2023 Fiscal Year Final Research Report
Identification of resistant clone for the chemotherapy of hepatocellular carcinoma using cell free DNA
Project/Area Number |
21K07950
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Review Section |
Basic Section 53010:Gastroenterology-related
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Research Institution | Kindai University |
Principal Investigator |
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Co-Investigator(Kenkyū-buntansha) |
西田 直生志 近畿大学, 医学部, 教授 (60281755)
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Project Period (FY) |
2021-04-01 – 2024-03-31
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Keywords | 肝細胞癌 / 免疫チェックポイント阻害剤 / アジュバント療法 / 腫瘍免疫微小環境 / cell-free DNA / ドライバー変異 |
Outline of Final Research Achievements |
We investigated the association between the circulating tumor DNA (ctDNA) in postoperative plasma and recurrence in 32 patients who received adjuvant immune checkpoint inhibitors (ICIs) after radical hepatocellular carcinoma (HCC) surgery. A valiant of 10 copies/ml or more was considered as ctDNA positive. Tumor immune microenvironment (TIME) was classified by examining immune-related molecules and β-catenin-associated molecules. Patients were classified into 2 groups (β-catenin pathway activated and inactivated), and TIME-hot/exhausted and cold/Treg types). Postoperative recurrence-free survival (RFS) on ICI was significantly longer in the β-catenin pathway inactivation group and in the hot/exhausted TIME group. The median RFS for ctDNA-positive cases was 26.2 months and NR for ctDNA-negative cases, with a trend toward shorter RFS in ctDNA-positive cases . The cases with copy number variation on the β-catenin-related loci showed significantly shorter RFS under ICI treatment.
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Free Research Field |
消化器内科
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Academic Significance and Societal Importance of the Research Achievements |
免疫チェックポイント阻害剤(ICI)は肝癌治療の重要な薬剤であるが、腫瘍免疫微小環境(TIME)が効果に影響する。TIMEの解析には腫瘍組織が必要であり、生検は侵襲的でリスクを伴う。一方、循環血液中の腫瘍由来DNA(ctDNA)は非侵襲的、かつ繰り返し採取可能である。近年、β-catenin 経路の活性化はnon-inflamed型のTIMEの誘因になることが報告されたが、本研究ではβ-catenin 経路異常をctDNAから検出でき、ICIの治療効果予測に応用できる可能性を示した。また、ICI治療中のctDNAは癌細胞残存の指標となることを示した。この成果は肝癌の治療戦略に意義がある。
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