb.
Article in English | MEDLINE | ID: mdl-10065139

ABSTRACT

BACKGROUND: Salivary gland impairment following high-dose radioiodine treatment is a well-recognized side effect, in general caused by free radicals. Therefore, it seemed promising to evaluate the radioprotective effect of the radical scavenger amifostine in patients receiving high-dose radioiodine therapy. PATIENTS AND METHOD: Quantitative salivary gland scintigraphy using 100 to 120 MBq Tc-99m-pertechnetate was performed in 17 patients with differentiated thyroid cancer prior to and 3 months after radioiodine treatment with 6 GBq I-131. Eight patients were treated with 500 mg/m2 amifostine prior to high-dose radioiodine treatment and compared retrospectively with 9 control patients. Xerostomia was graded according to WHO criteria. RESULTS: In 9 control patients high-dose radioiodine treatment significantly (p < 0.01) reduced Tc-99m-pertechnetate uptake by 35.4 +/- 22.0% and 31.7 +/- 21.1% in parotid and submandibular glands, respectively. Of these 9 patients, 3 exhibited xerostomia Grade I (WHO). In contrast, in 8 amifostine-treated patients, there was no significant (p = 0.878) decrease in parenchymal function following high-dose radioiodine treatment, and xerostomia did not occur in any of them. CONCLUSION: Parenchymal damage in salivary glands induced by high-dose radioiodine treatment can be reduced significantly by amifostine. This may help to increase patients' quality of life in differentiated thyroid cancer.


Subject(s)
Amifostine/therapeutic use , Carcinoma, Papillary/radiotherapy , Iodine Radioisotopes/administration & dosage , Radiation-Protective Agents/therapeutic use , Salivary Glands/drug effects , Thyroid Neoplasms/radiotherapy , Adult , Aged , Carcinoma, Papillary/complications , Carcinoma, Papillary/diagnostic imaging , Drug Evaluation , Female , Humans , Iodine Radioisotopes/adverse effects , Male , Middle Aged , Radionuclide Imaging , Radiopharmaceuticals , Retrospective Studies , Salivary Glands/diagnostic imaging , Salivary Glands/radiation effects , Sodium Pertechnetate Tc 99m , Thyroid Neoplasms/complications , Thyroid Neoplasms/diagnostic imaging , Time Factors , Xerostomia/etiology , Xerostomia/prevention & control
7.
J Nucl Med ; 40(12): 2021-4, 1999 Dec.
Article in English | MEDLINE | ID: mdl-10616880

ABSTRACT

UNLABELLED: The aim of this study was to compare the visual analysis of attenuation-corrected and noncorrected 18F-fluoro-2-deoxy-D-glucose (FDG) PET images in patients with primary or metastatic breast cancer using standardized film documentation and to evaluate the influence of attenuation correction on lesion detectability. METHODS: Standard FDG PET of the breasts and of the axillary regions was performed on 28 women with breast cancer. Transmission scans were acquired for attenuation correction after administration of FDG. Transverse and coronal slices and maximum intensity projections both with and without attenuation correction were documented in a standardized manner on film. Noncorrected images were displayed with an upper threshold of five times the mean activity in normal lung tissue. Attenuation-corrected images were documented with an upper threshold of a standardized uptake value of five. Two independent nuclear medicine physicians, who were unaware of the results of clinical investigation, other imaging modalities and histopathologic findings, interpreted the images visually, noncorrected images first. RESULTS: One hundred eighty-four of 189 lesions in 28 of 28 patients were found on attenuation-corrected and noncorrected images. Seventeen lesions were found in the breasts of 12 patients. In 18 patients, 31 axillary lesions were found. Moreover, 141 lesions representing distant metastases were detected in 18 patients. Attenuation-corrected images showed the same lesions in all patients but 2, in whom 5 of 189 small pulmonary lesions (2.6%) were not detected. Iterative reconstruction did not improve detectability of these lesions on attenuation-corrected images. These lesions were confirmed by CT, which revealed diameters of <1 cm. CONCLUSION: Attenuation correction by transmission measurement after injection may impair lesion detectability in PET for staging of breast cancer patients. When using the image modalities described, noncorrected PET images should be considered in image analysis.


Subject(s)
Breast Neoplasms/diagnostic imaging , Fluorodeoxyglucose F18 , Image Processing, Computer-Assisted , Radiopharmaceuticals , Tomography, Emission-Computed , Axilla/diagnostic imaging , Breast Neoplasms/pathology , Female , Humans , Lung Neoplasms/diagnostic imaging , Lung Neoplasms/secondary , Lymphatic Metastasis , Sensitivity and Specificity
8.
Dtsch Med Wochenschr ; 110(5): 163-7, 1985 Feb 01.
Article in German | MEDLINE | ID: mdl-3967602

ABSTRACT

Continuous ambulatory peritoneal dialysis (CAPD) is, next to conventional home dialysis, a world-wide method of treating chronic renal failure. This is the report of clinical experience of 34 CAPD patients who, from October 1978 to the end of 1983, had undergone 642 treatment months. The incidence of peritonitis after introduction of a new connector system in 1983 was reduced to 1 per 46 CAPD treatment months. In only 7 patients was it necessary to discontinue CAPD for reasons connected with the type of dialysis. No patient requested discontinuance of CAPD. Suitable bag and tube materials, adequate space, and well trained personnel are decisive for a successful CAPD programme, in addition to careful selection of patients. The latter aims at optimal patient motivation for the treatment method which, in principle, is more cost effective than home dialysis. In so far as patients fulfil the requirements for home dialysis they can be excellently rehabilitated.


Subject(s)
Peritoneal Dialysis, Continuous Ambulatory/psychology , Peritoneal Dialysis/psychology , Adolescent , Adult , Aged , Child , Diabetes Complications , Female , Humans , Male , Middle Aged , Patient Dropouts , Patient Education as Topic , Peritoneal Dialysis, Continuous Ambulatory/adverse effects , Peritonitis/etiology , Time Factors , Uremia/therapy
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