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1.
Eur J Nucl Med Mol Imaging ; 43(13): 2401-2412, 2016 Dec.
Article in English | MEDLINE | ID: mdl-27596984

ABSTRACT

PURPOSE: The diagnosis of prosthetic valve (PV) infective endocarditis (IE) and infection of cardiac implantable electronic devices (CIEDs) remains challenging. The aim of this study was to assess the usefulness of 18F-FDG PET/CT in these patients and analyse the interpretation criteria. METHODS: We included 41 patients suspected of having IE by the Duke criteria who underwent 18F-FDG PET/CT. The criteria applied for classifying the findings as positive/negative for IE were: (a) visual analysis of only PET images with attenuation-correction (AC PET images); (b) visual analysis of both AC PET images and PET images without AC (NAC PET images); (c) qualitative analysis of NAC PET images; and (d) semiquantitative analysis of AC PET images. 18F-FDG PET/CT was considered positive for IE independently of the intensity and distribution of FDG uptake. The gold standard was the Duke pathological criteria (if tissue was available) or the decision of an endocarditis expert team after a minimum 4 months follow-up. RESULTS: We studied 62 areas with suspicion of IE, 28 areas (45 %) showing definite IE and 34 (55 %) showing possible IE. Visual analysis of only AC PET images showed poor diagnostic accuracy (sensitivity 20 %, specificity 57 %). Visual analysis of both AC PET and NAC PET images showed excellent sensitivity (100 %) and intermediate specificity (73 %), focal uptake being more frequently associated with IE. The accuracy of qualitative analysis of NAC PET images depended on the threshold: the maximum sensitivity, specificity and accuracy achieved were 88 %, 80 %, 84 %, respectively. In the semiquantitative analysis of AC PET images, SUVmax was higher in areas of confirmed IE than in those without IE (∆SUVmax 2.2, p < 0.001). When FDG uptake was twice that in the liver, IE was always confirmed, and SUVmax 5.5 was the optimal threshold for IE diagnosis using ROC curve analysis (area under the curve 0.71). CONCLUSION: The value of 18F-FDG PET/CT in the diagnosis of suspected IE of PVs and CIEDs is highly dependent on patient preparation and the method used for image interpretation. Based on our results, the best method is to consider a study positive for IE when FDG uptake is present in both AC PET and NAC PET images.


Subject(s)
Electrodes, Implanted/adverse effects , Endocarditis/diagnostic imaging , Fluorodeoxyglucose F18 , Heart Valve Prosthesis/adverse effects , Positron Emission Tomography Computed Tomography/methods , Prosthesis-Related Infections/diagnostic imaging , Adult , Aged , Aged, 80 and over , Diagnosis, Differential , Endocarditis/etiology , Female , Humans , Male , Middle Aged , Prosthesis-Related Infections/etiology , Radiopharmaceuticals , Reproducibility of Results , Sensitivity and Specificity , Young Adult
2.
Rev. esp. med. nucl. imagen mol. (Ed. impr.) ; 33(1): 14-21, ene.-feb. 2014.
Article in English | IBECS | ID: ibc-118726

ABSTRACT

Purpose. To prospectively study the value of PET-CT with fluorine-18 fluorodeoxyglucose (FDG) to predict neoadjuvant chemotherapy (NAC) response of locoregional disease of stages II and III breast cancer patients. Material and methods. A written informed consent and approval were obtained from the Ethics Committee. PET-CT accuracy in the prediction of pathologic complete response (pCR) after NAC was studied in primary tumors and lymph node metastasis in 43 women (mean age: 50 years: range: 27-71 years) with histologically proven breast cancer between December 2009 and January 2011. PET-CT was performed at baseline and after NAC. SUVmax percentage changes (ΔSUVmax) were compared with pathology findings at surgery. Receiver-operator characteristic (ROC) analysis was used to discriminate between locoregional pCR and non-pCR. In patients not achieving pCR, it was investigated if ΔSUVmax could accurately identify the residual cancer burden (RCB) classes: RCB-I (minimal residual disease (MRD)), RCB-II (moderate RD), and RCB-III (extensive RD). Results. pCR was obtained in 11 patients (25.6%). Residual disease was found in 32 patients (74.4%): 16 (37.2%) RCB-I, 15 (35.6%) RCB-II and 2 (4.7%) RCB-III. Sensitivity, specificity, and accuracy to predict pCR were 90.9%, 90.6%, and 90.7%, respectively. Specificity was 94.1% in the identification of a subset of patients who had either pCR or MRD. Conclusion. Accuracy of ΔSUVmax in the locoregional disease of stages II and III breast cancer patients after NAC is high for the identification of pCR cases. Its specificity is potentially sufficient to identify a subgroup of patients who could be managed with conservative surgery (AU)


