The combination of circulating IgM and geriatric nutritional risk index predicts the prognostic of hepatocellular carcinoma patients who underwent immune checkpoint inhibitors

•IgM level was associated with the prognosis of patients with HCC receiving ICIs.•GNRI-IgM provided prognostic value in predicting survival in HCC patients receiving ICIs.•Non-invasive immunoglobulin biomarkers aided HCC prognosis. Immune checkpoint inhibitors (ICIs) have shown promise in hepatocell...

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Veröffentlicht in:International immunopharmacology 2023-10, Vol.123, p.110704-110704, Article 110704
Hauptverfasser: Liu, Chunxun, Zhao, Haoran, Wang, Peng, Guo, Zuoming, Qu, Zhaowei
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Sprache:eng
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Zusammenfassung:•IgM level was associated with the prognosis of patients with HCC receiving ICIs.•GNRI-IgM provided prognostic value in predicting survival in HCC patients receiving ICIs.•Non-invasive immunoglobulin biomarkers aided HCC prognosis. Immune checkpoint inhibitors (ICIs) have shown promise in hepatocellular carcinoma (HCC) treatment. With the increasing use of ICIs in cancer treatment, identifying biomarkers that can predict the prognosis of patients receiving ICIs is of great importance. We aimed to investigate the potential of circulating immunoglobulins and the combination of Geriatric Nutritional Risk Index (GNRI) with IgM to predict prognosis in patients with HCC who received ICIs. Clinical and pathological data were collected from 101 patients with HCC who were administered ICIs and underwent circulating immunoglobulin testing between January 2018 and December 2021. Survival analysis, Cox regression analysis, and nomogram construction were performed to evaluate the prognostic value of the indicators. In the preliminary survival analysis, we observed a significant correlation between patient prognosis and IgM levels. Patients with low IgM had shorter survival times. Upon combining the GNRI with IgM, patients with low GNRI and IgM levels had shorter progression-free survival (PFS) and overall survival (OS) (P 
ISSN:1567-5769
1878-1705
DOI:10.1016/j.intimp.2023.110704