Benefit of Gene Expression Profiling in Gastrointestinal Neuroendocrine Tumors of Unknown Primary Origin
- PMID: 35220231
- DOI: 10.21873/anticanres.15608
Benefit of Gene Expression Profiling in Gastrointestinal Neuroendocrine Tumors of Unknown Primary Origin
Abstract
Background/aim: Cancer of unknown primary (CUP), representing 3-5% of all newly diagnosed cancers in the United States, is a presumptive, non-definitive diagnosis rendered when a primary tumor site cannot be identified after exhaustive diagnostic evaluation, including cases of neuroendocrine neoplasms (NENs). CUPs are characterized by findings that are challenging to reconcile, including inconclusive immunohistochemical (IHC) stains, an undifferentiated morphologic phenotype, history of multiple cancers, a clinical presentation that is discordant from histologic findings, an atypical distribution of metastases, or lack of expected response to treatment. For a significant subset of NENs (10%), traditional diagnostic evaluation is unable to determine a primary tumor site using histomorphology and IHC stains. Gene expression profiling (GEP) of either mRNA or microRNA is the technique utilized in the three commercially available platforms that provide a prediction of tumor type in cases of diagnostic uncertainty of CUPs, including those with neuroendocrine differentiation. Case Series Report: Here we present four cases of NENs, where the diagnosis based upon histomorphological and IHC features presented a unique challenge that ultimately benefited from the integration of molecular tumor classification using the validated assay. CancerTYPE ID by Biotheranostics is based on a quantitative RT-PCR assay that uses a computational algorithm to measure the collective expression of 92 genes (87 cancer-related genes and 5 control genes). This case series reports five appropriate clinical scenarios that highlight the utility of a GEP-based assay to effectively provide a molecular tumor classification to identify NEN subtypes and tumor primary site of origin.
Conclusion: These cases demonstrated that the CancerTYPE ID test was able to resolve challenging diagnoses for primary and metastatic NENs. These cases emphasize the clinical need of utilizing a GEP-based assay for determining the anatomic site of origin and NEN subtyping, both essential for the appropriate clinical management of NENs.
Keywords: Cancer unknown primary; RT-PCR; gene expression profiling; neuroendocrine.
Copyright © 2022 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.
Similar articles
-
A 92-gene cancer classifier predicts the site of origin for neuroendocrine tumors.Mod Pathol. 2014 Jan;27(1):44-54. doi: 10.1038/modpathol.2013.105. Epub 2013 Jul 12. Mod Pathol. 2014. PMID: 23846576
-
Assigning site of origin in metastatic neuroendocrine neoplasms: a clinically significant application of diagnostic immunohistochemistry.Adv Anat Pathol. 2013 Sep;20(5):285-314. doi: 10.1097/PAP.0b013e3182a2dc67. Adv Anat Pathol. 2013. PMID: 23939147 Review.
-
Molecular profiling diagnosis in unknown primary cancer: accuracy and ability to complement standard pathology.J Natl Cancer Inst. 2013 Jun 5;105(11):782-90. doi: 10.1093/jnci/djt099. Epub 2013 May 2. J Natl Cancer Inst. 2013. PMID: 23641043
-
Comparison of histopathology to gene expression profiling for the diagnosis of metastatic cancer.Diagn Pathol. 2012 Aug 21;7:110. doi: 10.1186/1746-1596-7-110. Diagn Pathol. 2012. PMID: 22909314 Free PMC article.
-
Gene expression profiling in patients with carcinoma of unknown primary site: from translational research to standard of care.Virchows Arch. 2014 Apr;464(4):393-402. doi: 10.1007/s00428-014-1545-2. Epub 2014 Feb 1. Virchows Arch. 2014. PMID: 24487792 Review.
Cited by
-
Emerging Treatment Options for Neuroendocrine Neoplasms of Unknown Primary Origin: Current Evidence and Future Perspectives.Cancers (Basel). 2024 May 27;16(11):2025. doi: 10.3390/cancers16112025. Cancers (Basel). 2024. PMID: 38893145 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources