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Molecular profiling...
Molecular profiling of neuroendocrine tumours to predict response and toxicity to peptide receptor radionuclide therapy
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- Bodei, Lisa (author)
- Mem Sloan Kettering Canc Ctr, Dept Radiol, Mol Imaging & Therapy Serv, New York, NY 10065 USA.
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- Schoeder, Heiko (author)
- Mem Sloan Kettering Canc Ctr, Dept Radiol, Mol Imaging & Therapy Serv, New York, NY 10065 USA.
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- Baum, Richard P. (author)
- Ctr Adv Radiomol Precis Oncol, CURANOSTICUM, Wiesbaden, Germany.
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- Herrmann, Ken (author)
- Univ Duisburg Essen, Essen Univ Hosp, Dept Nucl Med, Essen, Germany.
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- Strosberg, Jonathan (author)
- H Lee Moffitt Canc Ctr & Res Inst, Dept Gastrointestinal Oncol, Tampa, FL USA.
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- Caplin, Martyn (author)
- Royal Free Hosp, Dept Gastroenterol, Neuroendocrine Tumour Unit, London, England.
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- Öberg, Kjell, 1946- (author)
- Uppsala universitet,Endokrin tumörbiologi
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- Modlin, Irvin M. (author)
- Yale Univ, Yale Univ Sch Med, Dept Surg, New Haven, CT USA.
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Mem Sloan Kettering Canc Ctr, Dept Radiol, Mol Imaging & Therapy Serv, New York, NY 10065 USA Ctr Adv Radiomol Precis Oncol, CURANOSTICUM, Wiesbaden, Germany. (creator_code:org_t)
- Elsevier, 2020
- 2020
- English.
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In: The Lancet Oncology. - : Elsevier. - 1470-2045 .- 1474-5488. ; 21:9, s. E431-E443
- Related links:
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https://urn.kb.se/re...
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https://doi.org/10.1...
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Abstract
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- Peptide receptor radionuclide therapy (PRRT) is a type of radiotherapy that targets peptide receptors and is typically used for neuroendocrine tumours (NETs). Some of the key challenges in its use are the prediction of efficacy and toxicity, patient selection, and response optimisation. In this Review, we assess current knowledge on the molecular profile of NETs and the strategies and tools used to predict, monitor, and assess the toxicity of PRRT. The few mutations in tumour genes that can be evaluated (eg, ATM and DAXX) are limited to pancreatic NETs and are most likely not informative. Assays that are transcriptomic or based on genes are effective in the prediction of radiotherapy response in other cancers. A blood-based assay for eight genes (the PRRT prediction quotient [PPQ]) has an overall accuracy of 95% for predicting responses to PRRT in NETs. No molecular markers exist that can predict the toxicity of PRRT. Candidate molecular targets include seven single nucleotide polymorphisms (SNPs) that are susceptible to radiation. Transcriptomic evaluations of blood and a combination of gene expression and specific SNPs, assessed by machine learning with algorithms that are tumour-specific, might yield molecular tools to enhance the efficacy and safety of PRRT.
Subject headings
- MEDICIN OCH HÄLSOVETENSKAP -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
- MEDICIN OCH HÄLSOVETENSKAP -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)
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