Focus on PET nanoparticles: Welch and colleagues highlight current approaches to and future challenges in the design of nanomaterials with optimized composition for tissue-selective PET imaging.
Page 1743
Quantitative studies of bone: Blake and colleagues provide perspective on current biochemical, radiographic, and radionuclide techniques for assessment of bone remodeling and preview a related article in this issue of JNM.
Page 1747
PET/CT in obstructive Crohn disease: Jacene and colleagues explore the accuracy of PET/CT in identifying active inflammation in patients with Crohn disease before surgical resection for obstructive symptoms and discuss implications for improved management.
Page 1751
SUV and CT measurement reproducibility: Jacene and colleagues estimate and compare across different readers and institutions the reproducibility of 18F-FDG PET standardized uptake values and CT size measurements in malignant tumors before and during therapy.
Page 1760
18F-FMT and lung cancer outcomes: Kaira and colleagues report on the prognostic abilities of this amino-acid tracer in PET assessment of primary tumors in patients with non–small cell lung cancer.
Page 1770
Monitoring liver metastasis response: Vriens and colleagues use dynamic contrast-enhanced MRI and 18F-FDG PET to examine the relationship between functional tumor vasculature and tumor metabolism during chemotherapy in patients with colorectal liver metastases.
Page 1777
99mTc-MIBI and MRP1 in thyroid lesions: Saggiorato and colleagues investigate the usefulness of visual and semiquantitative analyses of 99mTc-MIBI scintigraphy for preoperative characterization of thyroid nodules with indeterminate cytologic diagnoses and explore the associated relevance of P-glycoprotein/multidrug resistance–associated protein-1 expression.
Page 1785
18F-FCWAY PET in epilepsy: Giovacchini and colleagues report on the use of cerebral white matter as a reference region in 18F-FCWAY PET detection of differences in 5-HT1A binding in patients with temporal lobe epilepsy and healthy controls.
Page 1794
PET, neuroinflammation, and schizophrenia: Doorduin and colleagues use 11C-(R)-PK11195 PET to investigate the role of focal neuroinflammation during psychotic phases in patients with schizophrenia.
Page 1801
18F-fluoride PET in osteoporosis: Uchida and colleagues examine changes in regional bone remodeling and turnover measured by 18F-fluoride PET, the relationship between these measured changes and conventional bone metabolism parameters, and the effects of biphosphonate treatment.
Page 1808
PET and everolimus treatment: Nogová and colleagues assess the utility of 18F-FDG PET measurement of glucose metabolism inhibition as a pharmacodynamic marker in patients with everolimus-treated non–small cell lung cancer.
Page 1815
18F-FDG uptake molecular correlates: Jadvar and colleagues provide an educational overview of current data on correlations between underlying molecular biology and clinical observations of tumor 18F-FDG accumulation in human lung, breast, and colon cancers.
Page 1820
89Zr-cmAb U36 immuno-PET: Börjesson and colleagues present first-in-human assessments of safety, biodistribution, radiation dose, and quantification of this 89Zr-labeled chimeric monoclonal antibody in patients with head and neck squamous cell carcinoma.
Page 1828
90Y-ibritumomab dosimetry: Bischof Delaloye and colleagues document the radiation exposure associated with 90Y-ibritumomab tiuxetan when used as consolidation therapy in adults with low or minimal tumor burden after first-line therapy of advanced follicular lymphoma.
Page 1837
Real-time 3D-RD treatment planning: Hobbs and colleagues describe patient-specific 3D Monte Carlo–based dosimetry, with 124I PET for pharmacokinetics, for 131I treatment planning in a child with differentiated papillary thyroid cancer, lung involvement, and cerebral metastases.
Page 1844
PET and trastuzumab response: McLarty and colleagues report on a mouse study designed to determine whether changes in 18F-FDG uptake on PET can be associated with responses to trastuzumab treatment in breast cancer.
Page 1848
Dual-tracer PET in colorectal cancer: Hui and colleagues investigate whether 18F-FDG and 18F-FLT can be used complementarily in PET monitoring of the biologic characteristics of colorectal cancer and prediction of outcomes.
Page 1857
18F metallopeptides for melanoma imaging: Ren and colleagues assess the utility of an 18F-labeled probe for PET imaging of melanocortin type 1 receptor–positive malignant melanoma.
Page 1865
Imaging of osteolytic bone metastases: Wadas and colleagues describe the evaluation of a 64Cu-labeled agent for imaging osteolytic bone metastases and associated inflammation by targeting the αvβ3 integrin on osteoclasts and proinflammatory cells involved at the bone metastatic site.
Page 1873
Cell survival imaging after pretreatment: Higuchi and colleagues determine whether reporter gene PET can be used to detect the effects of atorvastatin and vascular endothelial growth factor on survival of endothelial progenitor cells after transplantation in the rat heart.
Page 1881
18F-AV-45 and Aβ plaques: Choi and colleagues describe small-animal studies of the properties of this agent for PET imaging of β-amyloid as a biomarker of pathogenesis processes in Alzheimer disease.
Page 1887
A new ribonucleoside radiotracer: Zlatopolskiy and colleagues report on the synthesis and preclinical evaluation of IV-14, a 131I-labeled ribonucleoside radiotracer, as a uridine-cytidine kinase–specific marker for tumor visualization.
Page 1895
PET and neurogenic inflammation: Cui and colleagues describe a PET technique using 11C-PK11195, a PET ligand for peripheral type–benzodiazepine receptors, to evaluate microglial activation in rat brain in an experimental model of migraine.
Page 1904
ON THE COVER
A study was undertaken of the in vivo relationship between functional tumor vasculature, determined by dynamic contrast-enhanced MRI, and tumor metabolism, determined by dynamic 18F-FDG PET, during cytotoxic treatment of patients with colorectal liver metastases. Cytotoxic chemotherapy was found not to alter the properties of tumor vasculature but to decrease glucose consumption by tumor cells.
See page 1780.