يعرض 1 - 4 نتائج من 4 نتيجة بحث عن '"blood-based diagnostic biomarker"', وقت الاستعلام: 0.77s تنقيح النتائج
  1. 1
    دورية أكاديمية

    المصدر: Cancers; Volume 14; Issue 4; Pages: 863

    الوصف: Current blood-based biomarkers for neuroendocrine neoplasms (NENs) lack both sensitivity 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).

    وصف الملف: application/pdf

    العلاقة: Tumor Microenvironment; https://dx.doi.org/10.3390/cancers14040863Test

  2. 2
    دورية أكاديمية

    المصدر: Cancers, Vol 14, Iss 863, p 863 (2022)

    الوصف: Current blood-based biomarkers for neuroendocrine neoplasms (NENs) lack both sensitivity and specificity. Human circulating progastrin (hPG 80 ) is a novel biomarker that can be easily measured in plasma by ELISA. This study is the first to examine hPG 80 in NENs. Plasma hPG 80 was quantified from 95 stage IV NEN patients, using DxPG 80 technology (ECS Progastrin, Switzerland) and compared with hPG 80 concentrations in two cohorts of healthy donor controls aged 50–80 ( n = 252) and 18–25 ( n = 137). Median hPG 80 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 hPG 80 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 hPG 80 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 hPG 80 as a means of monitoring disease (NCT04750954).

  3. 3
    دورية أكاديمية

    المصدر: Markey Cancer Center Faculty Publications

    الوصف: Current blood-based biomarkers for neuroendocrine neoplasms (NENs) lack both sensitivity 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).

    وصف الملف: application/pdf

    العلاقة: All data generated or analyzed during this study are included in this published article. Individual deidentified patient data can be shared upon request and IRB approval.; https://uknowledge.uky.edu/markey_facpub/177Test; https://uknowledge.uky.edu/cgi/viewcontent.cgi?article=1176&context=markey_facpubTest

  4. 4
    دورية أكاديمية

    المصدر: Cancers, Vol 14, Iss 863, p 863 (2022)

    الوصف: Current blood-based biomarkers for neuroendocrine neoplasms (NENs) lack both sensitivity and specificity. Human circulating progastrin (hPG 80 ) is a novel biomarker that can be easily measured in plasma by ELISA. This study is the first to examine hPG 80 in NENs. Plasma hPG 80 was quantified from 95 stage IV NEN patients, using DxPG 80 technology (ECS Progastrin, Switzerland) and compared with hPG 80 concentrations in two cohorts of healthy donor controls aged 50–80 ( n = 252) and 18–25 ( n = 137). Median hPG 80 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 hPG 80 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 hPG 80 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 hPG 80 as a means of monitoring disease (NCT04750954).