Immunotherapy for Advanced Hepatocellular Carcinoma-a Large Tertiary Center Experience

被引:4
|
作者
Raj, Roma [1 ]
Aykun, Nihal [1 ]
Wehrle, Chase J. [1 ]
Maspero, Marianna [1 ]
Krishnamurthi, Smitha [2 ]
Estfan, Bassam [2 ]
Kamath, Suneel [2 ]
Aucejo, Federico [1 ]
机构
[1] Cleveland Clin Fdn, Digest Dis & Surg Inst, Dept Hepatopancreatobiliary & Liver Transplant Su, 9500 Euclid Ave, Cleveland, OH 44195 USA
[2] Cleveland Clin Fdn, Dept Hematol & Oncol, Taussig Canc Inst, 9500 Euclid Ave, Cleveland, OH 44195 USA
关键词
advanced hepatocellular carcinoma; immunotherapy; alpha fetoprotein; tyrosine kinase inhibitors; immune checkpoint inhibitors; vascular endothelial growth factor antagonist; IMMUNE CHECKPOINT INHIBITORS; CHANGING LANDSCAPE; MECHANISMS; THERAPY;
D O I
10.1007/s11605-023-05783-w
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Introduction Combination of immune-checkpoint inhibitor (ICI) and vascular endothelial growth factor (VEGF) antagonist has become the first line systemic treatment for advanced hepatocellular carcinoma (HCC). However, two-thirds of patients do not respond to ICI-based treatments and biomarkers for response remain elusive. Methods Patients with advanced HCC who received Atezolizumab/Bevacizumab combination or Nivolumab during 2016-2022 were identified in our Liver Cancer Database. Retrospective review of their clinical data was performed to investigate parameters that could be predictive of immunotherapy response. Results 96 patients received Atezolizumab/Bevacizumab (n=60) or Nivolumab (n=36). Median age at diagnosis was 67.1 years. 70 patients had received treatment and 26 patients were treatment naive before starting immunotherapy. Mean pretreatment AFP was 9780.7 (+/- 32035) ng/mL. Confirmed objective response (complete or partial) was seen in 29% of the population (n=27). Disease remained stable in 12% (n=11) and progressed in 60% (n=56). On univariate analysis, pretreatment AFP>400 ng/mL was associated with objective response (OR=4.5, 95% CI:1.7-11.9, p=0.0015), while white race (OR=0.35, 95% CI:0.13-0.92, p=0.030) and prior radiotherapy (OR=0.14, 95% CI:0.01-1.1, p=0.033) or systemic therapy with TKIs (OR=0.25, 95% CI:0.08-0.81, p=0.017) were associated with poor response. On multivariate analysis only AFP>400 ng/mL remained associated with response (OR=3.7, 95% CI:1.3-10.5, p=0.014). Overall survival (OS) at one and three years was 86% and 43% in responders, and 45% and 29% in non-responders, respectively. Conclusion In our institutional experience, treatment naivety and pre-treatment AFP>400 ng/mL were associated with objective response. Prospective studies aimed at identifying factors associated with response to immunotherapy will aide patient selection.
引用
收藏
页码:2126 / 2134
页数:9
相关论文
共 50 条
  • [21] THE DISPARITY IN THE DELIVERY OF IMMUNOTHERAPY FOR ADVANCED HEPATOCELLULAR CARCINOMA
    Yeo, Yee Hui
    Kaur, Bhupinder
    Liang, Jeff
    Luu, Michael
    Ayoub, Walid S.
    Kuo, Alexander
    Trivedi, Hirsh D.
    Sankar, Kamya
    Gong, Jun
    Hendifar, Andrew
    Osipov, Arsen
    Kosari, Kambiz
    Nissen, Nicholas N.
    Abou-Alfa, Ghassan K.
    Singal, Amit G.
    Yang, Ju Dong
    GASTROENTEROLOGY, 2023, 164 (06) : S1392 - S1393
  • [22] Advanced development of biomarkers for immunotherapy in hepatocellular carcinoma
    Peng, Xuenan
    Gong, Caifeng
    Zhang, Wen
    Zhou, Aiping
    FRONTIERS IN ONCOLOGY, 2023, 12
  • [23] Immunotherapy for advanced hepatocellular carcinoma, where are we?
    Zhang, Li
    Ding, Jia
    Li, Hui-Yan
    Wang, Zhong-Hua
    Wu, Jian
    BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2020, 1874 (02):
  • [24] TERTIARY LYMPHOID STRUCTURES PROMOTE HEPATOCELLULAR CARCINOMA IMMUNOTHERAPY
    Li, Jinyang
    Yang, Xinxiang
    Zhu, Jiye
    Man, Kwan
    GUT, 2022, 71 : A19 - A21
  • [25] Hepatocellular carcinoma: A one year experience at a tertiary referral center in the united states.
    Schwartz, JM
    Larson, AM
    Gold, PJ
    Taylor, SL
    Yeung, RS
    Freeny, PC
    Schmiedl, UP
    Perkins, JD
    Kris, KV
    Robert, CL
    HEPATOLOGY, 1999, 30 (04) : 278A - 278A
  • [26] A tertiary cancer center experience with yttrium-90 radioembolization in hepatocellular carcinoma.
    Schaffer, Kerry
    Noel, Marcus Smith
    Hezel, Aram F.
    Katz, Alan W.
    Sharma, Ashwani
    Baran, Andrea
    Connolly, Gregory Clayton
    Tejani, Mohamedtaki Abdulaziz
    JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (03)
  • [27] Clinicopathological Study on Morphological Subtypes of Hepatocellular Carcinoma: A Single Tertiary Referral Center Experience
    Saler, C. H. A.
    Shuai, S.
    Beckervordersandforth, J. C.
    Rennspiess, D.
    Roemen, G.
    Gevers, T.
    Stoehr-Kleinegris, M. C. F.
    Bouwense, S. A. W.
    Dewulf, M. J. L.
    Coolsen, M. M. E.
    Bemelmans, M. H. A.
    Damink, S. W. Olde
    Winnepenninckx, V.
    zur Hausen, A.
    Kramer, M.
    Samarska, I. V.
    CANCER REPORTS, 2025, 8 (02)
  • [28] Safety and efficacy of sorafenib in the treatment of advanced hepatocellular carcinoma: a single center experience
    Rodrigo Imedio, Esteban
    Diaz Beveridge, Roberto
    Aparicio Urtasun, Jorge
    Bruixola Campos, Gema
    Lorente Estelles, David
    Fonfria Esparcia, Maria
    Caballero Daroqui, Javier
    Segura Huerta, Angel
    Gimenez Ortiz, Alejandra
    Montalar Salcedo, Joaquin
    MEDICAL ONCOLOGY, 2014, 31 (05) : 1 - 6
  • [29] Complications of transarterial chemoembolization for hepatocellular carcinoma-10 years' experience of a tertiary center
    Iliescu, Laura
    Ioanitescu, Simona
    Rababoc, Razvan
    Simu, Andreea
    Toma, Mihai
    Dumitru, Radu
    Grasu, Cristian Mugur
    JOURNAL OF HEPATOLOGY, 2024, 80 : S446 - S447
  • [30] Atezolizumab and bevacizumab in the treatment of advanced hepatocellular carcinoma - a single-center experience
    Adzic, G.
    Prejac, J.
    Librenjak, N.
    Kekez, D.
    Gorsic, I.
    Plestina, S.
    ANNALS OF ONCOLOGY, 2023, 34 : S115 - S115