Objetivo. Estudiar de forma prospectiva el valor de la PET-TC con fluor-18-desoxiglucosa (FDG) para predecir la respuesta a la quimioterapia neoadyuvante (NAC) de la enfermedad locoregional en pacientes con cáncer de mama en estadios II y III.Material y métodos. Se obtuvo un consentimiento informado por escrito y la aprobación del Comité Ético. Se estudió la precisión de la PET-TC para predecir la respuesta completa patológica (pCR) tras la NAC en los tumores y en los ganglios de 43 mujeres (edad media: 50 años; rango: 27-71 años) que presentaban cáncer de mama diagnosticado por histología entre diciembre del 2009 y Enero del 2011. Los estudios PET-TC se realizaron al diagnóstico y tras la NAC. Los cambios en el porcentaje del SUVmax (delta-SUVmax) se compararon con los hallazgos de la anatomía patológica de la pieza quirúrgica. Se realizaron análisis de Característica Operativa del Receptor (ROC) para discriminar entre pCR y no-pCR en la enfermedad locoregional. En las pacientes que no alcanzaron la pCR, se investigó si el delta-SUVmax podía identificar de forma precisa las siguientes categorías de carga tumoral residual: RCB-I (enfermedad mínima residual (MRD)), RCB-II (moderada RD), y RCB-III (extensa RD).Resultados. Se obtuvo pCR en 11 pacientes (25,6%). Se encontró enfermedad residual en 32 pacientes (74,4%): 16 (37,2%) RCB-I, 15 (35,6%) RCB-II y 2 (4,7%) RCB-III. La sensibilidad, especificidad y precisión para predecir la pCR fueron 90,9%, 90,6%, y 90,7%, respectivamente. En la identificación del subgrupo de pacientes con pCR o MRD la especificidad fue del 94,1%.Conclusión. El delta-SUVmax identifica con elevada precisión la pCR en la enfermedad locoregional de las pacientes con cáncer de mama en estadios II y III tras la NAC. La especificidad es potencialmente suficiente para identificar un subgrupo de pacientes que podrían ser candidatas a cirugía conservadora (AU)


Subject(s)
Humans , Female , Adult , Middle Aged , Positron Emission Tomography Computed Tomography/instrumentation , Positron Emission Tomography Computed Tomography/methods , Positron Emission Tomography Computed Tomography , Breast Neoplasms/diagnosis , Positron Emission Tomography Computed Tomography/trends , Neoadjuvant Therapy/methods , Neoadjuvant Therapy/trends , Neoadjuvant Therapy , Breast Neoplasms , Neoplasm Staging/methods , Neoplasm Staging , Sensitivity and Specificity , Nuclear Medicine/methods
3.
Rev Esp Med Nucl Imagen Mol ; 33(1): 14-21, 2014.
Article in English | MEDLINE | ID: mdl-23809513

