Molecular profiling of neuroendocrine tumours to predict response and toxicity to peptide receptor radionuclide therapy Review


Authors: Bodei, L.; Schöder, H.; Baum, R. P.; Herrmann, K.; Strosberg, J.; Caplin, M.; Öberg, K.; Modlin, I. M.
Review Title: Molecular profiling of neuroendocrine tumours to predict response and toxicity to peptide receptor radionuclide therapy
Abstract: 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. © 2020 Elsevier Ltd
Keywords: single nucleotide polymorphism; genetics; polymorphism, single nucleotide; pancreatic neoplasms; neoplasm proteins; pathology; radiation response; neuroendocrine tumor; gene expression regulation; gene expression regulation, neoplastic; pancreas tumor; tumor protein; radioisotope; radioisotopes; transcriptome; neuroendocrine tumors; humans; human; male; female; formylpeptide receptor; receptors, formyl peptide
Journal Title: Lancet Oncology
Volume: 21
Issue: 9
ISSN: 1470-2045
Publisher: Elsevier Science, Inc.  
Date Published: 2020-09-01
Start Page: e431
End Page: e443
Language: English
DOI: 10.1016/s1470-2045(20)30323-5
PUBMED: 32888472
PROVIDER: scopus
PMCID: PMC8385643
DOI/URL:
Notes: Review -- Source: Scopus
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MSK Authors
  1. Heiko Schoder
    542 Schoder
  2. Lisa   Bodei
    205 Bodei
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