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OtherThis Month in JNM

This Month in JNM

Journal of Nuclear Medicine April 2010, 51 (4) 11A-12A;
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Of mice and humans: de Jong and Maina provide an overview of the positive aspects as well as the shortcomings of laboratory animals as translational models for human studies, with a focus on tumor scintigraphy and radionuclide therapy.
Page 501

Myocardial viability assessment: Allman offers perspective on the history and status of 18F-FDG PET viability imaging in directing management of patients with coronary artery disease and poor left ventricular function and previews a related study in this issue of JNM.
Page 505

Bowel prep and PET/CT: Soyka and colleagues investigate the usefulness of bowel preparation before 18F-FDG PET/CT imaging to reduce physiologic intestinal uptake.
Page 507

Figure

PET in schizophrenia: Patel and colleagues review the use of PET tracers and kinetic modeling in identifying regional brain abnormalities associated with cognitive functioning in schizophrenia, including challenges and future investigational directions in dopaminergic function.
Page 511

Figure

PET and breast cancer metastases: Doot and colleagues evaluate the accuracy of 18F-fluoride model parameter estimates for characterizing regional kinetics in metastases and normal bone in breast cancer patients, with implications for PET assessment of bone turnover during therapy.
Page 521

PET/CT and tumor cell proliferation: Yue and colleagues determine whether serial 18F-FLT uptake on PET/CT can monitor the biologic response of esophageal squamous cell carcinoma and normal tissues to radiotherapy.
Page 528

Dual-phase PET in lung adenocarcinoma: Houseni and colleagues investigate the prognostic value of glucose metabolism dynamics as assessed by dual-phase 18F-FDG PET in patients with adenocarcinoma of the lung.
Page 535

PET, breast cancer, and molecular markers: Osborne and colleagues explore the relationship between specific markers (estrogen and progesterone receptors and HER2 status) and tumor glucose use as measured by PET in patients with breast cancer.
Page 543

Figure

PET monitoring in sarcomas: Dimitrakopoulou-Strauss and colleagues evaluate the effect of early dynamic 18F-FDG PET imaging on management and outcomes in patients with soft-tissue sarcomas who received neoadjuvant chemotherapy.
Page 551

Figure

Quantifying P-gp function: Kreisl and colleagues look at the ability of 11C-dLop PET to quantify permeability-glycoprotein function at the blood–brain barrier in humans.
Page 559

Figure

PET in viability evaluation: Abraham and colleagues from the PET and Recovery Following Revascularization (PARR 2) study report on a subanalysis of PET cardiac management in a center with experience, ready access to 18F-FDG, and integration with clinical teams.
Page 567

Reducing artifacts in cardiac PET/CT: Lubberink and colleagues assess the accuracy of myocardial blood flow and coronary flow reserve measurement by 15O-water PET in the absence of attenuation correction.
Page 575

Figure

18F-DMFP PET and parkinsonian syndromes: la Fougère and colleagues describe the utility of the selective dopamine receptor ligand 18F-desmethoxyfallypride for differential PET diagnosis of patients with idiopathic and nonidiopathic parkinsonian syndromes.
Page 581

Figure

11C-raclopride PET and parkinsonism: Van Laere and colleagues explore potential improvements in 11C-raclopride PET differentiation between Parkinson disease and multiple-system atrophy with predominant parkinsonism through addition of dynamic scan analysis combining striatal dopamine-2 binding and regional tracer influx.
Page 588

Figure

Imaging approaches to Parkinson disease: Brooks provides an educational overview of the current roles of structural and functional imaging for diagnosing and managing different parkinsonian syndromes.
Page 596

Figure

Positron emitters and small-animal PET: Disselhorst and colleagues report on detailed image quality assessments for several positron emitters using national standards in a high-resolution small-animal PET lutetium-oxyorthosilicate scanner.
Page 610

Vitamin C and salivary 131I dosimetry: Liu and colleagues investigate the effect of vitamin C administered at various times on salivary absorbed dose of therapeutic radioiodine in patients with differentiated thyroid cancer.
Page 618

Antiangiogenic agents and RIT efficacy: Kraeber-Bodéré and colleagues evaluate the results of combining anti–carcinoembryonic antigen 131I-F6 monoclonal antibody radioimmunotherapy with thalidomide or a cyclopeptic vascular endothelial growth inhibitor in a mouse model of thyroid cancer.
Page 624

Figure

18F-FDG uptake in micrometastases: Li and colleagues examine 18F-FDG uptake in microscopic tumors grown intraperitoneally in mice and relate this to physiologic hypoxia and glucose transporter-1 expression.
Page 632

Figure

68Ga-siderophores for PET: Petrik and colleagues evaluate the potential of radiolabeled iron-complexing ferric ion siderophobes in PET diagnosis of invasive pulmonary aspergillosis.
Page 639

Gated PET of regional lung volume change: Wellman and colleagues present a method using respiratory-gated PET images of inhaled 13N-nitrogen to measure regional specific lung volume change, a key variable in lung mechanics and pathogenesis of ventilator-induced lung injury.
Page 646

Figure

3D-based patient-specific dosimetry: Amro and colleagues describe the development of a 3-dimensional imaging–based dosimetry methodology incorporating antitumor biologic effects with biologically effective dose and equivalent uniform dose and present an example in patients with non-Hodgkin lymphoma undergoing radioimmunotherapy.
Page 654

Figure

ON THE COVER

18F-FLT uptake can be used to monitor the biologic response of esophageal squamous cell carcinoma to radiotherapy and may have an advantage over 18F-FDG in differentiating inflammation from tumor. Increased uptake of 18F-FLT after treatment interruption, as occurred in the patient shown here, may reflect accelerated repopulation. After the interruption, tumoral uptake rose above baseline whereas uptake in irradiated bone marrow decreased.

See page 532.

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Journal of Nuclear Medicine: 51 (4)
Journal of Nuclear Medicine
Vol. 51, Issue 4
April 2010
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