ABSTRACT

PURPOSE: To prospectively study the value of PET-CT with fluorine-18 fluorodeoxyglucose (FDG) to predict neoadjuvant chemotherapy (NAC) response of locoregional disease of stages II and III breast cancer patients. MATERIAL AND METHODS: A written informed consent and approval were obtained from the Ethics Committee. PET-CT accuracy in the prediction of pathologic complete response (pCR) after NAC was studied in primary tumors and lymph node metastasis in 43 women (mean age: 50 years: range: 27-71 years) with histologically proven breast cancer between December 2009 and January 2011. PET-CT was performed at baseline and after NAC. SUV(max) percentage changes (ΔSUV(max)) were compared with pathology findings at surgery. Receiver-operator characteristic (ROC) analysis was used to discriminate between locoregional pCR and non-pCR. In patients not achieving pCR, it was investigated if ΔSUV(max) could accurately identify the residual cancer burden (RCB) classes: RCB-I (minimal residual disease (MRD)), RCB-II (moderate RD), and RCB-III (extensive RD). RESULTS: pCR was obtained in 11 patients (25.6%). Residual disease was found in 32 patients (74.4%): 16 (37.2%) RCB-I, 15 (35.6%) RCB-II and 2 (4.7%) RCB-III. Sensitivity, specificity, and accuracy to predict pCR were 90.9%, 90.6%, and 90.7%, respectively. Specificity was 94.1% in the identification of a subset of patients who had either pCR or MRD. CONCLUSION: Accuracy of ΔSUV(max) in the locoregional disease of stages II and III breast cancer patients after NAC is high for the identification of pCR cases. Its specificity is potentially sufficient to identify a subgroup of patients who could be managed with conservative surgery.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Breast Neoplasms/diagnostic imaging , Carcinoma, Ductal, Breast/diagnostic imaging , Positron-Emission Tomography/methods , Taxoids/administration & dosage , Tomography, X-Ray Computed/methods , Adult , Aged , Antibodies, Monoclonal, Humanized/administration & dosage , Breast Neoplasms/therapy , Carcinoma, Ductal, Breast/secondary , Carcinoma, Ductal, Breast/therapy , Carcinoma, Lobular/diagnostic imaging , Carcinoma, Lobular/secondary , Carcinoma, Lobular/therapy , Combined Modality Therapy , Docetaxel , Female , Fluorodeoxyglucose F18 , Humans , Lymphatic Metastasis/diagnostic imaging , Mastectomy , Middle Aged , Multimodal Imaging , Neoplasm Staging , Neoplasm, Residual , Prospective Studies , ROC Curve , Radiopharmaceuticals , Sensitivity and Specificity , Trastuzumab , Tumor Burden
4.
Eur J Nucl Med Mol Imaging ; 37(2): 284-300, 2010 Feb.
Article in English | MEDLINE | ID: mdl-19727717

ABSTRACT

INTRODUCTION: The aim of this study was to perform a systematic review of the literature to evaluate the accuracy of FDG-PET in staging and restaging of cutaneous melanoma. METHODS: Systematic methods were used to identify, select, and evaluate the methodologic quality of the studies as well as to summarize the overall findings of sensitivity and specificity. The search strategy consisted of identifying studies published between 2000 and 2006. Inclusion criteria were studies that evaluated the diagnostic performance of FDG-PET in staging/restaging of cutaneous melanoma. The results were compared and pooled with a meta-analysis published previously that included studies published until 1999. The meta-analysis included 95% confidence intervals (CI) of sensitivity, specificity, likelihood-ratio (LR), and diagnostic-odds-ratio (DOR). RESULTS: The quantitative meta-analysis included 24 studies that were analysed in two groups: eight studies were included only in the regional staging analysis (group I), 13 studies were included only in the detection of distant metastases analysis (group II), and three studies were included in both analyses. Compliance with the methodologic-quality criteria was acceptable. We analysed the results of data presented in patients, lesions, basins, lymph-nodes, areas, and scans. Regarding the performance of FDG-PET in the detection of metastases, the pooled studies presented homogeneity for the negative-LR (0.15; 95% CI, 0.10-0.22) when analyzing lesions. When analyzing scans, there was global homogeneity for specificity (0.86; 95% CI, 0.77-0.92), positive-LR (5.86; 95% CI, 3.64-9.43), and DOR (37.89; 95% CI, 15.80-90.86). The pooled studies presented heterogeneity for the other items analysed. Regarding the detection of regional metastases, when analyzing lymph-nodes there was global homogeneity for specificity (0.99; 95% CI, 0.97-0.99; P = 0.101). The meta-regression evidenced that the variable that most influenced the DOR of the different studies and that can explain the heterogeneity was the year of publication; this may be related to the evolution of PET technology and an improvement of sensitivity/specificity. CONCLUSION: FDG-PET is not useful in the evaluation of regional metastases, as it does not detect microscopic disease. However, FDG-PET could be useful in the detection of distant metastases, and could suggest its utility in the management of patients with cutaneous melanoma.


