01-10-2008 | Editorial
What oncologists need and require from nuclear medicine
Published in: European Journal of Nuclear Medicine and Molecular Imaging | Issue 10/2008
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The detection of biological abnormalities of the solid tumours seems to be a crucial point in which targeted agents can be applied to cancer care. The methods to define a molecular profile of the tumour lesions are not very well-defined yet. Recent innovations on molecular basis, both the development of new technologies and the introduction to clinical practice of new biologic drugs, increase the benefits but also have some limitations (Table 1). The aim of this manuscript is to focus on the success and difficulties related to the application of new laboratory technologies and to the large use of biological drugs in medical oncology and also to discuss the potential research perspectives in collaboration between medical oncology and nuclear medicine to overcome some open clinical questions.
Tumour biological characterization
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Molecular drugs development
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Benefits
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Benefits
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High level technologies development:
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Several new drugs available in clinical practice for:
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Genomics
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Advanced disease
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DNA sequencing
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Untreated and pre-treated patients
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FISH
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Alone or in combination with chemotherapy, radiotherapy, hormonal therapy
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Real-time PCR
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Adjuvant setting
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Gene expression profiling
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Neoadjuvant setting
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SNPs array
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Action on specific molecular targets o biological pathway
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Proteomics
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Mild toxicity
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q-RT-PCR
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Oral administration
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Western blotting
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ELISA
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IHC
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Comprehensive and more precise biological information
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Limitations
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Limitations
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Small tissue specimens studies: no information of global tumour lesion’s background
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Activity and efficacy
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Biological tumour heterogeneity: difference between primary tumour and metastases
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Results often controversial
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Biological changes during the natural history of diseases especially in long survival and heavily pre-treated patients
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Acquired resistance
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Invasive, not repeatable and time-consuming procedures for the patient and physicians
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Not well-known mechanism of action
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Not well-known optimal dose level
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Different combination schedules with chemotherapy
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Therapeutical response evaluation: combined morphological and functional criteria are not available
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Therapeutical response prediction: validated tumour markers in clinical practice are not available
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