TY - JOUR
T1 - hPG80 (Circulating Progastrin), a Novel Blood-Based Biomarker for Detection of Poorly Differentiated Neuroendocrine Carcinoma and Well Differentiated Neuroendocrine Tumors
AU - Chauhan, Aman
AU - Prieur, Alexandre
AU - Kolesar, Jill
AU - Arnold, Susanne
AU - Payen, Léa
AU - Mahi, Younes
AU - Vire, Berengere
AU - Sands, Madison
AU - Evers, B. Mark
AU - Joubert, Dominique
AU - Anthony, Lowell
N1 - Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2022/2/1
Y1 - 2022/2/1
N2 - Current blood-based biomarkers for neuroendocrine neoplasms (NENs) lack both sen-sitivity and specificity. Human circulating progastrin (hPG80 ) is a novel biomarker that can be easily measured in plasma by ELISA. This study is the first to examine hPG80 in NENs. Plasma hPG80 was quantified from 95 stage IV NEN patients, using DxPG80 technology (ECS Progastrin, Switzerland) and compared with hPG80 concentrations in two cohorts of healthy donor controls aged 50–80 (n = 252) and 18–25 (n = 137). Median hPG80 in NENs patients was 5.54 pM compared to 1.5 pM for the 50–80 controls and 0.29 pM the 18–25 cohort (p < 0.0001). Subgroup analysis revealed median hPG80 levels significantly higher than for either control cohort in neuroendocrine carcinoma (NEC; n = 25) and neuroendocrine tumors (NET; n = 70) including the small-cell lung cancer (SCLC) sub-cohort (n = 13). Diagnostic accuracy, estimated by AUCs, was high for NENs, as well as both sub-groups (NEC/NET) when compared to the younger and older control groups. Plasma hPG80 in NENs may be a diagnostic blood biomarker for both low-and high-grade NENs; further study is warranted. A prospective multi-center trial is ongoing in NET to evaluate hPG80 as a means of monitoring disease (NCT04750954).
AB - Current blood-based biomarkers for neuroendocrine neoplasms (NENs) lack both sen-sitivity and specificity. Human circulating progastrin (hPG80 ) is a novel biomarker that can be easily measured in plasma by ELISA. This study is the first to examine hPG80 in NENs. Plasma hPG80 was quantified from 95 stage IV NEN patients, using DxPG80 technology (ECS Progastrin, Switzerland) and compared with hPG80 concentrations in two cohorts of healthy donor controls aged 50–80 (n = 252) and 18–25 (n = 137). Median hPG80 in NENs patients was 5.54 pM compared to 1.5 pM for the 50–80 controls and 0.29 pM the 18–25 cohort (p < 0.0001). Subgroup analysis revealed median hPG80 levels significantly higher than for either control cohort in neuroendocrine carcinoma (NEC; n = 25) and neuroendocrine tumors (NET; n = 70) including the small-cell lung cancer (SCLC) sub-cohort (n = 13). Diagnostic accuracy, estimated by AUCs, was high for NENs, as well as both sub-groups (NEC/NET) when compared to the younger and older control groups. Plasma hPG80 in NENs may be a diagnostic blood biomarker for both low-and high-grade NENs; further study is warranted. A prospective multi-center trial is ongoing in NET to evaluate hPG80 as a means of monitoring disease (NCT04750954).
KW - Blood-based diagnostic biomarker
KW - Circulating progastrin
KW - HPG
KW - Neuroendocrine carcinoma
KW - Neuroendocrine neoplasms
KW - Neuroendocrine tumors
KW - Small-cell carcinoma
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U2 - 10.3390/cancers14040863
DO - 10.3390/cancers14040863
M3 - Article
AN - SCOPUS:85124150079
SN - 2072-6694
VL - 14
JO - Cancers
JF - Cancers
IS - 4
M1 - 863
ER -