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Conventional and novel PET tracers for imaging in oncology in the era of molecular therapy
Authors:Pantaleo M A  Nannini M  Maleddu A  Fanti S  Ambrosini V  Nanni C  Boschi S  Biasco G
Affiliation:Institute of Hematology and Medical Oncology L. & A. Seragnoli, Sant'Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy. pantaleo@med.unibo.it
Abstract:In the last ten years, the development of several novel targeted drugs and the refinement of state of the art technologies such as the genomics and proteomics and their introduction to clinical practice have revolutionized the management of patients affected by cancer. However, everyday practice points out several clinical questions: the difficulty of response assessment to new drugs especially using standard RECIST criteria that do not provide information on biological, vascular or metabolic variations; the inadequate selection of patients who are likely to benefit from a targeted therapy excluding those with breast cancer and gastrointestinal stromal tumours; the need to know the global biological background of diseases especially in metastatic setting using repeatable non-invasive procedures. Molecular imaging could provide information on in vivo distribution of biological markers in response to targeted therapy and could improve the selection of patients before therapies. The aim of this review is to analyze the current role of conventional and innovative positron emission tomography (PET) radiotracers in clinical practice and to explore the promising perspectives of molecular imaging in cancer research.
Keywords:17AAG, 17-(Allylamino)-17-demethoxygeldanamycin   ARs, androgen receptors   ASCO, Annual Meeting of Clinical Oncology   11C-acetate, 11Carbon acetate   11C-choline, 11Carbon choline   CEUS, contrast-enhanced ultrasound   11C-methionine, 11Carbon methionine   CT, computed tomography   DNA, deoxyribonucleic acid   DOTATOC, [1,4,7,10-tetraazacy-clododecane-N,NN″,N?-tetraacetic-acid-d-Phe1-Tyr3]-octreotide   DSS, disease-specific survival   DTPA, diethylene triamine pentaacetate   EGFr, epidermal growth factor receptor   FDG, fluorodeoxyglucose   18F-FDG, 18fluorine-fluorodeoxyglucose   18F-FHBG, (9-[4-18F-fluoro-3-(hydroxymethyl)butyl]guanine)   18F-FLT, 18fluorine-3-fluoro-3-deoxy-thymidine   FDHT, 16β-fluoro-5α-dyhidrotestosterone   18F–fluoride, 18fluorine–fluoride   18F-fluoro-l-DOPA, 18F-fluoro-l-dihydroxyphenylalanine   FLT, fluoro-3-deoxy-thymidine   18F-PCV, 18fluorine fluoropenciclovir PCV   68Ga-DOTANOC, 68 gallium tetraazacyclododecanetetraacetic acid-[1-Nal3]-octreotide   68Ga-DOTATOC, 68gallium [1,4,7,10-tetraazacy-clododecane-N,NN″,N?-tetraacetic-acid-d-Phe1-Tyr3]-octreotide   68Ga, gallium68   GEP, gastro-enteropancreatic tumours   GIST, gastrointestinal stromal tumours   HCC, hepatocellular carcinoma   HNSCC, head and neck squamous cell carcinoma   IHC, immunohistochemistry   111In, indium 111   111In DOTANOC, 111indium tetraazacyclododecanetetraacetic acid-[1-Nal3]-octreotide   124I HuMV833, 124 iodinate humanized mouse monoclonal anti-VEGF antibody   I, iodium   HuMV833, humanized mouse monoclonal anti-VEGF antibody   IRG, imaging of reporter gene   HSV1-tk, herpes simplex virus type 1 thymidine kinase   MEN1, multiple endocrine neoplasm 1   Met, methionine   MIBG, metaiodobenzylguanidine   MR, magnetic resonance   NET, neuroendocrine tumour   NSCLC, non-small cell lung cancer   OS, overall survival   PDGFr-α, platelet-derived growth factors receptor   PDGFR, platelet-derived growth factor receptor   FOLFOX, fluorouracil, leucovorin calcium, oxaliplatin   PET, positron emission tomography   PSA, prostate specific antigen   RCC, renal cell carcinoma   RECIST, response evaluation criteria in solid tumours   SCLC, small cell lung cancer   SPECT, single photon computed tomography   SSTR, somatostatin receptor   SU11248, sunitinib   TGF-α, transforming growth factor-α   TK, tyrosin kinase   TTP, time to progression   VEGFr, vascular endothelial growth factor receptor   86Y, yttrium 86
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