Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request

Triple combination of HAIC-FO plus tyrosine kinase inhibitors and immune checkpoint inhibitors for advanced hepatocellular carcinoma: A systematic review and meta-analysis.

Item request has been placed! ×
Item request cannot be made. ×
loading   Processing Request
  • Additional Information
    • Source:
      Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE
    • Publication Information:
      Original Publication: San Francisco, CA : Public Library of Science
    • Subject Terms:
    • Abstract:
      Background: The triple combination of hepatic arterial infusion chemotherapy (HAIC) with fluorouracil, leucovorin, and oxaliplatin (FOLFOX) plus tyrosine kinase inhibitor (TKI) and immune checkpoint inhibitors (ICIs) is expected to have a synergistic anticancer effect in HCC. We conducted this meta-analysis to evaluate the efficacy and safety of the triple combination treatment in advanced HCC patients.
      Methods: PubMed, Embase, Cochrane Library, Web of Science databases were systematically searched for relevant studies from the inception of each database to May 10, 2023. All articles focusing the triple combination treatment of HAIC-FO plus TKI and ICIs for advanced HCC were eligible. The meta-analysis was conducted following the PRISMA guidelines. The risk of bias was assessed using the Joanna Briggs Institute (JBI) for case series and Newcastle-Ottawa Scale (NOS) for cohort studies. The primary outcomes were overall survival (OS), progression-free survival (PFS), objective response rate (ORR) and disease control rate (DCR). The secondary results were adverse events. Further meta-analysis of control studies demonstrated the superiority of the triple combination modality to TKI plus ICIs, and TKI alone.
      Results: Nine articles (four cohort studies and five one-arm studies) involving 777 advanced HCC patients were included in this meta-analysis. In terms of survival analysis, the pooled median PFS was 11 months (95% CI: 10.1-12.0 months) with low heterogeneity (I2 = 0%, p = 0.97). With regard to tumor response, the pooled ORR and DCR was 61.6% (I2=0%, p = 0.71) and 87.9% (I2 = 13%, p = 0.33) with low heterogeneity, respectively. As compared with TKIs plus ICIs, and TKIs alone, the triple combination thrapy was associated with improved median OS (HR=0.51, 95%CI 0.41-0.62) with low heterogeneity across studies (I2 = 0%, p = 0.47), median PFS (HR=0.51, 95%CI 0.41-0.64) with low heterogeneity across studies (I2 = 0%, p = 0.41), ORR (RR = 0.56, 95% CI: 0.42-0.74) with high heterogeneity across studies (I2 = 69%, p = 0.02), and DCR (RR = 0.38, 95%CI 0.27-0.54) with low heterogeneity across studies (I2 = 14%, p = 0.32). The most common 3/4 AEs were elevated ALT and AST, thrombocytopenia, hypertension, nausea and vomiting in this meta-analysis.
      Conclusions: The triple combination therapy of HAIC-FO plus TKI and ICIs showed promising efficacy and safety in patients with advanced HCC.
      Registration: The protocol was registered with PROSPERO (ID:CRD42023424281).
      Competing Interests: The authors have declared that no competing interests exist.
      (Copyright: © 2023 Tan et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)
    • References:
      Ther Adv Med Oncol. 2021 Mar 25;13:17588359211002720. (PMID: 33854567)
      J Gastroenterol. 2023 Apr;58(4):413-424. (PMID: 36894804)
      Signal Transduct Target Ther. 2023 Feb 8;8(1):58. (PMID: 36750721)
      J Gastroenterol Hepatol. 2020 Aug;35(8):1277-1287. (PMID: 32052876)
      J Hepatol. 2017 Nov;67(5):999-1008. (PMID: 28687477)
      CA Cancer J Clin. 2021 May;71(3):209-249. (PMID: 33538338)
      Eur J Cancer. 2022 May;167:1-12. (PMID: 35364421)
      Gut. 2018 Feb;67(2):395-396. (PMID: 28592441)
      Front Oncol. 2021 Feb 25;11:618206. (PMID: 33718175)
      Semin Liver Dis. 2010 Feb;30(1):52-60. (PMID: 20175033)
      J Hepatol. 2022 Mar;76(3):681-693. (PMID: 34801630)
      Front Oncol. 2022 Sep 23;12:1004652. (PMID: 36237309)
      JBI Evid Synth. 2020 Oct;18(10):2127-2133. (PMID: 33038125)
      J Clin Oncol. 2022 Feb 10;40(5):468-480. (PMID: 34905388)
      Lancet Oncol. 2021 Jul;22(7):977-990. (PMID: 34143971)
      Immunotherapy. 2021 Dec;13(17):1395-1405. (PMID: 34607482)
      Front Oncol. 2021 Nov 12;11:729764. (PMID: 34868921)
      Front Immunol. 2022 Aug 05;13:929141. (PMID: 35990634)
      Korean J Radiol. 2022 Dec;23(12):1126-1240. (PMID: 36447411)
      Front Pharmacol. 2022 Apr 26;13:849189. (PMID: 35559260)
      J Gastroenterol Hepatol. 2023 Apr;38(4):486-495. (PMID: 36516040)
      Liver Cancer. 2021 Jun;10(3):181-223. (PMID: 34239808)
      N Engl J Med. 2020 May 14;382(20):1894-1905. (PMID: 32402160)
      Front Med (Lausanne). 2022 Sep 01;9:919069. (PMID: 36117969)
      BMC Cancer. 2021 Oct 19;21(1):1126. (PMID: 34670506)
      J Clin Oncol. 2022 Jan 10;40(2):150-160. (PMID: 34648352)
    • Accession Number:
      0 (Antineoplastic Agents)
      0 (Immune Checkpoint Inhibitors)
      0 (Tyrosine Kinase Inhibitors)
      0 (Protein Kinase Inhibitors)
    • Publication Date:
      Date Created: 20231016 Date Completed: 20231023 Latest Revision: 20231213
    • Publication Date:
      20250114
    • Accession Number:
      PMC10578571
    • Accession Number:
      10.1371/journal.pone.0290644
    • Accession Number:
      37844117