Subject(s)
Fluorodeoxyglucose F18 , Melanoma/diagnostic imaging , Melanoma/epidemiology , Positron-Emission Tomography/statistics & numerical data , Skin Neoplasms/diagnostic imaging , Skin Neoplasms/epidemiology , Humans , Incidence , Radiopharmaceuticals , Reproducibility of Results , Sensitivity and Specificity
5.
Actas Urol Esp ; 33(1): 11-23, 2009 Jan.
Article in Spanish | MEDLINE | ID: mdl-19462720

ABSTRACT

PET has demonstrated its utility in management decisions in several types of tumors. In urologic tract tumors and prostate cancer its diagnostic performance has been lower due to the urinary excretion of the radiotracer, which can mask the presence of lesions. However, specific protocols must be applied that improve the diagnostic performance of PET with 18F-FDG in the evaluation of pelvic lesions. Furthermore, prostate cancer is a low-grade tumor with low avidity for 18F-FDG. In spite of these limitations, with PET new and interesting possibilities have been presented. The availability of PET-CT systems has improved its diagnostic performance. On the other hand, the development of new radiotracers that allow targeting other molecular processes and that are metabolized by pathways different to the urinary tract signifies an important advantage compared to 18F-FDG and has evidenced interesting results.


Subject(s)
Carcinoma, Renal Cell/diagnosis , Kidney Neoplasms/diagnosis , Neoplasm Recurrence, Local/diagnosis , Positron-Emission Tomography , Prostatic Neoplasms/diagnosis , Tomography, X-Ray Computed , Urinary Bladder Neoplasms/diagnosis , Humans , Male
6.
Actas urol. esp ; 33(1): 11-23, ene. 2009.
Article in Spanish | IBECS | ID: ibc-115011

ABSTRACT

La PET ha demostrado su utilidad en la toma de decisiones diagnóstico-terapéuticas en diversos tipos de tumores. En los tumores del tracto urinario y del cáncer de próstata su rendimiento diagnóstico ha sido menor debido a la eliminación urinaria del radiotrazador que puede enmascarar la presencia de lesiones. No obstante, deben aplicarse protocolos específicos que mejoran el rendimiento diagnóstico de la PET con 18F-FDG en la valoración de lesiones pélvicas. Además, el cáncer de próstata es un tumor de bajo grado con escasa avidez por la 18F-FDG. A pesar de estas limitaciones, con la PET se han planteado nuevas e interesantes posibilidades diagnósticas. La disponibilidad de equipos PET-TAC ha mejorado su rendimiento diagnóstico. Por otra parte, el desarrollo de nuevos radiotrazadores que permiten marcar otros procesos moleculares y que son metabolizados por vías diferentes de la urinaria, supone una ventaja importante respecto a la 18F-FDGy han proporcionado resultados interesantes (AU)


PET has demonstrated its utility in management decisions in several types of tumors. In urologic tract tumors and prostate cancer its diagnostic performance has been lower due to the urinary excretion of the radiotracer, which can mask the presence of lesions. However, specific protocols must be applied that improve the diagnostic performance of PET with 18FFDGin the evaluation of pelvic lesions. Furthermore, prostate cancer is a low-grade tumor with low avidity for 18F-FDG. Inspite of these limitations, with PET new and interesting possibilities have been presented. The availability of PET-CT systems has improved its diagnostic performance. On the other hand, the development of new radiotracers that allow targeting other molecular processes and that are metabolized by pathways different to the urinary tract signifies an important advantage compared to 18F-FDG and has evidenced interesting results (AU)


Subject(s)
Humans , Male , Middle Aged , Aged, 80 and over , Positron-Emission Tomography/instrumentation , Positron-Emission Tomography/methods , Positron-Emission Tomography , Positron Emission Tomography Computed Tomography/methods , Prostatic Neoplasms , Urologic Neoplasms , Prostate/pathology , Prostate , Urinary Tract/pathology , Urinary Tract , Kidney/pathology , Kidney , Carcinoma , Urinary Bladder Neoplasms
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