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  1. Article: Identification of the Best Cut-Off Value of PIVKA-II for the Surveillance of Patients at Risk of Hepatocellular Carcinoma Development.

    Caviglia, Gian Paolo / Abate, Maria Lorena / Troshina, Giulia / Carucci, Patrizia / Rolle, Emanuela / Risso, Alessandra / Burlone, Michela Emma / Albè, Alice / Crevola, Martina / Musso, Emma Clara / Rosso, Chiara / Armandi, Angelo / Olivero, Antonella / Minisini, Rosalba / Saracco, Giorgio Maria / Bugianesi, Elisabetta / Pirisi, Mario / Ciancio, Alessia / Gaia, Silvia

    Biology

    2023  Volume 12, Issue 1

    Abstract: Patients with cirrhosis are at risk of hepatocellular carcinoma (HCC) development and, according to current guidelines, should undergo surveillance by ultrasound at six month intervals. Due to the known limitations of surveillance strategies based on ... ...

    Abstract Patients with cirrhosis are at risk of hepatocellular carcinoma (HCC) development and, according to current guidelines, should undergo surveillance by ultrasound at six month intervals. Due to the known limitations of surveillance strategies based on ultrasonography, the use of tumor biomarkers, although debated, is common practice in many centers. The aim of the study was to identify the best cut-off value for one of such biomarkers, protein induced by vitamin K absence, or antagonist-II (PIVKA-II). We retrospectively enrolled 1187 patients with liver cirrhosis: 205 with a diagnosis of HCC (median age 67 years, 81.0% males) and 982 without tumor (median age 64 years, 56.2% males). During a median follow-up (FU) of 34.6 (11.4−43.7) months, 118 out of 982 (12.0%) patients developed HCC. Serum PIVKA-II was assessed by chemiluminescence immunoassay on the Lumipulse® G600 II platform (Fujirebio, Tokyo, Japan). In the overall cohort (n = 1187), PIVKA-II showed an area under the curve (AUC) of 0.802 for HCC detection. The best cut-off value that maximized sensitivity was 50 mAU/mL (sensitivity = 80%, specificity = 64%). In the 982 patients without HCC at baseline, PIVKA-II > 50 mAU/mL was associated with an increased risk of HCC development during the FU (HR = 1.74, 95% CI 1.21−2.51; p = 0.003)). In conclusion, the evaluation of serum PIVKA-II showed a good performance for HCC detection; a cut-off value > 50 mAU/mL could be suitable for the surveillance of patients who are at risk of developing HCC.
    Language English
    Publishing date 2023-01-07
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2661517-4
    ISSN 2079-7737
    ISSN 2079-7737
    DOI 10.3390/biology12010094
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Identification of the Best Cut-Off Value of PIVKA-II for the Surveillance of Patients at Risk of Hepatocellular Carcinoma Development

    Caviglia, Gian Paolo / Abate, Maria Lorena / Troshina, Giulia / Carucci, Patrizia / Rolle, Emanuela / Risso, Alessandra / Burlone, Michela Emma / Albè, Alice / Crevola, Martina / Musso, Emma Clara / Rosso, Chiara / Armandi, Angelo / Olivero, Antonella / Minisini, Rosalba / Saracco, Giorgio Maria / Bugianesi, Elisabetta / Pirisi, Mario / Ciancio, Alessia / Gaia, Silvia

    Biology (Basel). 2023 Jan. 07, v. 12, no. 1

    2023  

    Abstract: Patients with cirrhosis are at risk of hepatocellular carcinoma (HCC) development and, according to current guidelines, should undergo surveillance by ultrasound at six month intervals. Due to the known limitations of surveillance strategies based on ... ...

    Abstract Patients with cirrhosis are at risk of hepatocellular carcinoma (HCC) development and, according to current guidelines, should undergo surveillance by ultrasound at six month intervals. Due to the known limitations of surveillance strategies based on ultrasonography, the use of tumor biomarkers, although debated, is common practice in many centers. The aim of the study was to identify the best cut-off value for one of such biomarkers, protein induced by vitamin K absence, or antagonist-II (PIVKA-II). We retrospectively enrolled 1187 patients with liver cirrhosis: 205 with a diagnosis of HCC (median age 67 years, 81.0% males) and 982 without tumor (median age 64 years, 56.2% males). During a median follow-up (FU) of 34.6 (11.4–43.7) months, 118 out of 982 (12.0%) patients developed HCC. Serum PIVKA-II was assessed by chemiluminescence immunoassay on the Lumipulse® G600 II platform (Fujirebio, Tokyo, Japan). In the overall cohort (n = 1187), PIVKA-II showed an area under the curve (AUC) of 0.802 for HCC detection. The best cut-off value that maximized sensitivity was 50 mAU/mL (sensitivity = 80%, specificity = 64%). In the 982 patients without HCC at baseline, PIVKA-II > 50 mAU/mL was associated with an increased risk of HCC development during the FU (HR = 1.74, 95% CI 1.21–2.51; p = 0.003)). In conclusion, the evaluation of serum PIVKA-II showed a good performance for HCC detection; a cut-off value > 50 mAU/mL could be suitable for the surveillance of patients who are at risk of developing HCC.
    Keywords Japan ; biomarkers ; blood serum ; chemiluminescence immunoassays ; hepatoma ; liver cirrhosis ; monitoring ; risk ; ultrasonics ; ultrasonography ; vitamin K
    Language English
    Dates of publication 2023-0107
    Publishing place Multidisciplinary Digital Publishing Institute
    Document type Article ; Online
    ZDB-ID 2661517-4
    ISSN 2079-7737
    ISSN 2079-7737
    DOI 10.3390/biology12010094
    Database NAL-Catalogue (AGRICOLA)

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  3. Article: Interplay of

    De Benedittis, Carla / Bellan, Mattia / Crevola, Martina / Boin, Elena / Barbaglia, Matteo Nazzareno / Mallela, Venkata Ramana / Ravanini, Paolo / Ceriani, Elisa / Fangazio, Stefano / Sainaghi, Pier Paolo / Burlone, Michela Emma / Minisini, Rosalba / Pirisi, Mario

    Gastroenterology research and practice

    2020  Volume 2020, Page(s) 4216451

    Abstract: A single-nucleotide polymorphism causing a C to G change in ... ...

    Abstract A single-nucleotide polymorphism causing a C to G change in the
    Language English
    Publishing date 2020-04-24
    Publishing country Egypt
    Document type Journal Article
    ZDB-ID 2435460-0
    ISSN 1687-630X ; 1687-6121
    ISSN (online) 1687-630X
    ISSN 1687-6121
    DOI 10.1155/2020/4216451
    Database MEDical Literature Analysis and Retrieval System OnLINE

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